Photosensitive imaging devices and associated methods

Abstract
Photosensitive devices and associated methods are provided. In one aspect, for example, a photosensitive imager device can include a semiconductor substrate having multiple doped regions forming at least one junction, a textured region coupled to the semiconductor substrate and positioned to interact with electromagnetic radiation, and an electrical transfer element coupled to the semiconductor substrate and operable to transfer an electrical signal from the at least one junction. In one aspect, the textured region is operable to facilitate generation of an electrical signal from the detection of infrared electromagnetic radiation. In another aspect, interacting with electromagnetic radiation further includes increasing the semiconductor substrate's effective absorption wavelength as compared to a semiconductor substrate lacking a textured region.
Description
BACKGROUND

The interaction of light with semiconductor materials has been a significant innovation. Silicon imaging devices are used in various technologies, such as digital cameras, optical mice, video cameras, cell phones, and the like. Charge-coupled devices (CCDs) were widely used in digital imaging, and were later improved upon by complementary metal-oxide-semiconductor (CMOS) imagers having increased performance. CMOS sensors are typically manufactured from silicon and can covert visible incident light into a photocurrent and ultimately into a digital image. Silicon-based technologies for detecting infrared incident electromagnetic radiation have been problematic, however, because silicon is an indirect bandgap semiconductor having a bandgap of about 1.1 eV. Thus the absorption of electromagnetic radiation having wavelengths of greater than about 1100 nm is, therefore, very low in silicon.


SUMMARY

The present disclosure provides photosensitive devices and associated methods. In one aspect, for example, a photosensitive imager device can include a semiconductor substrate having multiple doped regions forming at least one junction, a textured region coupled to the semiconductor substrate and positioned to interact with electromagnetic radiation, and an electrical transfer element coupled to the semiconductor substrate and operable to transfer an electrical signal from the at least one junction. In one aspect, the textured region is operable to facilitate generation of an electrical signal from the detection of infrared electromagnetic radiation. In another aspect, interacting with electromagnetic radiation further includes increasing the semiconductor substrate's effective absorption length as compared to a semiconductor substrate lacking a textured region. In one specific aspect, the transfer element is selected from the group consisting of a transistor, a sensing node, a transfer gate, and combinations thereof.


The textured region can be positioned in a variety of locations relative to the doped regions. In one aspect, for example, the textured region is positioned on a surface of the semiconductor substrate that is opposite the multiple doped regions. In one specific aspect, the textured region has a surface morphology operable to direct electromagnetic radiation into or out of the semiconductor substrate. The surface morphology of the textured region relative to the semiconductor substrate can include a variety of configurations, including, without limitation, sloping, pyramidal, inverted pyramidal, spherical, parabolic, asymmetric, symmetric, and the like, including combinations thereof.


In another aspect, the textured region can be positioned on a surface of the semiconductor substrate that is adjacent the multiple doped regions. In a more specific aspect, an additional textured region can be positioned on a surface of the semiconductor substrate that is opposite the multiple doped regions. In this manner, textured regions can thus be positioned adjacent to multiple doped regions and opposite the multiple doped regions.


Various aspects of the textured region can vary depending on the desired configuration of the device. In one aspect, however, the textured region includes surface features having a size selected from the group consisting of micron-sized, nano-sized, and combinations thereof. Numerous surface feature morphologies are contemplated, nonlimiting examples of which include cones, pillars, pyramids, microlenses, quantum dots, inverted features, and combinations thereof. Additionally, the textured region can be formed by a variety of processes. Nonlimiting examples of such texturing processes can include lazing, chemical etching (e.g. anisotropic etching, isotropic etching), nanoimprinting, material deposition, and combinations thereof.


Additional layers and/or structures can be included in various devices according to aspects present disclosure. In one aspect, for example, a reflective layer can be coupled to the semiconductor substrate and positioned to maintain the electromagnetic radiation in the semiconductor substrate. In another aspect, a lens can be optically coupled to the semiconductor substrate and positioned to focus incident electromagnetic radiation into the semiconductor substrate.


In another aspect of the present disclosure, a method of making a photosensitive imager device is provided. Such a method can include forming a textured region on a semiconductor substrate having multiple doped regions forming a least one junction, wherein the textured region is formed in a position to interact with electromagnetic radiation and coupling an electrical transfer element to the semiconductor substrate such that the electrical transfer element is operable to transfer an electrical signal from the at least one junction.


In one aspect, the photosensitive imager device can be tuned to be selected to filter out specific electromagnetic radiation wavelengths. In one specific aspect, tuning includes forming surface features to have dimensions that selectively diffuse or selectively absorb a desired wavelength of electromagnetic radiation. In another aspect, tuning is accomplished through a factor selected from the group consisting of placement of the textured region, material type and/or thickness of the textured region, dopant type of the textured region, doping profile of the texture region, dopant profile of the semiconductor substrate, material type and/or thickness of the semiconductor substrate, and combinations thereof.


In another aspect of the present disclosure, a photosensitive imager device is provided. Such a device can include a semiconductor substrate having multiple doped regions forming a least one junction, a textured region coupled to the semiconductor substrate and positioned to interact with electromagnetic radiation, and at least 4 transistors coupled to the semiconductor substrate and with at least one of the transistors electrically coupled to the at least one junction.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a schematic view of a photosensitive device in accordance with one aspect of the present disclosure;



FIG. 2 is a schematic view of a photosensitive device in accordance with another aspect of the present disclosure;



FIG. 3 is a schematic view of a photosensitive device in accordance with yet another aspect of the present disclosure;



FIG. 4 is a schematic view of a photosensitive device in accordance with a further aspect of the present disclosure;



FIG. 5 is a schematic view of a photosensitive device in accordance with yet a further aspect of the present disclosure;



FIG. 6 is a schematic view of a photosensitive device in accordance with another aspect of the present disclosure;



FIG. 7 is a schematic view of a photosensitive pixel device in accordance with yet another aspect of the present disclosure;



FIG. 8 is a schematic view of a photosensitive pixel device in accordance with a further aspect of the present disclosure;



FIG. 9 is a schematic view of a photosensitive pixel device in accordance with yet a further aspect of the present disclosure;



FIG. 10 is a schematic view of a photosensitive pixel device in accordance with another aspect of the present disclosure;



FIG. 11 is a schematic view of a photosensitive pixel device in accordance with yet another aspect of the present disclosure;



FIG. 12 is a schematic view of a photosensitive pixel device in accordance with a further aspect of the present disclosure;



FIG. 13 is a schematic view of a photosensitive pixel device in accordance with another aspect of the present disclosure;



FIG. 14 is a schematic view of a photosensitive imager device in accordance with yet another aspect of the present disclosure;



FIG. 15 is a schematic view of a photosensitive pixel device in accordance with a further aspect of the present disclosure;



FIG. 16 is a schematic view of a photosensitive pixel device in accordance with another aspect of the present disclosure; and



FIG. 17 is a depiction of a method of making a photosensitive imager device in accordance with yet another aspect of the present disclosure.





DETAILED DESCRIPTION

Before the present disclosure is described herein, it is to be understood that this disclosure is not limited to the particular structures, process steps, or materials disclosed herein, but is extended to equivalents thereof as would be recognized by those ordinarily skilled in the relevant arts. It should also be understood that terminology employed herein is used for the purpose of describing particular embodiments only and is not intended to be limiting.


Definitions

The following terminology will be used in accordance with the definitions set forth below.


It should be noted that, as used in this specification and the appended claims, the singular forms “a,” and, “the” include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to “a dopant” includes one or more of such dopants and reference to “the layer” includes reference to one or more of such layers.


As used herein, the term “low oxygen content” refers to any material having an interstitial oxygen content that is less than or equal to about 60 ppm atomic.


