Cesium-zinc halide phosphors, phosphor screens, and preparation methods

FIELD OF THE INVENTION
The invention relates to radiography and radiographic phosphors. The invention more particularly relates to cesium-zinc halide phosphors, phosphor screens, and preparation methods.
BACKGROUND OF THE INVENTION
Phosphors have long been used in a variety of articles that can be referred to as "phosphor screens" or "phosphor-based radiation converters", articles that include a support and a phosphor-containing luminescent portion, and function to screen or capture X-rays and other high energy radiation for emission at a longer wavelength, either immediately or on a delayed basis following secondary stimulation. Information represented by the modulation of the captured radiation is reproduced in the emitted longer wavelength radiation. (As a matter of convenience, these articles are referred to generically herein as "phosphor screens" or "screens". A variety of different types of phosphor screens are commonly used including, for example, phosphor-based radiographic panels or screens, dosimeter elements, and optical information storage elements.
Many types of phosphor screen are used to detect image-wise X-radiation absorption by a target interposed between the phosphor screen and an X-ray source. A widely used variety of phosphor screen is a radiographic phosphor panel or screen. These articles are rigid or flexible sheet or plates having a thin luminescent layer that contains a radiographic phosphor. Flexible radiographic phosphor screens are generally exposed while flat, but can be utilized while bent into a cylinder or more complex shape, particularly for industrial applications. Like many other crystalline materials, radiographic phosphors have a crystal matrix which allows for the replacement of some atoms by other similar atoms, but does not readily accept other atoms or moieties. Radiographic phosphor screens can be classified, based upon their phosphors, as prompt emission screens and image storage screens.
Intensifying screens are the most common prompt emission screens. Intensifying screens are used to generate visible light upon exposure of the intensifying screen to X-radiation. A sheet of photographic film is positioned to intercept the visible light generated and commonly is pressed against the intensifying screen within a light-tight cassette. Other prompt emission screens operate similarly, but in place of the photographic film have some other means for visualizing the X-radiation.
Storage screens have storage phosphors, that have the capability of storing latent X-ray images for later release, apparently by locally trapping electron-hole pairs created by incident X-rays. Storage phosphors are distinguishable from the phosphors used in X-ray intensifying or conversion screens. In the latter, a latent image is not stored and X-radiation causes the immediate release of visible light from irradiated phosphor crystals. Storage phosphors generally exhibit some prompt emission, but at relatively low levels in comparison to phosphors intended for that purpose.
Radiation image storage screens are used in computed radiography. The screen is first exposed to X-radiation to create a latent image. The screen is then stimulated with longer wavelength radiation, resulting in the emission of radiation at a third wavelength. Typically a laser having a red or infrared beam is scanned over the screen, resulting in the emission of green or blue radiation. The emitted light is collected and the resulting signal is processed electronically to produce a final image.
X-ray storage phosphors and image storage screens are characterized by a number of properties including sensitivity, efficiency, linearity, resolution, noise, dark decay (the ability of the phosphor or screen to retain the image over time), and emission lifetime. It is generally desired that the sensitivity of the photostimulated luminescence of the screen or screen be made as high as possible to decrease the exposure dose for the patient while maintaining high image quality.
In phosphor screens, differences in the average index of refraction between phosphor crystals and the polymeric binder in which the crystals are dispersed, lead to light scattering, resulting in lower resolution and increased noise in the visible light image produced by the screen. Light scattering is greatly reduced if the phosphor and binder have substantially the same refractive index.
E.P. Patent Application No. 0 290 289 A1 discloses a digital radiographic imaging system including a phosphor screen in which a luminescent layer is optically coupled to a charge coupled device or the like. The luminescent layer has barium fluorohalide storage phosphor and a refractive index matched binder.
U.S. Pat. No. 4,637,898 discloses x-ray intensifying screens in which phosphor crystals and the polymeric binder have substantially the same index of refraction. One of the phosphors disclosed is RbI:Tl.
A variety of types of compounds containing cesium or rubidium and halide are known. Characteristics vary among the different materials.
"Phase Relationships in the Cs--Br--MBr.sub.2 (M=Zn, Cd, Hg) Systems", Kovaleva, et al., Inorganic Materials, Vol. 31, (1995) pp. 1442-1446 discloses crystal data for a variety of different cesium-metal bromides.
"New F-Type Color Center in CsBr", L. Pelsers, et al., Physical Review, Vol. 188, (1969) pp. 1324-1328; discloses luminescent CsBr crystals doped with Cl.sup.- or F.sup.-.
"Thermoluminescence of CsCl:Eu Crystals Irradiated with .gamma.-Rays", J. K. Radhakrishinan et al., Phys. Stat. Sol. (a), Vol. 141, (1994) pp. 457-462; discloses CsCl:Eu phosphors which exhibit thermoluminescence.
"Laser-stimulable transparent CsI:Na film for a high quality x-ray imaging sensor", Tsuyoshi Kano, et al., Appl. Phys. Lett., Vol. 48, (1986) pp. 1117-1118; discloses an x-ray sensor having a transparent film of the phosphor CsI:Na.
U.S. Pat. No. 4,780,376 discloses storage panels having phosphors defined by the formula:
CsX.aRbX':xEu.sup.2+
where X and X' are halogen selected from Cl, Br, and I; and 0<a.ltoreq.10.0 and 0<x.ltoreq.0.2.
U.S. Pat. No. 5,028,509 discloses storage panels having phosphors defined by the formula:
(M.sub.1-x.M'.sub.x)X.aM"X'.sub.2.bM'"X".sub.3.cA:dB (formula "(I)")
and by the formula:
M'.sub.x X.aM"X'.sub.2.bM'"X".sub.3.cA:dB (formula "(I")")
In the formulas, M is Cs or Rb. M' is at least one of Li, Na, K, Cs, and Rb. Phosphors including at least one of Cs and Rb are preferred. M" is selected from Be, Mg, Ca, Sr, Ba, Cd, Zn, Cu, or Ni, preferable Be, Mg, Ca, Sr, or Ba; M'" is a trivalent cation, A is a metal oxide; B is an activator ion like Tl, or Eu; X, X', and X" are each the same or different and are each selected from F, Cl, Br, or I. The ranges are 0.ltoreq.x.ltoreq.1; 0.ltoreq.a.ltoreq.1 preferably 0.ltoreq.a.ltoreq.0.4; 0.ltoreq.b.ltoreq.0.5 preferably 0.ltoreq.b.ltoreq.10.sup.-2 ; 0.ltoreq.c.ltoreq.0.5 preferably 0.ltoreq.c.ltoreq.0.2; 0.ltoreq.d.ltoreq.0.2 preferably 10.sup.-6 .ltoreq.d.ltoreq.0.1. There are no examples of any storage phosphors containing Zn.
"Luminescence Spectra of Mn(II) in Different Symmetries", U. Lanver and G. Lehmann, Journal of Luminescence, 17, (1978) pp. 225-235 describes the luminescence of Cs.sub.3 ZnBr.sub.5 :Mn and Cs.sub.3 ZnBr.sub.5 :Mn under UV excitation. No photostimulable luminescence is reported.
A continuing need exists for phosphor screens which can provide useful storage characteristics in combination with reduced light scattering. It would thus be desirable to provide such screens, phosphors, and preparation methods.
SUMMARY OF THE INVENTION
The invention is defined by the claims. The invention, in its broader aspects, provides phosphor screens, cesium-zinc halide phosphors, and preparation methods. The phosphor screens comprising a support and a luminescent portion including phosphor comprising oxygen and a combination of species characterized by the relationship:
(Cs.sub.1-r Rb.sub.r).sub.3+v-n (Zn.sub.1-m Mg.sub.m).sub.1-o (Li.sub.a Na.sub.b K.sub.c)(Ca.sub.f Sr.sub.g Ba.sub.h)Br.sub.5+v-z-i Cl.sub.z I.sub.i :jA
wherein A is selected from the group consisting of Eu, Th, Ce, Tm, Dy, Pr, Ho, Nd, Yb, Er, Gd, Lu, Sm, Y, Tl, Na, Ag, Cu, Mg, Pb, Bi, Mn, and In, and combinations thereof; r is from 0 to 1; v is from about -0.01 to about +1; n is from 0 to about 1.5; n=a+b+c; m is from 0 to 0.5; o=f+g+h; a is from 0 to 0.3; b is from 0 to 0.75; c is from 0 to 0.75; f is from 0 to 0.25; g is from 0 to 0.5; h is from 0 to 0.5; z+i is from 0 to 5; z is from 0 to 5; i is from 0 to 0.5; and j is from 0 to 0.15.
It is an advantageous effect of at least some of the embodiments of the invention that phosphor screens, phosphors, and preparation methods are provided which can provide useful storage characteristics in combination with reduced light scattering.
DESCRIPTION OF PARTICULAR EMBODIMENTS
The phosphor screen of the invention is an article of manufacture that includes a support and a phosphor-containing luminescent portion. The phosphor screen is generally described herein as if the phosphor screen were in the shape of a horizontally disposed flat plate. It is to be understood, however, that the phosphor screen is not limited to any particular shape and that directional terms refer only to relative positions, not an absolution orientation relative to the environment For example, the phosphor screen can have the form of a rigid planar panel, or a flexible sheet able to assume a variety of shapes, or a rigid cylindrical tube, or a complex three dimensional shape. Similarly, the luminescent portion can have small or large crystals or even a single crystal; held in place by a layer of binder, or adhered in place, or held in place mechanically by fasteners or the like.
The photostimulable phosphors of this invention show a high degree of photostimulated luminescence. Peak photostimulation varies with the relative concentrations of Cl and Br from the infrared to the visible spectrum. This allows the use of various phosphors of the invention with semiconductor diode lasers as well as He--Ne lasers as stimulation sources. For example, the stimulation spectrum of the photostimulated luminescence of Cs.sub.3 ZnCl.sub.5 and phosphors of the invention is extremely well matched to the He--Ne laser, so these materials are compatible with scanning devices used in computed radiography which currently employ other known storage phosphors like BaFBr:Eu. The stimulation spectrum of the photostimulated luminescence of the Cs.sub.3 ZnBr.sub.5 phosphors of the invention is in the infrared, allowing the use of semiconductor diode lasers as the stimulation source.
The phosphors of this invention also have an unexpectedly low refractive index at the stimulation wavelength and can be employed in high resolution photostimulable imaging plates where the index of refraction of the binder equals the average index of refraction of the photostimulable phosphor at the stimulation wavelength. The practical advantage of this is to minimize the amount of scattered stimulating radiation during the readout of the imaging plate. When the scatter of the interrogating stimulating light is minimized, an advantage in resolution (MTF) is realized in the digitized image.
The phosphors of the invention include oxygen and a combination of species characterized by the relationship:
(Cs.sub.1-r Rb.sub.r).sub.3+v-n (Zn.sub.1-m Mg.sub.m).sub.1-o-j (Li.sub.a Na.sub.b K.sub.c)(Ca.sub.f Sr.sub.g Ba.sub.h)Br.sub.5-z+v-i Cl.sub.z I.sub.i :jA (formula 1)
Each of the designations in this formula are explained below in detail. The same designations appearing elsewhere herein have the same meanings unless specifically stated to the contrary.
Most phosphors can be represented by a stoichiometric formula defining what is generally called a "host lattice", having a particular crystal structure, and possible substitutions within that host lattice. Surprisingly, this is not strictly the case for the phosphor of the invention (hereafter also referred to, for convenience, as "cesium-zinc halide phosphor"). The cesium-zinc halide phosphor has a host lattice that has a variable stoichiometry. This is represented in formula 1 by the term "v". The value of v can vary over a range of from about -0.01 to about +1.
Values of v which are negative are not preferred. The range of v is from 0 to 1.2. For phosphors in which a homogeneous index of refraction is desired so that scattering due to mismatch between the binder and the phosphor is minimized a value of z near 0 is desired. The range of z for this application is from -0.001 to 0.25. The preferred range of z for matched index applications is from 0.0 to 0.1. Satifactory phosphors can be made for use with binders where the index mismatch between the binder and the phosphor is not critical where the range of v is from 0 to 1.2. The preferred range of v for this application is from 0 to 1.
Crystal structure of such materials is similarly not simple and straightforward. These characteristics could be theorized as being incompatible with luminescence; however, in reality the cesium-zinc halide phosphor has good luminescence properties. It has been determined that a preferred value for v, from the viewpoint of storage properties is from about 0.001 to about 1. In most of the following discussion, v will be assumed to be 0 and phosphor having the formula:
Cs.sub.3 ZnX.sub.5 (formula 2)
where X is Br, or Cl, or a combination of Br and Cl, is sometimes referred to or otherwise considered herein as if it were the host lattice of the phosphor (hence the term "cesium-zinc halide"). This is a matter of convenience and it will be understood that structural formulas that ignore the value of v are approximations for the sake of discussion and do not preclude embodiments in which v has a non-zero value.
The cesium-zinc halide phosphor is a storage phosphor without an activator. Cs.sub.3 ZnCl.sub.5, Cs.sub.3 ZnBr.sub.5, and Cs.sub.3 ZnBr.sub.5-z Cl.sub.z, where 0<z<5 all exhibited intrinsic photostimulable luminescence. The mixed Br and Cl material appears to be a solid solution of the other two materials. This "host lattice" crystallizes in a tetragonal crystal structure like that of cesium cobalt choride. If j is substantially equal to 0, that is, less than about 0.0001, then z is preferably either from 0 to about 2.5 or z is 5. If j is substantially equal to zero and z ranges from 0 to 5 there is a maximum in the photostimulated luminescent response at around z=2.5 which is totally unexpected.
The cesium-zinc halide phosphor can include activator ("A" in formula 1). Inclusion of an activator will generally improve photostimulated luminescence relative to the unactivated phosphor, and as discussed below in some cases causes differing characteristics with substitutions into the host lattice. A in formula 1 is selected from the group consisting of Eu, Tb, Ce, Tm, Dy, Pr, Ho, Nd, Yb, Er, Gd, Lu, Sm, Y, Tl, Na, Ag, Cu, Mg, Pb, Bi, Mn, and In, and combinations thereof. A suitable concentration range (value of j in formula 1) for the activator is from about 0.0001 to about 0.15, with the range of about 0.0005 to about 0.05 (more particularly 0.0025 to about 0.02) being preferred. Greater concentrations of activator can degrade performance. With activator, the preferred values of z are from about 0 to 1 and about 4.75 to about 5. In formula 1, the value of j is charge compensated by removing an equivalent number of moles of divalent cation for every mole of activator substituted into the phosphor and in the following examples the value of v is considered to be essentially 0; however, it is known to one skilled in the art of phosphor preparation that equivalent phosphors can be prepared without charge compensation just by adding j moles of activator to the phosphor composition because when j is small (0.ltoreq.j.ltoreq.0.05) the compositional correction for charge compensation becomes negliable. Therefore, all compositions in which j is not specifically charge compensated are considered equivalent to those in which j is charge compensated when 0.ltoreq.j.ltoreq.0.05. When the value of v is greater than 0 then when 0.ltoreq.j.ltoreq.0.05 the charge compensated value of j is also considered to be essentially equal to the non-charge compensated value of j for small values of j.
In Cs.sub.3 ZnBr.sub.5-z Cl.sub.z :Eu there was a region of maximum photostimulated luminescent response in the composition region where 0.ltoreq.z.ltoreq.1.0. In the composition region where 1.0<z.ltoreq.5, the best response is found in the composition region where 4<z.ltoreq.5. The maximum in the composition region where 0.ltoreq.z.ltoreq.1.0 is completely unexpected. The maximum in the composition region where 40.ltoreq.z.ltoreq.5.0 is completely unexpected.
The stimulation spectra of Cs.sub.3 ZnCl.sub.5 :Eu, Cs.sub.3 ZnBr.sub.5 :Eu, and Cs.sub.3 ZnBr.sub.5-z Cl.sub.z showed that these phosphors are well matched to the He--Ne laser which emits as 633 nm, and that the primary emitting site is Eu.sup.2+ in the phosphor lattice. Cs.sub.3 ZnBr.sub.5 :Eu and Cs.sub.3 ZnBr.sub.5-z Cl.sub.z exhibited extended response in the infrared, beyond 650 nm, and can also be used with semiconductor laser diodes which emit in the infrared. With Cs.sub.3 ZnBr.sub.5 :Eu and Cs.sub.3 ZnBr.sub.5-z Cl.sub.z, the maximum in the stimulated emission spectrum was centered around 450 nm.
The measured lifetimes of the stimulated emission from Eu.sup.2+ in Cs.sub.3 ZnCl.sub.5 :Eu, Cs.sub.3 ZnBr.sub.5 :Eu, and Cs.sub.3 ZnBr.sub.5-z Cl.sub.z :Eu are competitive with currently known storage phosphors used in single point flying spot scanners.
The phosphor can include some I in place of some of the Br and/or Cl ions. In formula 1, z+i is from 0 to 5 and i is from 0 to about 0.5.
Some or all of the Cs in the phosphor can be substituted for by Rb. In formula 1, r can have a value from 0 to 1. In the non-activated phosphors of the invention, the value of r is less than about 0.001. In the activated phosphors of the invention, the value of r is from 0 to 1. This result is surprising. In the activated phosphors of the invention, when z=0, r is either r.ltoreq.0.25 or r.gtoreq.0.85 The effect of Rb in the activated phosphor when z=0 is unpredictable and surprising. When z=5, r ranges from 0 to 1. The preferred values of z and r in the activated phosphor are r is either .ltoreq.0.25 or r.gtoreq.0.85 when z.ltoreq.1 and 0.ltoreq.r.ltoreq.1 when z.gtoreq.4. It is obvious that phosphors where r=1, z ranges from 0 to 5 and n (n=a+b+c) does not equal zero will also be storage phosphors. In the case where r=1, when z.ltoreq.2.5 the materials crystallize in the same structure type as when z=0.
There is a complete solid solution between the compound Cs.sub.3 ZnCl.sub.5 and the compound Rb.sub.3 ZnCl.sub.5. This means that all compounds of the composition (Cs.sub.1-r Rb.sub.r).sub.3 ZnCl.sub.5 where 0.ltoreq.r.ltoreq.1 crystallize with the same structure type.
The examples demonstrate that all compounds in the system (Cs.sub.1-r Rb.sub.r).sub.3 ZnCl.sub.5 show a dramatic enhancement of the PSL when an activator cation like Eu.sup.2+ is present. It should be noted that Rb.sub.3 ZnCl.sub.5 :Eu is itseft a storage phosphor and all the previously shown (Li,Na,K) substitution chemistry shown, for instance, in Examples 10, 11, and 35 as well as the chemistry shown in Examples 40, 41, 64, 65, 70, and 75 can be done with Rb.sub.3 ZnCl.sub.5 also. It is understood in the art that materials which crystallise with very minor distortions in the lattice, for example, a monoclinic distortion of a tetragonal unit cell, are considered to be closely enough related to the undistorted structure as to be considered members of the same structural family and therefore are often called isostructural. In other words, a material does not have to be strictly tetragonal to be considered isostructural with the Cs.sub.3 CoCl.sub.5 structure.
