The invention relates in general to scintillators. In particular, the invention relates to implementation of high-energy radiation scintillator detectors.
Most scintillators known in the prior art are implemented in wide-gap insulating materials doped (“activated”) with radiation centers. A classical example of a solid-state scintillator is sodium iodide activated with thallium (NaI:Tl), introduced by Hofstadter more than 60 years ago. Because of the much longer wavelength of the scintillation associated with the activator energy levels, compared to the interband absorption threshold, the insulating scintillators are very transparent to their own luminescence. However, this advantage comes at a price in the transport of carriers to the activator site. Individual carriers have a poor mobility in insulators and transport efficiency requires that the generated electrons and holes form excitons and travel to the radiation site as neutral entities. The energy resolution even in the best modern scintillators does not compare well with that in semiconductors. One of the fundamental reasons for poor resolution is that the luminescent yield in dielectric scintillators is controlled by reactions that are nonlinear in the density of generated electron-hole pairs, such as the formation of excitons at low densities and the Auger recombination at high densities.
Such nonlinear processes do not exist in direct-gap doped semiconductors, where interaction with gamma radiation induces minority carriers while the concentration of majority carriers does not measurably change. Every reaction on the way to luminescence, including Auger recombination, is linear with respect to the concentration of minority carriers. One can therefore expect that doped semiconductor scintillators will not exhibit effects of non-proportionality and their ultimate energy resolution could be on par with that of diode detectors implemented in the same material.
Typically, scintillators are not made of semiconductor materials. The key issue in implementing a semiconductor scintillator is how to make the material transmit its own infrared luminescence, so that photons generated deep inside the semiconductor slab could reach its surface without tangible attenuation. However, semiconductors are usually opaque at wavelengths corresponding to their radiative emission spectrum. The inventors have been working on the implementation of radiation detectors based on direct-gap semiconductor scintillator wafers, like InP or GaAs. For the exemplary case of InP the scintillation spectrum is a band of wavelengths near 920 nm. The initial approach was to make InP relatively transparent to this radiation by doping it heavily with donor impurities, so as to introduce the Burstein shift between the emission and the absorption spectra. Because of the heavy doping, the edge of absorption is blue-shifted relative to the emission edge by the carrier Fermi energy. However, Burstein's shift by itself does not provide adequate transparency at room temperature. The problem is that attenuation of the signal depends on depth of the interaction site into the semiconductor (see Serge Luryi and Arsen Subashiev, “Semiconductor Scintillator for 3-Dimensional Array of Radiation Detectors” in Future Trends in Microelectronics: From Nanophotonics to Sensors to Energy, ed. by S. Luryi, J. M. Xu, and A. Zaslaysky, Wiley Interscience, Hoboken, N.J. (2010) pp. 331-346.)
The transparency issue is of critical importance and one is concerned with new ways to enhance the photon delivery to the semiconductor surface.
One possibility is to implement a semiconductor version of activated scintillator, similar in principle to NaI:Tl, by doping the semiconductor with high efficiency radiative centers that emit below-bandgap light. It is important that the excited electron-hole pairs be efficiently transferred to the radiative center. In the case of InP, this energy transfer probability was shown to be high for certain trivalent luminescent ions incorporated in the host lattice. The system InP:Yb3+ seems to work at cryogenic temperatures, producing emission near 1 μm—well below the bandgap of InP. However, at room temperature, its performance is degraded by fast non-radiative de-excitation of Yb ions.
Other ideas for implementing transparent semiconductor scintillators include replacing luminescent ions by semiconductor wells or “impregnations” of lower bandgap. This idea was proposed in Kastalsky, Luryi, et al. publication, (see “Semiconductor high-energy radiation scintillation detector,” Nucl. Instr. and Meth. in Phys. Research A 565, pp. 650-656 (2006) and in U.S. Pat. No. 7,265,354 to Kastalsky et al. and further discussed by Luryi (see “Impregnated Semiconductor Scintillator,” International Journal of High Speed Electronics and Systems, vol. 18, No 4 pp. 973-982 (2008)).
The epitaxially grown structure comprises two alternating materials that are lattice-matched to each other. The materials are assumed to have different energy gaps, with the second material having the lower bandgap, EG1>EG2. The essential idea is that the total volume occupied by the second material is small compared to that occupied by the first material. The ratio of these volumes defines a “duty cycle” factor S and the absorption coefficient of the composite structure is reduced by this factor. For example, if a 2 μm-thick InP layers are alternated by a 20 nm-thick layers of InGaAsP, the volume ratio is 100 (δ=0.01).