As used herein, the terms “disordered surface” and “textured surface” can be used interchangeably, and refer to a surface having a topology with nano- to micron-sized surface variations formed by the irradiation of laser pulses. While the characteristics of such a surface can be variable depending on the materials and techniques employed, in one aspect such a surface can be several hundred nanometers thick and made up of nanocrystallites (e.g. from about 10 to about 50 nanometers) and nanopores. In another aspect, such a surface can include micron-sized structures (e.g. about 2 μm to about 60 μm). In yet another aspect, the surface can include nano-sized and/or micron-sized structures from about 5 nm and about 500 μm.


As used herein, the term “fluence” refers to the amount of energy from a single pulse of laser radiation that passes through a unit area. In other words, “fluence” can be described as the energy density of one laser pulse.


As used herein, the terms “surface modifying” and “surface modification” refer to the altering of a surface of a semiconductor material using laser radiation. In one specific aspect, surface modification can include processes using primarily laser radiation or laser radiation in combination with a dopant, whereby the laser radiation facilitates the incorporation of the dopant into a surface of the semiconductor material. Accordingly, in one aspect surface modification includes doping of a semiconductor material.


As used herein, the term “target region” refers to an area of a semiconductor material that is intended to be doped or surface modified using laser radiation. The target region of a semiconductor material can vary as the surface modifying process progresses. For example, after a first target region is doped or surface modified, a second target region may be selected on the same semiconductor material.


As used herein, the term “detection” refers to the sensing, absorption, and/or collection of electromagnetic radiation.


As used herein, the team “substantially” refers to the complete or nearly complete extent or degree of an action, characteristic, property, state, structure, item, or result. For example, an object that is “substantially” enclosed would mean that the object is either completely enclosed or nearly completely enclosed. The exact allowable degree of deviation from absolute completeness may in some cases depend on the specific context. However, generally speaking the nearness of completion will be so as to have the same overall result as if absolute and total completion were obtained. The use of “substantially” is equally applicable when used in a negative connotation to refer to the complete or near complete lack of an action, characteristic, property, state, structure, item, or result. For example, a composition that is “substantially free of” particles would either completely lack particles, or so nearly completely lack particles that the effect would be the same as if it completely lacked particles. In other words, a composition that is “substantially free of” an ingredient or element may still actually contain such item as long as there is no measurable effect thereof.


As used herein, the term “about” is used to provide flexibility to a numerical range endpoint by providing that a given value may be “a little above” or “a little below” the endpoint.


As used herein, a plurality of items, structural elements, compositional elements, and/or materials may be presented in a common list for convenience. However, these lists should be construed as though each member of the list is individually identified as a separate and unique member. Thus, no individual member of such list should be construed as a de facto equivalent of any other member of the same list solely based on their presentation in a common group without indications to the contrary.


Concentrations, amounts, and other numerical data may be expressed or presented herein in a range format. It is to be understood that such a range format is used merely for convenience and brevity and thus should be interpreted flexibly to include not only the numerical values explicitly recited as the limits of the range, but also to include all the individual numerical values or sub-ranges encompassed within that range as if each numerical value and sub-range is explicitly recited. As an illustration, a numerical range of “about 1 to about 5” should be interpreted to include not only the explicitly recited values of about 1 to about 5, but also include individual values and sub-ranges within the indicated range. Thus, included in this numerical range are individual values such as 2, 3, and 4 and sub-ranges such as from 1-3, from 2-4, and from 3-5, etc., as well as 1, 2, 3, 4, and 5, individually.


This same principle applies to ranges reciting only one numerical value as a minimum or a maximum. Furthermore, such an interpretation should apply regardless of the breadth of the range or the characteristics being described.


The Disclosure


Electromagnetic radiation can be present across a broad wavelength range, including visible range wavelengths (approximately 350 nm to 800 nm) and non-visible wavelengths (longer than about 800 nm or shorter than 350 nm). The infrared spectrum is often described as including a near infrared portion of the spectrum including wavelengths of approximately 800 to 1300 nm, a short wave infrared portion of the spectrum including wavelengths of approximately 1300 nm to 3 micrometers, and a mid to long wave infrared (or thermal infrared) portion of the spectrum including wavelengths greater than about 3 micrometers up to about 30 micrometers. These are generally and collectively referred to herein as “infrared” portions of the electromagnetic spectrum unless otherwise noted.


Traditional silicon photodetecting imagers have limited light absorption/detection properties. For example, infrared light is mostly transparent to such silicon based detectors. While other materials (e.g. InGaAs) can be used to detect infrared electromagnetic radiation having wavelengths greater than about 1000 nm, silicon is still commonly used because it is relatively cheap to manufacture and can be used to detect wavelengths in the visible spectrum (i.e. visible light, 350 nm-800 nm). Traditional silicon materials require substantial absorption depths to detect photons having wavelengths longer than approximately 700 nm. While visible light can be absorbed at relatively shallow depths in silicon, absorption of longer wavelengths (e.g. 900 nm) in silicon of a standard wafer depth (e.g. approximately 750 μm) is poor if at all. The devices of the present disclosure increase the absorption of semiconductor materials by decreasing the effective absorption length to longer wavelengths as compared to traditional materials. For example, the absorption depth of silicon can be reduced such that these longer wavelengths can be absorbed at depths of less than or equal to about 850 μm. In other words, by decreasing the effective absorption length these devices are able to absorb longer wavelengths (e.g. >1000 nm for silicon) within a thin semiconductor material. In addition to increasing the effective absorption length, the response rate or response speed can also be increased using thinner semiconductor materials.


The present disclosure additionally provides broadband photosensitive diodes, pixels, and imagers capable of detecting visible as well as infrared electromagnetic radiation, including associated methods of making such devices. A photosensitive diode can include a semiconductor substrate having multiple doped regions forming at least one junction, and at least one textured region coupled to the semiconductor substrate and positioned to interact with electromagnetic radiation. In one aspect the multiple doped regions can include at least one cathode region and at least one anode region. In some aspects, doped regions can include an n-type dopant and/or a p-type dopant as is discussed below, thereby creating a p-n junction. In other aspects, a photosensitive device can include an i-type region to form a p-i-n junction.


A photosensitive pixel can include a semiconductor substrate having multiple doped regions forming at least one junction, at least one textured region coupled to the semiconductor substrate and positioned to interact with electromagnetic radiation, and an electrical transfer element coupled to the semiconductor substrate and operable to transfer an electrical signal from the at least one junction. A photosensitive imager can include multiple photosensitive pixels. Additionally, an electrical transfer element can include a variety of devices, including without limitation, transistors, sensing nodes, transfer gates, transfer electrodes, and the like.


Photosensitive or photodetecting imagers include photodiodes or pixels that are capable of absorbing electromagnetic radiation within a given wavelength range. Such imagers can be passive pixel sensors (PPS), active pixel sensors (APS), digital pixel sensor imagers (DPS), or the like, with one difference being the image sensor read out architecture. For example, a semiconducting photosensitive imager can be a three or four transistor active pixel sensor (3T APS or 4T APS). Various additional components are also contemplated, and would necessarily vary depending on the particular configuration and intended results. As and example, a 4T configuration can additionally include, among other things, a transfer gate, a reset, a source follower, and row select transistors. Additionally, devices having greater than 4 transistors are also within the present scope.