Example 30d where r=1 and z=0 crystallized in a different structure which has been reported to be orthorhombic and isostructural with (NH.sub.4).sub.3 ZnCl.sub.5. (M. Heming, et L., Zeit. Naturforsch. vol. 36a, (1981) pp. 286-293) There is a complete solid solution between the compound Cs.sub.3 ZnBr.sub.5 and the compound Rb.sub.3 ZnBr.sub.5 up to at least 75 mole % substitution. This means that all compounds of the composition (Cs.sub.1-r Rb.sub.r).sub.3 ZnBr.sub.5 where 0<r.ltoreq.0.75 crystallize with the Cs.sub.3 ZnBr.sub.5 structure type. Examination of Example 30d using polarizarized optical microscopy showed that the major phase was uniaxial, indicating that the Bravais symmetry is either tetragonal or hexagonal, despite the report in the literature that the crystal system is orthorhombic. We cannot explain this discrepancy. DTA examination of Rb.sub.3 ZnBr.sub.5 showed that the melting point of the compound is 450.degree..+-.5.degree. C. The melting point of RbBr is 698.degree. C. and the melting point of ZnBr.sub.2 is 394.degree. C. The difference in melting points shows that Rb.sub.3 ZnBr.sub.5 is not an unreacted mixture of the starting materials.
It is clear from the examples that compounds in the system (Cs.sub.1-r Rb.sub.r).sub.3 ZnBr.sub.5 where 0.ltoreq.r.ltoreq.1 are all intrinsic storage phosphors. It should be noted specifically that example 30d demonstrates that Rb.sub.3 ZnBr.sub.5 itself is a storage phosphor which crystallizes with a new structure type.
Examples 30a-d demonstrate that the relative PSL decreases for Rb levels greater than 25 mole % Rb substitution (r=0.25). The lack of response in examples 31d and 31e demonstrates that (Cs.sub.1-r Rb.sub.r).sub.3 ZnBr.sub.5 :Eu where 0.5.ltoreq.r.ltoreq.0.75 do not show enhanced photostimulated luminescence when Eu is used as an activator. Example 31f demonstrates the Rb.sub.3 ZnBr.sub.5 :Eu is a photostimulable phosphor and demonstrates that related structure types can also show photostimulated luminscence. From Example 82 it is obvious that matched index screens can be prepared using this material.
There is a complete solid solution between the compound Cs.sub.3 ZnBr.sub.5-z Cl.sub.z and the compound Rb.sub.3 ZnCl.sub.5. This means that all compounds of the composition (Cs.sub.1-r Rb.sub.r).sub.3 ZnBr.sub.5-z Cl.sub.z crystallize with the same structure type. Examples 32a,b report the PSL of these materials. It is clear from examples 32a and b that compounds in the system (Cs.sub.1-r Rb.sub.r).sub.3 ZnBr.sub.5-z Cl.sub.z are all storage phosphors. It should be noted specifically that Rb.sub.3 ZnBr.sub.5-z Cl.sub.z itself is a storage phosphor and crystallizes with the Cs.sub.3 CoCl.sub.5 structure on the chloride rich end.
Examples 33a,b demonstrate that all compounds in the system (Cs.sub.1-r Rb.sub.r).sub.3 ZnBr.sub.5-z Cl.sub.z show an enhancement of the PSL when an activator cation like Eu.sup.2+ is present. It should be noted that Rb.sub.3 ZnCl.sub.5-z Br.sub.z :Eu is itself a storage phosphor and when z is less than 2.5 this materials crystallizes with the Cs.sub.3 CoCl.sub.5 structure. In preferred embodiments, r is 0, or greater than 0 and less than about 0.25, or about 1. In preferred embodiments 0.ltoreq.z.ltoreq.0.5 and in a more preferred embodiment 0.ltoreq.z.ltoreq.0.3.
Under some conditions, photostimulable luminescence can be observed in the phosphor doped with alkali metals, alkaline earth metals, or a combination of both. The alkali metals can be one or any combination of the following: Li, Na, K, or Rb. The alkaline earth metals can be one or any combination of the following: Mg, Ca, Sr, or Ba. Finally, the addition of both Eu.sup.2+ and alkali or alkaline earth metals or both alkali and alkaline earth metals in the phosphor can give an improvement in the photostimulated luminescent response.
The alkali metals Li, Na, and K are not preferred. A most preferred value for n in formula 1 is 0 (n=a+b+c). A preferred range for n is from 0 to about 0.005. Other, less preferred ranges for alkali metal ions are as follows. If j is about 0 and z is about 0.25, then a can be about 0.15. If j is about 0 and z is less than 5, then b can be about 0.3. If j is about 0 and z is from 0 to about 0.25, then b is about 0.15. If j is about 0, z is from 0 to about 0.25, then c is from 0 to about 0.75.
The phosphors of the invention have a concentration of (Li,Na,K) in which n is always less than 1.5. In an embodiment of the invention in which z is greater than about 2.5, n is less than about 0.15. In an embodiment in which z is less than 2.5, n is less than about 0.75, and preferably a is less than 0.15, b is less than 0.75, and c is less than 0.75. The effect of the (Li,Na,K) on PSL depends upon whether activator is present. The presence of (Li,Na,K) in activated phosphors of the invention in a concentration of greater than about 0.05 degrades photostimulated luminescence relative to the same phosphor absent the elevated (Li,Na,K) concentration. With the non-activated phosphor, the (Li,Na,K)s showed results supporting an increases in PSL, in the indicated composition ranges. The presence of lithium at the levels of 25 mole percent or greater is undesirable because it imparts undue water sensitivity to the sample.
It is not advantageous to have lithium present in the phosphor when z>0.25. The presence of Na or K in Cs.sub.3 ZnBr.sub.5-z Cl.sub.z decreases the response relative to the "host lattice" or activated host lattice. The presence of sodium or potassium in the compounds also results in an undesirable increase in the water sensitivity of the phosphor.
When r is not zero, preferred ranges are that n is less than about 0.75, and preferably a is less than 0.15, b is less than 0.75, and c is less than 0.75. If r is from 0 to 1 then a preferred range is a=b=c=0.0015 (in this case n=0.0045). When z is not equal to either 0 or 5, the influence of the activator when n is not equal to zero is completely unpredictable and does not follow the same behavior found when z=0 or z=5. This result is extremely surprising.
In this invention the value of m can range from 0 to 0.5. The behavior of Mg is the photostimulable phosphor is unpredictable with respect to z. When z=0 the preferred range of m is 0.ltoreq.m.ltoreq.0.25. When 0.ltoreq.z<2.5, the value of m is 0.ltoreq.m.ltoreq.0.25. When 2.5.ltoreq.z<5, the value of m is 0.ltoreq.m.ltoreq.0.10. When z=5, the preferred range of m is 0.ltoreq.m<0.05. This is surprising. The results demonstrate that all compositions Cs.sub.3 (Zn.sub.1-m Mg.sub.m)Br.sub.5-z Cl.sub.z where 0.ltoreq.m.ltoreq.0.25 and 0.ltoreq.z<5 are photostimulable phosphors.
Examples 40a-40d all crystallized in the same structure type as Cs.sub.3 ZnCl.sub.5, indicating that there is a complete solid solution between Cs.sub.3 ZnCl.sub.5 and Cs.sub.3 MgCl.sub.5 up to 50 mole % substitution of Mg.sup.2+ for Zn.sup.2+. All compounds in the solid solution Cs.sub.3 (Zn.sub.1-m Mg.sub.m)Cl.sub.5 are storage phosphors. Examples 42a-42d all crystallized in the same structure type as Cs.sub.3 ZnBr.sub.5, indicating that there is a complete solid solution between Cs.sub.3 ZnBr.sub.5 and Cs.sub.3 MgBr.sub.5 up to 50 mole % substitution of Mg.sup.2+ for Zn.sup.2+. When an activator such as Eu.sup.2+ is present in the phosphor, the photostimulated luminescence is markedly improved, as demonstrated in examples 41, 43, and 45. When j is nonzero, then 0.ltoreq.m.ltoreq.0.25.
The range of f in the present invention is 0.ltoreq.f.ltoreq.0.5 for 0.ltoreq.z.ltoreq.0.5. When no activator is present, the preferred range of f is 0.ltoreq.f.ltoreq.0.1 and 0.25.ltoreq.f.ltoreq.0.5 when z=5. When an activator is present, for the range of 0.ltoreq.z.ltoreq.5, the preferred range of f is 0.ltoreq.f.ltoreq.0.25 and more preferably 0.ltoreq.f.ltoreq.0.1. Compounds of the composition Cs.sub.3 (Zn.sub.1-f Ca.sub.f)Br.sub.5-z Cl.sub.z are storage phosphors. Enhanced photostimulated emission is observed with an activator cation like Eu.sup.2+ in Cs.sub.3 (Zn.sub.1-f Ca.sub.f)Br.sub.5-z Cl.sub.z.
The range for g in the present invention is 0.ltoreq.g.ltoreq.0.5. In the absence of activator, when z=0, the preferred range for g is 0.ltoreq.g.ltoreq.0.05. In the absence of activator, when z=5, the preferred range for g is 0.1.ltoreq.g.ltoreq.0.5. In the presence of activator when z=0 or z=5, the preferred range for g is also 0.ltoreq.g.ltoreq.0.05. It is completely unexpected that in the absence of an activator when 0<z<5 the range of g is 0.ltoreq.g<0.05 whereas in the presence of an activator when 0<z<5 the range of g is broadened to 0.ltoreq.g.ltoreq.0.1. Compounds of the composition Cs.sub.3 (Zn.sub.1-g Sr.sub.g)Br.sub.5-z Cl.sub.z are storage phosphors.
The value of h in the invention ranges from 0 to 0.5. In the absence of activator when z=0 the preferred range of h is 0.ltoreq.h.ltoreq.0.25. In the absence of activator when z=5 the preferred range of h is 0.ltoreq.h.ltoreq.0.5. In the absence of activator when 0<z.ltoreq.2.5 the preferred range for h is 0.ltoreq.h.ltoreq.0.05. In the absence of activator when 2.5<z<5, the preferred range for h is 0.ltoreq.h.ltoreq.0.1. When activator present and z=0 the preferred range for h is 0.ltoreq.h.ltoreq.0.1. When activator is present and z=5, the preferred range for h is 0.ltoreq.h.ltoreq.0.5. When 0<z.ltoreq.2.5 the preferred range for h is 0.ltoreq.h.ltoreq.0.2. When 2.5<h<5 the preferred range for h is 0.ltoreq.h.ltoreq.0.25. The range of h in the presence and absence of the activator is unpredictable. Cs.sub.3 (Zn.sub.1-h Ba.sub.h)Br.sub.5-z Cl.sub.z phosphors are intrinsic storage phosphors. Cs.sub.3 (Zn.sub.1-h Ba.sub.h)Cl.sub.5 and Cs.sub.3 (Zn.sub.1-h Ba.sub.h)Br.sub.5-z Cl.sub.z show photostimulated luminescent response which is superior to that of undoped Cs.sub.3 ZnCl.sub.5.
Phosphors in the system Cs.sub.3 (Zn.sub.1-m Mg.sub.m).sub.1-o (Ca.sub.f Sr.sub.g Ba.sub.h)Br.sub.5-z Cl.sub.z where o=(f+g+h) are all intrinsic storage phosphors. Any combination of alkaline earth metals can be used to prepare a wide variety of materials containing various ratios of alkaline earth metals, all of which crystallize with the Cs.sub.3 ZnBr.sub.5 structure, all of which are photostimulable phosphors. Compounds in the system Cs.sub.3 (Zn.sub.1-m Mg.sub.m).sub.1-o-j (Ca.sub.f Sr.sub.g Ba.sub.h)Br.sub.5-z Cl.sub.z :jEu where o=(f+g+h) and j>0 show dramatically enhanced photostimulated luminescence when the activator Eu.sup.2+ is present in the compound. The range for o in the present invention is 0.ltoreq.o<0.5 when0.ltoreq.z.ltoreq.5 and0.ltoreq.m<0.5 and 0.ltoreq.f<0.25, 0.ltoreq.g<0.5, and 0.ltoreq.h<0.5. The preferred ranges are 0.ltoreq.f<0.25, 0.ltoreq.g<0.05, and 0.ltoreq.h<0.25. The influence of activator when z=0 or z=5 and n>0 is completely unpredictable, as demonstrated by examples 64-67. Furthermore, when 0<z<5 then influence of activator when o>0 is completely unpredictable, as shown by examples 68 and 69.
Examples 70-75 show that for 0.ltoreq.z.ltoreq.5, o and n are not mutually exclusive variables and that both may have non-zero values within the previously discussed ranges. It is also shown that the influence of activator is to improve the photostimulated luminescence of these materials.
The average index of refraction of Cs.sub.3 ZnX.sub.5 based phosphors can be matched using polymers prepared from known photopolymerizable organic monomers, thereby demonstrating that a matched index screen can be prepared using the phosphors of this invention using methods described in the U.S. Pat. No. 4,637,898.
Cs.sub.3 ZnCl.sub.5, Cs.sub.3 ZnBr.sub.5, and Cs.sub.3 ZnBr.sub.5-z Cl.sub.z exhibited average refractive indexes which can be matched using known binders. The index of refraction of the polymer prepared by photopolymerization of the 1-(S-naphthylcarbinyl)thioacrylate monomer described in U.S. Pat. No. 4,637,898 is 1.67 at 633 nm, a commonly used stimulation wavelength. Each of the phosphors of Examples 7-9 has a lower refractive index at 633 nm than this polymer, therefore matched index screens can be prepared using the methods described in U.S. Pat. No. 4,637,898. The results also demonstrate that the index of refraction of the phosphor can be adjusted by changing the z value in Cs.sub.3 ZnBr.sub.5-z Cl.sub.z :Eu. Examples 78 through 82 demonstrate that both unactivated and activated phosphors of the present invention can be used to prepare index matched screens according to the methods described in U.S. Pat. No. 4,637,898. The values of the average refractive index of the phosphor is not substantially affected by the incorporation of addenda. For example, 0.ltoreq.v.ltoreq.0.3 will not substantially influence the averge refractive index of the phosphor. Similarly, the value of j may range from 0.ltoreq.j.ltoreq.0.05 and the phosphor will still be suitable for matched index applications. The addition of other addenda expressed by non-zero values of r, n, o, f, g, and h which range from 0 to 0.25 will not substantially affect the use of the phosphor for matched index applications.
The phosphors of the invention can be prepared by the procedures disclosed in the Examples or by other procedures. Materials crystallizing with the Cs.sub.3 ZnX.sub.5 structure can be prepared by dehydration of an aqueous solution containing the appropriate molar ratios of cations. Dehydration may be accomplished through various means including evaporation, freeze drying, spray drying, and similar methods. It is believed that the cesium-zinc halide phosphors can also be made as free-standing transparent or transluscent photostimulable imaging plates using the methods described in U.S. Pat. No. 2,851,612 and European Patent Application No. 0 369 049, dated 15 Nov. 1988. Both of these procedures utilize hot pressing to prepare highly transparent radiographic plates.
Some of the possible binders which can be used to index match the phosphors of this invention are described in European Patent Application 0 290 298 dated 6 May 1988, and U.S. Pat. No. 4,637,898. The former describes the use of polysulfone polymers to prepare index matched screens and the latter describes the use of photopolymerizable acrylate monomers to prepare the same. The invention includes an improved procedure for preparing a matched index storage phosphor screen for use with a stimulation light source having a predetermined wavelength band, such as in at least one monochromatic wavelength band in the range of from 450 to 1100 nm. A polymeric binder is selected having a specified index of refraction at a particular wavelength band, the phosphor of the invention is then made so that the value of z in the invention is determined by the formula
z=5((r.sup.1 -r.sup.a)/(r.sup.b -r.sup.a))
where r.sup.1 is the index of refraction of the binder at the wavelength band, r.sup.a is the index of refraction of the phosphor of the invention at the wavelength band when z=5, and r.sup.b is the index of refraction of the phosphor of the invention at the wavelength band when z=0. Negative values of (r.sup.1 -r.sup.a) preclude the use of the polymeric binder with the invention for matched index applications but do not preclude the use of the polymeric binder for preparation of a storage phosphor screen.
The luminescent layer includes the composite phosphor in the form of a polycrystalline mass. Typically, a mass of individual particles are distributed in a binder, which gives the mass structural coherence and retains the mass on the support. The size and shape of the phosphor particles are determined, in the same manner as other phosphors, by requirements of a particular use and factors such as manufacturing constraints. Convenient parameters for a phosphor particulate useful in radiographic screens are a median particle size of from 1 to 40 micrometers.
Any conventional ratio of phosphor to binder can be employed. Generally thinner phosphor layers and sharper images are realized when a high weight ratio of phosphor to binder is employed. Preferred phosphor to binder ratios are in the range of from about 7:1 to 25:1 for screen constructions intended to withstand commercial exposure repetitions without loss of structural integrity. For limited or single exposure applications, any minimal amount of binder consistent with structural integrity is satisfactory.
For the highest attainable speeds a white support, such as a titania or barium sulfate loaded or coated support can be employed. Particular reflective supports which offer a balance of speed and sharpness are those containing reflective microlenslets, such as are disclosed in United States Pat. No. 4,912,333 to Roberts, et al. In those instances in which it is desired to reduce the effective thickness of a phosphor layer below its actual thickness the phosphor layer is modified to impart a small, but significant degree of light absorption. If the binder is chosen to exhibit the desired degree of light absorption, then no other ingredient of the phosphor layer is required to perform the light attenuation function. It is specifically noted that the less structurally complex chromophores for ultraviolet absorption particularly lend themselves to incorporation in polymers. A separate absorber can be incorporated in the phosphor layer to reduce its effective thickness. The absorber can be a dye or pigment capable of absorbing light within a desired spectrum. Black dyes and pigments such as carbon black are, of course, generally useful with phosphors, because of their broad absorption spectra. With storage screens, it is preferable to include a dye or pigment which absorbs some of the stimulating radiation, generally provided by a laser; but mostly reflects emitted light. U.S. Pat. No. 4,491,736, to Teraoka, teaches the use of such materials in storage screens.
Apart from the phosphor layers and the assembly features described above, the screen can be of any conventional construction. Screens typically have one or more flexible or rigid support layers. Flexible layers are most commonly polymeric. The most common polymeric supports are films of high dimensional integrity, such as poly(ethylene terephthalate) film supports. In a nonflexible screen, support is provided by one or more polymeric layers and by a rigid plate of aluminum or the like.
