WO2015047492A2 - Photovoltaic lead-salt detectors - Google Patents
Photovoltaic lead-salt detectors Download PDFInfo
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- WO2015047492A2 WO2015047492A2 PCT/US2014/043487 US2014043487W WO2015047492A2 WO 2015047492 A2 WO2015047492 A2 WO 2015047492A2 US 2014043487 W US2014043487 W US 2014043487W WO 2015047492 A2 WO2015047492 A2 WO 2015047492A2
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- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/08—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof in which radiation controls flow of current through the device, e.g. photoresistors
- H01L31/10—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof in which radiation controls flow of current through the device, e.g. photoresistors characterised by potential barriers, e.g. phototransistors
- H01L31/101—Devices sensitive to infrared, visible or ultraviolet radiation
- H01L31/102—Devices sensitive to infrared, visible or ultraviolet radiation characterised by only one potential barrier
- H01L31/108—Devices sensitive to infrared, visible or ultraviolet radiation characterised by only one potential barrier the potential barrier being of the Schottky type
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/08—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof in which radiation controls flow of current through the device, e.g. photoresistors
- H01L31/10—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof in which radiation controls flow of current through the device, e.g. photoresistors characterised by potential barriers, e.g. phototransistors
- H01L31/101—Devices sensitive to infrared, visible or ultraviolet radiation
- H01L31/102—Devices sensitive to infrared, visible or ultraviolet radiation characterised by only one potential barrier
- H01L31/109—Devices sensitive to infrared, visible or ultraviolet radiation characterised by only one potential barrier the potential barrier being of the PN heterojunction type
Definitions
- Detection of light emitted in the infrared (IR) wavelength region of the spectrum may have wide spread applications that include missile defense, night vision imaging for security and soldiers, and trace gas sensing imaging, such as chemical detection and explosive detection.
- IR infrared
- LWIR long/low- wavelength infrared wavelengths
- Current detection technologies with high sensitivity are typically based on semiconductor photodetectors. In the past, many semiconductor material systems have been studied and progress has been made in developing semiconductor photodetectors.
- HgCdTe Mercury-Cadmium-Telluride
- InSb Indium-Antimonide
- QWIPs quantum well infrared photodetectors
- MCT is used for mid-IR Focal Plane Array (FPA) applications.
- MCT may be produced by using molecular beam epitaxy (MBE) on Cadmium-Zinc-Telluride (CdZnTe) substrates.
- CdZnTe substrates are often relatively costly, brittle and of relatively small size.
- the semiconductor industry is attempting to transfer the growth and processes of MCT to alternative substrates, such as Silicon (Si). Transferring the growth and processes of MCT to a Si substrate may encounter problems because of the about 19% lattice mismatch and about 100% thermal mismatch that may cause deleterious effects on the final FPA.
- FIG. 1 is a schematic diagram of a non-limiting embodiment of a type II band gap alignment for a PV Pb-salt detector.
- FIG. 2 is a schematic diagram of another non-limiting embodiment of a type II band gap alignment for a PV Pb-salt detector.
- FIG. 3 is a schematic diagram of a non-limiting embodiment of a type II band gap alignment for a double heterojunction PV Pb-salt detector.
- FIG. 4 is a schematic diagram of a top-down view of a non-limiting embodiment of a PV Pb-salt detector that comprises a two-dimensional charge separation junction structure.
- FIG. 5 is a cross-sectional view, taken along line 5-5 in FIG. 4, of the PV Pb-salt detector shown in FIG. 4.
- FIG. 6 is a cross-sectional view of a PV Pb-salt detector similar to the PV Pb-salt detector shown in FIG. 4, further comprising a plurality of dopant diffusion regions beneath element areas therein.
- FIG. 7 is a schematic diagram of a non-limiting embodiment of an FPA comprising a plurality of photodetectors of the present disclosure.
- FIG. 8 is a schematic diagram of a side view of a non-limiting embodiment of a PV Pb- salt detector that comprises a three dimensional charge separation junction structure.
- FIG. 9 is a cross-sectional view, taken along line 9-9 in FIG. 8, of the PV Pb-salt detector of FIG. 8.
- FIG. 10 illustrates an I-V curve for a PV Pb-salt detector that comprises a plurality of three-dimensional CSJs.
- FIG. 11 is a schematic diagram of a non-limiting embodiment of a PV Pb-salt detector that comprises a heterojunction.
- FIG. 12 is a schematic diagram of an embodiment of a PV Pb-salt detector with the Pb- salt layer grown prior to the non-Pb-salt layer.
- FIG. 13 is a schematic diagram of a non-limiting embodiment of a PV Cadmium-Sulfur (CdS)/ Pb-Selenide (Se) (PbSe) heterojunction detector.
- FIG. 14 illustrates a J-V curve for the PV CdS/PbSe heterojunction detector depicted in FIG. 13.
- FIG. 15 illustrates a temperature-dependent mid-IR spectrum-resolved photoresponses of the CdS/PbSe heterojunction detector depicted in FIG. 13.
- FIG. 16 illustrates the peak photoresponse intensities and the cutoff wavelengths versus the temperatures of the CdS/PbSe heterojunction detector depicted in FIG. 13. DETAILED DESCRIPTION
- the designated value may vary by plus or minus twenty-five percent, plus or minus twenty percent, plus or minus fifteen percent, plus or minus twelve percent, or plus or minus eleven percent, or plus or minus ten percent, or plus or minus nine percent, or plus or minus eight percent, or plus or minus seven percent, or plus or minus six percent, or plus or minus five percent, or plus or minus four percent, or plus or minus three percent, or plus or minus two percent, or plus or minus one percent, or plus or minus one-half percent.
- At least one will be understood to include one as well as any quantity more than one, including but not limited to, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, or more.
- the term "at least one” may extend up to 500 or 1000 or more, depending on the term to which it is attached; in addition, the quantities of 500/1000 are not to be considered limiting, as higher limits may also produce satisfactory results.
- any references to "one embodiment,” “an embodiment,” “certain embodiments”, or “some embodiments” means that a particular element, feature, structure, or characteristic described in connection with the embodiment is included in at least one embodiment.
- the appearances of the phrase “in one embodiment” in various places in the specification may not refer to the same embodiment.
- the term “or combinations thereof as used herein refers to all permutations and combinations of the listed items preceding the term. For example, "A, B, C, or combinations thereof is intended to include at least one of: A, B, C, AB, AC, BC, or ABC, and if order is important in a particular context, also BA, CA, CB, CBA, BCA, ACB, BAC, or CAB.
- the term “substantially” means that the subsequently described event or circumstance completely occurs or that the subsequently described event or circumstance occurs to a great extent or degree.
- the term “substantially” means that the subsequently described event or circumstance occurs at least 90% of the time, or at least 95% of the time, or at least 98% of the time.
- the term “substantially” will be understood to allow for minor variations and/or deviations that do not result in a significant impact thereto.
- PV detectors may detect light differently in comparison to photoconductive (PC) detectors.
- PV detectors may be detectors that comprise a p-n junction on which photoelectric current appears upon illumination. Specifically, changes in width of the depletion region at the p-n junction interface within the PV detectors affect the PV detector's generation of photoelectric voltage and/or photoelectric current. For example, when detecting the illumination of one or more wavelengths of light, the PV detector may absorb light photons (e.g. absorb in a Pb-salt layer of a Pb-salt PV detector) that dislodge electrons to create free electrons and holes.
- light photons e.g. absorb in a Pb-salt layer of a Pb-salt PV detector
- the dislodged electrons may have sufficient energy to jump out of the depletion region, which generates a photoelectric current and reduces the width of the depletion region.
- a PC detector detects light using a change of resistance within PC detectors.
- a PC detector may function as a resistor whose resistance depends on the detected light intensity.
- PV detectors may exhibit other differences when compared to PC detectors. For instance, PV detectors may have a faster response time than PC detectors. Response time for PV Pb-salt material may typically be in a range of tens to hundreds of nanoseconds (ns). Current commercial Pb-salt PC detectors may be resistor-capacitor (RC) lifetime limited, with response time of a PC PbSe detector that ranges about 2-20 microseconds ( ⁇ ) and a PC PbS detector of about several hundred ⁇ 8. Furthermore, pixel density with PV array could be relatively higher than its PC counterpart, which offers a relatively more compact FPA system with lower cost.