We are referring now to
The crucial requirement for the structure disclosed by Kastalsky et al. publication and patent and illustrated in
The short-period requirement in prior-art layered semiconductor scintillators results from the need to capture into the lower-gap wells most of the minority carriers generated in the wide-gap material. The present invention circumvents this requirement. As will be fully explained below, no travel of minority carriers is contemplated in the inventive structure. This is a radical departure from all prior art of scintillators endowed with special radiation sites that emit light at subband wavelengths. In all prior art scintillators, charge carriers were supposed to travel to these radiation sites and the distance to travel had to be minimized by increasing the concentration of radiation sites. Nevertheless, the finite travel distance leads to the above-mentioned non-proportionality of activated dielectric scintillators.
In the inventive structure, the minority carriers generated in the wide-gap material recombine there radiatively and the short-wavelength light thus generated is captured by the narrow-gap wells generating new minority carriers therein. Recombination of these new minority carriers in the narrow-gap wells generates longer wavelength scintillation, to which the entire layered structure is largely transparent. It is important that the separation between narrow-gap wells is no longer limited by the minority-carrier diffusion length and can be as large as hundreds of microns. The actual limitation on the well separation, according to the present invention, results from the need to capture most of the short-wavelength light by the narrow-gap wells. That in turn leads to an optimization strategy for the choice of the wide-gap host material and its doping. The primary requirement is high radiative efficiency of the host material. As will be fully explained below, the loss of short-wavelength light on the way to the narrow-gap wells is associated only with free-carrier absorption. The interband absorption of a photon merely generates a new minority carrier, which again recombines radiatively to produce another photon. The high radiative efficiency requirement ensures that non-radiative channels of recombination of minority carriers are minimized.
In the scintillator of the invention, the radiation sites are pumped by light and require no charge-carrier travel. An essential difference between the invention and the structure proposed by Kastalsky et al. and illustrated in
An embodiment of the scintillator structure of the invention best illustrated in
Because of the requirement b>>w, most of the interaction with incident high-energy radiation occurs in the barriers and results in the formation of a non-equilibrium population of minority carriers, exemplarily holes. The attendant increase in the population of majority carriers, exemplarily electrons, is of no particular importance, as their concentration may not appreciably vary from that provided by donors. Because of the high radiative efficiency, most of the minority carriers recombine radiatively and produce primary scintillating photons of energy hvb that is approximately equal to the bandgap Eb in the barrier region. These primary photons may be further absorbed in the barrier layer. This absorption merely produces another minority carrier that in turn recombines predominately in a radiative fashion, generating another primary photon of energy hvb. This process is referred to as the photon recycling. The loss of scintillating photons in the recycling process arises only due to two factors, namely the free-carrier absorption and the less than perfect radiative efficiency, η<100%. The need to optimize these two factors stems from the desire to minimize loss of the scintillation signal. Apart from the lost signal, the process of photon recycling in the barrier regions ends when the primary scintillating photon is absorbed in the well region.
Associated with the barrier material, is a quantity that has the dimension of length, which we shall refer to as the photon collection range R. This quantity depends primarily on the radiative efficiency of the barrier material and is defined as the maximum thickness b of a barrier layer, such that the collection efficiency ξ of the primary signal generated in said barrier layer in the two adjacent wells exceeds a desired value ξmin, exemplarily 75%. The meaning of ξ is the probability that the process of photon recycling in the barrier region resulting from an initial minority carrier generated in said region ends with a primary scintillating photon absorbed in one of the two adjacent wells. The higher is the desired primary collection efficiency ξ, the shorter is the range R. The photon collection range R depends on the radiative efficiency η and the desired ξmin; it sets an upper limit on the thickness of individual barriers. Thus, in the preferred embodiment of the invention, the thickness of barrier layers, while much larger than the diffusion length LD of minority carriers, is smaller than the photon collection range R, viz. LD<<b<R. The range R is estimated by detailed calculations for exemplary structures and is typically several hundreds of microns. For example, if the radiative efficiency η=99% and the desired ξmin=75%, then R≈0.5 mm.
The primary collection efficiency ξmin is not the only parameter that must be optimized to a desired value. In general, it is advantageous to minimize the dependence of ξ on the average position of the interaction within the barrier, i.e. on the center of the minority carrier cloud generated by gamma interaction. For this purpose, it is important to consider the typical size of this cloud, which we shall denote by R*. In first approximation, it is determined by the characteristic range of the plasmons, generated by the high-energy electron excited by the incident gamma photon. It is known, that the plasmon emission is the dominant energy loss mechanism for high-energy (higher than keV) electrons in semiconductors. This implies that the deposited energy of the gamma photon at an intermediate stage of the energy branching produces multiple plasmons of typical energy about 16 eV. These plasmons spread over the distance that is largely independent of the initial gamma energy and ultimately determines the radius R* of an approximately spherical minority-carrier cloud. It has been ascertained by calculations that the dependence of the primary collection efficiency ζ on the position of the center of this cloud is minimized when the thickness of the barrier layer b is larger than the radius R* of said cloud by about 40%. The typical value of R* is about 70 μm thus suggesting a preferred value of b≈100 μm, consistent with the range LD<<b<R, established above.