Metal layers, such as aluminum, enhance reflection. Paper supports, though less common than film supports, are known and can be used for specific applications. Dyes and pigments are commonly loaded into supports to enhance absorption or reflection of light. Air can be trapped in supports to reflect ultraviolet and visible light. Supports and the subbing layers used to improve coating adhesion can be chosen from among those employed for silver halide photographic and radiographic elements, as illustrated by Research Disclosure, Vol. 176, December 1978, Item 17643, Section XVII, and Research Disclosure, Vol. 184, August 1979, Item 18431, Section I.
In some applications it is desired to use a support whose optical properties allow discrimination between the stimulating radiation and the photostimulated emission. For example, preferential transmission of the stimulating radiation and reflection of the photostimulated emission can be provided by certain types of multilayer dielectric interference filters which may be disposed upon the rigid or flexible support. Similarly transmission of the photostimulated emission and absorption of the stimulating radiation can be provided by using appropriate optical filters as a support such as the commercially available BG-25 filter from the Schott corporation. In matched index applications it is desirable to use a support which provides discrimination between the stimulating radiation and the photostimulated emission to improve the resolution and response of the phosphor layer.
The overcoat layer comprises a binder chosen using the criteria described above for the binder in the luminescent layer. The overcoat binder can be the same binder as in the luminescent layer or different and can also be chosen from polymers useful for supports. Polymers conventionally employed for fill supports can be used in the overcoat layer. For example, cellulose acetate is an overcoat commonly used with the poly(urethane) binders. Overcoat polymers are often also used to seal the edges of the phosphor layer. A suitable overcoat is disclosed in U.S. Pat. No. 5,401,971.
While anticurl layers are not required for the screens, they are generally preferred for inclusion. The function of the anticurl layer is to balance the forces exerted by the layers coated on the opposite major surface of a support which, if left unchecked, could cause the support to assume a non-planar configuration, that is, to curl or roll up on itself. Materials forming the anticurl layers can be chosen from among those identified above for use as binders and overcoats. Generally an anticurl layer is formed of the same polymer as the overcoat on the opposite side of the support.
Any one or combination of conventional screen features compatible with the features described herein can, of course, be employed. Conventional storage screen constructions are disclosed in U.S. Pat. No. 4,380,702 to Takahashi et at, the disclosure of which is hereby incorporated by reference. Conventional intensifying screen constructions are disclosed in Research Disclosure, Vol. 184, August 1979, Item 18431, hereby incorporated herein by reference.
The radiographic screens are formed by conventional coating techniques. Phosphor powder and addenda are mixed with a solution of a resin binder material and coated by means such as blade coating onto a substrate. U.S. Pat. No. 4,505,989, to Umemoto et al, the disclosure of which is hereby incorporated herein by reference, describes suitable techniques known in the art for preparing a radiographic screen.
The phosphor screen of the invention, in some embodiments, is what can be referred to as a "large crystal device". In contrast to a radiographic screen, the mass of small phosphor particles is replaced by a relatively small number of large crystals or even a single very large crystal. The support and binder are replaced by a mechanical structure that holds the crystal or crystals in a desired orientation. The large crystal device can also include a light responsive element, such as an array of photodiodes. The crystals are arranged so that the longest dimension of each crystal is aligned with the direction of incident radiation. This maximizes the thickness, and thus the radiation stopping power, of the phosphor "layer". The crystals together define a surface that faces the direction or directions from which incident radiation is to be received. In many applications, such as computed tomography, it is desirable to capture only radiation incident from a single direction, the direction of the collimated beam used to image the subject matter. In these applications, the crystals define a plane. In some other applications, such as high energy physics detectors, it is desirable to capture radiation emitted in many directions from a particular location and the crystals therefore define a complex curved surface centered upon the site of origin of events to be detected. These multidirectional detectors are otherwise substantially similar to the unidirectional detectors previously described.

The following Examples and Comparative Examples are presented to further illustrate and elucidate some preferred modes of practice of the invention. Unless otherwise indicated, all starting materials were commercially obtained.
Stimulation Spectra:
The stimulation spectrum of the packed powder sample is obtained by exposing the sample for 1 minute to x-radiation from a tungsten target x-ray tube operated at 55 kV, 33 mA, filtered through 1/32" Al. After a delay of several minutes the sample is placed in a stimulation apparatus. The sample is subjected to sequential 15 ms long pulses of weak stimulation light. Stimulation measurements were taken every 10 nm. The stimulation radiation used here had a bandpass of 8 nm and was provided by light from a tungsten-halogen lamp which was passed through a monochromator and an order-sorting filter. An CS3-72 filter was used for stimulation wavelengths shorter than 700 nm. An OG550 filter was used for stimulation wavelengths greater than or equal to 700 nm. The stimulated emission is collected and detected by an R928 PMT after passing through CS4-96 and CS7-51 bandpass filters. The spectral correction curve was obtained under these conditions with an NBS-traceable radiometer detector.
Stimulated Emission Spectra:
The stimulated emission spectrum of the packed powder sample is obtained by exposing the sample for 1 minute to unfiltered x-radiation from a tungsten target tube operated at 70 kVp, 30 mA. After a delay of several minutes, the sample is loaded into a spectrofluorometer. 650 nm light from xenon arc lamp which had passed through a monochromator and a RG610 bandpass filter is used as the stimulating radiation. The photostimulated emission from the sample is collected and detected by a calibrated spectrometer. The spectrometer had been calibrated to within .+-.1 nm and had a resolution of approximately 4 nm (full width at half maximum). The intensity calibration of the spectrometer was performed using two NBS-traceable sources and yielded an arbitrary intensity scale proportional to Watts/nm/cm.sup.2 (different from the prompt emission spectra). The photostimulated emission at each wavelength are corrected for the emission filter transmission and spectrometer sensitivity.
X-Ray Powder Diffraction:
All preparations were characterized for phase purity using x-ray powder diffraction. Starting materials present in the x-ray powder diffraction pattern of the product were not considered as impurity phases. X-ray powder diffraction patterns were taken using an Enraf Nonius Guinier-DeWolff model 552 camera using Cu k.alpha..sub.1 radiation. When quantitative evaluation of the lattice constants from the x-ray pattern was desired, the pattern on the guinier film was digitized using a scanning densitometer and the line positions were corrected using silver as an internal standard. Lattice constants were calculated using a least squares method with a local computer program.
Evaluation of Reponse Time for Photostimulable Phosphors:
The response time (or lifetime) of materials is obtained by irradiating the sample with x-rays from a tungsten tube operating at 70 kVp and 3 mA for several seconds. After x-irradiation the sample is placed at the bottom port of an integrating sphere and subjected to very short pulses of 633 nm light. The stimulated emission is synchronously detected by a photomultiplier tube, (PMT), with appropriate filtration to block the red stimulating light. The signal from the PMT is amplified, then digitized at a rapid rate, (every 20 nanoseconds for a total time of 40 microseconds). The results of several stimulation pulses are averaged together for an improved signal-to-noise ratio. The response time (or lifetime) was taken as the time interval required for the post-stimulation signal to drop to 1/e of its peak value. The response time is measured in microseconds.
Index of Refraction Measurements:
The average index of refraction of a phosphor powder was determined using an optical microscope with a tungsten halogen light source, bandpass filters, and Cargille.TM. Certified Refractive Index Liquids (R. P. Cargille Laboratories, Inc.) The following procedure was used to determine the average refractive index of a phosphor powder. A microscope slide was prepared containing a small amount of the ground sample immersed in one of the Certified Refractive Index Liquids. The sample was examined on the microscope using illumination from the tungsten halogen light source which had passed through a bandpass filter, (50 nm bandwidth interference type). The average refractive index of the sample was taken to be equal to the value of the Certified Refractive Index Liquid when the sample showed a minimum of optical scatter when immersed in the fluid. The actual refractive index of the immersion fluid at the wavelength of the bandpass filter was calculated using the Cauchy Equations relating refractive index as a function of wavelength supplied by R. P. Cargille Laboratories for the particular set of Refractive Index Liquid used. The average refractive index measurements were double checked by the Becke method. (Optical Crystallography (Fifth Edition) by E. E. Wahlstrom, John Wiley and Sons, New York, N.Y., (1979) pp 120-123)
Evaluation of Photostimulable Luminescence:
Photostimulable luminescent response of the packed powder sample is obtained by first exposing the sample for 3 minutes to a heat lamp to eliminate any residual signal which might be present, then exposing the sample for several seconds to x-radiation from a tungsten target x-ray tube operated at 70 kV, 2.5 mA. The normal filtration conditions used 13/8" Al as a filter. On occasion the filters were removed for samples with extremely low sensitivity. The typical sample dose varied from 1.5 mRem to 18 Rem. The radiation dose was measured using a Radcal Corp. model 2025 x-ray monitor and probe. After exposure to x-rays, the sample was stimulated with a 4 millisecond pulse from a 12 mW He--Ne laser. The stimulated emission is collected and detected by a PMT with an S-4 response after passing through a Schott BG-25 filter. The peak voltage obtained from the PMT was measured, and the ratio of peak voltage from the PMT divided by the radiation dose was used as a measure of the photostimulable luminescent response.
Differential Thermal Analysis:
The melting point of a sample was determined using differential thermal analysis (DTA) with a Thermit 10C DTA unit. The heating rate was 5.degree. C./min and high purity alumina was used as the reference material.
Preparation of Starting Materials:
Zinc chloride, all alkali metal bromides and chlorides, and all alkaline earth metal bromides and chlorides were dehydrated under vacuum between 100.degree. C. and 200.degree. C. before use. Anhydrous ZnBr.sub.2 was prepared by the following two step procedure. In the first step, 15 grams of high purity zinc metal (Atomergic Chemetals Corp. 99.999% zinc shot) is dissolved in 100 mls of concentrated HBr (Eastman Kodak Company ACS reagent) with stirring. The solution is then evaporated to near dryness by gently boiling the liquid. The remaining water on the material is removed by drying under vacuum. In the second step, the zinc bromide is heated under argon saturated with bromine in three steps: 1.5 hours at 90.degree. C., 1.5 hours at 180.degree. C., and finally two hours at 400.degree. C. The melt is cooled to room temperature and the anhydrous product removed from the tube in a glove bag.
Anhydrous EuBr.sub.2 was prepared by the method of Cox and Fong (Journal of Crystal Growth, 20, (1973), 233-238) from high purity Eu.sub.2 O.sub.3, HBr and NH.sub.4 Br. In a typical preparation, 1 g of Eu.sub.2 O.sub.3 and 1.5 g NH.sub.4 Br is dissolved in 20 mls of concentrated HBr with heat. The solution is evaporated to dryness then transferred to a sublimation tube. The sample is placed under vacuum and successively heated at 90.degree. C. for 6 hrs, 180.degree. C. for 6 hrs, then 400.degree. C. for 12 hrs to dehydrate the material and remove the excess NH.sub.4 Br. TGA analysis of the product in air verified the composition as anhydrous EuBr.sub.2.
Anhydrous EuCl.sub.3 was prepared by the method of Cox and Fong (Journal of Crystal Growth, 20, (1973), 233-238) from high purity Eu.sub.2 O.sub.3, HCl and NH.sub.4 Cl. In a typical preparation, 1 g of Eu.sub.2 O.sub.3 and 1.5 g NH.sub.4 Cl were dissolved in 20 mls of concentrated HCL with heat. The solution was evaporated to dryness then transferred to a sublimation tube. The sample was placed under vacuum and successively heated at 90.degree. C. for 6 hrs, 180.degree. C. for 6 hrs, then 400.degree. C. for 12 hrs to dehydrate the material and remove the excess NH.sub.4 Cl. TGA analysis of the product in air verified the composition as anhydrous EuCl.sub.3.
Photostimulated luminescence response (PSL) values
Generally, the photostimulated luminescence response of phosphors having species inclusive of the formula, Cs.sub.3 ZnCl.sub.5 or the formula Cs.sub.3 ZnBr.sub.5-z Cl.sub.z (where z is greater than 0 and less than 5), are reported herein normalized to the response of Cs.sub.3 ZnCl.sub.5 in Example 4 (normalizing conversion factor=1726.12198) or in Example 6e (normalizing conversion factor=2316.147605), as indicated. These photostimulated luminescence responses are indicated in the tables by the heading: "PSL (1)". Generally, the response of phosphors having species inclusive of the formula, Cs.sub.3 ZnBr.sub.5, are reported herein normalized to the response of Cs.sub.3 ZnBr.sub.5 in Example 5. These photostimulated luminescence responses are indicated in the tables by the heading: "PSL (2)". The PSL (2) normalizing conversion factor is 384.3985444. Any departures from these practices in the following will be understandable from context.
EXAMPLES 1-3
CRYSTAL STRUCTURE OF Cs.sub.3 ZnX.sub.5
Cs.sub.3 ZnBr.sub.5 and Cs.sub.3 ZnCl.sub.5 were determined to crystallize in the Cs.sub.3 CoCl.sub.5 structure and the tetragonal space group I 4/mcm. This is different from reported alkali halides. Compounds in the system Cs.sub.3 ZnBr.sub.5-z Cl.sub.z were also determined to crystallize in the same structure. A solid solution was found across the composition region from z=0 to z=5. The unit cell volume of the compounds Cs.sub.3 ZnBr.sub.5-z Cl.sub.z varied linearly with z. This strongly suggests that, surprisingly, the smaller chloride anion substitutes directly for the larger bromide anion in the solid solution.
Example 1
Cs.sub.3 ZnCl.sub.5
The sample container for this experiment was a pyrex tube for melt filtration consisting of a small piece of capillary tubing connected to 1/2" o.d. pyrex tubing on both ends. A plug of glass wool was inserted into one side of the tube to use as a filter for the molten salt. 2.525 g of CsCl and 0.6814 g of ZnCl.sub.2 were sealed in the side of the tube equipped with the glass wool plug. The sample was evacuated to better than 10 microns and sealed off. The entire assembly was heated in the vertical position at 624.degree. C. for at least 18 hrs to allow the melt to filter. The product was cooled and removed from the tube, whereupon several clear crystals were separated from the mass.
The crystals were examined using a precession camera and Cu k.alpha. radiation. The precession photographs of the single crystal demonstrated that the material was tetragonal with approximate lattice parameters of a=9.12 .ANG. and c=14.45 .ANG.. X-ray powder diffraction photographs taken with a Guinier camera gave precision lattice constants of a=9.240 .ANG. and c=14.487 .ANG.. Results are reported in Table 1. The extinctions observed in the powder diffraction pattern and the single crystal photographs were consistent with the tetragonal space group I 4/mcm.
As a further check for the structure type, the guinier film was digitized and the intensities of the x-ray powder diffraction fines were measured. The intensity of a reflection was taken as the maximum value of the optical density above the baseline for each reflection profile observed during digitization. Values are reported as "I(obs)" in Table 1. Theoretical intensities for the powder pattern were calculated using the computer program LAZYPULVERIX (J. Appl. Cryst. (1977) 10, 73-74) available from Klaus Yvon, Wolfgang Jeitschko, and Erwin Parthe of The Laboratoire de Cristallographie aux Rayons X, Universite de Geneve, 24 quai Ernest-Ansermet, CH-1211, Geneve 4, Switzerland, making the assumption that Cs.sub.3 ZnCl.sub.5 crystallizes with the Cs.sub.3 CoCl.sub.5 structure. The theoretical intensities for the powder pattern were calculated using previously refined lattice parameters from guinier films. The atomic positions for the Cs.sub.3 CoCl.sub.5 structure type were taken from a structure of Cs.sub.3 MnCl.sub.5 reported in "Crystal Structure of Cs.sub.3 MnCl.sub.5 ", by J. Goodyear and D. J. Kennedy, Acta Cryst, B32 (1976) p. 631. The intensities of the reflections with calculated intensities from the program LAZYPULVERIX using the Guinier diffraction geometry is listed in Table 1 as "I(calc)". The agreement between calculated and observed values shown in Table 1 demonstrates that Cs.sub.3 ZnCl.sub.5 crystallizes with the Cs.sub.3 CoCl.sub.5 structure. This crystal structure is not the alkali halide crystal structure seen in reported alkali halide storage phosphors.
Cs.sub.3 ZnCl.sub.5 was examined using differential thermal analysis (DTA). The DTA of Cs.sub.3 ZnCl.sub.5 showed a discrete endotherm on the heating cycle which was indicative of melting. The melting point of Cs.sub.3 ZnCl.sub.5 was 540.degree..+-.5.degree. C., which is different from that of either CsCl (645.degree. C.) or ZnCl.sub.2 (283.degree. C.) demonstrating that the material is a true compound, not a physical mixture of starting materials.
TABLE 1______________________________________X-ray Powder Diffraction Results for Cs.sub.3 ZnCl.sub.5(H K L) D-spacing I(calc) I(obs)______________________________________(1 1 2) 4.8488 76 96(2 0 0) 4.6173 43 62(2 1 1) 3.9722 317 411(2 0 2) 3.8947 652 658(0 0 4) 3.6206 274 342(2 2 0) 3.2668 263 411(2 1 3) 3.1396 1000 1000(2 2 2) 2.9769 49 68(3 1 0) 2.9214 436 575(2 0 4) 2.8494 76 96(3 1 2) 2.7098 42 68(2 2 4) 2.4259 213 274(2 1 5)(0 0 6) 2.3719 159 123(3 1 4) 2.2741 131 178(1 1 6) 2.2648 46 89(4 1 1) 2.2148 102 164(4 0 2) 2.2015 131 137(3 3 0) 2.1783 74 110(2 0 6) 2.1402 179 219(3 3 2) 2.0859 104 123(4 2 0) 2.0663 179 192(4 1 3) 2.0331 172 65(3 1 6) 1.8618 76 107(2 1 7) 1.8511 27 41(0 0 8) 1.8117 72 110(4 2 4) 1.7953 173 178(4 1 5) 1.7730 70 89(4 0 6) 1.6697 158 137(4 4 0) 1.6337 76 68(5 2 3)(3 3 6) 1.6176 314 260(2 2 8) 1.5840 94 96(6 0 0) 1.5399 122 137(4 1 7) 1.5210 31 41(2 1 9) 1.5001 106 96(4 4 4) 1.4890 35 27(5 2 5) 1.4760 47 55(5 3 4) 1.4517 70 82______________________________________
EXAMPLE 2
Cs.sub.3 ZnBr.sub.5
3.179 g of CsBr and 1.126 g of ZnBr.sub.2 were placed into a quartz tube and dehydrated under flowing argon at 200.degree. C. to remove excess water. The sample was then evacuated to better than 10 microns and sealed off. The entire assembly was heated in the vertical position using a moving zone furnace which translated over the length of the tube over a period of 36 hours. The temperature at the midpoint of the moving zone furnace was 600.degree. C. The product was cooled and removed from the tube, whereupon several clear crystals were separated from the mass.