- RC resistor-capacitor
- IV- VI Pb-salt material may offer low Auger recombination that result in relatively high detectivity for detectors and operating temperature that do not require cooling.
- Pb- salt material may have greater tolerance of defects in comparison to MCT, optimal growth temperature of Pb-salt materials that are below 400 degrees Celsius (°C), and easier to handle thin film growth (e.g. PbSnSe) than MCT.
- IV- VI refers to a semiconductor material constructed from at least one Group IV element and at least one Group VI element and is not intended to be interpreted as including a Group V element.
- Uncooled PV detectors in the mid-IR wavelength range may be less expensive and more compact than detectors with cooled systems.
- Auger recombination may cause major loss channel at relatively high temperature for current semiconductor mid-IR detectors, and thus may be a hurdle in developing the semiconductor mid-IR detectors.
- Auger coefficient in Pb-salt materials is more than an order of magnitude lower than those in type-II QWIPs and may suppress Auger recombination relatively to other III-V and II- VI semiconductors with about the same energy band gaps.
- uncooled PbSe PC detectors have demonstrated improvement in specific detectivity (D*) of 2.8xl0 10 centimeters (cm) hertz- (Hz) 1/2 /watt (W) and 4.2xl0 10 cm- Hz 1"/27W at -3.8 ⁇ , without and with antireflective coating, respectively.
- D* specific detectivity
- Hz centimeters
- W hertz-
- W 4.2xl0 10 cm- Hz 1"/27W at -3.8 ⁇
- IV- VI semiconductors such as Pb-salt materials (e.g. Pb- sulfide (PbS), PbSe, and Pb 1-X -Tin (Sn) x Se) may offer high sensitivity similar to MCT.
- Auger recombination may be one factor in loss channel for mid- wavelength IR (MWIR) and long- wavelength IR (LWIR) (e.g. wavelengths from about 8-15 ⁇ ) detectors.
- Auger coefficient in IV- VI structures may be more than an order of magnitude lower than those in type-II QWIPs, which in turn may be more suppressed relative to other III-V and II- VI semiconductors with the same energy gaps.
- previous IV- VI semiconductors have not been fully realized for detector fabrication because of the inability to produce a relatively high quality p-n junction from diffusion, defects, and/or other material related issues.
- PV Pb-salt detector is a metal semiconductor junction detector that comprises a Pb or Pb-salt Schottky contact junction.
- the performance of such a PV Pb- salt detector is generally below the theoretical limit of Auger recombination.
- Possible performance enhancement includes improving the Pb-salt material quality improvement or the device junction engineering.
- the Schottky contact junction may be replaced with a p-n homojunction to lower Auger recombination.
- developing p-n homojunction mid-IR PV detectors may encounter difficulties because of the impurity of inter-diffusion and other material related issues.
- Another alternative is to construct a larger band gap semiconductor with Pb-salt material to form a p-n heterojunction with proper band offset that is able to offer relatively higher R 0 A values by allowing minority carrier transport and blocking the majority carrier leak.
- a PV Pb-salt detector configured to detect light emitted in at least the IR wavelength region of the spectrum, such as mid- IR wavelengths and long/low- wavelength IR wavelengths.
- the PV Pb-salt detector may comprise a CSJ structure configured to separate the electrons and holes flowing during illumination of the PV Pb-salt detector.
- CSJs can be introduced in PV Pb-salt detectors with a IV- VI Pb-salt layer that comprises polycrystalline material or mono-crystalline material.
- CSJs may be implemented within PV Pb-salt detectors that comprise a homojunction, a heterojunction, and/or a Schottky contact junction.
- the PV Pb-salt detector may be a heterojunction PV detector that comprises a non- Pb-salt layer.
- the non-Pb-salt layer may be an n-type material that can be selected from a group consisting of, for example, group II- VI materials, such as Cadmium-Sulfur (CdS), Cadmium-Selenide (CdSe), and Zinc-Oxide (ZnO), oxides, such as Titanium Dioxide (Ti0 2 ), and any other materials that satisfy the type II band gap as shown in FIG. 1.
- group II- VI materials such as Cadmium-Sulfur (CdS), Cadmium-Selenide (CdSe), and Zinc-Oxide (ZnO)
- oxides such as Titanium Dioxide (Ti0 2 )
- Ti0 2 Titanium Dioxide
- II-VI is intended to refer to a semiconductor material comprising at least one Group II element and at least one Group VI element and is not intended to be interpreted as including a Group V, Group III, Group TV, or Group V element unless explicitly included.
- polycrystalline may refer to a solid material (e.g. Pb-salt layer) that comprises a plurality of crystallites of varying size and orientation. Areas where the crystallites meet may be known by persons of ordinary skill in the art as grain boundaries. Persons of ordinary skill in the art are also aware that the term “crystallites” may be interchangeably referred to as grains or microcrystals.
- the layer of polycrystalline material is a thin film material defined as having boundary domains existing along at least one dimension between crystallites therein. The size of crystallites in the layer of polycrystalline material can be in micro- or nano-meter scale.
- thin films comprising one dimensional column crystals (either in micro- or nano-scale) are considered polycrystalline thin film materials.
- a polycrystalline IV- VI Pb-salt layer in some embodiments, may comprise crystallites with sizes that range from about 1 nm to about 10 ⁇ .
- the plurality of microcrystals of the polycrystalline layer may have boundary domains, due to different orientations of the microcrystals, forming divisions between the plurality of microcrystals.
- the plurality of microcrystals, forming the layer of polycrystalline material 40 may be about ⁇ in size and about ⁇ in thickness. It should be noted that the shape of the microcrystal (crystallite) is cubic or near-cubic. The "size" of such crystallite (e.g., length, width or height) could range from lOOnm to a few micrometers, and common sizes are in a range from about lOOnm to about lOOOnm.
- the size can be controlled using known techniques, to grow one-dimensional column-like crystals, in which the crystallite has a square base with a length and/or width in the range of about lnm to about 2000nm and a height in a range from about 1 nm to about 10,000 nm (10 mm). In principle, height can be even higher than 10 mm.
- the plurality of microcrystals forming the layer of polycrystalline material may be about lOOnm or about 500nm in size.
- each microcrystal of the plurality of microcrystals forming the layer of polycrystalline material may have a width in a range of from about 50 nm to about ⁇ (in the horizontal direction). In some embodiments, each microcrystal of the plurality of microcrystals may have a height in a range of from about ⁇ to about ⁇ (in the vertical direction), such that the polycrystalline material comprising the microcrystals has a thickness in a range of from about 50 nm to about ⁇ to about ⁇ .
- the layer of polycrystalline material may be sensitized to enhance or create an ability to receive and interact with light.
- the layer of polycrystalline material may be sensitized for example by annealing the polycrystalline material under a predetermined atmosphere. In some embodiments, the predetermined atmosphere may be an Iodine atmosphere follow by an Oxygen atmosphere.
- the layers of polycrystalline material may be sensitized by heating for about 10-60 minutes at temperatures between 420°C and 450°C followed by iodine vapor carried by nitrogen gas or oxygen with a 5-50 seem flow at 350°C -390°C for 10- 30 min.
- the sensitization process uses pure oxygen in a first step to improve the crystal quality.
- the 0 2 annealing temperature in certain embodiments is in a range of about 375°C to about 385°C, for example about 380°C
- annealing time in certain embodiments, is in a range of about 20 min to about 30 min, for example about 25 min. The annealing time can vary depend on the size of the crystallites.
- I 2 is introduced for about 3 min to about 10 min, for example about 5 min, to sensitize the material.
- the optimized temperature for I 2 annealing may vary depending on the size of the crystallites and the surface conditions after the 0 2 annealing step.
- the temperature for the iodine step may be in a range of about 375°C to about 385°C, for example about 380°C.
- the sensitization method includes exposing a lead salt-coated substrate to an oxygen atmosphere or nitrogen atmosphere or an oxygen-nitrogen atmosphere for a duration of time in a range of about 10 minutes to about 30 minutes at a temperature in a range of about 350°C to about 390°C, followed by a step of exposing the lead salt- coated substrate to an iodine vapor for a duration of time in a range of about 3 minutes to about 10 minutes at a temperature in a range of about 350°C to about 390°C, forming a sensitized lead salt- coated substrate.