Photosensitive imagers can be front side illumination (FSI) or back side illumination (BSI) devices, and there are advantages and disadvantages to both architecture types. In a typical FSI imager, incident light enters the semiconductor device by first passing by transistors and metal circuitry. The light, however, can scatter off of the transistors and circuitry prior to entering the light sensing portion of the imager, thus causing optical loss and noise. A lens can be disposed on the topside of a FSI pixel to direct and focus the incident light to the light sensing active region of the device, thus partially avoiding the circuitry. In one aspect the lens can be a ulens. BSI imagers, one the other hand, are configured to have the depletion region of the junction extending to the opposite side of the device. In one aspect, for example, incident light enters the device via the light sensing portion and is mostly absorbed prior to reaching the circuitry. BSI designs allow for smaller pixel architecture and a high fill factor for the imager. As mentioned, the present disclosure can be adapted for either configuration. It should also be understood that devices according to aspects of the present disclosure can be incorporated into complimentary metal-oxide-semiconductor (CMOS) imager architectures or charge-coupled device (CCD) imager architectures.


In one aspect, as is shown in FIG. 1, a photosensitive diode 10 can include a semiconductor substrate 12 having multiple doped regions 14, 16 forming at least one junction, and at least one textured region 18 coupled to the semiconductor substrate and positioned to interact with electromagnetic radiation. The different doped regions can have the same doping profile or different doping profiles, depending on the device. Such an architecture is a FSI design where light enters the semiconductor substrate from the direction of the multiple doped regions. While the device shown in FIG. 1 contains three doped regions, it should be noted that aspects containing one or more doped regions are considered to be within the present scope. Additionally, the semiconductor substrate can be doped, and thus can be considered to be a doped region in some aspects. It should also be noted that the photosensitive diode can be configured with a BSI architecture, and thus electromagnetic radiation would enter the semiconductor substrate from the direction of the textured region.


The various devices according to aspects of the present disclosure can exhibit increased quantum efficiency over traditional photosensitive devices. Any increase in the quantum efficiency makes a large difference in the signal to noise ratio. More complex structures can provide not only increased quantum efficiency but also good uniformity from pixel to pixel. In addition, devices of the present disclosure exhibit increased responsivity as compared to traditional photosensitive devices. For example, in one aspect the responsivity can be greater than or equal to 0.8 A/W for wavelengths greater than 1000 nm for semiconductor substrate that is less than 100 μm thick.


Photosensitive imagers can be maintained under constant conditions (fixed voltage or current) to provide enhanced linearity and uniformity. Connections between the imager and the underlying device layers can be achieved using vias fabricated from a refractory metal, such as tungsten or tantalum. Placing storage elements under the imager may provide various photonic benefits. For example, the entire pixel array may be dedicated to signal processing. This may enable higher performance by permitting access to low level pixel signals. Furthermore, massively parallel operations can be performed by pixel processors. For example, analog to digital conversion, noise reduction (i.e., true correlated double sampling), power conditioning, nearest neighbor pixel processing, compression, fusion, and color multiplexing operations can be performed.


A variety of semiconductor materials are contemplated for use with the devices and methods according to aspects of the present disclosure. Non-limiting examples of such semiconductor materials can include group IV materials, compounds and alloys comprised of materials from groups II and VI, compounds and alloys comprised of materials from groups III and V, and combinations thereof. More specifically, exemplary group IV materials can include silicon, carbon (e.g. diamond), germanium, and combinations thereof. Various exemplary combinations of group IV materials can include silicon carbide (SiC) and silicon germanium (SiGe). In one specific aspect, the semiconductor material can be or include silicon. Exemplary silicon materials can include amorphous silicon (a-Si), microcrystalline silicon, multicrystalline silicon, and mono crystalline silicon, as well as other crystal types. In another aspect, the semiconductor material can include at least one of silicon, carbon, germanium, aluminum nitride, gallium nitride, indium gallium arsenide, aluminum gallium arsenide, and combinations thereof.


Exemplary combinations of group II-VI materials can include cadmium selenide (CdSe), cadmium sulfide (CdS), cadmium telluride (CdTe), zinc oxide (ZnO), zinc selenide (ZnSe), zinc sulfide (ZnS), zinc telluride (ZnTe), cadmium zinc telluride (CdZnTe, CZT), mercury cadmium telluride (HgCdTe), mercury zinc telluride (HgZnTe), mercury zinc selenide (HgZnSe), and combinations thereof.


Exemplary combinations of group III-V materials can include aluminum antimonide (AlSb), aluminum arsenide (AlAs), aluminum nitride (AlN), aluminum phosphide (AlP), boron nitride (BN), boron phosphide (BP), boron arsenide (BAs), gallium antimonide (GaSb), gallium arsenide (GaAs), gallium nitride (GaN), gallium phosphide (GaP), indium antimonide (InSb), indium arsenide (InAs), indium nitride (InN), indium phosphide (InP), aluminum gallium arsenide (AlGaAs, AlxGa1-xAs), indium gallium arsenide (InGaAs, InxGa1-xAs), indium gallium phosphide (InGaP), aluminum indium arsenide (AlInAs), aluminum indium antimonide (AlInSb), gallium arsenide nitride (GaAsN), gallium arsenide phosphide (GaAsP), aluminum gallium nitride (AlGaN), aluminum gallium phosphide (AlGaP), indium gallium nitride (InGaN), indium arsenide antimonide (InAsSb), indium gallium antimonide (InGaSb), aluminum gallium indium phosphide (AlGaInP), aluminum gallium arsenide phosphide (AlGaAsP), indium gallium arsenide phosphide (InGaAsP), aluminum indium arsenide phosphide (AlInAsP), aluminum gallium arsenide nitride (AlGaAsN), indium gallium arsenide nitride (InGaAsN), indium aluminum arsenide nitride (InAlAsN), gallium arsenide antimonide nitride (GaAsSbN), gallium indium nitride arsenide antimonide (GaInNAsSb), gallium indium arsenide antimonide phosphide (GaInAsSbP), and combinations thereof.


The semiconductor material can be of any thickness that allows electromagnetic radiation detection and conversion functionality, and thus any such thickness of semiconductor material is considered to be within the present scope. In some aspects the laser processed region of the semiconductor increases the efficiency of the device such that the semiconductor material can be thinner than has previously been possible. Decreasing the thickness of the semiconductor reduces the amount of semiconductor material required to make such a device. In one aspect, for example, the semiconductor material has a thickness of from about 500 nm to about 50 μm. In another aspect, the semiconductor material has a thickness of less than or equal to about 500 μm. In yet another aspect, the semiconductor material has a thickness of from about 1 μm to about 10 μm. In a further aspect, the semiconductor material can have a thickness of from about 5 μm to about 750 μm. In yet a further aspect, the semiconductor material can have a thickness of from about 5 μm to about 100 μm.


Additionally, various types of semiconductor material are contemplated, and any such material that can be incorporated into an electromagnetic radiation detection device is considered to be within the present scope. In one aspect, for example, the semiconductor material is monocrystalline. In another aspect, the semiconductor material is multicrystalline. In yet another aspect, the semiconductor material is microcrystalline. It is also contemplated that the semiconductor material can be amorphous. Specific nonlimiting examples include amorphous silicon or amorphous selenium.


The semiconductor materials of the present disclosure can also be made using a variety of manufacturing processes. In some cases the manufacturing procedures can affect the efficiency of the device, and may be taken into account in achieving a desired result. Exemplary manufacturing processes can include Czochralski (Cz) processes, magnetic Czochralski (mCz) processes, Float Zone (FZ) processes, epitaxial growth or deposition processes, and the like. Whether or not low oxygen content is desired in the device can also affect the choice of a manufacturing process for the semiconductor material. Various processes produce semiconductor materials containing varying amounts of oxygen, and as such, some applications having more stringent tolerances with respect to oxygen levels may benefit more from specific manufacturing procedures as compared to others. For example, during CZ crystal growth oxygen from the containment vessel, usually a quartz crucible, can become incorporated into the crystal as it is pulled. Additionally, other sources of oxygen contamination are also possible with the CZ process. Such contamination may be reduced, however, through the use of non oxygen-containing crucible materials, as well as the development of other crystal growth methods that do not utilize a crucible. One such process is the FZ process.