The crystals were examined using a precession camera and Cu K.alpha. radiation. The precession photographs of the single crystal demonstrated that the material was tetragonal with the same symmetry as Cs.sub.3 ZnCl.sub.5. X-ray powder diffraction photographs taken with a Guinier camera gave precision lattice constants of a=9.6384(10) .ANG. and c=15.1373(10) .ANG.. Results are reported in Table 2. The extinctions observed in the powder diffraction pattern and the single crystal photographs are consistent with the tetragonal space group I 4/mcm.
As a further check for the structure type, the guinier film was digitized and the intensities of the x-ray powder diffraction lines were measured and theoretical intensities were calculated in the same manner as in Example 1. Results are reported in Table 2. The results indicate that Cs.sub.3 ZnBr.sub.5 crystallizes with the same structure as Cs.sub.3 ZnCl.sub.5.
Cs.sub.3 ZnBr.sub.5 was examined using differential thermal analysis (DTA). The DTA of Cs.sub.3 ZnBr.sub.5 showed a discrete endotherm on the heating cycle which was indicative of melting. The melting point of Cs.sub.3 ZnBr.sub.5 was 515.degree..+-.5.degree. C., which is different from that of either CsBr (636.degree. C.) or ZnCl.sub.2 (394.degree. C.) demonstrating that the material is a true compound, not a physical mixture of starting materials.
TABLE 2______________________________________X-ray Powder Diffraction Results for Cs.sub.3 ZnBr.sub.5(H K L) D-spacing I(calc) I(obs)______________________________________(1 1 0) 6.80471 22 22(2 0 0) 4.81845 24 22(2 1 1) 4.14381 33 48(2 0 2) 4.06435 205 221(0 0 4) 3.78241 85 95(2 2 0) 3.40480 181 209(1 1 4) 3.30850 75 66(2 1 3) 3.27499 1000 1000(2 2 2) 3.10697 9 11(3 1 0) 3.04522 454 386(2 0 4) 2.97430 89 81(3 1 2) 2.82743 26 29(2 1 5) 2.47598 65 44(4 1 1) 2.30920 32 29(4 0 2) 2.29511 25 15(3 3 0) 2.26977 69 95(2 0 6) 2.23340 86 66(3 3 2) 2.17468 20 7(4 2 0) 2.15390 140 140(4 1 3) 2.11983 137 118(4 0 4) 2.03089 85 77(3 1 6) 1.94221 122 110(0 0 8) 1.89104 46 22(4 2 4) 1.87183 99 81(4 1 5) 1.84997 32 7(4 0 6) 1.74223 124 73(4 4 0) 1.70376 82 48(5 2 3) 1.68630 213 162(2 2 8) 1.65417 45 29(6 0 0) 1.60644 100 73(2 1 9) 1.56687 103 59______________________________________
EXAMPLES 3a-3g
Cs.sub.3 ZnBr.sub.5-z Cl.sub.z
Samples in the system Cs.sub.3 ZnBr.sub.5-z Cl.sub.z were prepared by adding CsCl, CsBr, ZnCl.sub.2, and ZnBr.sub.2 (in the amounts indicated in Table 3) into individual quartz tubes and drying under flowing argon for 2 hours at temperatures between 100.degree. C. and 200.degree. C., (except for example 3a, which had no dehydration treatment). The samples were then evacuated to better than 10 microns and sealed. The samples were placed in a moving zone furnace which was translated up and down the entire length of the sample twice in the period of time and at the temperature indicated in Table 3. After the heat treatment, the samples were cooled to room temperature and removed from their containers.
All samples were examined using x-ray powder diffraction. The x-ray diffraction patterns of all samples were strictly isostructural to Cs.sub.3 ZnCl.sub.5 and Cs.sub.3 ZnBr.sub.5. Refinement of the unit cells using a least squares method confirmed that all the samples were isostructural with the Cs.sub.3 CoCl.sub.5 structure type. A listing of the unit cell parameters for the compositions is given in Table 4. The error in the a and c unit cell dimensions is .+-.0.001 .ANG..
TABLE 3__________________________________________________________________________Preparation of Cs.sub.3 ZnBr.sub.5-z Cl.sub.zExample z CsCl (g) CsBr (g) ZnCl.sub.2 (g) ZnBr.sub.2 (g) Temp (.degree.C.) Time (hrs)__________________________________________________________________________3a 5.0 5.0510 -- 1.3630 -- 700 643b 4.0 3.3672 2.1281 1.3628 -- 693 83c 3.0 5.0508 -- -- 2.2519 600 83d 2.5 .8418 5.3202 1.3628 -- 693 83e 2.0 -- 6.3843 1.3628 -- 600 83f 1.0 1.6840 4.2560 -- 2.2519 693 83g 0.0 -- 3.1790 -- 1.1260 600 36__________________________________________________________________________
TABLE 4______________________________________Unit cell parameters for Cs.sub.3 ZnBr.sub.5-z Cl.sub.zExample z a (.ANG.) c (.ANG.) Cell volume (.ANG..sup.3)______________________________________3a 5.0 9.238 14.483 1235.913b 4.0 9.369 14.542 1276.433c 3.0 9.460 14.636 1309.803d 2.5 9.508 14.711 1329.973e 2.0 9.546 14.783 1347.193f 1.0 9.596 14.935 1375.233g 0.0 9.638 15.136 1405.88______________________________________
EXAMPLE 4
PSL of Cs.sub.3 ZnCl.sub.5
3.788 g of CsCl and 1.022 g of ZnCl.sub.2 were placed in a quartz tube and dehydrated under vacuum at between 100.degree. C. and 200.degree. C. The sample was then evacuated to better than 10 microns and sealed off. The sample was heated in the vertical position at 700.degree. C. for 3 hrs then cooled to room temperature over a period of 4 hrs. The product was removed from the tube and lightly ground. X-ray powder diffraction patterns taken of the sample showed that the material crystallized with the Cs.sub.3 CoCl.sub.5 structure type.
The photostimulated luminescence of the sample was measured as described above and the radiation dose was 15 Rems. The peak response was 869 V and the integrated response was 1.018 V. The ratio of peak response divided by dose is 0.058 V/Rem. This was considered the baseline response of the intrinsic storage properties of Cs.sub.3 ZnCl.sub.5 and was normalized to 100.
EXAMPLE 5
PSL of Cs.sub.3 ZnBr.sub.5
4.7882 g of CsBr and 1.6889 g of ZnBr.sub.2 were placed in a quartz tube and dehydrated under vacuum at between 100.degree. C. and 200.degree. C. The sample was then evacuated to better than 10 microns and sealed off. The sample was heated in the vertical position at 700.degree. C. for 3 hrs then cooled to room temperature over a period of 4 hrs. The product was removed from the tube and lightly ground. X-ray powder diffraction patterns taken of the sample showed that the material crystallized with the Cs.sub.3 CoCl.sub.5 structure type.
The photostimulated luminescence of the sample was measured as described above and the radiation dose was 15 Rems. The peak response was 3.9022 V and the integrated response was 3.6395 V. The ratio of peak response divided by dose was 0.26 V/Rem. This was considered the baseline response of the intrinsic storage properties of Cs.sub.3 ZnBr.sub.5 and was normalized to 100.
EXAMPLES 6a-6e
PSL of Cs.sub.3 ZnBr.sub.5-z Cl.sub.z
The samples were prepared as follows. The halides were placed in a quartz tube using the amounts of starting reagents reported in Table 5 and dehydrated under vacuum at between 100.degree. C. and 200.degree. C. The sample was then evacuated to better than 10 microns and sealed off. The sample was heated in the vertical position at 700.degree. C. for 3 hrs then cooled to room temperature over a period of 4 hrs. The product was removed from the tube and ground with a mortar and pestle. The samples were tested for photostimulated luminescence as described above. The photostimulated luminescent responses are listed in Table 5. Example 6e, Cs.sub.3 ZnCl.sub.5, was normalized to a value of 100.
TABLE 5______________________________________Cs.sub.3 ZnBr.sub.5-z Cl.sub.zEx z CsCl (g) CsBr (g) ZnCl.sub.2 (g) ZnBr.sub.2 (g) PSL (1)______________________________________6a 0.00 -- 4.7882 -- 1.6889 1080876b 1.25 1.5784 2.7931 -- 1.6889 1116386c 2.50 3.1568 .7980 -- 1.6889 5782656d 3.75 2.2097 1.9951 1.0221 -- 646e 5.00 3.7881 -- 1.0221 -- 100______________________________________
EXAMPLES 7a-7d
Cs.sub.3 ZnCl.sub.5 :Eu
The samples were prepared as described in Example 4. The amounts of materials used and nominal composition of the final compound are listed in Table 6. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substituted for Zn.sup.2+. Example 7d was prepared as in example 7a-7c except that EuBr.sub.2 was used instead of EuCl.sub.3 and the sample was heated as described in example 3b using two furnace translation cycles instead of one.
X-ray powder diffraction showed that examples 7a and 7b crystallized with the Cs.sub.3 CoCl.sub.5 structure. Example 7c gave a pattern which indicated that the basic Cs.sub.3 CoCl.sub.5 structure was intact but distorted. The PSL response of the samples is given in Table 6 and is relative to Example 4. The stimulation spectrum of Cs.sub.3 ZnCl.sub.5 :Eu was measured in the wavelength region from 500 nm to 1000 nm. The stimulation spectrum in this wavelength region consists of a single peak centered at 610 nm with a full width at half maximum of less than 200 nm. The photostimulated emission spectrum of Cs.sub.3 ZnCl.sub.5 :Eu was measured using 650 nm stimulation. The photostimulated emission spectrum in the wavelength region from 200 nm to 700 nm consists of a single emission band centered around 450 nm with a full width at half maximum of less than 100 nm. The measured lifetime of the Eu.sup.2+ emission in Example 7d was about 850 nsec. It was determined that the stimulation spectrum, the photostimulated emission spectrum, and the lifetime of the Eu.sup.2+ photostimulated emission does not change substantially when the concentration of europium changes in the phosphor.
TABLE 6______________________________________Cs.sub.3 ZnCl.sub.5 : jEuEx j CsCl (g) ZnCl.sub.2 (g) EuCl.sub.3 (g) PSL (1)______________________________________7a .0050 3.7881 1.0170 .0097 8181827b .0250 3.7881 .9966 .0484 13475267c 0.15 3.7881 .8688 .2906 4767d 0.001 7.5761 2.0443 .0048 --______________________________________
EXAMPLES 8a-8d
Cs.sub.3 ZnBr.sub.5 :Eu
The samples were prepared substantially according to the method described in Example 5. The amounts of materials used and nominal compositions of the final compounds are listed in Table. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+. Example 8d was prepared substantially according to the method described in example 7d.
Examples 8a-8c were examined ming x-ray powder diffraction. All samples crystallized with the Cs.sub.3 ZnBr.sub.5 structure. The PSL response of the samples is given in Table 7 and is relative to Example 5. The stimulation spectrum of Cs.sub.3 ZnBr.sub.5 :Eu in the wavelength region from 500 nm to 1000 nm consists of a single peak centered around 690 nm with a full width at half maximum of less than 200 nm. The photostimulated emission spectrum of Cs.sub.3 ZnBr.sub.5 :Eu was measured using 650 nm stimulation. The photostimulated emission spectrum in the wavelength region from 200 nm to 700 nm consists of a single emission band centered around 450 nm with a full width at half maximum of less than 100 nm. The measured lifetime of the Eu.sup.2+ emission in Example 8d was about 720 nsec. It was determined that the stimulation spectrum, the photostimulated emission spectrum, and the lifetime of the Eu.sup.2+ photostimulated emission does not change substantially when the concentration of europium changes in the phosphor.
TABLE 7______________________________________Cs.sub.3 ZnBr.sub.5 : jEuEx j CsBr (g) ZnBr.sub.2 (g) EuBr.sub.2 (g) PSL (2)______________________________________8a .005 4.7882 1.6805 .0117 2071398b .025 4.7882 1.6467 .0585 3641538c .15 4.7882 1.4356 .3508 168d .0014 6.3843 2.2519 .0043 --______________________________________
EXAMPLES 9a-9q
Cs.sub.3 ZnBr.sub.5-z Cl.sub.z :Eu
The samples were prepared substantially according to the method described in Examples 6a-6e. The amounts of materials used and nominal compositions of the final compounds are listed in Table 8. The Eu.sup.2+ concentration was 0.5 mole %. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+. The photostimulated luminescent response of Examples 9a-9q are listed in Table 8 and are relative to Example 6e. The stimulation and stimulated emission spectrum of Examples 9g and 9o are shown in FIGS. 7 and 8. The measured lifetimes of the stimulated emission from Eu.sup.2+ in Examples 9g and 9o were about 640 nsec and about 760 nsec, respectively.
TABLE 8______________________________________Cs.sub.3 ZnBr.sub.5-z Cl.sub.z : EuEx. CsCl (g) CsBr (g) ZnCl.sub.2 (g) ZnBr.sub.2 (g) EuBr.sub.2 (g) EuCl2______________________________________9a -- 4.7882 -- 1.6805 .0117 --9b .0316 4.7483 -- 1.6805 .0117 --9c .0631 4.7084 -- 1.6805 .0117 --9d .1263 4.6286 -- 1.6805 .0117 --9e .1894 4.5488 -- 1.6805 .0117 --9f .2525 4.4690 -- 1.6805 .0117 --9g .3157 4.3892 -- 1.6805 .0117 --9h .3788 4.3094 -- 1.6805 .0117 --9i .4419 4.2296 -- 1.6805 .0117 --9j .6314 3.9902 -- 1.6805 .0117 --9k 3.1568 .7980 -- 1.6805 .0117 --9l 2.8411 1.1971 1.0170 -- -- .00979m 3.1568 .7980 1.0170 -- -- .00979n 3.342 .5586 1.0170 -- -- .00979o 3.4724 .3990 1.0170 -- -- .00979p 3.6618 .1596 1.0170 -- -- .00979q 3.7881 -- 1.0170 -- -- .0097______________________________________
EXAMPLES 10a-10d
Cs.sub.3-a Li.sub.a ZnCl.sub.5
The samples were prepared substantially according to the method described in Example 4. The amounts of materials used and nominal composition of the final compounds are listed in Table 9. X-ray powder diffraction showed that Examples 10a and 10b crystallized in the same structure type as Cs.sub.3 ZnCl.sub.5. Examples 10c and 10d crystallized in a completely different structure type from Cs.sub.3 ZnCl.sub.5. The structure type was not identified. The PSL of the samples relative to Example 4 is listed in Table 9. The materials of Examples 10c (25 mole percent Li) and 10d (50 mole percent Li) were strongly hygroscopic and PSL measurements could not be obtained.
TABLE 9______________________________________Cs.sub.3-a Li.sub.a ZnCl.sub.5Ex a Li (mol %) CsCl (g) ZnCl.sub.2 (g) LiCl (g) PSL (1)______________________________________10a .15 5 3.5987 1.0221 .0477 .7810b .3 10 3.4093 1.0221 .0954 .7810c .75 25 2.8410 1.0221 .2385 --10d 1.50 50 1.8940 1.0221 .4769 --______________________________________
EXAMPLE 11
Cs.sub.3-a Li.sub.a ZnCl.sub.5 :0.005Eu
The sample was prepared substantially according to the method described in Example 4. The amounts of materials used and nominal composition of the final compound are listed in Table 10. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in Cs.sub.3-a Li.sub.a ZnCl.sub.5. The PSL is relative to Example 4.
TABLE 10______________________________________Cs.sub.3-a Li.sub.a ZnCl.sub.5 : 0.005 Eu LiEx a (mol %) CsCl (g) ZnCl.sub.2 (g) LiCl (g) EuCl.sub.3 (g) PSL (1)______________________________________11 .15 5 3.5987 1.0170 .0477 .0097 36248______________________________________
EXAMPLES 12a-12d
Cs.sub.3-a Li.sub.a ZnBr.sub.5
The samples were prepared substantially according to the method described in Example 5. The amounts of materials used and nominal compositions of the final compounds are listed in Table 11. X-ray powder diffraction was conducted. Examples 12a and 12b were isostructural with Cs.sub.3 ZnBr.sub.5. Example 12c showed two distinct phases and Example 12d crystallized in a different structure type from Cs.sub.3 ZnBr.sub.5. The structure type was not identified. The PSL of the samples, relative to Example 5, is listed in Table 11. The materials of Examples 12c (25 mole percent Li) and 12d (50 mole percent Li) were strongly hygroscopic and PSL measurements could not be obtained.
TABLE 11______________________________________Cs.sub.3-a Li.sub.a ZnBr.sub.5Ex a Li (mol %) CsBr (g) ZnBr.sub.2 (g) LiBr (g) PSL (2)______________________________________12a .15 5 4.5488 1.6889 .0977 3312b .3 10 4.3094 1.6889 .1954 .112c .75 25 3.5912 1.6889 .4885 --12d 1.50 50 2.3941 1.6889 .9770 --______________________________________
EXAMPLE 13
Cs.sub.3-a Li.sub.a ZnBr.sub.5 :0.005Eu
The sample was prepared substantially according to the method described in Example 5. The amounts of materials used and nominal composition of the final compound are listed in Table 12. The stoichiometry of the compound was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in Cs.sub.3-a Li.sub.a ZnBr.sub.5. The PSL of Example 13 is relative to Example 5.
TABLE 12______________________________________Cs.sub.3-a Li.sub.a ZnBr.sub.5 : 0.005 Eu LiEx a (mol %) CsBr (g) ZnBr.sub.2 (g) LiBr (g) EuBr.sub.2 (g) PSL (2)______________________________________13 .15 5 4.5488 1.6805 .0977 .0117 109682______________________________________
EXAMPLES 14a-14b
Cs.sub.3-a Li.sub.a ZnBr.sub.5-z Cl.sub.z
The samples were prepared substantially according to the method described in Examples 6. The amounts of materials used and nominal compositions of the final compounds are listed in Table 13. X-ray powder diffraction showed that Examples 14a and 14b both crystallized in the same structure type as Cs.sub.3 ZnBr.sub.5-z Cl.sub.z. The PSL of the samples relative to Example 6e is listed in Table 13. The material of Example 14b was strongly hygroscopic.
TABLE 13__________________________________________________________________________Cs.sub.3-a Li.sub.a ZnBr.sub.5-z Cl.sub.z (a = 0.15)Ex z CsBr (g) CsCl (g) ZnBr.sub.2 (g) ZnCl.sub.2 (g) LiCl (g) LiBr (g) PSL (1)__________________________________________________________________________14a .25 4.1498 .3157 1.6889 -- -- .0977 85414b 4.75 .3990 3.2830 -- 1.0221 .0477 -- 0__________________________________________________________________________
EXAMPLES 15a-15b
Cs.sub.3-a Li.sub.a ZnBr.sub.5-z Cl.sub.z :Eu
The samples were prepared substantially according to the method described in Example 6. The amounts of materials used are listed in Table 14. Stoichiometry was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in Cs.sub.3-a Li.sub.a ZnBr.sub.5-z Cl.sub.z. The PSL responses of Examples 15a-15b relative to the PSL of Example 6e, are listed in Table 14.