- the term "mono-crystalline” may refer to a solid material (e.g. Pb-salt layer) in which the crystal lattice of an entire sample is substantially continuous and substantially unbroken to the edges of the sample.
- the mono-crystalline material may include no or relatively little number of grain boundaries and may be substantially uniform.
- the term “heterojunction” may refer to a junction that occurs between layers or regions of dissimilar semiconductor material. In particular to a p-n junction, a heterojunction comprises different n-type and p-type material that have different energy band gaps.
- the term “homojunction” refers to a junction that occurs between layers or regions that have substantially similar semiconductor material. Typically, the substantially similar semiconductor materials may have about equal band gaps.
- a homojunction may comprise substantially the same n-type material (e.g. PbSe material layer) and p-type material (e.g. PbSe material layer).
- the detector is connected, e.g., via lead wires to an electrical system.
- the electrical system may be implemented as a readout integrated circuit (ROIC), electronics configured to receive information indicative of patterns in electron strikes, a computer system, or any other suitable electrical system capable of receiving electrical signals, voltages, and/or information generated from the detectors.
- the electrical system may include at least one processor capable of executing processor executable instructions, a non-transitory processor readable medium capable of storing processor executable instructions, an input device, an output device, and a communications device, all of which may be partially or completely network-based or cloud based, and may not necessarily be located in a single physical location.
- the processor of the electrical system can be implemented as a single processor or multiple processors working together to execute processor executable instructions including the logic described herein.
- Exemplary embodiments of the processor may include a digital signal processor (DSP), a central processing unit (CPU), a field programmable gate array (FPGA), a microprocessor, a multi-core processor, a quantum processor, application-specific integrated circuit (ASIC), a graphics processing unit (GPU), a visual processing unit (VPU) and combinations thereof.
- DSP digital signal processor
- CPU central processing unit
- FPGA field programmable gate array
- microprocessor a microprocessor
- a multi-core processor a quantum processor
- ASIC application-specific integrated circuit
- GPU graphics processing unit
- VPU visual processing unit
- the processor is operably coupled with the non- transitory processor readable medium via a path which can be implemented as a data bus allowing bi-directional communication between the processor and the non-transitory processor readable medium, for example.
- the processor is capable of communicating with the input device and with the output device via additional paths, which may be one or more data busses, for example.
- the processor may be further capable of interfacing and/or bi-directionally communicating with a network using the communications device, such as by exchanging electronic, digital, analogue, and/or optical signals via one or more physical, virtual, or logical ports using any desired network protocol such as TCP/IP, for example.
- TCP/IP network protocol
- the processor is capable of reading and or executing processor executable code stored in the one or more non-transitory processor readable medium and/or of creating, manipulating, altering, and storing computer data structures into the one or more non-transitory processor readable medium.
- the non-transitory processor readable medium of the electrical system may store a program having processor executable instructions configured to receive and interpret electrical signals, voltages, and or information received from two or more spaced apart electrical contacts.
- the processor executable instructions may also be configured to provide signal processing when the detector is implemented as an array, for example.
- the non- transitory processor readable medium may be implemented as any type of memory, such as random access memory (RAM), a CD-ROM, a hard drive, a solid state drive, a flash drive, a memory card, a DVD-ROM, a floppy disk, an optical drive, and combinations thereof, for example.
- non-transitory processor readable medium may be located in the same physical location as the processor, the non-transitory processor readable medium may also be located remotely from the processor and may communicate with the processor via the network. Additionally, when more than one non-transitory processor readable medium is used, one or more non-transitory processor readable medium may be located in the same physical location as the processor, and one or more non-transitory processor readable medium may be located in a remote physical location from the processor.
- the physical location of the non-transitory processor readable medium can be varied, and the non-transitory processor readable medium may be implemented as a "cloud memory" i.e., one or more non-transitory processor readable medium which is partially, or completely based on or accessed using the network, for example.
- the one or more processors may not communicate directly with the non-transitory processor readable medium, but may communicate with another processor communicating with the non-transitory processor readable medium over the network, for example.
- the processor may include a first processor communicating with a second processor executing processor executable instructions including the word recognition and media insertion program over the network.
- the second processor may be part of a computer station, or may be a part of a separate computer system or server configured to communicate with the computer system over the network or otherwise operably coupled with the computer system, for example.
- the input device may pass data to the processor, and may be implemented as a keyboard, a mouse, a touch-screen, a camera, a cellular phone, a tablet, a smart phone, a personal digital assistant (PDA), a microphone, a network adapter, the photodetector, and combinations thereof, for example.
- the input device may also be implemented as a stylus, a mouse, a trackball, and combinations thereof, for example.
- the input device may be located in the same physical location as the processor, or may be remotely located and/or partially or completely network-based.
- the disclosure includes an IR photovoltaic (PV) detector, comprising a IV- VI Lead (Pb)-salt layer disposed on a substrate; and a charge- separation-junction (CSJ) structure disposed on or embedded in the IV- VI Pb-salt layer, wherein the CSJ structure comprises a plurality of element areas disposed upon or within the IV- VI Pb-salt layer, wherein the plurality of element areas are substantially parallel to each other, wherein each element area is connected to a first Ohmic contact thereby forming a plurality of interconnected first Ohmic contacts, and wherein a second Ohmic contact is disposed upon a portion of the IV- VI Pb-salt layer.
- PV IR photovoltaic
- Pb IV- VI Lead
- CSJ charge- separation-junction
- the disclosure includes a photovoltaic PV detector, comprising a heterojunction region that comprises at least one IV- VI Pb-salt material layer coupled to at least one non-Pb-salt layer, wherein the at least one IV- VI Pb-salt layer and the at least one non-Pb-salt layer form a p-type-n-type (p-n) junction with a type II band gap alignment, and wherein the type II band gap alignment is arranged such that a conduction band of an n-type material of the p-n junction is about equal to or at a relatively lower energy level than the conduction band of the p-type material of the p-n junction.
- the disclosure includes an apparatus for detecting infrared light, comprising a IV- VI Pb-salt layer disposed on a substrate, a plurality of junction layers applied to an upper surface of the IV- VI Pb-salt layer to form a plurality of junctions that are either a p-n junction or a Schottky contact junction, one or more junction electrical contacts that are interconnected with each other and applied to the upper surface of the junction layers, one or more Pb-salt electrical contacts that are interconnected with each other and applied to the upper surface of the IV- VI Pb-salt layer, wherein the junctions generate a photoelectric current upon illumination of the junctions and absorbed by IV- VI Pb-salt layer, and wherein the junction electrical contacts and the Pb-salt electrical contacts collect a plurality of free electrons and a plurality of free holes upon illumination of the junctions and absorbed by IV- VI Pb-salt layer.
- FIG. 1 is a schematic diagram of a non-limiting embodiment of a type II band gap alignment for a PV Pb-salt detector 100.
- FIG. 1 illustrates an n-type non-Pb-salt layer band gap 102 and a p-type Pb-salt layer band gap 104 for the PV Pb-salt detector 100.
- the n-type non-Pb-salt layer may be coupled to the p-type Pb-salt layer.
- the p-type Pb-salt layer may be deposited as a mono-crystalline material, a polycrystalline material, or an amorphous material.
- the Pb-salt layer may comprise crystallites with sizes that range from about 1 nm to about 10 ⁇ , or other sizes described elsewhere herein.
- Using a polycrystalline Pb-salt material may provide for a relative higher material quality in comparison to a mono-crystalline Pb-salt layer.
- a mono-crystalline may provide for a relatively more uniform Pb-salt layer and typically produces a relatively easier contact surface.
- the non-Pb-salt layer or layers may have wider band gaps than the Pb-salt layer or layers therein.
- FIG. 1 illustrates that the p-n junction may have type II band gap alignment such that the energy level for the conduction band of the n-type non-Pb-salt layer is about equal to or less than the energy level for the conduction band of the p-type Pb-salt layer.
- the Pb- salt layer is a p-type layer
- the conduction band is relatively higher or more than the energy level of the conduction band of the n-type non-Pb-salt layer.
- the type II band gap alignment as shown in FIG.
- n-type non-Pb-salt layer may be used to perform photo-detection such that free electrons and holes may travel through the n-type non-Pb-salt layer and p-type Pb-salt layer, respectively, to generate photoelectric current.
- a different type II band gap alignment where the conduction band for the p-type Pb-salt layer is lower than n-type non-Pb-salt material layer may not be suitable for photo-detection.