Materials grown with the CZ method can also be made to have lowered oxygen concentration through enhancements to the crystal growth process, such as growing the crystal in the presence of a magnetic field (i.e. the mCz process). Also, gettering techniques can be employed to reduce the impact of oxygen or other impurities on the finished device. These gettering techniques can include thermal cycles to liberate or nucleate impurities, or selective ion implantation of species to serve as gettering sites for the impurities. For example, oxygen concentrated in the semiconductor can be removed by the performing a furnace cycle to form a denuded zone. During heating with an inert gas, oxygen near the surface of the semiconductor diffuses out of the material. During the furnace cycle but after the denuding step, nucleating and growing steps may be performed. Nucleating sites for precipitates are formed during the nucleating step, and the precipitates are grown from the nucleating sites during a growing step. The precipitates are formed from interstitial oxygen within the bulk of the semiconductor material and beneath the denuded zone. The precipitation of oxygen in the bulk of the semiconductor material can be desired because such precipitates can act as gettering sites. Such precipitate formation can also be performed to “lock up” interstitial oxygen into the precipitates and reduce the likelihood that such oxygen can migrates from the bulk of the semiconductor material into the denuded zone.


In those aspects where low oxygen content of the device is desired, further processing of the semiconductor material can be performed so as to minimize the introduction of oxygen. Oxygen can exist in different states or at different sites (for example, interstitially or substitutionally) within a semiconductor such as silicon, dependent upon the thermal processing the semiconductor has received. If the semiconductor is subjected to temperatures higher than, for example, about 1000° C., oxygen can form aggregates or clusters that serve as defect sites in the crystal lattice. These sites may result in trap states and a reduction in carrier lifetime within the semiconductor material and device can occur. At lower temperatures (for example, around 400° C. to 700° C.), oxygen can behave as electrically active thermal donors. Thus, oxygen can have a negative impact on carrier lifetime and on carrier mobility. In a device fabricated to have photoconductive gain, the presence of oxygen causing reduced carrier lifetime may result in reduced levels of photoconductive gain.


It may be beneficial, therefore, to produce semiconductor devices such that a low oxygen content is obtained or maintained. This can be accomplished in a variety of ways, including using semiconductor materials having low levels of oxygen contained therein to begin with, processing these materials in a manner that minimizes the uptake of oxygen into the semiconductor lattice, and utilizing techniques that eliminate or reduce oxygen that may be present in the semiconductor. Such processes and techniques can include, for example, annealing the semiconductor material and any laser treated region to lower temperatures as compared to previous annealing procedures. Annealing processes are discussed more fully below.


Additionally, texture processing of the semiconductor material and/or any annealing process can be performed in a substantially oxygen-depleted environment in order to minimize the introduction of oxygen into the semiconductor. An oxygen-depleted or substantially oxygen-depleted environment can include a variety of environments. In one aspect, for example, the oxygen-depleted environment can be an environment whereby oxygen from the air or other sources has been replaced with a gas or other fluid containing little to no oxygen. In another aspect, processing can occur in a vacuum environment, and thus contain little to no oxygen. Additionally, oxygen-containing materials or materials that introduce oxygen into the semiconductor, such as, for example, quartz crucibles, can be avoided. As a practical matter, the term “oxygen-depleted environment” can be used to describe an environment with low levels of oxygen, provided a semiconductor material can be processed therein within the desired tolerances. Thus, environments having low oxygen, or little to no oxygen, are environments in which a semiconductor can be processed as a low-oxygen content semiconductor while maintaining oxygen levels within the tolerances of the present disclosure. In one aspect, an oxygen-depleted environment can be an oxygen-free environment. Further details regarding low-oxygen content semiconductor materials can be found in U.S. patent application Ser. No. 12/771,848, filed on Apr. 30, 2010, which is incorporated herein by reference.


The semiconductor material can have varying levels of interstitial oxygen depending on the desired efficiency of the device. In some aspects, oxygen content may be of no concern, and thus any level of oxygen within the lattice is acceptable. In other aspects, a low oxygen content is desired. In one aspect a semiconductor material can have an oxygen content that is less than or equal to about 50 ppm atomic. In another aspect, a semiconductor material can have an oxygen content that is less than or equal to about 30 ppm atomic. In yet another aspect, the semiconductor material can have an oxygen content less than or equal to about 10 ppm atomic. In another aspect the semiconductor can have an oxygen content less than about 5 ppm atomic. In yet another aspect the semiconductor can have an oxygen content less than about 1 ppm atomic.


As has been described, the textured region can function to diffuse electromagnetic radiation, to redirect electromagnetic radiation, and to absorb electromagnetic radiation, thus increasing the quantum efficiency of the device. The textured region can include surface features to increase the effective absorption length of the photosensitive pixel. The surface features can be cones, pyramids, pillars, protrusions, microlenses, quantum dots, inverted features and the like. Factors such as manipulating the feature sizes, dimensions, material type, dopant profiles, texture location, etc. can allow the diffusing region to be tunable for a specific wavelength. In one aspect, tuning the device can allow specific wavelengths or ranges of wavelengths to be absorbed. In another aspect, tuning the device can allow specific wavelengths or ranges of wavelengths to be reduced or eliminated via filtering.


Tuning can also be accomplished through the location of the texture region within the device, modifying the dopant profile(s) of regions within the device, dopant selection, and the like. Additionally, material composition near the textured region can create a wavelength specific photosensing pixel device. It should be noted that a wavelength specific photosensing pixel can differ from one pixel to the next, and can be incorporated into an imaging array. For example a 4×4 array can include a blue pixel, a green pixel, a red pixel, and infrared light absorbing pixel, or a blue pixel, two green pixels, and a red pixel.


Textured regions according to aspects of the present disclosure can allow a photosensitive device to experience multiple passes of incident electromagnetic radiation within the device, particularly at longer wavelengths (i.e. infrared). Such internal reflection increases the effective absorption length to be greater than the thickness of the semiconductor substrate. This increase in absorption length increases the quantum efficiency of the device, leading to an improved signal to noise ratio.


The textured region can be formed by various techniques, including lasing, chemical etching (e.g. anisotropic etching, isotropic etching), nanoimprinting, additional material deposition, and the like. For example, pillar features can be incorporated into pixels by thinning or removing material from the backside of a FSI semiconductor substrate by using deep trench isolation and etching techniques. In one aspect material can be removed to a thickness of about 20 μm. Anisotropic etching can be used to produce a sloping backside pyramid structure, spherical, structure parabolic structure, a lens structure with reflectors, and the like. Such features on the backside of pillars will also serve to diffuse and reflect electromagnetic radiation.


In one aspect, the texturing process can be performed during the manufacture of the photosensitive device. In another aspect, the texturing process can be performed on a photosensitive device that has previously been made. For example, a CMOS, CCD, or other photosensitive element can be textured following manufacture. In this case, material layers may be removed from the photosensitive element to expose the semiconductor substrate or bulk material upon which a textured region may be formed.


One effective method of producing a textured region is through laser processing. Such laser processing allows discrete locations of the semiconductor substrate to be textured. A variety of techniques of laser processing to form a textured region are contemplated, and any technique capable of forming such a region should be considered to be within the present scope. Laser treatment or processing can allow, among other things, enhanced absorption properties and thus increased electromagnetic radiation focusing and detection. The laser treated region can be associated with the surface nearest the impinging electromagnetic radiation, or the laser treated surface can be associated with a surface opposite in relation to impinging electromagnetic radiation, thereby allowing the radiation to pass through the semiconductor material before it hits the laser treated region.