The requirement to well composition and thickness will be discussed now. The purpose of the wells is two-fold. Firstly, they must efficiently capture the primary scintillating photons and secondly, they serve as emitters of secondary scintillation photons at energy hvw that is approximately equal to the bandgap Ew in the well region. For the purpose of efficient capture, the wells must be not too thin, exemplarily larger than 0.5 μm. The wells should be made of direct-gap semiconductor, lattice-matched and otherwise compatible with the barrier material, with the well bandgap Ew narrower than the barrier bandgap Eb by at least 50 meV. The condition Eb Ew>50 meV guarantees not only the high absorption coefficient in the well for primary photons at energy hvb, but it also ensures low absorption coefficient in the barrier for secondary scintillation photons at energy hvw.
The secondary photons constitute the signal that is registered by the photoreceivers arranged at the surface of the entire scintillator structure in an optically tight fashion. In a preferred embodiment of the present invention, these photoreceivers are photodiodes sensitive to the secondary scintillation photons at energy hvw arranged on both sides of the layered scintillator structure. As initially disclosed by Abeles and Luryi, (see Slab Scintillator With Integrated Double-Sided Photoreceiver, PCT Application No PCT/US2010/01496), simultaneous detection and separate recording by both photoreceivers of the signal resulting from the same high-energy radiation event, enables one to adjust for the possible dependence of the total photon collection efficiency on the event position inside the scintillator and thus ensure higher energy resolution of the detector. This applies equally to the detector of the invention, as has been confirmed by detailed calculations.
We are referring now to the drawings in general, and
Detailed model calculations for a preferred embodiment illustrated in
Arrangements are provided to record the response of the top D1 and the bottom D2 photoreceivers individually and separately. It is essential that for a given energy deposition by a single high-energy particle, we have two signals D1 and D2 in the top and the bottom photodiodes, respectively. These signals in general depend on the position z of the interaction with the high-energy particle. The sum of the two diode signals D1(z)+D2(z) (per unit excitation) is referred to as the total photon collection efficiency, or the PCE. In general, the PCE is still dependent on the position z owing to possible optical attenuation of the signal. This dependence is taken into account in a scintillator system that aims at a high resolution of the deposited energy. In a preferred embodiment of the measurement system, the two signals D1 and D2 are further analyzed by computing the ratio D of their difference and their sum, viz.
The ratio D (z) varies in the range between −1 and +1, and it vanishes in the middle of the structure, at z=d/2, where D1=D2 by symmetry. The ratio D computed for a particular interaction can hence be used to ascertain its position z and thus correct for possible attenuation of the signal.
The scintillator performance of the invention is analyzed below by theoretical calculations, using the physical model, discussed above. Although the possible use of our scintillator is contemplated for a variety of high-energy radiation sources, the discussion presented herein below is confined to gamma spectroscopy. Interaction with a single gamma photon, which is either Compton scattering or photoelectric absorption, results in a large amount of energy E0 that is typically of order 100 keV, deposited (i.e. transferred to an electron) at a position z. The high-energy electron, initially excited by the gamma interaction, gives away its energy in a cascade process that ends up with a number N of thermalized electron-hole pairs. The average energy per pair Ei=E0/N is a characteristic of the material, called the ionization energy. In InP the average ionization energy is approximately Ei=4.2 eV. One of the purposes of the scintillator of the invention is to perform gamma spectroscopy, that is to quantify the deposited energy E0 by measuring N via the optical signals D1 and D2.
In order to conduct a quantitative analysis, it is necessary to specify the physical model further. Inasmuch as our scintillator body is an n-type semiconductor, the number of majority carriers (electrons) does not appreciably change as a result of a single gamma interaction, hence without any loss of generality we can regard the number N as the number of generated minority carriers (holes). The cascade energy branching process occurs at a much faster scale (picoseconds) than the recombination of minority carriers (nanoseconds). At the end of the cascade process, but before an appreciable recombination has taken place, there are N holes distributed in some region of the semiconductor, referred to as the minority-carrier (hole) cloud.