- band gap alignments may also exist that are not suitable for photo-detection as a type II band gap alignment.
- band gap alignments that have the energy level for the conduction band of the n-type layer relatively more or higher than the energy level for the conduction band of the p-type layer may not be used for photo-detection.
- One example of the type of band gap alignment that may not be suitable for PV photo-detection is a type-I band gap alignment.
- a type-I band gap alignment may occur when the band gap of one of the materials (e.g. the n-type non-Pb-salt layer) completely overlaps the band gap of another material (e.g. p-type Pb-salt material layer).
- the valence band for the n-type layer is at a relatively lower energy than the valence band of the p-type layer
- the conduction band for the n-type layer is at a relatively higher energy than the conduction band of the p-type layer.
- a heterojunction that comprises a p-type PbSe and an n-type ZnO structure may not be used for detector applications because the band gap of the n-type ZnO may have band gap that overlaps the p-type PbSe.
- the wider band gap n-type material could be replaced with Ohmic contact materials that contact the Pb-salt materials where wider band gap material is not used to form p-n junction within the PV Pb-salt detector 100.
- the Ohmic contact material which may have a narrower band gap than the Pb-salt layer, and the Pb-salt material may form an Ohmic contact.
- the PV Pb-salt detector 100 may have cutoff wavelengths that fall within the Pb-salt absorption range, which is typically about 0.5-32 ⁇ .
- the PV Pb- salt detector 100 or any detector described herein may be configured with cutoff wavelengths that fall within the ranges of about 0.5-5 ⁇ , 3-5 ⁇ , 3-8 ⁇ (e.g. mid-IR or MWIR), 3-12 ⁇ , 5-12 ⁇ , 8-12 ⁇ , 8-15 ⁇ (e.g. LWIR), 10-16 ⁇ , 12-18 ⁇ , 8-20 ⁇ or any other set of wavelengths that range from about 0.5-32 ⁇ .
- cutoff wavelengths that fall within the ranges of about 0.5-5 ⁇ , 3-5 ⁇ , 3-8 ⁇ (e.g. mid-IR or MWIR), 3-12 ⁇ , 5-12 ⁇ , 8-12 ⁇ , 8-15 ⁇ (e.g. LWIR), 10-16 ⁇ , 12-18 ⁇ , 8-20 ⁇ or any other set of wavelengths that range from about 0.5-32 ⁇ .
- the p-n junction may have type II band gap alignment, as shown in FIG. 1, using a heterojunction.
- the layers that create the junction may have dissimilar crystalline structure.
- a II- VI layer and a IV- VI layer could be used to form the heterojunction.
- heterojunctions may offer advantages over homojunctions. For example, in comparison to homojunctions, heterojunctions may have relatively less diffusion of dopant materials between heterojunction layers. The lesser diffusion of dopant material may maintain a well-defined interface between the two layers to maintain the p-n junction behavior of the semiconductor.
- heterojunctions may be easier to fabricate because certain n-type materials can be applied via wet chemical methods (e.g. chemical bath deposition (CBD)).
- CBD chemical bath deposition
- n-type materials that can be used include CdS, ZnO, and Titanium Dioxide (Ti0 2 ).
- CdS CdS
- ZnO ZnO
- Ti0 2 Titanium Dioxide
- the CdS layer may be grown directly on a substrate with a readout circuit via CBD to create relatively large format FPAs with relatively high detectivity.
- the PV detector 100 may also be constructed on a planar or non-planar (e.g., wire or quantum dot) substrate.
- the PV Pb-salt detector 100 may further comprise a charge-separation-junction (CSJ) structure comprising a plurality of charge-separation-junctions.
- the CSJ structure may be disposed on or embedded in a semiconductor layer, such as an epitaxial layer.
- the PV Pb-salt detector 100 may comprise IV- VI Pb-salt materials, which are used herein as non-limiting examples.
- IV- VI Pb-salt materials offer advantages in the long wavelength regime of enhancement of the Auger non-radiative lifetime. The low Auger recombination results in a relatively increase in detector performance, such as relatively high detectivity and relatively high operating temperature.
- CSJ structure within a PV Pb-salt detector 100 may be used to prevent low carrier lifetime because of, for example, Schokley-Reed-Hall recombination.
- the CSJs may in effect separate the electrons and holes in mono-crystalline, polycrystalline, or amorphous Pb-salt materials to prevent recombination.
- the PV Pb-salt detector 100 may be a single element detector that may comprise a plurality of CSJs embedded in a single semiconductor layer (e.g. Pb-salt layer), which could be a p- type or n-type material, and comprises a plurality of p-n junctions effectively embedded within the single semiconductor layer.
- the single semiconductor layer may be coupled substantially parallel to a substrate.
- Each p-n junction comprises a pair of Ohmic contacts isolated from each other, wherein all of the p-type contacts are interconnected and all of the n-type contacts are interconnected to form the single element detector, which may correspond to detecting a pixel.
- the photo-induced electrons and holes may be spatially separated by the built-in potential and carrier lifetimes to separate electron-hole pairs in space and lower the recombination rate.
- CSJs may alleviate short-carrier lifetime ( ⁇ 10 ns) which may be a problem for Pb-salt layers, such as a PbSe layer, grown on Si substrates. Introducing CSJs within PV Pb-salt detectors will be discussed in more detail in the description regarding FIGS. 4-9.
- FIG. 2 is a schematic diagram of a non-limiting embodiment of a type II band gap alignment for a PV Pb-salt detector 200.
- FIG. 2 illustrates an n-type Pb-salt layer band gap 202 and a p-type non-Pb-salt layer band gap 204 for the PV Pb-salt detector 200.
- the n-type Pb-salt layer and the p-type non-Pb-salt layer may be coupled together to form the p-n junction.
- the n-type Pb-salt material may be deposited as a mono-crystalline material, polycrystalline material, or an amorphous material.
- the Pb-salt layer may comprise crystallites with sizes as described elsewhere herein.
- a polycrystalline Pb-salt material may provide for a relative higher material quality in comparison to a mono-crystalline Pb-salt material.
- a mono-crystalline may provide for a relatively more uniform Pb-salt layer and typically produces a relatively easier contact surface.
- the PV Pb-salt detector 200 may further comprise a plurality of CSJs.
- the p-n junction formed between the n-type Pb-salt layer and the p- type non-Pb-salt layer may have type II band gap alignment such that the energy level for the conduction band of the n-type Pb-salt layer is about equal to or less than the energy level for the conduction of the p-type non-Pb-salt layer.
- the p-type layer's (e.g., p-type non-Pb-salt layer) conduction band may be about equal or relatively higher than the energy level of the conduction band of the n-type layer (e.g. n-type Pb-salt layer).
- the wider band gap p-type non-Pb-salt layer could be replaced with Ohmic contact materials that contact the Pb-salt layer when the wider band gap material is not used to form p-n junction within the PV Pb-salt detector 200.
- the Ohmic contact material which may have a narrower band gap than the Pb-salt layer, and the Pb-salt layer may form an Ohmic contact.
- FIG. 3 is a schematic diagram of a non-limiting embodiment of a type II band gap alignment for a double heterojunction PV Pb-salt detector 300.
- FIG. 3 illustrates a n-type layer band gap 302, a p/n-type Pb-salt layer band gap 304, and a p-type layer band gap 306 for the double heterojunction PV Pb-salt detector 300.
- the double heterojunction PV Pb-salt detector 300 may comprise a plurality of CSJs that form a CSJ structure. As shown in FIG. 3, the Pb-salt material could be p-type and n-type within the double heterojunction PV Pb-salt detector 300.
- two p-n junctions may be formed within the double heterojunction PV Pb-salt detector 300 when the Pb-salt layer is either a p-type or an n- type.
- the portion of the Pb-salt layer that is a p-type material may be coupled to an n- type material to form a p-n junction.
- the portion of the Pb-salt layer that is an n-type material may be coupled to a p-type material to form another p-n junction.
- PV detectors instead of a PV detector that comprises a p-n junction, one non-limiting embodiment of the PV detector may comprise a Schottky contact junction used for photo-detection.
- the PV detector with the Schottky contact junction may comprise a Pb-salt layer that may be n-type or p-type and may comprise polycrystalline material, mono-crystalline material, and amorphous material.
