Patent Application
20110147661
The present invention relates to persistent phosphors having a long decay period, and in particular, to persistent phosphor compositions based on (Ba,Sr,Ca,K,Na)3(Al,B,Ga,Co,Zn,Sc)10-x(Si,Ge)1+xO20-xNx:Eu2+, Er3+ and techniques for the manufacture and use of such phosphors.
A phosphor is a luminescent material that absorbs radiation energy in one portion of the electromagnetic spectrum and emits energy in another portion of the electromagnetic spectrum. One important class of phosphors includes crystalline inorganic compounds of very high chemical purity and of controlled composition, to which small quantities of other elements, called “activators,” have been added for fluorescent emission. With the right combination of activators and inorganic compounds, the color of the emission of these crystalline phosphors can be controlled. Most useful and well-known phosphors emit radiation in the visible portion of the electromagnetic spectrum in response to excitation by electromagnetic energy outside the visible range. Well known phosphors have been used in mercury vapor discharge lamps to convert the ultraviolet (UV) radiation emitted by the excited mercury to visible light. Other phosphors are capable of emitting visible light upon being excited by electrons, useful in photomultiplier tubes, or X-rays, such as scintillators used in imaging systems.
One important property of phosphors is the decay time, e.g., the time required for the phosphor to stop emitting light after the excitation is removed. Most phosphor compositions have extremely short decay times, with most of the stored energy emitted as light within seconds, or even a small fraction of a second after excitation ends. These phosphors may be useful in lighting type applications where continuous excitation is present. However, in many applications it would be worthwhile to have a phosphorescent material that continues to emit light for long periods of time after excitation has ended.
Persistent phosphors based on Sr3Al10SiO20 and doped with Ho3+, have been developed and commercialized to provide a blue persistent phosphor that has found wide application in both the aesthetic and functional markets, including, but not limited to entertainment, safety and emergency lighting and in exit signage. The applications of these materials are limited mainly due to their initial intensity and length of persistence as these materials have a relatively low initial intensity and decay relatively quickly.
Accordingly, it would be beneficial to provide a blue persistent phosphor having a higher initial intensity and slower rate of decay as compared to the prior art aluminosilicate based blue persistent phosphor materials. It would also be beneficial to provide methods of making these blue persistent phosphors as well as articles utilizing such persistent phosphors.
The present invention provides blue persistent phosphor materials having a higher initial intensity, a slower rate of decay and/or longer length of persistence. These phosphors are based on aluminosilicate that have been activated by the addition of combinations of lanthanoid metals, such as, but not limited to, europium, erbium, holmium, dysprosium, and neodymium. These phosphors have a higher initial intensity, a slower rate of decay and/or longer length of persistence as compared to the prior art.
Accordingly, in one aspect, the present invention provides a material including a phosphor having a general formula of, A3M10-xC1+x(O20-xNx):Eu, RE wherein A may be strontium (Sr), calcium (Ca), barium (Ba), potassium (K) or sodium (Na), or a combination thereof, M may be aluminum (Al), boron (B), zinc (Zn), cobalt (Co), gallium (Ga), scandium (Sc) or a combination thereof, and C may be silicon (Si) or germanium (Ge) or a combination thereof; x is between 0.001 and 5.0; and RE is dysprosium (Dy), neodymium (Nd), erbium (Er), holmium (Ho), terbium (Tm), ytterbium (Yb), samarium (Sm) or a combination thereof.
In another aspect, the present invention provides a method for producing a phosphor, the method including the steps of providing amounts of an oxy-nitride-containing compounds of europium, RE, at least one alkali metal or alkaline-earth metal selected from the group consisting of Ba, Sr, Ca, K, Na and combinations thereof, at least one metal or metalloid selected from the group consisting of Al, B, Zn, Co, Ga, Sc and combinations thereof, and at least one metalloid selected from the group consisting of Si, Ge and combinations thereof, wherein RE is at least one of Dy, Nd, Er, Ho, Tm, Yb, Sm or a combination thereof; mixing together the oxy-nitride-containing compounds to form a mixture; and then firing the mixture at a temperature between about 900° C. and about 1700° C. under a reducing atmosphere for a sufficient period of time to convert the mixture to a phosphor having a general formula of, A3M10-xC1+x(O20-xNx):Eu, RE wherein A may be Ba, Sr, Ca, K, Na or a combination thereof, M may be Al, B, Zn, Co, Ga, Sc or a combination thereof, and C may be Si or Ge or a combination thereof; x is between 0.001 and 5.0; and RE is Dy, Nd, Er, Ho, Tm, Yb, Sm or a combination thereof.