In the model calculations this region was considered to be substantially spherical and centered about the initial gamma interaction position. The radius R of the hole cloud is taken independent of the deposited energy E0. This assumption is reasonable when the dominant energy loss mechanism is plasmon emission. In this case, for any E0>>1 keV, the intermediate stage of the energy branching comprises multiple plasmons of typical energy about 16 eV that spread over the distance largely independent of E0.
We are referring now to
The radiative properties of semiconductors employed in the barrier and well layers, as illustrated in
Transport of the luminescent photons, both primary and secondary, across the material will be discussed in terms of the so-called on-the-spot approximation and used by the inventors to extract important parameters of InP. This model neglects entirely the diffusion of minority carriers and describes the transport of photons, as mediated by photon recycling, in terms of repeated emissions from the same spot.
The essential material parameters that limit photon recycling are the free-carrier absorption (FCA) characterized by an absorption coefficient αFCA and the radiative efficiency η defined in terms of the minority-carrier recombination times, radiative (τr) and nonradiative (τnr), or more precisely in terms of their ratio r=τr/τnr, viz.
The first step in the analysis is to consider the collection efficiency ζ of primary photons, defined as the probability that luminescence generated in the barrier by the recombination of an initial hole at some position z ends up being absorbed in one of the nearest wells. This probability is much larger than the probability that a typical primary photon (average over the emission spectrum) reaches one of the wells on the first try. That probability we refer to as the one-shot probability, and designate by small letters p1 (z) and p2 (z)=p1 (b−z) for the two nearest wells. In terms of these one-shot probabilities, the primary collection efficiency is given by
where pFCA is the single-shot probability that an emitted photon will lost to free-carrier absorption. The range R, such that for z<R one has ξ(z)<ξmin for some ξmin, is referred to as the photon collection range. The larger is the desired ξmin the more restricted is the photon collection range R. The photon collection range R depends on the radiative efficiency η and sets an upper limit on the thickness of individual barriers.
We are referring now to
In this calculation, the one-shot probabilities p1, p2 and pFCA were calculated using the experimental data for the absorption and the emission spectra, illustrated in FIG. 3. The main feature of the z dependence of p1 and p2 is that it is a power law, rather than an exponential, p1(z)˜1/zζ, except at very long distances, where the dependence becomes exponential due to free-carrier absorption. The theoretical value of the exponent ζ is ζ=1−Δ/kT≈0.4 for low-doped n-type InP at room temperature, where Δ≈10 meV is the Urbach tailing parameter for absorption spectra.9 Empirically, one can approximate the dependence p1 (z) very accurately by an expression of the form,
p
1(z)=0.5×exp(−αFCAz)/(1+z/z1)ζ
where for lightly-doped InP (ND=3×1017 cm−3) one has z1=0.09 μm, z2=0.82 μm, ζ1=0.2, and ζ2=0.23. The free-carrier absorption for this concentration is practically negligible (αFCA≈0.1 cm−1).
To estimate the actual value of the radiative efficiency η, the experimental data of the Semyonov, Subashiev et al. publication was used for the recombination rates in InP, as function of the free-carrier concentration n at room temperature, τr−1=1.2×10−10 n and τnr−1=0.4×10−6+1.5×10−30 n2 (both in units of s−1).
For the low-doped InP, the radiative efficiency η>0.99, so that r=(1−η)/η≦0.01. As seen from
Since ξ(z)≧ξmin, the primary collection efficiency will be still higher, when z is not in the middle of the barrier. This dependence of ξ(z) on the position of the interaction within a barrier is inherited by the ultimate PCE, as received by the surface photodiodes, and gives rise to an unwelcome phenomenon of “wiggles” in the dependence of the PCE on the fine-grained position of the interaction within a barrier. These wiggles will be discussed further below in this application. At this point, it is merely noted that the wiggle amplitude can be minimized by a judicial choice of the barrier thickness.
The point-like excitations, neglecting the spatial dimensions of the excited minority-carrier cloud have been considered above. Taking into account the finite size of the cloud, comparable to the barrier thickness, will have a quantitative effect on the results. The most important effect of the extended cloud is that it reduces the wiggle amplitude, compared to the point-like excitation. These effects are estimated in a model, where the excited holes are distributed homogeneously within a sphere of radius R*, i.e. ρ({right arrow over (r)})=3/4πR*3 for |{right arrow over (r)}|≦R* and zero otherwise. In order to obtain the z dependence of the distribution, we integrate over the plane parallel to the scintillator layers. This gives
The problem can be solved by using a kinetic equation. In a reasonably accurate simplified approach we can take into account the effect of the extended cloud by averaging the one-shot probabilities p1, p2 and pFCA in Eqs. (3) and (4) over the distribution (5).