- present disclosure is not limited in its application to the specific examples, experimentation, results and laboratory procedures described herein. Rather, the examples are simply provided as several of various embodiments and are meant to be exemplary and not exhaustive.
- FIG. 4 is a schematic diagram of a top-down view of a non-limiting embodiment of a PV Pb-salt detector 400 that comprises a two dimensional CSJ structure 402.
- PV Pb-salt detector 400 comprises a substrate 412, such as a silicon substrate (or other substrate material described herein), having disposed thereon a single Pb-salt layer 414.
- the substrate 412 could be any suitable material that include, but are not limited to Si, silica, Silicon Dioxide (Si0 2 ) , glass, Barium fluoride (BaF 2 ), quartz, sapphire, and conductive transparent oxides.
- the substrate 412 could be a planar or non-planar (e.g., wire, curved, or quantum dot) substrate.
- the PV Pb-salt detector 400 is also depicted in cross-section in FIG. 5.
- the single Pb-salt layer 414 may be mono-crystalline or polycrystalline material and may be epitaxial.
- the single Pb-salt layer 414 may be a continuous layer that is disposed on the substrate 412.
- the single Pb- salt layer 414 may be any IV- VI Pb-salt material described herein, such as PbSe, and may comprise a p-type dopant material.
- the CSJ structure 402 comprises a plurality of element areas 416, each comprising an n-type material, that are disposed upon the single Pb-salt layer 414.
- the plurality of element areas 416 are spaced apart and may be substantially parallel to each other and may be substantially parallel to the surface of the substrate 412 upon which the single Pb-salt layer 414 is disposed.
- the element areas 416 may have the shapes of, but are not limited to strips, wires (e.g., nanowires), tubes, or dots.
- the substrate 412 may be any substrate material discussed herein, including, but not limited to: a silicon substrate, such as a monocrystalline silicon substrate; a silicon micro-lens; a mid-infrared transparent substrate; an infrared transparent substrate; a substrate transparent to light in a visible portion of the light spectrum; a polyimide substrate developed for solar cell applications; a monocrystalline semiconductor material; or other monocrystalline or polycrystalline substrates.
- a silicon substrate such as a monocrystalline silicon substrate; a silicon micro-lens; a mid-infrared transparent substrate; an infrared transparent substrate; a substrate transparent to light in a visible portion of the light spectrum; a polyimide substrate developed for solar cell applications; a monocrystalline semiconductor material; or other monocrystalline or polycrystalline substrates.
- the substrate 412 can be constructed of a monocrystalline or polycrystalline material such as, but not limited to, silicon (e.g., monocrystalline silicon), glass, silica, Si0 2 , quartz, sapphire, CaF 2 , amorphous materials such as glass, conductive transparent (in visible) materials such as fluorine doped Tin Oxide, or Indium Tin Oxide.
- the substrate 412 may be constructed as a cylinder.
- the substrate 412 may be constructed in a variety of different manners and may have a variety of shapes, such as planar, curved, or a combination of planar and curved portions and may be rigid or flexible.
- the substrate 412 may be able to pass light of the wavelengths or wavelength ranges to be detected by the photodetector.
- Each element area 416 may have an n-type Ohmic contact 422 disposed thereon to form a plurality of interconnected n-type Ohmic contacts 422. Further, a p-type Ohmic contact 424 may be disposed upon a portion of the single Pb-salt layer 414 to form a plurality of interconnected p-type Ohmic contacts 424. As shown in FIG. 4, the layout of the n-type Ohmic contact 422 and the p-type Ohmic contact 424 may form a finger-like structure.
- the p-type Ohmic contacts 424 may be located between adjacent element areas 416 to form a plurality of interconnected p-type Ohmic contacts 424, and the n-type Ohmic contacts 422 may be located on top of each element area 416 to form a plurality of interconnected n-type Ohmic contacts 424. While the single Pb-salt layer 414 is referred to in this example as constructed of a p-type material, and the overlaying element areas 416 are referred to as constructed of an n-type material, it will be understood that the materials could be switched, such that the Pb salt layer 414 comprises an n- type material and the element areas 416 comprise a p-type material instead.
- the junctions of the present PV Pb-salt detectors can be formed by n-type doping, p- type doping, by having Schottky junctions, or by heterojunction.
- the Ohmic contacts 422 and 424 may be constructed of gold (Au), silver (Ag) or any other suitable conductive material known by persons having ordinary skill in the art of IV- VI semiconductor construction.
- the Pb-salt layer may be formed by any appropriate deposition method known in the art, including, but not limited to an epitaxial deposition method such as molecular beam epitaxy or chemical vapor deposition (CVD).
- the CSJs of any of the presently disclosed inventive concepts described herein can be used on planar or non-planar (e.g., curved) substrates.
- FIG. 5 is a cross-sectional view of the PV Pb-salt detector 400 that comprises a two dimensional CSJ structure 402.
- the CSJ structure 402 of the PV Pb-salt detector 400 comprises element areas 416 that comprise n-type (or p-type) material that may be shaped as strips, wires, tubes, or dots, for example.
- Each of the element areas 416 may be disposed on top of a portion of the single Pb-salt layer 414.
- a p-type Ohmic contact 424 may be positioned on the Pb-salt layer 414 between adjacent element areas 416.
- an n-type Ohmic contact 422 may be coupled to or contact the element area 416.
- the n- type material may be embedded in a layer of p-type single Pb-salt layer 414 (or n-type, respectively), such as PbSe, which form a plurality of p-n junctions within the p-type Pb-salt layer 414.
- Embedding n-type material in a layer of p-type single Pb-salt layer 414 (or n-type, respectively) is described in more detail below in FIGS. 8 and 9.
- the element areas 416 are a metal material
- Schottky contact junctions 420 are formed instead of p-n junctions 420.
- the built-in potential of the p-n junctions 420 may spatially separate the electrons and holes at a relatively faster rate than Auger and radiative recombination.
- the p-n junctions 420 may be used to enhance carrier lifetime.
- the photon-induced electrons and holes may subsequently be transported to the Ohmic contacts 422 and 424.
- the n-type Ohmic contact 422 may be used to collect the free holes and the p-type Ohmic contact 424 may be used to collect the free electrons.
- the p-n junctions 420 and the Ohmic contacts 422 and 424 may be located within the diffusion length of the majority carriers.
- FIG. 5 illustrates an embodiment wherein diffusion of dopant material from the n-type material into the p-type material, and vice-versa, is absent or minimal at the p-n junction 420.
- Minimal diffusion of dopant material may maintain a relatively well-defined interface between the element areas 416 and the Pb-salt layer 414 in order to maintain the p-n junction behavior of the semiconductor.
- heterojunctions and Schottky contact junctions generally have reduced diffusion of dopant materials at the junction layers in comparison to homojunctions.
- FIG. 6 is cross-sectional view taken through a PV Pb-salt detector 600, which is similar to PV Pb-salt detector 400 except it comprises a CSJ structure 402 comprising element areas 416 and a plurality of dopant diffusion regions 618.
- the CSJ structure may be able to separate out electrons and holes and avoid recombination when dopant diffusion regions 618 are embedded within the single Pb-salt layer 414.
- the dopant diffusion regions 618 may occur when the p-n junctions are homojunctions.
- each element area 416 with n-type material may diffuse into a portion of the single p-type Pb-salt layer 414 thereby forming a plurality of n-type dopant diffusion regions 618.
- the n-type dopant diffusion regions 618 in the p- type Pb-salt layer 414 may be located below and/or surround each element area 416 such that a plurality of substantially parallel p-n junctions 620 are formed in the p-type Pb-salt layer 414.
- the dopant diffusion regions 618 may also be referred to herein as charged zones or depletion zones.
- the p-n junctions 620 are located where the n-type dopant diffusion regions 618 meet the p-type Pb-salt layer 414.
- the element areas 618 may comprise a p-type material and the Pb- salt layer 414 may comprise an n-type material wherein the dopant diffusion regions 618 comprise p-type dopant.
- FIG. 7 is a schematic diagram of a non-limiting embodiment of a FPA 700 used for photo-detection.
- the FPA 700 may be constructed to comprise an array substrate 720, a plurality of PV Pb-salt detectors 702 that are disposed on an upper surface of the array substrate 720.
- the PV Pb-salt detectors 702 may correspond to the PV Pb-salt detectors 400 in FIG. 4 or the PV Pb- salt detector 800 in FIG. 8 or any other detectors described herein.