TABLE 14__________________________________________________________________________Cs.sub.3-a Li.sub.a ZnBr.sub.5-z Cl.sub.z : 0.01 Eu (a = 0.15)Ex CsBr (g) CsCl (g) ZnBr.sub.2 (g) ZnCl.sub.2 (g) LiCl (g) LiBr (g) EuBr.sub.2 (g) EuCl.sub.3 (g) z PSL (1)__________________________________________________________________________15a 4.1498 .3157 .6720 -- -- .0977 .0234 -- .25 108009715b .3990 3.2830 -- 1.0119 .0477 -- -- .0194 4.75 138__________________________________________________________________________
EXAMPLES 16a-16d: Cs.sub.3-b Na.sub.b ZnCl.sub.5
The samples were prepared substantially according to the method described in Example 4. The amounts of materials used and nominal composition of the final compounds are listed in Table 15. Examples 16a-16d were examined by x-ray powder diffraction. Examples 16a and 16b crystallized with the Cs.sub.3 ZnCl.sub.5 structure type. Example 16c showed a phase which was isostructural with Cs.sub.3 ZnCl.sub.5 and an additional unidentified phase. Example 16d crystallized in a completely different structure type from Cs.sub.3 ZnCl.sub.5. The structure type was not identified. The PSL of the samples relative to Example 4 is listed in Table 15.
TABLE 15______________________________________Cs.sub.3-b Na.sub.b ZnCl.sub.5Ex b Na (mol %) CsCl (g) ZnCl.sub.2 (g) NaCl (g) PSL (1)______________________________________16a .15 5 3.5987 1.0221 .0657 .9716b .3 10 3.4093 1.0221 .1315 .9716c .75 25 2.8410 1.0221 .3287 .9716d 1.50 50 1.8940 1.0221 .6575 4.87______________________________________
EXAMPLE 17
Cs.sub.3-b Na.sub.b ZnCl.sub.5 :Eu
The sample was prepared substantially according to the method described in Example A2. The amounts of materials used and nominal composition of the final compound are listed in Table 16. Stoichiometry was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in Cs.sub.3-b Na.sub.b ZnCl.sub.5. The PSL response of Example 17 is relative to Example 4. This demonstrates that enhanced stimulated emission is observed with an activator cation like Eu.sup.2+ in Cs.sub.3-b Na.sub.b ZnCl.sub.5.
TABLE 16______________________________________Cs.sub.3-b Na.sub.b ZnCl.sub.5 : 0.005 Eu Na EuCl.sub.3 PSLEx b (mol %) CsCl (g) ZnCl.sub.2 (g) NaCl (g) (g) (1)______________________________________17 .15 5 3.5987 1.0170 .0657 .0097 11507______________________________________
EXAMPLES 18a-18d
Cs.sub.3-b Na.sub.b ZnBr.sub.5
The samples were prepared substantially according to the method described in Example 5. The amounts of materials used and nominal compositions of the final compounds are listed in Table 17. X-ray powder diffraction showed that the major phase in Example 18a was isostructural with Cs.sub.3 ZnBr.sub.5. Examples 18b and 18c crystallized in a distorted Cs.sub.3 ZnBr.sub.5 lattice as shown by the splitting of various lines in the x-ray diffraction pattern. Example 18d crystallized in a different structure type from Cs.sub.3 ZnBr.sub.5. The structure type was not identified. The PSL of the samples relative to Example 5 is listed in Table 17.
TABLE 17______________________________________Cs.sub.3-b Na.sub.b ZnBr.sub.5Ex b Na (mol %) CsBr (g) ZnBr.sub.2 (g) NaBr (g) PSL (2)______________________________________18a .15 5 4.5488 1.6889 .1158 10718b .3 10 4.3094 1.6889 .2315 807218c .75 25 3.5912 1.6889 .5788 10318d 1.50 50 2.3941 1.6889 1.1576 45______________________________________
EXAMPLE 19
Cs.sub.3-b Na.sub.b ZnBr.sub.5 :Eu
The sample was prepared substantially according to the method described in Example 5. The amounts of materials used and nominal composition of the final compound are listed in Table 18. Stoichiometry was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in Cs.sub.3-b Na.sub.b ZnBr.sub.5. The PSL response of Example 19 was relative to Example 5.
TABLE 18______________________________________Cs.sub.3-b Na.sub.b ZnBr.sub.5 : 0.005 Eu Na ZnBr.sub.2 EuBr.sub.2Ex b (mol %) CsBr (g) (g) NaBr (g) (g) PSL (2)______________________________________19 .15 5 4.5488 1.6805 .1158 .0117 35800______________________________________
EXAMPLES 20a-20b
Cs.sub.3-b Na.sub.b ZnBr.sub.5-z Cl.sub.z
The samples were prepared substantially according to the method described in Examples 6. The amounts of materials used and nominal compositions of the final compounds are listed in Table 19. X-ray powder diffraction was performed. Examples 20a and 20b crystallized in the same structure type as Cs.sub.3 ZnBr.sub.5-z Cl.sub.z. The PSL of the samples is relative to Example 6e.
TABLE 19__________________________________________________________________________Cs.sub.3-b Na.sub.b ZnBr.sub.5-z Cl.sub.z (b = 0.15) PSLEx z CsBr (g) CsCl (g) ZnBr.sub.2 (g) ZnCl.sub.2 (g) NaCl (g) NaBr (g) (1)__________________________________________________________________________20a .25 4.1498 .3157 1.6889 -- -- .1158 37720b 4.75 .3990 3.2830 -- 1.0221 .0657 -- 91__________________________________________________________________________
EXAMPLES 21a-21b
Cs.sub.3-b Na.sub.b ZnBr.sub.5-z Cl.sub.z :Eu
The samples were prepared substantially according to the method described in Examples 6. The amounts of materials used and nominal compositions of the final compounds are listed in Table 20. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in Cs.sub.3-b Na.sub.b ZnBr.sub.5-z Cl.sub.z. The PSL of Examples 21a and 21b are relative to Example 6e.
TABLE 20__________________________________________________________________________Cs.sub.3-b Na.sub.b ZnBr.sub.5-z Cl.sub.z : 0.01 Eu (b = 0.15)Ex CsBr (g) CsCl (g) ZnBr.sub.2 (g) ZnCl.sub.2 (g) NaCl (g) NaBr (g) EuBr.sub.2 (g) EuCl.sub.3 (g) z PSL (1)__________________________________________________________________________21a 4.1498 .3157 1.6720 -- -- .1158 .0234 -- .25 105616321b .3990 3.2830 -- 1.0119 .0657 -- -- .0194 4.75 664__________________________________________________________________________
EXAMPLES 22a-22d
Cs.sub.3-c K.sub.c ZnCl.sub.5
The samples were prepared substantially according to the method described in Example 4. The amounts of materials used and nominal compositions of the final compounds are listed in Table 21. Examples 22a-22d were examined by x-ray powder diffraction. Example 22a showed the Cs.sub.3 ZnCl.sub.5 structure. The x-ray powder diffraction patterns of examples 22b and 22c showed split lines which can tentatively be explained as a distorted Cs.sub.3 ZnCl.sub.5 lattice type. Example 22d crystallized in a completely different structure type from Cs.sub.3 ZnCl.sub.5. The structure type was not identified. The PSL of the samples relative to Example 4 is listed in Table 21.
TABLE 21______________________________________Cs.sub.3-c K.sub.c ZnCl.sub.5Ex c K (mol %) CsCl (g) ZnCl.sub.2 (g) KCl (g) PSL (1)______________________________________22a .15 5 3.5987 1.0221 .0839 1422b .3 10 3.4093 1.0221 .1677 1022c .75 25 2.8410 1.0221 .4194 1122d 1.50 50 1.8940 1.0221 .8387 20______________________________________
EXAMPLE 23
Cs.sub.3-c K.sub.c ZnCl.sub.5 :Eu
The sample was prepared substantially according to the method described in Example 4. The amounts of materials used and nominal composition of the final compound are listed in Table 22. Stoichiometry was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in Cs.sub.3-c K.sub.c ZnCl.sub.5. The PSL response of Example 23 is relative to Example 4. This demonstrates that enhanced stimulated emission is observed with an activator cation like Eu.sup.2+ in Cs.sub.3-c K.sub.c ZnCl.sub.5.
TABLE 22______________________________________Cs.sub.3-c K.sub.c ZnCl.sub.5 : 0.005 Eu KEx c (mol %) CsCl (g) ZnCl.sub.2 (g) KCl (g) EuCl.sub.3 (g) PSL (1)______________________________________23 .15 5 3.5987 1.0170 .0839 .0097 72497______________________________________
EXAMPLES 24a-24d
Cs.sub.3-c K.sub.c ZnBr.sub.5
The samples were prepared substantially according to the method described in Example 5. The amounts of materials used and nominal compositions of the final compounds are listed in Table 23. Examples 24a-24d were examined using x-ray powder diffraction. Examples 24a and 24b were isostructural with Cs.sub.3 ZnBr.sub.5. Example 24c showed two distinct phases and Example 24d crystallized in a different structure type from Cs.sub.3 ZnBr.sub.5. The structure type was not identified. The PSL of the samples relative to Example 5 is listed in Table 23.
TABLE 23______________________________________Cs.sub.3-c K.sub.c ZnBr.sub.5Ex c K (mol %) CsBr (g) ZnBr.sub.2 (g) KBr (g) PSL (2)______________________________________24a .15 5 4.5488 1.6889 .1861 448524b .30 10 4.3094 1.6889 .3721 192224c .75 25 3.5912 1.6889 .9303 192224d 1.50 50 2.3941 1.6889 1.8605 78______________________________________
EXAMPLE 25
Cs.sub.3-c K.sub.c ZnBr.sub.5 :Eu
The sample was prepared substantially according to the method described in Example 5. The amounts of materials used and nominal composition of the final compound are listed in Table 24. Stoichiometry was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in Cs.sub.3-c K.sub.c ZnBr.sub.5. The PSL response of Example 25 is relative to Example 5.
TABLE 24______________________________________Cs.sub.3-c K.sub.c ZnBr.sub.5 : 0.005 Eu NaEx c (mol %) CsBr (g) ZnBr.sub.2 (g) KBr (g) EuBr.sub.2 (g) PSL (2)______________________________________25 .15 5 4.5488 1.6805 .1861 .0117 89309______________________________________
EXAMPLES 26a-26b
Cs.sub.3-c K.sub.c ZnBr.sub.5-z Cl.sub.z
The samples were prepared substantially according to the method described in Examples 6. The amounts of materials used and nominal compositions of the final compounds are listed in Table 25. Examples 26a and 26b crystallized in the same structure type as Cs.sub.3 ZnBr.sub.5-z Cl.sub.z. The PSL of the samples relative to Example 6e, is listed in Table 25.
TABLE 25__________________________________________________________________________Cs.sub.3-c K.sub.c ZnBr.sub.5-z Cl.sub.z (c = 0.15)Ex z CsBr (g) CsCl (g) ZnBr.sub.2 (g) ZnCl.sub.2 (g) KCl (g) KBr (g) PSL (1)__________________________________________________________________________26a .25 4.1498 .3157 1.6889 -- -- 1339 3366126b 4.75 .3990 3.2830 -- 1.0221 .0839 -- 39__________________________________________________________________________
EXAMPLES 27a-27b
Cs.sub.3-c K.sub.c ZnBr.sub.5-z Cl.sub.z :Eu
The samples were prepared substantially according to the method described in Examples 6. The amounts of materials used and nominal compositions of the final compounds are listed in Table 26. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in Cs.sub.3-c K.sub.c ZnBr.sub.5-z Cl.sub.z. The PSL of Examples 27a and 27b relative to Example 6e, are shown in Table 26.
TABLE 26__________________________________________________________________________Cs.sub.3-c K.sub.c ZnBr.sub.5-z Cl.sub.z : 0.01 Eu (c = 0.15)Ex CsBr (g) CsCl (g) ZnBr.sub.2 (g) ZnCl.sub.2 (g) KCl (g) KBr (g) EuBr.sub.2 (g) EuCl.sub.3 (g) z PSL (1)__________________________________________________________________________27a 4.1498 .3157 1.6720 -- -- .1339 .0234 -- .25 10422727b .3990 3.2830 -- 1.0119 .0839 -- -- .0194 4.75 63694__________________________________________________________________________
EXAMPLES 28a-28d
(Cs.sub.1-r Rb.sub.r).sub.3 ZnCl.sub.5
The samples were prepared substantially according to the method described in Example 4. The amounts of materials used and nominal compositions of the final compounds are listed in Table 27. X-ray powder diffraction showed that Examples 28a-28d all crystallized in the same structure type as Cs.sub.3 ZnCl.sub.5. DTA of Rb.sub.3 ZnCl.sub.5 showed that the compound melted at 500.degree..+-.5.degree. C. The PSL of the samples relative to Example 4, is listed in Table 27.
TABLE 27______________________________________(Cs.sub.1-r Rb.sub.r).sub.3 ZnCl.sub.5Ex r CsCl (g) ZnCl.sub.2 (g) RbCl (g) PSL (1)______________________________________28a .25 2.8410 1.0221 .6802 6628b .50 1.8940 1.0221 1.3604 8828c .75 0.9470 1.0221 2.0406 4728d 1.00 0.0000 1.0221 2.7208 70______________________________________
EXAMPLES 29a-29d
(Cs.sub.1-r Rb.sub.r).sub.3 ZnCl.sub.5 :0.005Eu
The samples were prepared substantially according to the method described in Example 4. The amounts of materials used and nominal compositions of the final compounds are listed in Table 28. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in (Cs.sub.1-r Rb.sub.r).sub.3 ZnCl.sub.5. X-ray powder diffraction showed that Examples 29a-29d crystallized in the Cs.sub.3 ZnCl.sub.5 structure. The PSL of the samples, relative to Example 4, is listed in Table 28.
TABLE 28______________________________________(Cs.sub.1-r Rb.sub.r).sub.3 ZnCl.sub.5 : 0.005 EuEx r CsCl (g) ZnCl.sub.2 (g) RbCl (g) EuCl.sub.3 (g) PSL (1)______________________________________29a .25 2.8410 1.0170 .6802 .0097 502029b .50 1.8940 1.0170 1.3604 .0097 762429c .75 0.9470 1.0170 2.0406 .0097 1323429d 1.00 0.0000 1.0170 2.7208 .0097 151273______________________________________
EXAMPLES 30a-30d
(Cs.sub.1-r Rb.sub.r).sub.3 ZnBr.sub.5
The samples were prepared substantially according to the method described in Example 5. The amounts of materials used and nominal compositions of the final compounds are listed in Table 29. X-ray powder diffraction was conducted. Examples 30a-30c had a major phase crystallizing in the same structure type as Cs.sub.3 ZnBr.sub.5. Example 30d crystallized in a different structure. Examination of Example 30d using polarizarized optical microscopy showed that the major phase was uniaxial, indicating that the Bravais symmetry is either tetragonal or hexagonal. DTA examination of Rb.sub.3 ZnBr.sub.5 showed that the melting point of the compound was 450.degree..+-.5.degree. C. The melting point of RbBr is 698.degree. C. and the melting point of ZnBr.sub.2 is 394.degree. C. The difference in melting points showed that the Rb.sub.3 ZnBr.sub.5 was not an unreacted mixture of the starting materials. The PSL of the samples, relative to Example 5, is listed in Table 29.
TABLE 29______________________________________(Cs.sub.1-r Rb.sub.r).sub.3 ZnBr.sub.5Ex r CsBr (g) ZnBr.sub.2 (g) RbBr (g) PSL (2)______________________________________30a .25 3.5912 1.6889 .9303 7230b .50 2.3941 1.6889 1.8605 1930c .75 1.1971 1.6889 2.7908 2830d 1.00 0.0000 1.6889 3.7210 228______________________________________
EXAMPLE 31a-31f
(Cs.sub.1-r Rb.sub.r).sub.3 ZnBr.sub.5 :0.005Eu
The samples were prepared substantially according to the method described in Example 5. The amounts of materials used and nominal compositions of the final compounds are listed in Table 30. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in (Cs.sub.1-r Rb.sub.r).sub.3 ZnBr.sub.5. X-ray powder diffraction showed that Examples 31a-31c crystallized in the Cs.sub.3 ZnBr.sub.5 structure. Examples 31d and 31e showed a phase which was isostructural with Cs.sub.3 ZnBr.sub.5 plus an additional phase which was not identified. Example 31f crystallized with a different structure type, that appeared to be the same as that of Example 30d. The PSL of the samples, relative to Example 5, is listed in Table 30.
TABLE 30______________________________________(Cs.sub.1-r Rb.sub.r).sub.3 ZnBr.sub.5 : 0.005 EuEx r CsBr (g) ZnBr.sub.2 (g) RbBr (g) EuBr.sub.2 (g) PSL (2)______________________________________31a .05 1.5488 1.6805 .1861 .0117 8423531b .10 4.3094 1.6805 .3721 .0117 6701331c .25 3.5912 1.6805 .9303 .0117 5271431d .50 2.3941 1.6805 1.8605 .0117 231e .75 1.1971 1.6805 2.7908 .0117 131f 1.00 0.0000 1.6805 3.7210 .0117 60684______________________________________
EXAMPLE 32a-32b
(Cs.sub.1-r Rb.sub.r).sub.3 ZnBr.sub.5-z Cl.sub.z
The samples were prepared substantially according to the method described in Examples 6. The amounts of materials used and nominal compositions of the final compounds are listed in Table 31. X-ray powder diffraction was conducted. Examples 32a and 32b crystallized in the same structure type as Cs.sub.3 ZnBr.sub.5-z Cl.sub.z. The PSL of the samples, relative to Example 6e, is listed in Table 31.
TABLE 31__________________________________________________________________________(Cs.sub.1-r Rb.sub.r).sub.3 ZnBr.sub.5-z Cl.sub.z (r = 0.05)Ex z CsBr (g) CsCl (g) ZnBr.sub.2 (g) ZnCl.sub.2 (g) RbCl (g) RbBr (g) PSL (1)__________________________________________________________________________32a .25 4.1498 .3157 1.6889 -- -- 1861 19032b 4.75 .3990 3.2830 -- 1.0221 1360 -- 93__________________________________________________________________________
EXAMPLES 33a-33b
(Cs.sub.1-r Rb.sub.r).sub.3 ZnBr.sub.5-z Cl.sub.z :Eu
The samples were prepared substantially according to the method described in Examples 6. The amounts of materials used and nominal compositions of the final compounds are listed in Table 32. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in (Cs.sub.1-r Rb.sub.r).sub.3 ZnBr.sub.5-z Cl.sub.z. X-ray powder diffraction showed that Examples 33a and 33b crystallized in the Cs.sub.3 ZnCl.sub.5 structure. The PSL of the samples, relative to Example 6e, is listed in Table 32.