The first stage of luminescence collection was described in the scintillator of the invention corresponding to the collection of primary scintillating photons generated in a barrier by the adjacent wells. Absorption of primary photons in the wells results in the generation of minority carriers in the wells, their number related to the initial number of holes generated by the gamma interaction by the function ξ(z) given by Eq. (3).
In the next stage, these minority carriers recombine in the wells, producing the longer wavelength radiation comprising secondary scintillation photons at energy hvw that is approximately equal to the bandgap Ew in the well region. The secondary photons are eventually absorbed in the surface photoreceivers, producing the signals D1 and D2. Inasmuch as the barrier material is substantially transparent to this radiation, the transport of secondary photons to the surface represents a sequence of random hops between different wells. Evaluation of the signals D1 and D2 becomes a discrete version of similar calculations for the homogeneous scintillator outlined in the Luryi and Subashiev publication.
We are referring now to
The diagram (a) of
Nevertheless, any positional dependence of the PCE is unwelcome, since it makes the determination of deposited energy uncertain. As disclosed by the Abeles and Luryi PCT patent publication, one can remedy this problem if one knows the position of the interaction. In this case, the measured value of the PCE can be adjusted. The diagram (b) of
It was previously mentioned that the PCE dependence on z can show wiggles on the fine scale, said wiggles originating from the dependence of the primary collection efficiency ξ(z) on the position of the interaction within the unit element of the structure. If the distribution of the minority carriers generated by a single interaction were point-like, then minima of ξ(z) would occur in the middle of barriers, ξmin=(b/2). For an extended cloud, there will remain in general some dependence of ξ(z) on the cloud position, but the minima may not necessarily occur when the cloud center is in the middle of a barrier.
We are referring now to
The value of R* is an important physical parameter that is determined by the initial high-energy processes at the early stages of energy-branching cascade. Inasmuch as the dominant interaction of high-energy electrons in semiconductors is plasmon emission, the radius R* is substantially independent of the energy transferred by the incident quantum to the electronic system and is controlled by the distance over which plasmon spread over. The estimated value of R* in InP is about 70 μM, but this value should not be considered definitive; in practice, one may be able to assess the value of R* from experimental date for a given semiconductor
From the analysis of basic equations, it is clear that the wiggle amplitude is a function of the ratio b/R* and therefore we have conveniently evaluated this amplitude by varying R* for a given b, rather than varying b for a given R*.
We are referring now to
There are actually two sets of curves provided in
We are referring now to
Curves similar to those in
Both sets of curves in
This consideration assumes that the precision of our measuring the signals D1 and D2 is insufficient for the function D (z) to discriminate the position within a single barrier. If the photodiode signals are measured sufficiently accurately, then the event position is also accurately known, enabling one to correct for the wiggles as well as for the overall position dependence of the PCE. In this case, one would be justified in growing thicker barriers.
The exemplary discussion is confined to the specific and preferred material system of lattice-matched InP and quaternary InGaAsP semiconductors. These direct-gap semiconductors are known to possess high radiative efficiency and at the same time produce scintillation at sufficiently short wavelengths (hv ≧1 eV) that the entire detector system can operate at room temperature. If one contemplates cooled operation of the inventive detector, the scope of possible semiconductor materials widens to include narrow bandgap systems, including those based on InAs, GaSb, and their alloys. Those skilled in the art will recognize multiple possibilities, limited primarily by the availability of rapid growth techniques.
A number of possibilities remain even if the contemplated operation is restricted to room temperature. Again, these possibilities are limited primarily by the availability of rapid growth techniques and are well-known to those skilled in the art. Instead of producing an exhaustive list, we mention one possibility here. The well material is GaAs and the barrier material (wide-gap) is AlGaAs with the aluminum content such that the alloy has direct bandgap, exceeding that of GaAs by at least 100 meV. The advantage of the GaAs/AlGaAs system is that one can contemplate growth of the entire heterostructure in the same growth chamber, including rapid growth of the barrier material with the wells produced by periodic cutting off the source of aluminum.
The reference is made now to
This application claims priority of U.S. Provisional Application Ser. No. 61/460,199 filed by the inventors on Dec. 28, 2010.
This invention was made with United States government support under grant number 2008-DNA-007-AR1002 awarded by the Department of Homeland Security and grant number HDTRA1-08-1-0011 awarded by the Defense Threat Reduction Agency. The government has certain rights in the invention.
Number | Date | Country | |
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61460199 | Dec 2010 | US |