- the PV Pb-salt detector 702 may correspond to a pixel of the FPA 700.
- Each of the PV Pb-salt detectors 702 may collect photons to correspond to a particular area of an image.
- the FPA 700 may further comprise a Readout Integrated Circuit (ROIC) or some other read out circuit (not shown in FIG. 7) configured to provide the analog electrical signals (e.g. photoelectric current and/or voltage) from the PV Pb-salt detectors 702 to one or more signal processors to generate digital images and determine which IR signatures the PV Pb-salt detectors 702 are receiving.
- ROI Readout Integrated Circuit
- FIG. 8 is a schematic diagram of a side view of a non-limiting embodiment of a PV Pb- salt detector 800 that comprises a three dimensional CSJ structure 806 that comprises a plurality of vertically oriented element areas 804.
- the PV Pb-salt detector 800 is constructed of a substrate 814, a conducting layer 812 (also referred to herein as an Ohmic contact layer) disposed upon the substrate 814, and a Pb-salt layer 802.
- Embedded within the Pb-salt layer 802 is the plurality of vertical element areas 804 (which may be, but are not limited to strips, wires (nanowires), tubes, stumps, rods, and dots) that extend substantially vertically (perpendicularly) into the Pb-salt layer 802 from a base 808.
- the base 808 may comprise substantially the same material as the vertical element area 804.
- Element areas 804 may be semiconductor or metal material or any material described herein for forming element areas of the CSJ structures described herein.
- the base 808 is disposed upon the conducting layer 812, and the Pb-salt layer 802 is disposed upon the base 808.
- the plurality of vertical element areas 804 of the CSJ structure 806 are embedded within the Pb-salt layer 802.
- Junctions such as p-n junctions and Schottky contact junctions, may be formed by embedding the element areas 804 within the Pb-salt layer 802.
- a first Ohmic contact 806, for example, constructed of Au or any suitable conductive material, is attached to a portion of the Pb-salt layer 802 and a second Ohmic contact 810, for example, constructed of Au, or any suitable conductive material, is attached to an exposed portion of the conducting layer 812.
- the first Ohmic contact 806 may be configured as a positive terminal that collects free electrons and the second Ohmic contact 810 may be configured as a negative terminal that collects free holes to avoid recombination.
- the Pb-salt layer 802 in one non-limiting embodiment, comprises a p-type material (e.g. PbSe, Pb-salt layer 414, and/or other Pb-salt materials as discussed elsewhere herein) and the vertical element areas 804 comprise an n-type material (e.g. element area 416 and/or any n-type material as discussed elsewhere herein).
- P-n junctions form at the interfaces between the vertical element areas 804 and the adjacent zones of the p-type Pb-salt layer 802, for example, as shown in FIG. 6.
- the Pb-salt layer 802 may comprise an n-type material, wherein the vertical element areas 804 correspondingly comprise a p-type material.
- the conducting layer 812 may comprise a transparent conducting oxide (TCO) film, such as, but not limited to indium tin oxide (tin-doped indium oxide), fluorine doped tin oxide, carbon nanotube networks, graphene, polymers such as poly (3,4-ethylenedioxy thiophene) (PEDOT), and derivatives thereof, copolymers such as PEDOT:PSS (polystyrene sulfonate), aluminum doped zinc oxide (AZO), and indium-doped cadmium oxide.
- the substrate 814 may be constructed of, but is not limited to, any suitable substrate material described elsewhere herein. [0077]
- FIG. 9 is a cross-sectional view taken through line 9-9 of the PV Pb-salt detector 800.
- each of the vertical element areas 804 are spaced apart from each other such that the Pb-salt layer 802 surrounds each of the element areas 804.
- the vertical element areas 804 may be constructed to have a cylindrical-like shape or any other suitable rod-like or stump-like shape.
- Design criteria of the PV Pb-salt detector 800 of the presently disclosed inventive concepts include, but are not limited to optimization of the distance between p-and n-region based on the carrier lifetime. In principle, photo-induced electrons and holes should be spatially separated by the p-n junction. At the same time, the distances apart should not be too small to avoid "sweep- out" effect. These dimensions can be designed based on the material parameters such as dielectric constant and doping concentration. For example, for PbSe, the distance can be in a range of about 0.5 ⁇ to about 5 ⁇ . In other embodiments, the Pb-salt distance may range from about 10 nm to about one millimeter.
- FIG. 10 illustrates a J-V curve for the PV Pb-salt detector 800 depicted in FIG. 8.
- Detectivities of the PV Pb-salt detector 800 may be in the range (at room temperature) of about lxlO 10 cmHz ⁇ W "1 to about lxlO 11 cmHz 1/2 W _1 .
- the detectivities may output perform typical currently available photoconductive (PC) detectors.
- the response times of the PV Pb-salt detector 800 may generally be in the range of about 100 ns to about 600 ns, which may be faster than typical PC detector counterparts (which is generally about several ⁇ 8).
- the fabrication process for a CSJ detector of the presently disclosed devices start with an MBE growth of a p-type Pb-salt layer (such as, but not limited to PbSe or PbSnSe or other suitable IV- VI materials described herein) on a substrate material, such as a Si substrate.
- a p-type Pb-salt layer such as, but not limited to PbSe or PbSnSe or other suitable IV- VI materials described herein
- Photolithography, the deposition of Si0 2 , and the lift-off may be used to form a Si0 2 mask (grid) on the p-type layer.
- n-type dopant could comprise n- type doped Pb-salt materials, thermal deposition of n-type dopants, or a simple Schottky contact, or other materials described herein).
- etching may be used to remove most of the Si0 2 mask layer to expose p-type grid pattern with interleaved n-type grid pattern.
- Annealing may be used for impurity diffusion followed by 0 2 passivation. Ohmic contact formation may subsequently occur on exposed n-type and p-type grid elements.
- FIG. 11 is a schematic diagram of another non-limiting embodiment of a PV Pb-salt detector of the presently disclosed inventive concepts, designated by the general reference numeral 1100 and which comprises a heterojunction region 1102, which may comprise at least one Pb-salt layer 802 and at least one non-Pb-salt layer 1104.
- the non-Pb-salt layer 1104 may be disposed on a conducting layer 812 (as discussed above), and the conducting layer 812 may be disposed on substrate 814 (as discussed above).
- the Pb-salt layer 802 may be a p-type material (e.g. more holes concentration) and the non-Pb-salt layer 1104 may be an n-type material (e.g. more electrons concentration).
- the Pb-salt layer 802 may be an n-type material and the non-Pb-salt layer 1104 may be a p-type material.
- the band gaps for the Pb-salt layer 802 and the non-Pb-salt layer 1104 may have type II band gap as shown in FIGS. 1 or 2.
- the heterojunction region 1102 may comprise Pb-salt layer (e.g., PbSe) 802 that is coupled to and deposited upon a non-Pb- salt layer (e.g. an n-type CdS layer) 1104.
- Pb-salt layer 802 when fabricating the p-n junction, the Pb-salt layer 802 may be grown upon the non-Pb-salt layer (e.g., the n-type CdS layer) 1104.
- the PV Pb-salt detector 1100 may comprise at least one n-type non-Pb-salt layer (e.g., CdS) and at least one p-type Pb-salt layer 802.
- FIG. 12 is a schematic diagram of an alternate embodiment of a PV Pb-salt detector 1200 having the Pb-salt layer 802 (e.g., PbSe) grown prior to the non-Pb-salt layer 1104 (e.g., n-type CdS layer).
- the p-n junction could be formed by growing a non-Pb-salt layer 1104 (e.g., CdS) on top of the Pb-salt layer 802.
- the conducting layer 812 may comprise substantially the same material as the Pb-salt layer 802.
- the Pb-salt layer 802 may comprise a p-type material and the non-Pb-salt layer may comprise an n-type material.
- the Pb-salt layers of the PV Pb-salt detectors 400, 500, 600, 800, 1100, and 1200 or any other detector embodiment described herein, the Pb-salt layer may comprise of any of the following: PbSe, PbS, PbTe, PbXSelenium (Se), PbXTellurium (Te), and PbXSulfur (S), where X represents a chemical element with a composition that is configured to form ternary compound semiconductors.