TABLE 32__________________________________________________________________________(Cs.sub.1-r Rb.sub.r).sub.3 ZnBr.sub.5-z Cl.sub.z : 0.01 Eu (r = 0.05)Ex CsBr (g) CsCl (g) ZnBr.sub.2 (g) ZnCl.sub.2 (g) RbCl (g) RbBr (g) EuBr.sub.2 (g) EuCl.sub.3 (g) z PSL (1)__________________________________________________________________________33a 4.1498 .3157 1.6720 -- -- .1861 .0234 -- .25 37367233b .3990 3.2830 -- 1.0119 .1360 -- -- .0194 4.75 164060__________________________________________________________________________
EXAMPLE 34
(Cs.sub.1-r Rb.sub.r).sub.3-n (Li.sub.a Na.sub.b K.sub.c)ZnCl.sub.5 where n=(a+b+c)
The sample was prepared substantially according to the method described in Example 4. The amounts of materials used and nominal composition of the final compound are listed in Table 33. X-ray powder diffraction showed that Example 34 crystallized in the same structure type as Cs.sub.3 ZnCl.sub.5. The PSL of the Example 34 is relative to Example 4.
TABLE 33______________________________________(Cs.sub.1-r Rb.sub.r).sub.3-n (Li.sub.a Na.sub.b K.sub.c)ZnCl.sub.5 wheren = (a + b + c) = 0.0045,r = 0.0005, a = 0.0015, b = 0.0015, c = 0.0015 CsCl ZnCl.sub.2 RbClEx (g) (g) (g) KCl (g) NaCl (g) LiCl (g) PSL (1)______________________________________34 3.7805 1.0221 .0014 .0008 .0007 .0005 2970______________________________________
EXAMPLE 35
(Cs.sub.1-r Rb.sub.r).sub.3-n (Li.sub.a Na.sub.b K.sub.c)ZnCl.sub.5 :Eu where n=(a+b+c)
The sample was prepared substantially according to the method described in Example 4. The amounts of materials used and nominal composition of the final compound are listed in Table 34. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in the compounds. The PSL of Example 35 is relative to Example 4.
TABLE 34__________________________________________________________________________(Cs.sub.1-r Rb.sub.r).sub.3-n (Li.sub.a Na.sub.b K.sub.c)ZnCl.sub.5 :0.005 Eu where n = (a + b + c) = 0.0045,r = 0.0005, a = 0.0015, b = 0.0015, c = 0.0015Ex CsCl (g) ZnCl.sub.2 (g) RbCl (g) KCl (g) NaCl (g) LiCl (g) EuCl.sub.3 (g) PSL (1)__________________________________________________________________________35 3.7805 1.0170 .0014 .0008 .0007 .0005 .0097 367434__________________________________________________________________________
EXAMPLE 36
(Cs.sub.1-r Rb.sub.r).sub.3-n (Li.sub.a Na.sub.b K.sub.c)ZnBr.sub.5 where n=(a+b+c)
The sample was prepared substantially according to the method described in Example 5. The amounts of materials used and nominal composition of the final compound are listed in Table 35. X-ray powder diffraction showed that Example 36 crystallized in the same structure type as Cs.sub.3 ZnBr.sub.5. The PSL of the Example 36 is relative to Example 5.
TABLE 35______________________________________(Cs.sub.1-r Rb.sub.r).sub.3-n (Li.sub.a Na.sub.b K.sub.c)ZnBr.sub.5 wheren = (a + b + c) = 0.0045,r = 0.0005, a = 0.0015, b = 0.0015, c = 0.0015 CsBr ZnBr.sub.2 NaBrEx (g) (g) RbBr (g) KBr (g) (g) LiBr (g) PSL (2)______________________________________36 4.7858 1.6889 .0019 .0013 .0012 .0010 1845______________________________________
EXAMPLE 37
(Cs.sub.1-r Rb.sub.r).sub.3-n (Li.sub.a Na.sub.b K.sub.c)ZnBr.sub.5 :Eu where n=(a+b+c)
The sample was prepared substantially according to the method described in Example 5. The amounts of materials used and nominal composition of the final compound are listed in Table 36. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in the compounds. The PSL of Example 37 is relative to Example 5.
TABLE 36__________________________________________________________________________(Cs.sub.1-r Rb.sub.r).sub.3-n (Li.sub.a Na.sub.b K.sub.c)ZnBr.sub.5 :0.005 Eu where n = (a + b + c) = 0.0045,r = 0.0005, a = 0.0015, b = 0.0015, c = 0.0015Ex CsBr (g) ZnBr.sub.2 (g) RbBr (g) KBr (g) NaBr (g) LiBr (g) EuBr.sub.2 (g) PSL (2)__________________________________________________________________________37 4.7858 1.6805 .0019 .0013 .0012 .0010 .0117 141894__________________________________________________________________________
EXAMPLES 38a-38b
(Cs.sub.1-r Rb.sub.r).sub.3-n (Li.sub.a Na.sub.b K.sub.c)ZnBr.sub.5-z Cl.sub.z
The samples were prepared substantially according to the method described in Examples 6, except that the alkali metals other than Cs were added as mixtures which were prepared and dehydrated by heating under vacuum in advance. The amounts of alkali halides used to prepare the mixtures are shown in Table 37. The amounts of materials used and nominal compositions of the final compounds of Examples 38a-38b are listed in Table 38. X-ray powder diffraction examination of Examples 38a and 38b showed that both crystallized with the Cs.sub.3 CoCl.sub.5 structure type. The PSL of Examples 38a and 38b are relative to Example 6e and are shown in Table 38.
TABLE 37______________________________________Preparation of Anhydrous Alkali Halide Mixtures______________________________________Mixture 1 LiBr (g) NaBr (g) KBr (g) RbBr (g)______________________________________ .0977 .1158 .1339 .1860______________________________________Mixture 2 LiCl (g) NaCl (g) KCl (g) RbCl (g)______________________________________ .0477 .0657 .0839 .1360______________________________________
TABLE 38__________________________________________________________________________(Cs.sub.1-r Rb.sub.r).sub.3-n (Li.sub.a Na.sub.b K.sub.c)ZnBr.sub.5-zCl.sub.z where n = (a + b + c) = 0.0045,r = 0.0005, a = 0.0015, b = 0.0015, c = 0.0015Ex z CsBr (g) CsCl (g) ZnBr.sub.2 (g) ZnCl.sub.2 (g) Mixt. #1 (g) Mixt. #2 (g) PSL (1)__________________________________________________________________________38a .25 4.3796 .3157 1.6889 -- .0053 -- 149422438b 4.75 .3990 3.4648 -- 1.0221 -- .0033 632__________________________________________________________________________
EXAMPLES 39a-39b
(Cs.sub.1 -Rb.sub.r).sub.3-n (Li.sub.a Na.sub.b K.sub.c)ZnBr.sub.5-z Cl.sub.z :Eu where n=(a+b+c)
The samples were prepared substantially according to the method described in Examples 38a-38b, except that Eu was added as EuBr.sub.2 or EuCl.sub.3. The amounts of materials used and nominal compositions of the final compounds are listed in Table 39. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in the compounds. The PSL of Examples 39a and 39b relative to Example 6e are shown in Table 39.
TABLE 39__________________________________________________________________________(Cs.sub.1-r Rb.sub.r).sub.3-n (Li.sub.a Na.sub.b K.sub.c)ZnBr.sub.5-zCl.sub.z : 0.01 Eu wheren = (a + b + c) = 0.0045, r = 0.0005, a = 0.0015, b = 0.0015, c = 0.0015Ex CsBr (g) CsCl (g) ZnBr.sub.2 (g) ZnCl.sub.2 (g) Mixture #1 (g) Mixture #2 (g) EuBr.sub.2 (g) EuCl.sub.3 (g) z PSL(1)__________________________________________________________________________39a 4.3796 .3157 1.6720 -- .0053 -- .0234 -- .25 62767639b .3990 3.4648 -- 1.0119 -- .0033 -- .0194 4.75 1173052__________________________________________________________________________
EXAMPLE 40a-40d
Cs.sub.3 (Zn.sub.1-m Mg.sub.m)Cl.sub.5
The samples were prepared substantially according to the method described in Example 4 except that the samples were heated at 775.degree. C. The amounts of materials used and nominal compositions of the final compounds are listed in Table 40. X-ray powder diffraction was conducted. Examples 40a-40d all crystallized in the same structure type as Cs.sub.3 ZnCl.sub.5. The PSL of the samples, relative to Example 4, is listed in Table 40.
TABLE 40______________________________________Cs.sub.3 (Zn.sub.1-m Mg.sub.m)Cl.sub.5Ex m CsCl (g) ZnCl.sub.2 (g) MgCl.sub.2 (g) PSL (1)______________________________________40a .05 3.7881 0.9710 .0357 1990840b .10 3.7881 0.9199 .0714 632940c .25 3.7881 0.7666 .1785 886140d .50 3.7881 0.5111 .3571 12______________________________________
EXAMPLE 41
Cs.sub.3 (Zn.sub.1- Mg.sub.m)Cl.sub.5 :0.01Eu
The sample was prepared substantially according to the method described in Example 40a. The amounts of materials used and nominal composition of the final compound are listed in Table 41. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in Cs.sub.3 (Zn.sub.1-m Mg.sub.m)Cl.sub.5. The PSL response of Example 41 is relative to Example 4.
TABLE 41______________________________________Cs.sub.3 (Zn.sub.1-m Mg.sub.m)Cl.sub.5 : 0.01 EuEx m CsCl (g) ZnCl.sub.2 (g) MgCl.sub.2 (g) EuCl.sub.3 (g) PSL (1)______________________________________41 .05 3.7881 0.9608 .0357 .0194 625719______________________________________
EXAMPLE 42a-42d
Cs.sub.3 (Zn.sub.1-m Mg.sub.m)Br.sub.5
The samples were prepared substantially according to the method described in Example 5. The amounts of materials used and nominal compositions of the final compounds are listed in Table 42. X-ray powder diffraction was conducted. Examples 42a-42d all crystallized in the same structure type as Cs.sub.3 ZnBr.sub.5. The PSL of the samples, relative to Example 5, is listed in Table 42.
TABLE 42______________________________________Cs.sub.3 (Zn.sub.1-m Mg.sub.m)Br.sub.5Ex m CsBr (g) ZnBr.sub.2 (g) MgBr.sub.2 (g) PSL (2)______________________________________42a .05 4.7884 1.6045 .0690 1237842b .10 4.7884 1.5200 .1381 11339742c .25 4.7884 1.2667 .3452 1673442d .50 4.7884 0.8445 .6905 6868______________________________________
EXAMPLE 43
Cs.sub.3 (Zn.sub.1-m Mg.sub.m)Br.sub.5 :Eu
The sample was prepared substantially according to the method described in Example 5. The amounts of materials used and nominal composition of the final compound are listed in Table 43. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in Cs.sub.3 (Zn.sub.1-m Mg.sub.m)Br.sub.5. The PSL response is relative to Example 5.
TABLE 43______________________________________Cs.sub.3 (Zn.sub.1-m Mg.sub.m)Br.sub.5 : 0.01 EuEx m CsBr (g) ZnBr.sub.2 (g) MgBr.sub.2 (g) EuBr.sub.2 (g) PSL (2)______________________________________43 .05 4.7884 1.5876 .0690 .0234 1809800______________________________________
EXAMPLE 44a-44b
Cs.sub.3 (Zn.sub.1-m Mg.sub.m)Br.sub.5-z Cl.sub.z
The samples were prepared substantially according to the method described in Examples 6 except that the samples were heated at 775.degree. C. The amounts of materials used and nominal compositions of the final compounds are listed in Table 44. X-ray powder diffraction showed that Examples 44a and 44b crystallized in the same structure type as Cs.sub.3 ZnCl.sub.5. The PSL of the samples, relative to Example 6e, is listed in Table 44.
TABLE 44__________________________________________________________________________Cs.sub.3 (Zn.sub.1-m Mg.sub.m)Br.sub.5-z Cl.sub.z (m = 0.05)Ex CsBr (g) CsCl (g) ZnBr.sub.2 (g) ZnCl.sub.2 (g) MgCl.sub.2 (g) MgBr.sub.2 (g) z PSL (1)__________________________________________________________________________44a 4.3892 .3157 1.6045 -- -- .0690 .25 13510944b .3990 3.4724 -- .9710 .0357 -- 4.75 59448__________________________________________________________________________
EXAMPLE 45a-45b
Cs.sub.3 (Zn.sub.1-m Mg.sub.m)Br.sub.5-z Cl.sub.z :Eu
The samples were prepared substantially according to the method described in Examples 44. The amounts of materials used and nominal compositions of the final compounds are listed in Table 45. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in Cs.sub.3 (Zn.sub.1-m Mg.sub.m)Br.sub.5-z Cl.sub.z. X-ray powder diffraction showed that Examples 45a and 45b crystallized with the Cs.sub.3 CoCl.sub.5 structure. The PSL of Examples 45a and 45b, relative to Example 6e, are shown in Table 45.
TABLE 45__________________________________________________________________________Cs.sub.3 (Zn.sub.1-m Mg.sub.m)Br.sub.5-z Cl.sub.z : 0.01 Eu (m = 0.05)Ex CsBr (g) CsCl (g) ZnBr.sub.2 (g) ZnCl.sub.2 (g) MgCl.sub.2 (g) MgBr.sub.2 (g) EuBr.sub.2 (g) EuCl.sub.3 (g) z PSL (1)__________________________________________________________________________45a 4.3892 .3157 1.5876 -- -- .0690 .0234 -- .25 279173045b .3990 3.4724 -- .9608 .0357 -- -- .0194 4.75 1314028__________________________________________________________________________
EXAMPLES 46a-46d
Cs.sub.3 (Zn.sub.1-f Ca.sub.f)Cl.sub.5
The samples were prepared substantially according to the method described in Example 40. The amounts of materials used and nominal compositions of the final compounds are listed in Table 46. X-ray powder diffraction patterns of Examples 46a-46d showed that a major phase crystallized with the Cs.sub.3 ZnCl.sub.5 structure type. Examples 46b-46d showed extra lines which were not from the Cs.sub.3 ZnCl.sub.5 structure. The PSL of the samples relative to Example 4, is listed in Table 46.
TABLE 46______________________________________Cs.sub.3 (Zn.sub.1-f Ca.sub.f)Cl.sub.5Ex f CsCl (g) ZnCl.sub.2 (g) CaCl.sub.2 (g) PSL (1)______________________________________46a .05 3.7881 0.9710 .0416 1438446b .10 3.7881 0.9199 .0832 1150746c .25 3.7881 0.7666 .2081 2531646d .50 3.7881 0.5111 .4162 52589______________________________________
EXAMPLE 47
Cs.sub.3 (Zn.sub.1-f Ca.sub.f)Cl.sub.5 :Eu
The sample was prepared substantially according to the method described in Example 40. The amounts of materials used and nominal composition of the final compound are listed in Table 47. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in Cs.sub.3 (Zn.sub.1-f Ca.sub.f)Cl.sub.5. The PSL response of the sample, relative to Example 4, is given in Table 47.
TABLE 47______________________________________Cs.sub.3 (Zn.sub.1-f Ca.sub.f)Cl.sub.5 : 0.01 EuEx f CsCl (g) ZnCl.sub.2 (g) CaCl.sub.2 (g) EuCl.sub.3 (g) PSL (1)______________________________________47 .05 3.7881 0.9608 .0416 .0194 2767894______________________________________
EXAMPLE 48a-48d
Cs.sub.3 (Zn.sub.1-f Ca.sub.f)Br.sub.5
The samples were prepared substantially according to the method described in Example 5. The amounts of materials used and nominal compositions of the final compounds are listed in Table 48. X-ray powder diffraction showed that the major phase present in Examples 48a-48d crystallized with the Cs.sub.3 ZnBr.sub.5 structure. The PSL of the samples, relative to Example 5, is listed in Table 48.
TABLE 48______________________________________Cs.sub.3 (Zn.sub.1-f Ca.sub.f)Br.sub.5Ex f CsBr (g) ZnBr.sub.2 (g) CaBr.sub.2 (g) PSL (2)______________________________________48a .05 4.7884 1.6045 .0750 930248b .10 4.7884 1.5200 .1499 435748c .25 4.7884 1.2667 .3748 807248d .50 4.7884 0.8445 .7496 11199______________________________________
EXAMPLE 49
Cs.sub.3 (Zn.sub.1-f Ca.sub.f)Br.sub.5 :Eu
The sample was prepared substantially according to the method described in Example 5. The amounts of materials used and nominal composition of the final compound are listed in Table 49. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in Cs.sub.3 (Zn.sub.1-f Ca.sub.f)Br.sub.5. The PSL response of Example 49 is relative to Example 5.
TABLE 49______________________________________Cs.sub.3 (Zn.sub.1-f Ca.sub.f)Br.sub.5 : 0.01 EuEx f CsBr (g) ZnBr.sub.2 (g) CaBr.sub.2 (g) EuBr.sub.2 (g) PSL (2)______________________________________49 .05 4.7884 1.5876 .0750 .0234 679488______________________________________
EXAMPLE 50a-50b
Cs.sub.3 (Zn.sub.1-f Ca.sub.f)Br.sub.5-z Cl.sub.z
The samples were prepared substantially according to the method described in Example 44. The amounts of materials used and nominal compositions of the final compounds are listed in Table 50. X-ray powder diffraction showed that Examples 50a and 50b crystallized with the Cs.sub.3 CoCl.sub.5 structure. The PSL of the samples, relative to Example 6e, is listed in Table 50.
TABLE 50__________________________________________________________________________Cs.sub.3 (Zn.sub.1-f Ca.sub.f)Br.sub.5-z Cl.sub.z (f = 0.05)Ex z CsBr (g) CsCl (g) ZnBr.sub.2 (g) ZnCl.sub.2 (g) CaCl.sub.2 (g) CaBr.sub.2 (g) PSL (1)__________________________________________________________________________50a .25 4.3892 .3157 1.6045 -- -- .0750 3427950b 4.75 .3990 3.4724 -- .9710 .0416 -- 632__________________________________________________________________________
EXAMPLES 51a-51b
Cs.sub.3 (Zn.sub.1-f Ca.sub.f)Br.sub.5-z Cl.sub.z :Eu
The samples were prepared substantially according to the method described in Example 44. The amounts of materials used and nominal compositions of the final compounds are listed in Table 51. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in Cs.sub.3 (Zn.sub.1-f Ca.sub.f)Br.sub.5-z Cl.sub.z. The PSL responses, relative to Example 6e, are shown in Table 51.