In one aspect, for example, a target region of the semiconductor material can be irradiated with laser radiation to form a textured region. Examples of such processing have been described in further detail in U.S. Pat. Nos. 7,057,256, 7,354,792 and 7,442,629, which are incorporated herein by reference in their entireties. Briefly, a surface of a semiconductor material is irradiated with laser radiation to form a textured or surface modified region. Such laser processing can occur with or without a dopant material. In those aspects whereby a dopant is used, the laser can be directed through a dopant carrier and onto the semiconductor surface. In this way, dopant from the dopant carrier is introduced into the target region of the semiconductor material. Such a region incorporated into a semiconductor material can have various benefits in accordance with aspects of the present disclosure. For example, the target region typically has a textured surface that increases the surface area of the laser treated region and increases the probability of radiation absorption via the mechanisms described herein. In one aspect, such a target region is a substantially textured surface including micron-sized and/or nano-sized surface features that have been generated by the laser texturing. In another aspect, irradiating the surface of semiconductor material includes exposing the laser radiation to a dopant such that irradiation incorporates the dopant into the semiconductor. Various dopant materials are known in the art, and are discussed in more detail herein.


Thus the surface of the semiconductor material is chemically and/or structurally altered by the laser treatment, which may, in some aspects, result in the formation of surface features appearing as microstructures or patterned areas on the surface and, if a dopant is used, the incorporation of such dopants into the semiconductor material. In some aspects, the features or microstructures can be on the order of 50 nm to 20 μm in size and can assist in the absorption of electromagnetic radiation. In other words, the textured surface can increase the probability of incident radiation being absorbed by the semiconductor material.


The type of laser radiation used to surface modify a semiconductor material can vary depending on the material and the intended modification. Any laser radiation known in the art can be used with the devices and methods of the present disclosure. There are a number of laser characteristics, however, that can affect the surface modification process and/or the resulting product including, but not limited to the wavelength of the laser radiation, pulse width, pulse fluence, pulse frequency, polarization, laser propagation direction relative to the semiconductor material, etc. In one aspect, a laser can be configured to provide pulsatile lasing of a semiconductor material. A short-pulsed laser is one capable of producing femtosecond, picosecond and/or nanosecond pulse durations. Laser pulses can have a central wavelength in a range of about from about 10 nm to about 8 μm, and more specifically from about 200 nm to about 1200 nm. The pulse width of the laser radiation can be in a range of from about tens of femtoseconds to about hundreds of nanoseconds. In one aspect, laser pulse widths can be in the range of from about 50 femtoseconds to about 50 picoseconds. In another aspect, laser pulse widths can be in the range of from about 50 picoseconds to 100 nanoseconds. In another aspect, laser pulse widths are in the range of from about 50 to 500 femtoseconds.


The number of laser pulses irradiating a target region can be in a range of from about 1 to about 2000. In one aspect, the number of laser pulses irradiating a semiconductor target region can be from about 2 to about 1000. Further, the repetition rate or frequency of the pulses can be selected to be in a range of from about 10 Hz to about 10 μHz, or in a range of from about 1 kHz to about 1 MHz, or in a range from about 10 Hz to about 1 kHz. Moreover, the fluence of each laser pulse can be in a range of from about 1 kJ/m2 to about 20 kJ/m2, or in a range of from about 3 kJ/m2 to about 8 kJ/m2.


A variety of dopant materials are contemplated, and any such material that can be used in the laser treatment process to surface modify a semiconductor material according to aspects of the present disclosure is considered to be within the present scope. It should be noted that the particular dopant utilized can vary depending on the semiconductor material being laser treated, as well as the intended use of the resulting semiconductor material. For example, the selection of potential dopants may differ depending on whether or not tuning of the photosensitive device is desired.


A dopant can be either electron donating or hole donating. In one aspect, non-limiting examples of dopant materials can include S, F, B, P, N, As, Se, Te, Ge, Ar, Ga, In, Sb, and combinations thereof. It should be noted that the scope of dopant materials should include, not only the dopant materials themselves, but also materials in forms that deliver such dopants (i.e. dopant carriers). For example, S dopant materials includes not only S, but also any material capable being used to dope S into the target region, such as, for example, H2S, SF6, SO2, and the like, including combinations thereof. In one specific aspect, the dopant can be S. Sulfur can be present at an ion dosage level of between about 5×1014 and about 1×1016 ions/cm2. Non-limiting examples of fluorine-containing compounds can include ClF3, PF5, F2SF6, BF3, GeF4, WF6, SiF4, HF, CF4, CHF3, CH2F2, CH3F, C2F6, C2HF5, C3F8, C4F8, NF3, and the like, including combinations thereof. Non-limiting examples of boron-containing compounds can include B(CH3)3, BF3, BCl3, BN, C2B10H12, borosilica, B2H6, and the like, including combinations thereof. Non-limiting examples of phosphorous-containing compounds can include PF5, PH3, and the like, including combinations thereof. Non-limiting examples of chlorine-containing compounds can include Cl2, SiH2Cl2, HCl, SiCl4, and the like, including combinations thereof. Dopants can also include arsenic-containing compounds such as AsH3 and the like, as well as antimony-containing compounds. Additionally, dopant materials can include mixtures or combinations across dopant groups, i.e. a sulfur-containing compound mixed with a chlorine-containing compound. In one aspect, the dopant material can have a density that is greater than air. In one specific aspect, the dopant material can include Se, H2S, SF6, or mixtures thereof. In yet another specific aspect, the dopant can be SF6 and can have a predetermined concentration range of about 5.0×10−8 mol/cm3 to about 5.0×10−4 mol/cm3. SF6 gas is a good carrier for the incorporation of sulfur into the semiconductor material via a laser process without significant adverse effects on the semiconductor material. Additionally, it is noted that dopants can also be liquid solutions of n-type or p-type dopant materials dissolved in a solution such as water, alcohol, or an acid or basic solution. Dopants can also be solid materials applied as a powder or as a suspension dried onto the wafer.


The semiconductor substrate can be annealed for a variety of reasons, including dopant activation, semiconductor material damage repair, and the like. In those aspects including a laser textured region, the semiconductor material can be annealed prior to laser treatment, following laser treatment, during laser treatment, or both prior to and following laser treatment. Annealing can enhance the semiconductive properties of the device, including increasing the photoresponse properties of the semiconductor materials. Additionally, annealing can reduce damage done by the lasing process. Although any known anneal can be beneficial and would be considered to be within the present scope, annealing at lower temperatures can be particularly useful. Such a “low temperature” anneal can greatly enhance the photoconductive gain and external quantum efficiency of devices utilizing such materials. In one aspect, for example, the semiconductor material can be annealed to a temperature of from about 300° C. to about 1100° C. In another aspect, the semiconductor material can be annealed to a temperature of from about 500° C. to about 900° C. In yet another aspect, the semiconductor material can be annealed to a temperature of from about 700° C. to about 800° C. In a further aspect, the semiconductor material can be annealed to a temperature that is less than or equal to about 850° C.


The duration of the annealing procedure can vary according to the specific type of anneal being performed, as well as according to the materials being used. For example, rapid annealing processes can be used, and as such, the duration of the anneal may be shorter as compared to other techniques. Various rapid thermal anneal techniques are known, all of which should be considered to be within the present scope. In one aspect, the semiconductor material can be annealed by a rapid annealing process for a duration of greater than or equal to about 1 μs. In another aspect, the duration of the rapid annealing process can be from about 1 μs to about 1 ms. As another example, a baking or furnace anneal process can be used having durations that may be longer compared to a rapid anneal. In one aspect, for example, the semiconductor material can be annealed by a baking anneal process for a duration of greater than or equal to about 1 ms to several hours. As has been described, if low oxygen content semiconductor materials are used it may be beneficial to anneal such materials in a substantially oxygen-depleted environment.