- X could include, but is not limited to Sn, Strontium (Sr), Europium (Eu), Germanium (Ge), and Cd (e.g., PbSnSe, PbSnTe, PbSrSe, PbSrTe, PbEuSe, PbEuTe, PbCdSe, or PbCdTe,
- the Pb-salt layer could also be a quaternary compound, such as, but not limited to, PbXSeTe, PbXSeS, PbXTeS.
- the Pb-salt layer could be in mono-crystalline, polycrystalline or amorphous form.
- the Pb-salt layer could also be in bulk form, microcrystalline form, or nano-structures such as quantum dots, quantum wire or quantum well.
- the Pb-salt layer could be in two-dimensional form or three-dimensional form, such as a "forest" of wires.
- the Pb-salt or non-Pb-salt layers described herein could comprise a two dimensional layer, or three-dimensional elements embedded within another layer, such as the PV detector 800 as described in FIGS. 8 and 9.
- the substrate upon which the layers are disposed could be any suitable material, such as, but not limited to Si, silica, Si0 2, glass, Barium fluoride (BaF 2 ), quartz, sapphire, and conductive transparent oxides.
- the conductive film may be a Pb-salt mono-crystalline material.
- Certain non-Pb-salt materials, such as but not limited to CdS can be grown on different surfaces including metals, thus could be grown directly on a readout circuit.
- the Pb-salt arrays could then be grown on the non-Pb-salt layer (e.g., CdS).
- the chemical growth method for growing the non-Pb-salt layer and the Pb-salt arrays may be scaled up to fabricate relatively large format arrays.
- CdS is a wide band gap semiconductor material with energy gap (E g ) at about 2.4 electron volts (eV) and may be an n-type and window material with relatively high efficiency thin film solar cells based on CdTe and CIGS ((Cu(In,Ga)Se 2 )), and other optoelectronic devices.
- the electron affinity of CdS may be around 4.5 eV, which is relatively close to PbSe material. Therefore, CdS may form a heterojunction with a Pb-salt layer (e.g. PbSe layer) for IR photodiode detector fabrication.
- an epitaxial PbSe thin film is used to demonstrate the feasibility of n-CdS/p-PbSe heterostructure (e.g., where CdS has a larger band gap energy than PbSe) for mid-IR detector applications.
- the chemical growth method e.g. fabrication
- Pb-salt materials and CdS as well as the form of materials (mono- crystalline, polycrystalline, amorphous); however, is not limited to the specific fabrication method or material form.
- two consecutive material growth steps may be used in the chemical growth method to form the Pb-salt layer and the n-CdS layer.
- the growth method may be performed in a two- growth-chamber MBE system.
- the first material growth step may involve PbSe thin film growth or any other Pb-salt material.
- a double polished high resistant Si wafer (-3500 Q » cm) (or any other suitable substrate described herein) may be cleaned, such as a modified Shiraki cleaning method known by persons skilled in the art, prior to the growth.
- the Si wafer may be dried with a high purity nitrogen gas (N 2 ) purge and transferred into the MBE system.
- N 2 nitrogen gas
- a buffer layer such as an ultrathin CaF 2 ( ⁇ 2 nm) may be grown in the first growth chamber, to compensate for the lattice and thermal mismatch between PbSe and Si.
- Other materials may be used as the buffer layer if the other materials are substantially similar to the lattice of Si and have a thermal expansion coefficient that is substantially similar to PbSe.
- the substrate temperature during growth of the PbSe layer may be controlled at about 800 °C in order to obtain surface reconstruction of Si substrate for epitaxial growth of calcium fluoride (CaF 2 ).
- the PbSe film (e.g. about 1.2 ⁇ in thickness) may then be deposited in the second growth chamber of the MBE system.
- Substrate temperature may be about 390 °C for PbSe growth with a PbSe deposition rate of about 25 nm/minute.
- An additional Se source may be used to adjust the p-type carrier concentration of the film and also to control material quality because of the high Se vapor pressure during growth.
- the second material growth step may grow a CdS film on top of the PbSe film by using a CBD method.
- the PbSe film on Si substrate (or other suitable substrate) may be divided into one or more relatively smaller samples.
- the relatively smaller samples may be fixed on a Teflon® holder and kept vertically in the CBD solution during growth.
- the chemicals used in the CBD solution may comprise analytic grade reagents without further purification.
- a 15 milliliters (ml) mixed aqueous solution that comprises Cadmium Acetate (Cd(CH 3 COO) 2 ) (e.g. 24 millimoles (mmol)) and Ammonium Acetate (NH 4 CH 3 COO) (e.g.
- a 15 ml thiourea (e.g. 30 mmol) may be used as a sulfur precursor.
- the two solutions may be mixed together in another 60 ml glass bottle and 7.5 ml ⁇ 3 ⁇ 2 0 may be introduced into the bottle as a complexing agent.
- the PbSe samples in the Teflon holder are immersed in the aqueous solution, and the bottle may then be heated up and stabilized for about an hour in the 60 °C water bath for subsequent CdS film deposition (thickness is about 100 nm).
- the as-grown CdS/PbSe samples may be rinsed in deionized water and may then be purged to dry out under high purity N 2 .
- the carrier concentrations of CdS and PbSe thin films prepared using the CBD as described above may be about n ⁇ lxl0 16 cm “3 and p ⁇ 3xl0 17 cm “3 , respectively.
- the electron concentration of CdS may be about one order of magnitude lower than the hole concentration of PbSe at room temperature, which means that major depletion region may fall on the CdS side.
- the junction area may be formed using similar photolithographic technology and thermal vapor deposition of gold (Au) contacts for both CdS and PbSe layers.
- Au gold
- Other conductive materials may be used besides Au when forming the contacts for both the CdS and PbSe layers.
- the lift-off procedure may be performed after the metal deposition.
- FIG. 13 depicts a schematic diagram of a PV CdS/PbSe heterojunction detector 1300.
- the PV CdS/PbSe heterojunction detector 1300 may comprise a Si substrate 1312, a CaF 2 conducting layer 1310, a p-type PbSe layer 1308, and an n- type CdS layer 1306.
- An n-type Ohmic contact 1302 may contact the n-type CdS layer 1306 and a p-type Ohmic contact 1304 may contact the p-type PbSe layer 1308. As shown in FIG.
- the Si substrate 1312 may have a thickness of about 350 ⁇
- the CaF 2 conducting layer 1310 may have a thickness of about 2 nm
- the p-type PbSe layer 1308 may have a thickness of about 1.2 ⁇
- the n-type CdS layer may have a thickness of about 100 nm.
- the quantum efficiency of the PV CdS/PbSe heterojunction detector 1300 determines the response intensity behavior of the detector with the temperature. There are two regions in p- type PbSe layer 1308 that produce photo-generated carriers, including neutral p-type region and junction region on p-type PbSe layer 1308 side. In the back illumination case, the incident light intensity decays exponentially in the p-type PbSe layer 1308 (about 1.2 ⁇ ), and thus most of photo- generated carriers are in neutral p-type PbSe region. On the other hand, as mentioned previously, due to carrier concentration difference, most of the depletion region drops in n-type CdS layer 1306.
- the calculated depletion width in PbSe side at room temperature is about ⁇ 2.7 nm. Although depletion width may change with temperature, it is relatively small compared to the p-type PbSe layer 1308 thickness.
- the carrier collection efficiency affected by bias condition may not a factor to be considered because of the zero bias photovoltaic mode operation method.
- photo-generated carriers in neutral p-type PbSe region dominate the photodetector quantum efficiency, which can be described as follows, assuming there is no potential barrier for minority carrier transport due to hetero unction band offset as shown in equation 1:
- the variable r is the illuminated junction surface reflection coefficient
- a is the absorption coefficient
- L e is the electron diffusion length as mentioned
- x p is the distance from backside of PbSe film to the p side junction boundary.
- the temperature dependent parameters including diffusion length L e and absorption coefficient a play may affect the quantum efficiency and eventually photoresponse.
- diffusion length L e Carrier mobility i in lead-salt semiconductor is proportionally to T " mainly due to the decrease of phonon scattering.