TABLE 51__________________________________________________________________________Cs.sub.3 (Zn.sub.1-f Ca.sub.f)Br.sub.5-z Cl.sub.z : 0.01 Eu (f = 0.05)Ex CsBr (g) CsCl (g) ZnBr.sub.2 (g) ZnCl.sub.2 (g) CaCl.sub.2 (g) CaBr.sub.2 (g) EuBr.sub.2 (g) EuCl.sub.3 (g) z PSL (1)__________________________________________________________________________51a 4.3892 .3157 1.5876 -- -- .0750 .0234 -- .25 737924651b .3990 3.4724 -- .9608 .0416 -- -- .0194 4.75 2572468__________________________________________________________________________
EXAMPLES 52a-52d
Cs.sub.3 (Zn.sub.1-g Sr.sub.g)Cl.sub.5
The samples were prepared substantially according to the method described in Example 40. The amounts of materials used and nominal compositions of the final compounds are listed in Table 52. X-ray powder diffraction of Examples 52a-52d showed that the major phase in each case crystallized with the Cs.sub.3 ZnCl.sub.5 structure. Examples 52c and 52d showed extra lines which could not be attributed to the Cs.sub.3 ZnCl.sub.5 structure. The PSL of the samples relative to example 4 is listed in Table 52.
TABLE 52______________________________________Cs.sub.3 (Zn.sub.1-g Sr.sub.g)Cl.sub.5Ex g CsCl (g) ZnCl.sub.2 (g) SrCl.sub.2 (g) PSL (1)______________________________________52a .05 3.7881 0.9710 .0594 4652b .10 3.7881 0.9199 .1189 1150752c .25 3.7881 0.7666 .2972 3049552d .50 3.7881 0.5111 .5945 21864______________________________________
EXAMPLE 53
Cs.sub.3 (Zn.sub.1-g Sr.sub.g)Cl.sub.5 :0.01Eu
The sample was prepared substantially according to the method described in Example 40. The amounts of materials used and nominal composition of the final compound are listed in Table 53. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in Cs.sub.3 (Zn.sub.1-g Sr.sub.g)Cl.sub.5. The PSL response of the sample, relative to Example 4, is shown in Table 53.
TABLE 53______________________________________Cs.sub.3 (Zn.sub.1-g Sr.sub.g)Cl.sub.5 : 0.01 EuEx g CsCl (g) ZnCl.sub.2 (g) SrCl.sub.2 (g) EuCl.sub.3 (g) PSL (1)______________________________________53 .05 3.7881 .9608 .0594 .0194 41979______________________________________
EXAMPLES 54a-54d
Cs.sub.3 (Zn.sub.1-g Sr.sub.g)Br.sub.5
The samples were prepared substantially according to the method described in Example 5. The amounts of materials used and nominal compositions of the final compounds are listed in Table 54. X-ray powder diffraction of Examples 54a-54d showed that the major phase is each case crystallized with the same structure type as Cs.sub.3 ZnBr.sub.5. The PSL of the samples, relative to Example 5, is listed in Table 54.
TABLE 54______________________________________Cs.sub.3 (Zn.sub.1-g Sr.sub.g)Br.sub.5Ex g CsBr (g) ZnBr.sub.2 (g) SrBr.sub.2 (g) PSL (2)______________________________________54a .05 4.7884 1.6045 .0928 2854b .10 4.7884 1.5200 .1856 2054c .25 4.7884 1.2667 .4639 2154d .50 4.7884 0.8445 .9279 16______________________________________
EXAMPLE 55
Cs.sub.3 (Zn.sub.1-g Sr.sub.g)Br.sub.5 :Eu
The sample was prepared substantially according to the method described in Example 5. The amounts of materials used and nominal composition of the final compound are listed in Table 55. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in Cs.sub.3 (Zn.sub.1-g Sr.sub.g)Br.sub.5. The PSL response of the sample, relative to Example 5, is shown in Table 55.
TABLE 55______________________________________Cs.sub.3 (Zn.sub.1-g Sr.sub.g)Br: 0.01 EuEx g CsBr (g) ZnBr.sub.2 (g) SrBr.sub.2 (g) EuBr.sub.2 (g) PSL (2)______________________________________55 .05 4.7884 1.5876 .0928 .0234 41132______________________________________
EXAMPLES 56a-56b
Cs.sub.3 (Zn.sub.1-g Sr.sub.g)Br.sub.5-z Cl.sub.z
The samples were prepared substantially according to the method described in Example 44. The amounts of materials used and nominal compositions of the final compounds are listed in Table 56. X-ray powder diffraction of showed that both Examples 56a and 56b crystallized with the Cs.sub.3 CoCl.sub.5 structure. The PSL of the samples, relative to Example 6e, is listed in Table 56.
TABLE 56__________________________________________________________________________Cs.sub.3 (Zn.sub.1-g Sr.sub.g)Br.sub.5-z Cl.sub.z (g = 0.05)Ex z CsBr (g) CsCl (g) ZnBr.sub.2 (g) ZnCl.sub.2 (g) SrCl.sub.2 (g) SrBr.sub.2 (g) PSL (1)__________________________________________________________________________56a .25 4.3892 3157 1.6045 -- -- .0928 47956b 4.75 .3990 3.4724 -- .9710 .0594 -- 157__________________________________________________________________________
EXAMPLES 57a-57b
Cs.sub.3 (Zn.sub.1-g Sr.sub.g)Br.sub.5-z Cl.sub.z :Eu
The samples were prepared substantially according to the method described in Example 44. The amounts of materials used and nominal compositions of the final compounds are listed in Table 57. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in Cs.sub.3 (Zn.sub.1-g Sr.sub.g)Br.sub.5-z Cl.sub.z. The PSL responses, relative to Example 6e, are listed in Table 57.
TABLE 57__________________________________________________________________________Cs.sub.3 (Zn.sub.1-g Sr.sub.g)Br.sub.5-z Cl.sub.z : 0.01 Eu (g = 0.05)Ex CsBr (g) CsCl (g) ZnBr.sub.2 (g) ZnCl.sub.2 (g) SrCl.sub.2 (g) SrBr.sub.2 (g) EuBr.sub.2 (g) EuCl.sub.3 (g) z PSL (1)__________________________________________________________________________57a 4.3892 .3157 1.5876 -- -- .0928 .0234 -- .25 256320357b .3990 3.4724 -- .9608 .0594 -- -- .0194 4.75 1385056__________________________________________________________________________
EXAMPLES 58a-58d
Cs.sub.3 (Zn.sub.1-h Ba.sub.h)Cl.sub.5
The samples were prepared substantially according to the method described in Example 40. The amounts of materials used and nominal compositions of the final compounds are listed in Table 58. X-ray powder diffraction indicated that Examples 58a-58d crystallized in the same structure type as Cs.sub.3 ZnCl.sub.5. The PSL of the samples, relative to Example 4, is listed in Table 58.
TABLE 58______________________________________Cs.sub.3 (Zn.sub.1-h Ba.sub.h)Cl.sub.5Ex h CsCl.sub.2 (g) ZnCl.sub.2 (g) BaCl.sub.2 (g) PSL(1)______________________________________58a .05 3.7881 .9710 .0781 17261______________________________________58b .10 3.7881 .9199 .1562 2013858c .25 3.7881 .7666 .3905 4753658d .50 3.7881 .5111 .7809 60989______________________________________
EXAMPLE 59
Cs.sub.3 (Zn.sub.1-h Ba.sub.h)Cl.sub.5 :Eu
The sample was prepared substantially according to the method described in Example 40. The amounts of materials used and nominal composition of the final compound are listed in Table 59. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in Cs.sub.3 (Zn.sub.1-h Ba.sub.h)Cl.sub.5. The PSL response of the sample, relative to Example 4, is shown in Table 59.
TABLE 59______________________________________Cs.sub.3 (Zn.sub.1-h Ba.sub.h)Cl.sub.5 : 0.01 EuEx h CsCl (g) ZnCl.sub.2 (g) BaCl.sub.2 (g) EuCl.sub.3 (g) PSL (1)______________________________________59 .05 3.7881 .9608 .0781 .0194 1629459______________________________________
EXAMPLES 60a-60d
Cs.sub.3 (Zn.sub.1-h Ba.sub.h)Br.sub.5
The samples were prepared substantially according to the method described in Example 5. The amounts of materials used and nominal compositions of the final compounds are listed in Table 60. X-ray powder diffraction showed that in Examples 60a-60d the major phase crystallized in the same structure type as Cs.sub.3 ZnBr.sub.5. The PSL of the samples, relative to Example 5, is listed in Table 60.
TABLE 60______________________________________Cs.sub.3 (Zn.sub.1-h Ba.sub.h)Br.sub.5Ex h CsBr (g) ZnBr.sub.2 (g) BaBr.sub.2 (g) PSL (2)______________________________________60a .05 4.7884 1.6045 .1114 743260b .10 4.7884 1.5200 .2229 1601760c .25 4.7884 1.2667 .5572 376760d .50 4.7884 .8445 1.1143 3844______________________________________
EXAMPLE 61
Cs.sub.3 (Zn.sub.1-h Ba.sub.h)Br.sub.5 :Eu
The sample was prepared substantially according to the method described in Example 5. The amounts of materials used and nominal composition of the final compound are listed in Table 61. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in Cs.sub.3 (Zn.sub.1-h Ba.sub.h)Br.sub.5. The PSL response, relative to Example 5, is shown in Table 61.
TABLE 61______________________________________Cs.sub.3 (Zn.sub.1-h Ba.sub.h)Br.sub.5 : 0.01 EuEx h CsBr (g) ZnBr.sub.2 (g) BaBr.sub.2 (g) EuBr.sub.2 (g) PSL (2)______________________________________61 .05 4.7884 1.5876 .1114 .0234 265927______________________________________
EXAMPLES 62a-62b
Cs.sub.3 (Zn.sub.1-h Ba.sub.h)Br.sub.5-z Cl.sub.z
The samples were prepared substantially according to the method described in Example 44. The amounts of materials used and nominal compositions of the final compounds are listed in Table 62. X-ray powder diffraction showed that Examples 62a and 62b crystallized in the same structure type as Cs.sub.3 ZnCl.sub.5. The PSL of the samples, relative to Example 6e, is listed in Table 62.
TABLE 62__________________________________________________________________________Cs.sub.3 (Zn.sub.1-h Ba.sub.h)Br.sub.5-z Cl.sub.zEx h CsBr (g) CsCl (g) ZnBr.sub.2 (g) ZnCl.sub.2 (g) BaCl.sub.2 (g) BaBr.sub.2 (g) z PSL (1)__________________________________________________________________________62a .05 4.3892 .3157 1.6045 -- -- .1114 .25 37362b .05 .3990 3.4724 -- .9710 .0781 -- 4.75 493031__________________________________________________________________________
EXAMPLES 63a-63b
Cs.sub.3 (Zn.sub.1-h Ba.sub.h)Br.sub.5-z Cl.sub.z :Eu
The samples were prepared substantially according to the method described in Example 44. The amounts of materials used and nominal compositions of the final compounds are listed in Table 63. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in Cs.sub.3 (Zn.sub.1-h Ba.sub.h)Br.sub.5-z Cl.sub.z. The PSL of the samples, relative to Example 6e, is listed in Table 63.
TABLE 63__________________________________________________________________________Cs.sub.3 (Zn.sub.1-h Ba.sub.h)Br.sub.5-z Cl.sub.z : 0.01 Eu (h = 0.05)Ex CsBr (g) CsCl (g) ZnBr.sub.2 (g) ZnCl.sub.2 (g) BaCl.sub.2 (g) BaBr.sub.2 (g) EuBr.sub.2 (g) EuCl.sub.3 (g) z PSL (1)__________________________________________________________________________63a 4.3892 .3157 1.5876 -- -- .1114 .0234 -- .25 492135063b .3990 3.4724 -- .9608 .0781 -- -- 0.194 4.75 1534062__________________________________________________________________________
EXAMPLE 64
Cs.sub.3 (Zn.sub.1-m Mg.sub.m).sub.1-o (Ca.sub.f Sr.sub.g Ba.sub.h)Cl.sub.5 where o=(f+g+h)
The sample was prepared substantially according to the method described in Example 40, except that a mixture of alkaline earth halides was added by first preparing and dehydrating a mixture of alkaline earth halide under vacuum with heat. The amounts of alkaline earth halides used to prepare the mixture are shown in Table 64. The amounts of materials used and nominal composition of the final compound are listed in Table 65. X-ray powder diffraction showed that Example 64 crystallized in the same structure type as Cs.sub.3 ZnCl.sub.5. The PSL of the sample, relative to Example 4, is shown in Table 65.
TABLE 64______________________________________Preparation of Anhydrous Alkaline Earth Halide MixturesMixture 2 MgCl.sub.2 (g) CaCl.sub.2 (g) SrCl.sub.2.6H.sub.2 O (g) BaCl.sub.2.2H.sub.2 O______________________________________ (g).1071 .1249 .2779 .2748______________________________________
TABLE 65______________________________________Cs.sub.3 (Zn.sub.1-m Mg.sub.m).sub.1-o (Ca.sub.f Sr.sub.g Ba.sub.h)Cl.sub.5 where o = (f + g + h) = 0.0015 andm = 0.0005, f = 0.0005, g = 0.0005, h = 0.0005Ex CsCl (g) ZnCl.sub.2 (g) Mixture 2 (g) PSL (1)______________________________________64 3.7881 1.0201 .0021 275______________________________________
EXAMPLE 65
Cs.sub.3 (Zn.sub.1-m Mg.sub.m).sub.1-o (Ca.sub.f Sr.sub.g Ba.sub.h)Cl.sub.5 :Eu where o=(f+g+h)
The sample was prepared substantially according to the method described in Example 64. The amounts of materials used and nominal composition of the final compound are listed in Table 66. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in the compounds. The PSL of the sample, relative to Example 4, is shown in Table 66.
TABLE 66______________________________________Cs.sub.3 (Zn.sub.1-m Mg.sub.m).sub.1-o (Ca.sub.f Sr.sub.g Ba.sub.h)Cl.sub.5 : 0.01 Eu where o =(f + g + h) = 0.0015 and m = 0.0005, f = 0.0005,g = 0.0005, h = 0.0005Ex CsCl(g) ZnCl.sub.2 (g) Mixture 2 (g) EuCl.sub.3 (g) PSL (1)______________________________________65 3.7881 1.0099 .0021 .0194 332______________________________________
EXAMPLE 66
Cs.sub.3 (Zn.sub.1-m Mg.sub.m).sub.1-o (Ca.sub.f Sr.sub.g Ba.sub.h)Br.sub.5 where o=(f+g+h)
The sample was prepared substantially according to the method described in Example 5, except that a mixture of alkaline earth halides was added by first preparing and dehydrating a mixture of alkaline earth halide under vacuum with heat. The amounts of alkaline earth halides used to prepare the mixture are shown in Table 67. The amounts of materials used and nominal composition of the final compound are listed in Table 68. X-ray powder diffraction showed that Example 66 crystallized in the same structure type as Cs.sub.3 ZnBr.sub.5. The PSL response, relative to Example 5, is shown in Table 66.
TABLE 67______________________________________Preparation of Anhydrous Alkaline Earth Halide Mixtures______________________________________Mixture 2: .2072 grams .2654 grams .2784 grams .3748 grams MgBr.sub.2 CaBr.sub.2 :2H.sub.2 O SrBr.sub.2 BaBr.sub.2 :2H.sub.2 O______________________________________
TABLE 68______________________________________Cs.sub.3 (Zn.sub.1-m Mg.sub.m).sub.1-o (Ca.sub.f Sr.sub.g Ba.sub.h)Br.sub.5 where o = (f = g + h) =0.0015 and m = 0.0005, f = 0.0005, g = 0.0005, h = 0.0005Ex CsBr (g) ZnBr.sub.2 (g) Mixture 2 (g) PSL (2)______________________________________66 4.7882 1.6855 .0035 46______________________________________
EXAMPLE 67
Cs.sub.3 (Zn.sub.1-m Mg.sub.m).sub.1-o (Ca.sub.f Sr.sub.g Ba.sub.h)Br.sub.5 :Eu where o=(f+g+h) and m=0.0005
The sample was prepared substantially according to the method described in Example 66. The amounts of materials used and nominal composition of the final compound are listed in Table 69. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in the compounds. The PSL response, relative to Example 5, is shown in Table 69.
TABLE 69______________________________________Preparation of Cs.sub.3 (Zn.sub.1-m Mg.sub.m).sub.1-o (Ca.sub.f Sr.sub.gBa.sub.h)Br.sub.5 : 0.01 Eu whereo = (f + g + h) = 0.0015 and m = 0.0005, f = 0.0005,g = 0.0005, h = 0.0005Ex CsBr (g) ZnBr.sub.2 (g) Mixture 2 (g) EuBr.sub.2 (g) PSL (2)______________________________________67 4.7882 1.6686 .0035 .0234 237558______________________________________
EXAMPLES 68a-68b
Cs.sub.3 (Zn.sub.1-m Mg.sub.m).sub.1-o (Ca.sub.f Sr.sub.g Ba.sub.h)Br.sub.5-z Cl.sub.z :0.01Eu where o=(f+g+h) and m=0.0005
The samples were prepared substantially according to the method described in Example 44, except that a mixture of alkaline earth halides was substituted for the individual of alkaline earth halide compound. The addendum mixture was prepared in advance by dehydrating a mixture of alkaline earth halide under vacuum with heat. The amounts of alkaline earth halides used to prepare the mixture are shown in Table 70. The amounts of materials used and nominal compositions of the final compounds are listed in Table 71. X-ray powder diffraction showed that Examples 68a and 68b crystallized in the same structure type as Cs.sub.3 ZnCl.sub.5. The PSL of the samples, relative to Example 6e, is listed in Table 71.
TABLE 70______________________________________Preparation of Anhydrous Alkaline Earth Halide Mixtures (Mixture 3and Mixture 4)______________________________________Mixture 3: .2072 grams .2654 grams .2784 grams .3748 grams MgBr.sub.2 CaBr.sub.2.2H.sub.2 O SrBr.sub.2 BaBr.sub.2.2H.sub.2 OMixture 4: .1071 grams .1249 grams .2779 grams .2748 grams MgCl.sub.2 CaCl.sub.2 SrCl.sub.2.6H.sub.2 O BaCl.sub.2.2H.sub.2 O______________________________________
TABLE 71__________________________________________________________________________Cs.sub.3 (Zn.sub.1-m Mg.sub.m).sub.1-o (Ca.sub.f Sr.sub.g Ba.sub.h)Br.sub.5-z Cl.sub.z where o = (f + g + h) = 0.0015and m = 0.0005, f = 0.0005, g = 0.0005, h = 0.0005Ex CsBr (g) CsCl (g) ZnBr.sub.2 (g) ZnCl.sub.2 (g) Mixture #3 (g) Mixture #4 (g) z PSL (1)__________________________________________________________________________68a 4.3892 .3157 1.6855 -- .0035 -- .25 7844068b .3990 3.4724 -- 1.0201 -- .0021 4.75 38__________________________________________________________________________
EXAMPLE 69a-69b
Cs.sub.3 (Zn.sub.1-m Mg.sub.m).sub.1-o (Ca.sub.f Sr.sub.g Ba.sub.h)Br.sub.5-z Cl.sub.z :Eu where o=(f+g+h) and m=0.0005
The samples were prepared substantially according to the method described in Examples 68a-68b, except that Eu was added as an activator cation. The amounts of materials used and nominal compositions of the final compounds are listed in Table 72. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in the compounds. The PSL responses, relative to Example 6e, are listed in Table 72.