As has been described, annealing can help reduce defects inherent to the semiconductor substrate and otherwise reduce electron/hole recombination. In other words, the annealing can help create electron states that effectively reduce the undesirable recombination processes. Annealing the semiconductor material may also improve the responsivity or photoconductive gain of the device. Photoconductive devices can have dopants, impurities, or defects that can introduce energy levels that can trap carriers. Trapping carriers and reducing recombination of photocarriers can lead to an increase in photoconductive gain of the device. The relationship of photoconductive gain and trapping time can be represented by Equation (I):

Gain=τLt  (I)

where “τL” is the lifetime of an excess carrier and “τt” is the transit time of the carriers across the device. It is understood that the lifetime of an excess carrier can be increased by trapping a carrier species and reducing the recombination rate. An increase in gain can be achieved by trapping centers in the semiconductor that have millisecond trapping times at room temperature and short transit times in thinned lightly doped wafers. These trapping locations can decrease the recombination of carriers and therefore improve or increase the photoconductive gain of the device by allowing more electrons to traverse the different regions without being recombined.


Turning to FIG. 2, a reflecting layer 20 can be coupled to the semiconductor substrate 12. The reflecting layer can be coupled to any side or portion of the semiconductor substrate in order to reflect electromagnetic radiation back into the device. Accordingly, in one aspect the reflecting layer can be located on the semiconductor substrate opposite the incoming electromagnetic radiation. Thus, as is shown in FIG. 2, electromagnetic radiation passing though the semiconductor substrate and the textured region 16 can be reflected back into the semiconductor substrate. Additionally, a passivation layer 22 can be coupled to the semiconductor substrate. The passivation layer is shown coupled to the side of the semiconductor substrate facing the incoming electromagnetic radiation, however a passivation layer can be located anywhere on the device and still be within the present scope.


As has been described, location of the textured region can be used to provide enhancement and/or filtering of the incoming electromagnetic radiation. For example, a textured region located at the point of entry of the electromagnetic radiation into the photosensitive device tends to bend the electromagnetic radiation, particularly the blue wavelengths. Accordingly, one level of tuning can be accomplished by locating the textured region on the surface adjacent the incident electromagnetic radiation to purposely effectuate the filtering of blue wavelengths. Additionally, absorption of particular wavelengths of electromagnetic radiation occurs at different depths in the semiconductor layer and/or textured region. By increasing the absorption to green wavelengths, for example, the electrical signal as a result of green wavelengths can be increased in a diode or pixel. Certain traditional 4 pixel imagers have one red, one blue, and two green pixels, with the greater number of green pixels to account for increased sensitivity of the human eye to green colors. Thus in one aspect, a 4 pixel imager can have one blue, one red, and one green pixel having an increased green wavelength absorption. The fourth pixel can be used for an IR or other wavelength selective pixel depending on the desired application of the imager.



FIG. 3 shows a photosensitive device having textured regions 30 located on the sides of the semiconductor substrate 12. Such a configuration allows electromagnetic radiation normally exiting through the sides of the device to be further defused and absorbed within semiconductor substrate. The textured region(s) can be located on one or more sides to facilitate the enhanced absorption.



FIG. 4 shows a photosensitive device having a textured region 40 having a nonparallel surface with respect to the semiconductor substrate 12. Thus the overall configuration of the textured region can be designed to further enhance absorption and/or selectively tune the device. As has been described, the nonparallel surface can have a variety of configurations, such as, without limitation, nonparallel slope, a pyramid, an inverted pyramid, a concave shape, a convex shape, and the like. In some cases the configuration of the textured region can function to direct or focus electromagnetic radiation into the semiconductor substrate, and in other cases the configuration of the textured region can function to direct or focus electromagnetic radiation away from the semiconductor substrate.


As is shown in FIG. 5, a lens 50 can be coupled to the semiconductor substrate 12 on a side facing incoming electromagnetic radiation. Thus the lens can focus the electromagnetic radiation into the semiconductor substrate. In those aspects having circuitry or other structures disposed on the incoming electromagnetic radiation surface, the lens can further focus light around such structures, thereby reducing optical scattering and noise.


As is shown in FIG. 6, a textured region 60 is located on the semiconductor substrate 12 adjacent to the multiple doped regions 14, 16. The textured region can be associated with at least one of the doped regions as is shown, or the textured region can be distinct from the doped regions (not shown). Electromagnetic radiation can enter the photosensitive device at the side adjacent the doped regions, or alternatively at the side opposite the doped regions.



FIGS. 7-11 show various steps in the manufacture of a photosensitive pixel according to aspects of the present disclosure. FIG. 7 shows a cross-section of a front side illumination (FSI) photosensitive pixel device. The photosensitive pixel device can include a semiconductor substrate 72, and can be referred to as bulk semiconductor material. The semiconductor substrate includes at least one doped region 74 that can be doped with an electron donating or hole donating species to cause the region to become more positive or negative in polarity as compared to the semiconductor substrate. In one aspect, for example, the doped region can be p doped. In another aspect the doped region can be n doped. A highly doped region 76 can be formed on or near the doped region to create a pinned diode. In one example, the semiconductor substrate can be negative in polarity, and the doped region and the highly doped region can be doped with p+ and n− dopants respectively. In some aspects, variations of n(−−), n(−), n(+), n(++), p(−−), p(−), p(+), or p(++) type doping of the regions can be used. It should be noted that in one aspect the highly doped region can be the textured region. In other words, textured surface features can be formed on or in the highly doped region.


The device of FIG. 7 can further include various metal regions 78, at least one via 80, a passivation layer 82, trench isolation 84, and an electrical transfer element 86. Trench isolation elements can maintain pixel to pixel uniformity by reducing optical and electrical crosstalk. The trench isolation can be shallow (FIG. 7) or deep (FIG. 12) trench isolation. The trench isolation can include various materials, including, without limitation, dielectric materials, reflective materials, conductive materials, light diffusing features, and the like. These trench isolation regions can be configured to reflect incident light until it is absorbed, thereby increase the effective absorption length of the device.


As is shown in FIG. 8, a carrier substrate or carrier wafer 88 can be coupled to the photosensing pixel. In one aspect, the carrier substrate can be disposed on the passivation layer 82, although the carrier substrate can be disposed on any surface of the device. In one aspect, for example, the carrier substrate can be disposed on the semiconductor substrate (not shown). The carrier substrate can be coupled to the photosensing pixel by various techniques, and any such coupling mechanism is within the present scope. In one aspect, for example, the coupling can occur by way of a bonding layer or adhesive layer disposed on the device, for example, on the passivation layer. The support substrate can provide support to the semiconductor device both during and after manufacture, depending on whether or not the support is removed. The carrier substrate can be made of a semiconductor material that is the same or similar to the bulk semiconductor material, or it can be made of a different material.


As is shown in FIG. 9, a textured region 90 is coupled to the semiconductor substrate 72 opposite the doped regions 74,76. Thus light entering from the direction of the doped regions passes through the semiconductor substrate prior to contacting the textured region. The textured region can be disposed across an entire surface of the semiconductor substrate, as is shown in FIG. 9, or it can be disposed on one or more discrete regions (not shown).


As is shown in FIG. 10, an additional carrier support substrate 100 can be coupled to the device on an opposing side from the carrier support substrate 88. The additional carrier support substrate can be utilized for a variety of purposes, including providing additional support to the device, facilitating the removal of the first carrier support substrate, and the like. A reflective layer 102 can be disposed between the textured region 90 and the carrier support substrate. Thus the reflective layer can reflect electromagnetic radiation that passes through the textured region back toward the semiconductor substrate 72, thus reducing optical loss and backscattering. Thus, in some aspects a reflective layer can increase the quantum efficiency of the device. The reflective layer material can be any reflective material that can be incorporated into such a device. Nonlimiting examples can include materials such as silver, aluminum, and the like.