- the minority carrier lifetime, especially at lower temperatures, in the p-type PbSe layer 1308 may be dominated by the Shockley-Rheed-Hall recombination process, which is not substantially affected by temperature. Therefore, the diffusion length increases at lower temperature. Not only are the absorption edge red-shifts to longer wavelength, but also the absorption coefficient increases slightly in the photoresponse spectral range at lower temperature. Therefore, temperature-dependent quantum efficiency can be estimated by using the discussed diffusion length and absorption parameters. The simulation based on the theory described above shows that quantum efficiency increases from about 20% to about 70% while temperature drops from room temperature down to about 140 K. As a result, the photoresponse intensity may typically increase at lower temperature, which is shown in FIG. 15.
- FIG. 14 illustrates a current density/voltage (J-V) curve for the PV CdS/PbSe heterojunction detector 1300 of FIG. 13.
- FIG. 14 illustrates the room temperature joules-volts (J- V) characteristic of an n-type CdS/p-type PbSe heterojunction detector 1300.
- the rectifying ratio measured at about +0.3 V is about 178.
- the dark current density is about 1.15x10 -4 A/cm 2 at about 10 milli-V (mV) and a forward turn-on voltage is about 0.12 V.
- the forward J-V characteristic of a p-n junction may be described by the exponential relation J o ⁇ ( ⁇ / ⁇ 13 ⁇ 4 ⁇ ), where ⁇ is the ideality factor, when exp(qV ⁇ k B T) » 1.
- ⁇ is the ideality factor, when exp(qV ⁇ k B T) » 1.
- the ideality factor ⁇ is determined by curve fitting to be about 1.79, which indicates the recombination current may play a major role in this range.
- the inset box in FIG. 14 shows a curve which is the same J-V characteristic but wherein the current density is in logarithm.
- the PV CdS/PbSe heterojunction detector 1300 performance may be evaluated by a detectivity measurement system.
- a detectivity measurement system For example, a calibrated 800 Kelvin (K) blackbody from Infrared System Development may be used as the standard infrared light source.
- K Kelvin
- a Thorlabs mechanical chopper is integrated in order to provide a frequency-modulated heat source.
- PV mode may be used, which means zero bias is applied on the heterojunction diode during the measurement.
- signal and noise currents from the device are directly collected by a Stanford Research System SR830 lock-in amplifier.
- the responsivity R and specific detectivity * are obtained by using the definition as shown below in equation 2:
- the cutoff wavelength is obtained from the spectral response measurement described as follows.
- FIG. 15 illustrates temperature-dependent mid-IR spectrum-resolved photoresponses of the CdS/PbSe heterojunction detector 1300 from 320 K to 200 K and from 200K to 140 K. The measurements are taken by a Bruker IFS-66v Fourier Transform Infrared Spectroscope system. As seen in FIG. 15, when temperature decreases from 320 K to 200 K, both photoresponse and the cutoff wavelength increase gradually. After the temperature drops below 200 K, the cutoff wavelength is still increasing with the decreasing temperature, but the peak photoresponse intensity decreases as illustrated.
- FIG. 16 illustrates normalized peak photoresponse intensities and the cutoff wavelengths at temperatures ranging from 140K to 320 K. In FIG. 16, the maximum photoresponse intensity is obtained at around 200 K.
- examples of Pb-salts which can be used in the PV Pb-salt detectors throughout the present disclosure include, but are not limited to combinations of Group IV and Group VI elements: PbS, PbSe, PbTe, PbSnSe, PbSnTe, PbSrSe, PbSrTe, PbEuSe, PbEuTe, PbCdSe, PbCdTe, and any Pb-salt containing a combination of two, three, four, or more Group IV and Group VI elements.
- Substrates that may be used in the devices of the presently disclosed inventive concepts include, but are not limited to silicon, glass, silica, quartz, sapphire, CaF 2 , and other substrates commonly used by persons having ordinary skill in the art to construct photodetectors.
- Examples of p-type and n-type doping materials which can be used in the presently disclosed detectors include, but are not limited to: Se, Tl, BaF 2 , Na, Pb, Bi, Sb, In, and I.
- the presently disclosed detectors may be implemented for mid-/far IR sensing and imaging applications.
- the PV Pb-salt photodetectors enable a relatively low-cost, relatively large- format detector focal plane array having high detectivity at ambient temperatures.
- Examples of the utilities of the PV Pb-salt detectors and FPAs of the presently disclosed inventive concepts include, but are not limited to thermal imaging and environmental uses (e.g. gas detection and control, and pollution measurements).
- compositions, devices, and/or methods disclosed herein can be made and executed without undue experimentation in light of the present disclosure. While the compositions, devices and methods of this presently disclosed inventive concepts have been described in terms of particular examples and embodiments, it will be apparent to those of skill in the art that variations may be applied to the devices, compositions and/or methods and in the steps or in the sequence of steps of the method described herein without departing from the concept, spirit and scope of the presently disclosed inventive concepts. All such similar substitutes and modifications apparent to those skilled in the art are deemed to be within the spirit, scope and concept of the inventive concepts as defined by the appended claims. Moreover, the following claims are exemplary claims supported by the present disclosure and are not intended to be limiting of the claims which can be pursued in subsequent patent applications based on the present application.
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CN201480034918.6A CN105324856B (zh) | 2013-06-20 | 2014-06-20 | 光伏铅盐检测器 |
US14/975,404 US9887309B2 (en) | 2012-12-13 | 2015-12-18 | Photovoltaic lead-salt semiconductor detectors |
US14/975,285 US10109754B2 (en) | 2012-12-13 | 2015-12-18 | Photovoltaic lead-salt detectors |
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US201361837490P | 2013-06-20 | 2013-06-20 | |
US61/837,490 | 2013-06-20 | ||
PCT/US2013/075110 WO2014093877A1 (en) | 2012-12-13 | 2013-12-13 | Polycrystalline photodetectors and methods of use and manufacture |
USPCT/US2013/075110 | 2013-12-13 | ||
US201461969975P | 2014-03-25 | 2014-03-25 | |
US61/969,975 | 2014-03-25 |
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US14/975,285 Continuation US10109754B2 (en) | 2012-12-13 | 2015-12-18 | Photovoltaic lead-salt detectors |
US14/975,404 Continuation US9887309B2 (en) | 2012-12-13 | 2015-12-18 | Photovoltaic lead-salt semiconductor detectors |
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CN109920863A (zh) * | 2019-01-28 | 2019-06-21 | 电子科技大学 | 窄禁带半导体薄膜、光敏二极管及制备方法 |
CN109873046B (zh) * | 2019-01-28 | 2020-09-11 | 电子科技大学 | 双异质结光敏二极管及制备方法 |
CN112331737B (zh) * | 2020-10-30 | 2022-05-03 | 苏州大学 | 一种紫外-可见-近红外硅基光电探测器及其制备方法 |
CN113206184B (zh) * | 2021-04-30 | 2023-04-07 | 河北大学 | 一种基于硒化铅薄膜的自驱动紫外光探测器 |
CN113838964B (zh) * | 2021-09-15 | 2023-11-24 | 北京量子信息科学研究院 | 超导-半导体纳米线异质结及其制备方法和包含其的器件 |
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US3716424A (en) * | 1970-04-02 | 1973-02-13 | Us Navy | Method of preparation of lead sulfide pn junction diodes |
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US3911469A (en) * | 1974-02-25 | 1975-10-07 | Texas Instruments Inc | Method of forming P-N junction in PbSnTe and photovoltaic infrared detector provided thereby |
US4154631A (en) * | 1977-05-27 | 1979-05-15 | The United States Of America As Represented By The Secretary Of The Navy | Equilibrium growth technique for preparing PbSx Se1-x epilayers |
US4183035A (en) * | 1978-06-26 | 1980-01-08 | Rockwell International Corporation | Inverted heterojunction photodiode |
US4996579A (en) * | 1983-02-04 | 1991-02-26 | The United States Of America As Represented By The Secretary Of The Navy | Design for electronic spectrally tunable infrared detector |
US4870027A (en) * | 1988-07-27 | 1989-09-26 | The United States Of America As Represented By The Secretary Of The Navy | Sensitization pretreatment of Pb-salt epitaxial films for Schottky diodes by sulfur vapor exposure |
US4962303A (en) * | 1989-06-27 | 1990-10-09 | The United States Of America As Represented By The Secretary Of The Navy | Infrared image detector utilizing Schottky barrier junctions |
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US20110146766A1 (en) * | 2008-02-26 | 2011-06-23 | Solar Cells Based On Quantum Dot Or Colloidal Nanocrystal Films | Solar cells based on quantum dot or colloidal nanocrystal films |
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