In yet another aspect, the present invention provides an article of manufacture containing a phosphor, including a structure; and a phosphor having a general formula of A3M10-xC1+x(O20-xNx):Eu, RE wherein A may be Ba, Sr, Ca, K, Na or a combination thereof, M may be Al, B, Zn, Co, Ga, Sc or a combination thereof, and C may be Si or Ge or a combination thereof; x is between 0.001 and 5.0; and RE is Dy, Nd, Er, Ho, Tm, Yb, Sm or a combination thereof.
These and other features, aspects, and advantages of the present techniques will become better understood when the following detailed description is read with reference to the accompanying drawings in which like characters represent like parts throughout the drawings, wherein:
The present invention is more particularly described in the following description and example that are intended to be illustrative only since numerous modifications and variations therein will be apparent to those skilled in the art. As used in the specification and in the claims, the term “comprising” may include the embodiments “consisting of” and “consisting essentially of.” All ranges disclosed herein are inclusive of the endpoints and are independently combinable. The endpoints of the ranges and any values disclosed herein are not limited to the precise range or value; they are sufficiently imprecise to include values approximating these ranges and/or values.
As used herein, approximating language may be applied to modify any quantitative representation that may vary without resulting in a change in the basic function to which it is related. Accordingly, a value modified by a term or terms, such as “about” and “substantially,” may not be limited to the precise value specified, in some cases. In at least some instances, the approximating language may correspond to the precision of an instrument for measuring the value.
The present invention addresses the problems of prior art materials and provides blue persistent phosphor materials having a higher initial intensity, a slower rate of decay and/or longer length of persistence. These phosphors are based on oxy-nitrides of aluminosilicates activated by the addition of combinations of lanthanoid metals, such as europium, dysprosium, neodymium, erbium, holmium, terbium, ytterbium, samarium or a combination thereof. In select embodiments, the phosphors are based on oxides or oxy-nitrides of aluminosilicates activated by the addition of europium and erbium.
The phosphors contained in embodiments of the present techniques may have a general formula of, A3M10-xC1+x(O20-xNx):Eu, RE wherein A may be Ba, Sr, Ca, K, Na or a combination thereof, M may be Al, B, Zn, Co, Ga, Sc or a combination thereof, and C may be Si or Ge or a combination thereof; x is between 0.001 and 5.0; and RE is Dy, Nd, Er, Ho, Tm, Yb, Sm or a combination thereof. Select embodiments utilize Sr, Al and Si. Other select embodiments utilize Sr, Si and a combination of Al and B. Phosphors made according to this formulation have a blue luminescence and a longer persistence than other types of phosphors.
The phosphors of the present invention are based on aluminosilicates wherein a small portion of the oxide component has been replaced by a nitride component. It has been found that these oxy-nitride embodiments provide better results than the oxide-based prior art phosphors. The amount of nitride substituted for oxide is relatively small, but the use of the nitride helps provide a phosphor having a higher initial intensity, a slower rate of decay and/or longer length of persistence as compared to oxide-based prior art phosphors. In one embodiment, the amount of nitride substituted for oxide is from 0.001 to 5.0 moles. In another embodiment, the amount of nitride substituted for oxide is from 0.001 to 3.0 moles. In still another embodiment, the amount of nitride substituted for oxide is from 0.001 to 2.0 moles.
The phosphors of the present invention are activated as per prior art phosphor materials using one or more lanthanoid metals. In one embodiment, europium is used along with erbium as the lanthanoid metals.
The phosphors of the present invention may be made using various techniques. In one embodiment, they may be made into particles of about 1 to 20 microns, or larger, using standard firing techniques.