As is shown in FIG. 11, the carrier support substrate can be removed to expose the passivation layer 82 or any other material layer that was previously covered by the carrier support substrate. The additional carrier substrate 100 can be maintained in the device, removed from the device, or thinned to reduce the thickness of the substrate depending on the intended use of the device. The removal of material from the device, including the carrier support substrate and the additional carrier substrate, can be accomplished by a variety of methods including, without limitation, etching, chemical mechanical polishing, ion implanting (i.e. smart cut), and the like.


Various types of trench isolation are contemplated, and any such isolation is considered to be within the present scope. As has been described, trench isolation can be shallow (FIG. 7, 84) or deep (FIG. 12, 120) trench isolation. The trench isolation can also include depths between shallow and deep, depending on the device design. Trench isolation can include dielectric materials, reflective materials, conductive materials, and combinations thereof, including textured regions and other light diffusing features. Thus the trench isolation layer can be configured to reflect incident electromagnetic radiation, in some cases until it is absorbed, thereby increasing the effective absorption length of the device. Additionally, in some aspects pillar features can be incorporated into pixels by thinning or removing material from the semiconductor substrate using deep trench isolation and etching techniques. As is shown in FIG. 13, the textured region 130 can have a nonparallel surface with respect to the semiconductor substrate 72 as has been described. This nonparallel morphology, when included with the deep trench isolation 120, can effectively focus electromagnetic radiation into the semiconductor substrate from multiple sides.


It is also contemplated, that a non-bulk material can be formed or disposed near a doped region in the device. The addition of the non-bulk material can allow for electromagnetic radiation diffusing features to be formed on or in the non-bulk material. A metal layer defining an aperture can also be included in one aspect of the present disclosure. The metal layer can be formed near the doped regions and can have a light entering region that defines an aperture. This light entering region can also include an antireflecting material.



FIG. 14 shows a photosensitive imager comprising two photosensitive pixels 140. Each photosensitive pixel includes a boundary region 142 that can include metal circuitry and a textured region 144. Each photosensitive pixel can include at least one transistor 146 or other electrical transfer element. Additional read out and circuitry elements 148 can be utilized and shared by both photosensitive pixels.


Turning to FIG. 15, a backside illuminated (BSI) photosensitive pixel according to one aspect present disclosure is provided. A lens 150 and an anti-reflective coating 152 are disposed on the backside of the pixel following thinning and trench isolation. A color filter 154 can be optically coupled to the lens to allow specific wavelengths filtering of the electromagnetic radiation. A textured region 156 can be coupled to the semiconductor substrate 72 opposite the lens in order to provide diffusive scattering and reflection of the incident electromagnetic radiation that passes through to the front side of the pixel. Thus the electromagnetic radiation can be focused within the semiconductor substrate to the combined action of the textured region and the trench isolation 120



FIG. 16 shows a front side illuminated (FSI) imager according to another aspect of the present disclosure. A lens 160 and an antireflecting passivation layer on 62 are coupled to the front side of the pixel. A textured region 90 and a reflecting layer 102 are coupled to the semiconductor substrate 72 opposite the lens to provide diffusive scattering and reflection of the incident electromagnetic radiation that passes through the semiconductor substrate. An aperture 164 formed in a metal or other reflective material layer 166 can increase the effectiveness of the optical cavity. Thus the lens focuses electromagnetic radiation through the aperture.


In other aspects of the present disclosure, various methods of making photosensitive diodes, pixels, and imagers, are contemplated. In one aspect, as is shown in FIG. 17, a method of making a photosensitive imager device can include forming a textured region on a semiconductor substrate having multiple doped regions forming a least one junction, wherein the textured region is formed in a position to interact with electromagnetic radiation 170. The method also includes coupling an electrical transfer element to the semiconductor substrate such that the electrical transfer element is operable to transfer an electrical signal from the at least one junction 172. In one aspect, multiple pixels can be associated together to form an imager. A passivation layer can also be disposed on the photosensitive imager device to protect and/or reduce the dark current of the device.


In another aspect of the present disclosure, a method for making a photosensitive diode is provided. Such a method can include forming at least one cathode and at least one anode on a surface of a semiconductor substrate, coupling a textured region to the semiconductor substrate, and coupling a support substrate to the semiconductor substrate. The textured region can be located adjacent to the anode and cathode, opposite the anode and cathode, or both adjacent and opposite the anode and cathode. An electrical transfer on the can be electrically coupled to at least one of the anode and cathode to form a photosensitive pixel. In another aspect, the semiconductor substrate can be thinned to improve the response rate and/or speed of the device. A passivation layer can also be disposed on the photosensitive diode to protect and/or reduce the dark current of the device. An additional support substrate can be attached to the device to provide additional support. In one aspect, the additional support substrate can be located on the opposite side of the photosensitive diode from the support substrate. The support substrate can subsequently be removed to allow for further processing.


Of course, it is to be understood that the above-described arrangements are only illustrative of the application of the principles of the present disclosure. Numerous modifications and alternative arrangements may be devised by those skilled in the art without departing from the spirit and scope of the present disclosure and the appended claims are intended to cover such modifications and arrangements. Thus, while the present disclosure has been described above with particularity and detail in connection with what is presently deemed to be the most practical embodiments of the disclosure, it will be apparent to those of ordinary skill in the art that numerous modifications, including, but not limited to, variations in size, materials, shape, form, function and manner of operation, assembly and use may be made without departing from the principles and concepts set forth herein.

Claims
  • 1. A photosensitive imager device, comprising: a semiconductor substrate having a light-incident surface, a back surface opposed to said light-incident surface and at least one side surface, said semiconductor substrate having multiple doped regions forming at least one junction, said side surface having at least a textured region coupled to the semiconductor substrate and positioned to interact with electromagnetic radiation to provide reflection of radiation so as to increase effective absorption of radiation in the semiconductor substrate; wherein said textured region comprises surface features with sizes in a range of about 50 nm to about 2 microns, andan electrical transfer element coupled to the semiconductor substrate and operable to transfer an electrical signal from the at least one junction.
  • 2. The device of claim 1, wherein the textured region is operable to facilitate generation of an electrical signal from the detection of infrared electromagnetic radiation.
  • 3. The device of claim 1, wherein the transfer element is selected from the group consisting of a transistor, a sensing node, a transfer gate, and combinations thereof.
  • 4. The device of claim 1, further comprising a reflective layer coupled to the semiconductor substrate and positioned to maintain the electromagnetic radiation in the semiconductor substrate.
  • 5. The device of claim 1, wherein the textured region has been formed by a process selected from the group consisting of lasing, chemical etching, nanoimprinting, material deposition, and combinations thereof.
  • 6. The device of claim 1, further comprising a lens optically coupled to the semiconductor substrate and positioned to focus incident electromagnetic radiation into the semiconductor substrate.
  • 7. A photosensitive image array, comprising at least two photosensitive imager devices of claim 1.
  • 8. The photosensitive image array of claim 7, further comprising at least one trench isolation positioned between the at least two photosensitive imager device.
  • 9. A photosensitive imager device, comprising: a semiconductor substrate having a light-incident surface, a back surface opposed to said light-incident surface and at least one side surface, said semiconductor substrate further having multiple doped regions forming at least one junction, said side surface having at least a textured region coupled to the semiconductor substrate and positioned to interact with electromagnetic radiation to provide reflection of radiation so as to increase effective absorption of radiation in the semiconductor substrate, wherein said textured region comprises surface features with sizes in a range of about 50 nm to about 2 microns; andat least 4 transistors coupled to the semiconductor substrate and with at least one of the transistors electrically coupled to the at least one junction.
  • 10. The photosensitive imager device of claim 1, wherein said semiconductor substrate includes multiple side surfaces each of which has a textured region.
  • 11. A photosensitive imager device, comprising: a semiconductor substrate having a light-incident surface, a back surface opposed to said light-incident surface and at least one side surface, said semiconductor substrate having multiple doped regions forming at least one junction, said side surface having at least a textured region coupled to the semiconductor substrate and positioned to interact with electromagnetic radiation; wherein said textured region comprises surface features with sizes in a range of about 50 nm to about 2 microns, andan electrical transfer element coupled to the semiconductor substrate and operable to transfer an electrical signal from the at least one junction,wherein the transfer element is selected from the group consisting of a transistor, a sensing node, a transfer gate, and combinations thereof.
  • 12. The device of claim 11, wherein the textured region is operable to facilitate generation of an electrical signal from the detection of infrared electromagnetic radiation.
  • 13. The device of claim 11, further comprising a reflective layer coupled to the semiconductor and positioned to maintain the electromagnetic radiation in the semiconductor substrate.
  • 14. The device of claim 11, wherein said surface features are selected from the group consisting of cones, pillars, pyramids, microlenses, quantum dots, inverted features, and combinations thereof.
PRIORITY DATA