TABLE 72__________________________________________________________________________Cs.sub.3 (Zn.sub.1-m Mg.sub.m).sub.1-o (Ca.sub.f Sr.sub.g Ba.sub.h)Br.sub.5-z Cl.sub.z : 0.01 Eu whereo = (f + g + h) = 0.0015 and m = 0.0005, f = 0.0005, g = 0.0005, h =0.0005Ex CsBr (g) CsCl (g) ZnBr.sub.2 (g) ZnCl.sub.2 (g) Mixture #3 (g) Mixture #4 (g) z PSL (1)__________________________________________________________________________69a 4.3892 .3157 .6686 -- 0035 -- .25 112904569b .3990 3.4724 -- 1.0099 -- .0021 4.75 1195904__________________________________________________________________________
EXAMPLE 70
(Cs.sub.1-r Rb.sub.r).sub.3-n (Zn.sub.1-m Mg.sub.m).sub.1-o (Li.sub.a Na.sub.b K.sub.c)(Ca.sub.f Sr.sub.g Ba.sub.h)Cl.sub.5 where n=(a+b+c), o=(f+g+h)
The sample was prepared substantially according to the method described in Example 64, except that the alkali metal halides were added in addition to the alkaline earth metal halides. The alkali metal halide mixtures were prepared by the methods described in Example 38. The amounts used to prepare the alkali halide mixtures are shown in Table 73. The amounts of materials used and nominal composition of the final compound are listed in Table 74. In table 74, mixture 2 refers to mixture 2 from example 64. X-ray powder diffraction showed that Example 70 crystallized in the same structure type as Cs.sub.3 ZnCl.sub.5. The PSL response, relative to Example 4, is given in Table 74.
TABLE 73______________________________________Preparation of Anhydrous Alkali Halide MixturesMixture 1 LiCl (g) NaCl (g) KCl (g) RbCl (g)______________________________________ .0477 .0657 .0839 .1360______________________________________
TABLE 74______________________________________(Cs.sub.1-r Rb.sub.r).sub.3-n (Zn.sub.1-m Mg.sub.m).sub.1-o (Li.sub.aNa.sub.b K.sub.c)(Ca.sub.f Sr.sub.g Ba.sub.h)Cl.sub.5 wherer = .0005, n = (a + b + c) = 0.0045, a = 0.0015, b = 0.0015,c = 0.0015, m = 0.0005, o = (f + g + h) = 0.0015, and f = 0.0005,g = 0.0005, h = 0.0005 Mixture 1 Mixture 2Ex CsCl (g) ZnCl.sub.2 (g) (g) (g) PSL (1)______________________________________70 3.7805 1.0201 .0033 .0021 1102417______________________________________
EXAMPLE 71
(Cs.sub.1-r Rb.sub.r).sub.3-n (Zn.sub.1-m Mg.sub.m).sub.1-o-j (Li.sub.a Na.sub.b K.sub.c)(Ca.sub.f Sr.sub.g Ba.sub.h)Cl.sub.5 :jEu where r=0.0005, n=(a+b+c), m=0.0005, o=(f+g+h), j=0.01
The sample was prepared substantially according to the method described in Example 70. The amounts of materials used and nominal composition of the final compound are listed in Table 75. In table 75 mixture 1 refers to mixture 1 from example 70 and mixture 2 refers to mixture 2 from example 64. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in the compounds. The PSL response, relative to Example 4, is given in Table 75.
TABLE 75______________________________________(Cs.sub.1-r Rb.sub.r).sub.3-n (Zn.sub.1-m Mg.sub.m).sub.1-o-0.01 (Li.sub.a Na.sub.b K.sub.c)(Ca.sub.f Sr.sub.g Ba.sub.h)Cl.sub.5 : 0.01 Euwhere r = .0005, n = (a + b + c) = 0.0045, a = 0.0015, b = 0.0015,c = 0.0015, m = 0.0005, o = (f + g + h) = 0.0015, and f = 0.0005,g = 0.0005, h = 0.0005, j = 0.01 CsCl MixtureEx (g) ZnCl.sub.2 (g) 1 (g) Mixture 2 (g) EuCl.sub.3 (g) PSL (1)______________________________________71 3.7805 1.0099 .0033 .0021 .0194 888032______________________________________
EXAMPLE 72
(Cs.sub.1-r Rb.sub.r).sub.3-n (Zn.sub.1-m Mg.sub.m).sub.1-o (Li.sub.a Na.sub.b K.sub.c)(Ca.sub.f Sr.sub.g Ba.sub.h)Br.sub.5 where r=0.0005, n=(a+b+c), m=0.0005, o=(f+g+h)
The sample was prepared substantially according to the method described in Example 66 except that the alkali metal halides were added in addition to the alkaline earth metal halides. The alkali metal halide mixtures were prepared by the methods described in Example 38. The amounts used to prepare the alkali halide mixtures are shown in Table 76. The amounts of materials used and nominal composition of the final compound are listed in table 77. In table 77 mixture 2 refers to mixture 2 from example 66 and mixture 1 refers to mixture 1 from example 72 as described in table 76. X-ray powder diffraction showed that Example 72 crystallized in the same structure type as Cs.sub.3 ZnBr.sub.5. The PSL response, relative to Example 5, is given in Table 77.
TABLE 76______________________________________Preparation of Anhydrous Alkali Halide MixturesMixture 1 LiBr (g) NaBr (g) KBr (g) RbBr (g)______________________________________ .0977 .1158 .1339 .1860______________________________________
TABLE 77______________________________________(Cs.sub.1-r Rb.sub.r).sub.3-n (Zn.sub.1-m Mg.sub.m).sub.1-o (Li.sub.aNa.sub.b K.sub.c)(Ca.sub.f Sr.sub.g Ba.sub.h)Br.sub.5 wherer = .0005, n = (a + b + c) = 0.0045, a = 0.0015, b = 0.0015,c = 0.0015, m = 0.0005, o = (f + g + h) = 0.0015, and f = 0.0005,g = 0.0005, h = 0.0005Ex CsBr (g) ZnBr.sub.2 (g) Mixture 1 (g) Mixture 2 (g) PSL (2)______________________________________72 4.7786 1.6855 .0053 .0035 14171______________________________________
EXAMPLE 73
(Cs.sub.1-r Rb.sub.r).sub.3-n (Zn.sub.1-m Mg.sub.m).sub.1-o-j (Li.sub.a Na.sub.b K.sub.c)(Ca.sub.f Sr.sub.g Ba.sub.h)Br.sub.5 :jEu where r=0.0005, n=(a+b+c), m=0.0005, o=(f+g+h)
The sample was prepared substantially according to the method described in Example 72. The amounts of materials used and nominal composition of the final compound are listed in Table 78. In table 78 mixture 1 refers to mixture 1 from example 72 and mixture 2 refers to mixture 2 from example 66. The stoichiometry of the compounds was calculated assuming that Eu2+ substitutes for Zn.sup.2+ in the compounds. The PSL response, relative to Example 5, is given in Table 78.
TABLE 78______________________________________(Cs.sub.1-r Rb.sub.r).sub.3-n (Zn.sub.1-m Mg.sub.m).sub.1-o-0.01 (Li.sub.a Na.sub.b K.sub.c)(Ca.sub.f Sr.sub.g Ba.sub.h)Br.sub.5 : 0.01 Euwhere r = .0005, n = (a + b + c) = 0.0045, a = 0.0015, b = 0.0015,c = 0.0015, m = 0.0005, o = (f + g + h) = 0.0015, and f = 0.0005,g = 0.0005, h = 0.0005, j = 0.01 CsBr MixtureEx (g) ZnBr.sub.2 (g) 1 (g) Mixture 2 (g) EuBr.sub.2 (g) PSL (2)______________________________________73 4.7786 1.6686 .0053 .0035 .0234 164266______________________________________
EXAMPLE 74a-74b
(Cs.sub.1-r Rb.sub.r).sub.3-n (Zn.sub.1-m Mg.sub.m).sub.1-o (Li.sub.a Na.sub.b K.sub.c)(Ca.sub.f Sr.sub.g Ba.sub.h)Br.sub.5-z Cl.sub.z where r=0.0005, n=(a+b+c), m=0.0005, o=(f+g+h), z=0.025 or 4.75
The samples were prepared substantially according to the method described in Example 68 except that a mixture of alkali metal halides were added in addition to the alkaline earth metal halide mixture and the samples were heated at 700.degree. C. The alkaline earth metal halide mixtures were prepared according the method described in Example 68. The alkali halide mixture were prepared as described in example 38 The amounts of materials used and nominal compositions of the final compounds are listed in Table 79. In table 79 mixture 1 and 2 refer to mixtures 1 and 2 prepared according to example 38. In table 79 mixtures 3 and 4 refer to mixtures 3 and 4 from example 68. X-ray powder diffraction showed that Examples 74a and 74b crystallized in the same structure type as Cs.sub.3 ZnCl.sub.5. The PSL of the samples, relative to Example 6e, is listed in Table 79.
TABLE 79__________________________________________________________________________Cs.sub.3-n Li.sub.a Na.sub.b K.sub.c Rb.sub.d Zn.sub.1-m Mg.sub.eCa.sub.f Sr.sub.g Ba.sub.h Br.sub.5-z Cl.sub.z wheren = (a + b + c + d) = 0.006 and m = (e + f + g + h) = 0.002Ex CsCl (g) CsBr (g) ZnBr.sub.2 (g) ZnCl.sub.2 (g) Mixture #3 (g) Mixture #1 (g) Mixture #4 (g) Mixture #2 (g) z PSL__________________________________________________________________________ (1)74a .3157 4.3796 1.6855 -- .0035 .0053 -- -- .25 42174b 3.4648 .3990 -- 1.0201 -- -- .0021 .0033 4.75 38__________________________________________________________________________
EXAMPLES 75a-75b
(Cs.sub.1-r Rb.sub.r).sub.3-n (Zn.sub.1-m Mg.sub.m).sub.1-o-j (Li.sub.a Na.sub.b K.sub.c)(Ca.sub.f Sr.sub.g Ba.sub.h)Br.sub.5-z Cl.sub.z :jEu where r=0.0005, n=(a+b+c), a=0.0015, b=0.0015, c=0.0015, m=0.0005, o=(f+g+h), and f=0.0005, g=0.0005, h=0.0005, j=0.01, z=0.25 or 4.75
The samples were prepared substantially according to the method described in Examples 74, except that Eu was added as an activator cation. The amounts of materials used and nominal compositions of the final compounds are listed in Table 80. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in the compounds. The PSL of the samples, relative to Example 6e, is listed in Table 80.
TABLE 80__________________________________________________________________________(Cs.sub.1-r Rb.sub.r).sub.3-n (Zn.sub.1-m Mg.sub.m).sub.1-o-0.01 (Li.sub.a Na.sub.b K.sub.c)(Ca.sub.f Sr.sub.g Ba.sub.h)Br.sub.5-z Cl.sub.z : 0.01Eu wherer = .0005, n = (a + b + c), a = 0.0015, b = 0.0015, c = 0.0015, m =0.0005,o = (f + g + h), and f = 0.0005, g = 0.0005, h = 0.0005, j = 0.01, z =0.25 or 4.75 Mixture MixtureEx CsCl (g) CsBr (g) ZnBr.sub.2 (g) ZnCl.sub.2 (g) Mixture #3 (g) Mixture #1 (g) #4 (g) #2 (g) EuCl.sub.3 EuBr.sub.2 (g) z PSL__________________________________________________________________________ (1)75a .3157 4.3796 1.6686 -- .0035 .0053 -- -- -- .0234 .25 25786475b 3.4648 .3990 -- 1.0099 -- -- .0021 .0033 .0194 -- 4.75 7653324__________________________________________________________________________
EXAMPLE 76
Cs.sub.3 ZnBr.sub.5-i I.sub.i :Eu
The samples were prepared substantially according to the method described in Examples 6. The amounts of materials used and nominal composition of the final compound are listed in Table 81. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in Cs.sub.3 ZnBr.sub.5-i I.sub.i. X-ray powder diffraction showed that Example 76 crystallized with the Cs.sub.3 CoCl.sub.5 structure type. The PSL response, relative to Example 6e, is reported in Table 81.
TABLE 81______________________________________Cs.sub.3 ZnBr.sub.5-z I.sub.z : 0.005 EuExample z CsI (g) ZnBr.sub.2 (g) CsBr (g) EuBr.sub.2 (g) PSL (1)______________________________________76 .25 .4871 1.6805 4.3892 .0117 37830______________________________________
EXAMPLE 77
Cs.sub.3 ZnBr.sub.5-z-i Cl.sub.z I.sub.i :Eu
The samples were prepared substantially according to the method described in Examples 6. The amounts of materials used and nominal composition of the final compound are listed in Table 82. The stoichiometry of the compounds was calculated assuming that Eu.sup.2+ substitutes for Zn.sup.2+ in Cs.sub.3 ZnBr.sub.5-z-i Cl.sub.z I.sub.i. X-ray ray powder diffraction showed that Example 77 crystallized with the Cs.sub.3 CoCl.sub.5 structure type. The PSL response, relative to Example 6e, is shown in Table 82.
TABLE 82______________________________________ CsCl EuBr.sub.2Ex z i (g) CsI (g) ZnBr.sub.2 (g) CsBr (g) (g) PSL (1)______________________________________77 .25 .25 .3157 .4871 1.6805 3.9902 .0117 59757______________________________________
EXAMPLE 78
Average refractive index of Cs.sub.3 ZnCl.sub.5
The average refractive index of the Cs.sub.3 ZnCl.sub.5 phosphor of Example 4 was measured as a function of wavelength using the methods previously described. Results are given in Table 83.
TABLE 83______________________________________The average refractive index of Cs.sub.3 ZnCl.sub.5Wavelength (anstroms) refractive index______________________________________6500 1.5876000 1.5915500 1.5975000 1.6034500 1.610______________________________________
EXAMPLE 79
Average refractive index of Cs.sub.3 ZnBr.sub.5
The average refractive index of the Cs.sub.3 ZnBr.sub.5 phosphor of Example 5 was measured as a function of wavelength using the methods previously described. Results are given in Table 84.
TABLE 84______________________________________The average refractive index of Cs.sub.3 ZnBr.sub.5wavelength (angstroms) refractive index______________________________________6500 1.6656000 1.6705500 1.6775000 1.6864500 1.700______________________________________
EXAMPLES 80a-80b
The average refractive index of the Cs.sub.3 ZnBr.sub.5-z Cl.sub.z :Eu phosphor of Examples 9g and 9o was measured as a function of wavelength using the methods previously described. Results are given in Tables 85 and 86, respectively.
TABLE 85______________________________________Refractive index as a function of wavelength for Cs.sub.3 ZnBr.sub.5-zCl.sub.z : Euwhere z = .25wavelength(angstroms) refractive index______________________________________6500 1.6606000 1.6645500 1.6735000 1.6844500 1.695______________________________________
TABLE 86______________________________________Refractive index as a function of wavelength for Cs.sub.3 ZnBr.sub.5-zCl.sub.z : Euwhere z = 4.75wavelength(angstroms) refractive index______________________________________6500 1.5926000 1.5955500 1.5995000 1.6054500 1.615______________________________________
EXAMPLE 81
The average refractive index of the Rb.sub.3 ZnCl.sub.5 phosphor of Example 28d was measured using the methods previously described. The average refractive index of Rb.sub.3 ZnCl.sub.5 is 1.575 at 600 nm and is 1.571 at 650 nm.
EXAMPLE 82
The average refractive index of the Rb.sub.3 ZnBr.sub.5 phase of example B10d was determined at 600 nm and 650 nm. The refractive index of the uniaxial phase of Rb.sub.3 ZnBr.sub.5 is 1.648 at 600 nm and is 1.643 at 650 nm.
EXAMPLE 83.1-83.34
(Cs.sub.1-r Rb.sub.r).sub.3-n+v (Zn.sub.1-m Mg.sub.m).sub.1-o-j (Li.sub.a Na.sub.b K.sub.c)(Ca.sub.f Sr.sub.g Ba.sub.h)Br.sub.5-z+v Cl.sub.z :Eu where r=0, n=(a+b+c)=0, m is variable, o=(f+g+h)=0, z=0, j is variable
Examples 83.1 through 83.34 were prepared substantially according to the method described in Example 43 except that the value of v, m and j for each sample are as listed in Table 87. The PSL of each sample, given in units of 100.times. (PMT peak volts/rem exposure) is listed in table 87.
TABLE 87______________________________________ RelativeEx response v j m______________________________________83.1 .007 -.20 .0025 0.000083.2 .0453 -.15 .0214 .011883.3 .0221 -.15 .0072 .047183.4 1.9333 -.01 .0072 .011883.5 .3919 -.01 .0214 .047183.6 .0081 -.01 .0214 .011883.7 38.4167 .07 .0135 .043283.8 41.1167 .13 .0119 .035383.9 119.88 .18 .0025 .058983.10 100.55 .27 .0072 .047183.11 160.2667 .36 .0083 .087783.12 425.1 .46 .0025 .094283.13 236.467 .51 .0020 .138783.14 311.7333 .54 .0088 .125683.15 505.6 .65 .0025 .127183.16 369.167 .71 .0098 .127983.17 138.3 .75 .0001 .148783.18 418.26 .75 .0107 .163083.19 538.18 .77 .0054 .150383.20 624.54 .79 .0036 .142683.21 516.033 .83 .0063 .180183.22 617.63 .83 .0049 .154883.23 489.72 .85 .0065 .156883.24 417.7 .87 .0035 .137783.25 595.16 .88 .0010 .134983.26 423.67 .91 .0017 .147783.27 553.53 .92 .0011 .151083.28 528.4 .93 .0111 .168483.29 512.3 .97 .0049 .179483.30 781.57 .98 .0009 .143383.31 539.4 1.06 .0070 .198383.32 444.47 1.06 .0028 .224583.33 595.01 1.16 .0083 .240883.34 453.4 1.16 .0058 .2100______________________________________
While specific embodiments of the invention have been shown and described herein for purposes of illustration, the protection afforded by any patent which may issue upon this application is not strictly limited to a disclosed embodiment; but rather extends to all modifications and arrangements which fall fairly within the scope of the claims which are appended hereto:

Number	Name	Date
4637898	DeBoer et al.	Jan 1987
4780376	Nakamura	Oct 1988
5028509	Shimada et al.	Jul 1991

Cesium-zinc halide phosphors, phosphor screens, and preparation methods

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