The benefits of an oxy-nitride persistent phosphor may be seen in
The benefits of incorporating boron into the persistent phosphor, both oxide and oxy-nitride embodiments, may be seen in
The persistent phosphors of the present techniques may be used in any number of applications requiring long term light in locations that have no energy source for powered lighting. In embodiments of the present techniques a plastic matrix may contain embedded particles of a persistent phosphor. In other embodiments, the phosphor particles may be incorporated into the plastic matrix of a film or surface layer attached to the body of a structure. In either of these embodiments, incorporation of the phosphor particles into the matrix or surface layer may be implemented using normal plastics processing techniques. Such techniques could include compression molding, injection molding, sheet forming, film blowing, or any other plastics processing technique that can incorporate a dry powder into a plastic matrix. One skilled in the art will recognize that the plastic matrix material used in these techniques may be any thermoplastic material with sufficient translucency to allow light transfer through thin layers, including, but not limited to, polystyrene, high impact polystyrene (HIPS), styrene-butadiene copolymers, polycarbonate, polyethylene, polyurethane, polyethylene terephthalate (PET), polyethylene terephthalate glycol (PETG), and polypropylene, among others. Furthermore, thermoset materials may also be used for the plastic matrix, including such compounds as silicon room temperature vulcanized (RTV) compounds and epoxies, among others. In embodiments, the phosphors are incorporated into the thermoset resins by mixing the phosphor with one of the two reactant portions. Further, the matrix does not need to be plastic. One of ordinary skill in the art will recognize that the phosphors of the present techniques may be incorporated into glass or ceramic matrices as well. Other applications include use in paints, tapes or other substrates such as textiles.
Particles of the phosphor may lack compatibility with the matrix leading to agglomeration during processing. This effect may be especially severe for smaller particles, such as nano-scale particles. For both types of phosphor particles, this effect may be lessened by coating the particles prior to incorporation in the matrix. The coating may include either small molecule ligands or polymeric ligands. Exemplary small molecule ligands may include octyl amine, oleic acid, trioctylphosphine oxide, or trialkoxysilane. Those skilled in the art will realize that other small molecule ligands may be used in addition to, or in place of, those listed here. The particles may also be coated with polymeric ligands, which may be either synthesized from the surface of the particles or added to the surface of the nano-scale particles.
In one embodiment, a particle is coated by growing polymer chains from the surface of the particle. In this embodiment, the particle may be functionalized by the addition of polymer initiation compounds to form polymer initiation sites on the particle. In certain embodiments, such polymer initiation compounds may include amines, carboxylic acids, or alkoxy silanes, among others. Those skilled in the art will recognize that other polymer initiation compounds may work in addition to, or in place of, those listed here. Once the particle has been functionalized with the initiation compounds, monomers may be added to the solution to grow polymeric or oligomeric chains from the initiation sites. The final size of the shell that is formed around the particle will depend on the number of initiation sites and the amount of monomer added to the solution. Those skilled in the art will recognize that these parameters may be adjusted for the results selected.
In an alternative embodiment, a particle is coated with a polymer. In this embodiment, the polymer chain may be chosen to interact with the particle, and may include random copolymers and block copolymers. In the latter embodiment, one monomer chain may be chosen to interact with the particle, while the other may be chosen to interact with the matrix. In certain embodiments, the polymer coating may include such groups as amines, carboxylic acids, and alkoxy silanes, among others. One of ordinary skill in the art will recognize that other functional groups may also be effective.
Fixing mixtures of precursor powders under a reducing atmosphere may produce the persistent phosphors of the present invention in various manners. In one embodiment, the persistent phosphors may be produced by mixing powders or co-precipitated mixtures of oxygen-containing compounds of europium, dysprosium, neodymium, erbium, holmium, terbium, ytterbium, samarium, an alkali metal or alkaline-earth metal, one or more group metal or metalloid elements, nitrogen-containing compounds and other metal oxygen-containing compounds, in accordance with the formulations shown above, and then firing the mixture under a reducing atmosphere. The oxygen-containing compounds may be but are not limited to, oxides, carbonates, nitrates, citrates, carboxylates, or combinations of these compounds. The nitrogen-containing compounds are solid nitrides.
In other embodiments, the mixture of starting materials for producing the phosphor may also include a flux. The flux, for example, may include materials such as, but not limited to, lithium tetraborate, lithium carbonate, boron oxide, or a mixture of these compounds.
The oxygen-containing compounds and the nitrogen-containing compounds may be mixed together by any appropriate mechanical method or chemical method. In one embodiment, such methods may include stirring or blending the powders in a high-speed blender, ball mill or a ribbon blender. Those skilled in the art will recognize that any number of other techniques may be used to make a well-blended mixture of powders.
The mixture of oxide powders and nitride powders may be fired in a reducing atmosphere at a temperature in a range from about 900° C. to about 1,700° C. for a time sufficient to convert the mixture to the phosphor. In one embodiment the temperature may be in the range from about 1300° C. to about 1700° C. The firing may be conducted in a batch or continuous process, beneficially with stirring or mixing to promote good gas-solid contact. The firing time required may range from about one minute to ten hours, depending on the amount of the mixture being fired, the extent of contact between the solid and the gas of the atmosphere, and the degree of mixing while the mixture is fired or heated. The mixture may rapidly be brought to and held at the final temperature, or the mixture may be heated to the final temperature at a lower rate such as from about 1° C./minute to about 200° C./minute. In select embodiments, the temperature is raised to the final temperature at rates of about 3° C./minute to about 25° C./minute.
The firing is performed under a reducing atmosphere, which may include such compounds as hydrogen, carbon monoxide, ammonia, or a mixture of these compounds with an inert gas such as nitrogen, helium, argon, krypton, xenon, or a mixture thereof. In one embodiment, a mixture of hydrogen and nitrogen containing hydrogen in an amount from about 0.1 volume percent to about 10 volume percent may be used as a reducing gas. In another embodiment, the reducing gas may be carbon monoxide, generated in situ in the firing chamber by the reaction between residual oxygen and carbon particles placed in the firing chamber. In yet another embodiment, the reducing atmosphere is generated by the decomposition of ammonia or hydrazine.
The fired phosphor may be milled to form smaller particles and break up aggregates. The final phosphor may then be incorporated into the matrix to form the final product.
The phosphors of the present invention may be incorporated into numerous products used in low light applications. Such applications include, but are not limited to, cell phones and keyboards, such as in the keypad, front faceplate or in the controls attached to the faceplate. Additionally, the low toxicity of the phosphors of the present techniques makes applications such as textiles, toys and other commercial or consumer goods a possibility.
Furthermore, the long persistence of the phosphors of the present techniques makes them useful for applications in emergency equipment. Examples of such equipment include, but are not limited to, hard hats, stickers or decals applied to safety equipment, emergency exit signs, such as lettering or the sign itself, articles of clothing, such as in the fabric or in lettering or symbols applied to the clothing, and the like. In alternative embodiment, the phosphors may be included in lettering, such as an “EXIT” sign and may either be colored, so as to be visible at all times, or clear, so as to be visible only in low light conditions, when the glow from the incorporated phosphors may be visible.
The applications above are but a few examples of embodiments of the present techniques and are not intended to limit its application to those uses. Those skilled in the art will recognize that a long-lived persistent phosphor may be useful in a large variety of applications beyond the ones listed above.
The present invention is further illustrated by the following non-limiting examples.
The present invention will now be illustrated in more detail by reference to the following specific, non-limiting examples. Unless otherwise indicated, all percentages are by weight.
This composition requires the starting materials be blended together. The intimate mixture of the aforementioned starting raw materials are placed in an open alumina crucible and heated to a temperature of 1450 deg C. for a period of five hours in 1% forming gas.
One example of a composition according to the concepts of the present invention is (Sr2.96Eu0.01Er0.03)Al9.4B0.4Si1.2O19.8N0.2 Phosphor. In this example, 2.49 g of SrCO3, 0.01 g of Eu2O3, 0.03 g of Er2O3, 2.73 g of Al2O3, 0.14 g H3BO3, 0.39 g of SiO2 and 0.04 g of Si3N4 were blended together to form a blue persistent phosphor according to one embodiment of the present invention. The intimate mixture of the aforementioned starting raw materials were placed in an open alumina crucible and heated to a temperature of 1450 deg C. for a period of five hours in 1% forming gas.
On completion of the firing, the phosphor was obtained in the form of a sintered cake. This cake was reduced to a powder using a ball mill until the mean particle size (d50) reached the desired size. The resultant phosphor exhibited an improved initial intensity and longer persistence as compared to standard silicate analog. The oxy-nitride phosphor persistence was measured relative to the standard silicate phosphor. The results of the optical measurements are shown in Table 1 and graphically in
Table 1 shows that phosphors produced with the oxy-nitride composition have an initial intensity and persistent emission exceeding that of the standard silicate sample as well as a slightly lower rate of decay. As such, the initial efficiency of the resultant phosphor exceeds that of the standard composition. In addition, the persistent intensity also exceeds that of the standard composition.
While typical embodiments have been set forth for the purpose of illustration, the foregoing descriptions should not be deemed to be a limitation on the scope of the invention. Accordingly, various modifications, adaptations, and alternatives may occur to one skilled in the art without departing from the spirit and scope of the present invention.