This application is a continuation of U.S. patent application Ser. No. 12/885,158, filed on Sep. 17, 2010, now issued as U.S. Pat. No. 8,680,591, which claims the benefit of U.S. Provisional Patent Application Ser. No. 61/243,434, filed on Sep. 17, 2009, U.S. Provisional Patent Application Ser. No. 61/311,004 filed on Mar. 5, 2010, and U.S. Provisional Patent Application Ser. No. 61/311,107, filed on Mar. 5, 2010, each of which is incorporated herein by reference.

US Referenced Citations (546)
Number Name Date Kind
3487223 St. John Dec 1969 A
3922571 Smith Nov 1975 A
3973994 Redfield Aug 1976 A
3994012 Warner, Jr. Nov 1976 A
4017887 Davies et al. Apr 1977 A
4149174 Shannon Apr 1979 A
4176365 Kroger Nov 1979 A
4201450 Trapani May 1980 A
4242149 King et al. Dec 1980 A
4253882 Dalal Mar 1981 A
4277793 Webb Jul 1981 A
4322571 Stanbery Mar 1982 A
4419533 Czubatyj et al. Dec 1983 A
4452826 Shields et al. Jun 1984 A
4493942 Sheng et al. Jan 1985 A
4514582 Tiedje et al. Apr 1985 A
4536608 Sheng et al. Aug 1985 A
4568960 Petroff et al. Feb 1986 A
4593303 Dyck et al. Jun 1986 A
4593313 Nagasaki Jun 1986 A
4617593 Dudley Oct 1986 A
4630082 Sakai Dec 1986 A
4648936 Ashby et al. Mar 1987 A
4663188 Kane May 1987 A
4672206 Suzuki Jun 1987 A
4673770 Mandelkorn Jun 1987 A
4679068 Lillquist et al. Jul 1987 A
4751571 Lillquist Jun 1988 A
4775425 Guha et al. Oct 1988 A
4777490 Sharma et al. Oct 1988 A
4829013 Yamazaki May 1989 A
4883962 Elliot Nov 1989 A
4886958 Merryman Dec 1989 A
4887255 Handa et al. Dec 1989 A
4894526 Bethea et al. Jan 1990 A
4910568 Taki et al. Mar 1990 A
4910588 Kinoshita et al. Mar 1990 A
4964134 Westbrook et al. Oct 1990 A
4965784 Land et al. Oct 1990 A
4968372 Maass Nov 1990 A
4999308 Nishiura et al. Mar 1991 A
5021100 Ishihara et al. Jun 1991 A
5021854 Huth Jun 1991 A
5080725 Green et al. Jan 1992 A
5081049 Green et al. Jan 1992 A
5100478 Kawabata Mar 1992 A
5101260 Nath Mar 1992 A
5114876 Weiner May 1992 A
5127964 Hamakawa et al. Jul 1992 A
5164324 Russell et al. Nov 1992 A
5208822 Haus et al. May 1993 A
5223043 Olson et al. Jun 1993 A
5234790 Lang et al. Aug 1993 A
5236863 Iranmanesh Aug 1993 A
5244817 Hawkins et al. Sep 1993 A
5296045 Banerjee et al. Mar 1994 A
5309275 Nishimura et al. May 1994 A
5322988 Russell et al. Jun 1994 A
5346850 Kaschmitter et al. Sep 1994 A
5351446 Langsdorf Oct 1994 A
5370747 Noguchi et al. Dec 1994 A
5373182 Norton Dec 1994 A
5381431 Zayhowski Jan 1995 A
5383217 Uemura Jan 1995 A
5390201 Tomono et al. Feb 1995 A
5410168 Hisa Apr 1995 A
5413100 Barthelemy et al. May 1995 A
5449626 Hezel Sep 1995 A
5454347 Shibata et al. Oct 1995 A
5502329 Pezzani Mar 1996 A
5523570 Hairston Jun 1996 A
5559361 Pezzani Sep 1996 A
5569615 Yamazaki et al. Oct 1996 A
5578858 Mueller et al. Nov 1996 A
5580615 Itoh et al. Dec 1996 A
5589008 Kepper Dec 1996 A
5589704 Levine Dec 1996 A
5597621 Hummel et al. Jan 1997 A
5600130 VanZeghbroeck Feb 1997 A
5626687 Campbell May 1997 A
5627081 Tsuo et al. May 1997 A
5635089 Singh et al. Jun 1997 A
5640013 Ishikawa et al. Jun 1997 A
5641362 Meier Jun 1997 A
5641969 Cooke et al. Jun 1997 A
5705413 Harkin et al. Jan 1998 A
5705828 Noguchi et al. Jan 1998 A
5708486 Miyawaki et al. Jan 1998 A
5710442 Watanabe et al. Jan 1998 A
5714404 Mititsky et al. Feb 1998 A
5727096 Ghirardi et al. Mar 1998 A
5731213 Ono Mar 1998 A
5751005 Wyles et al. May 1998 A
5758644 Diab et al. Jun 1998 A
5766127 Pologe et al. Jun 1998 A
5766964 Rohatgi et al. Jun 1998 A
5773820 Osajda et al. Jun 1998 A
5779631 Chance Jul 1998 A
5781392 Clark Jul 1998 A
5792280 Ruby et al. Aug 1998 A
5808350 Jack et al. Sep 1998 A
5859446 Nagasu et al. Jan 1999 A
5861639 Bernier Jan 1999 A
5923071 Saito Jul 1999 A
5935320 Graef et al. Aug 1999 A
5942789 Morikawa Aug 1999 A
5943584 Shim et al. Aug 1999 A
5963790 Matsuno et al. Oct 1999 A
5977603 Ishikawa Nov 1999 A
6071796 Voutsas Jun 2000 A
6072117 Matsuyama et al. Jun 2000 A
6080988 Ishizuya et al. Jun 2000 A
6082858 Grace et al. Jul 2000 A
6097031 Cole Aug 2000 A
6106689 Matsuyama Aug 2000 A
6107618 Fossum et al. Aug 2000 A
6111300 Cao et al. Aug 2000 A
6147297 Wettling et al. Nov 2000 A
6160833 Floyd et al. Dec 2000 A
6168965 Malinovich et al. Jan 2001 B1
6194722 Fiorini et al. Feb 2001 B1
6204506 Akahori et al. Mar 2001 B1
6229192 Gu May 2001 B1
6252256 Ugge et al. Jun 2001 B1
6290713 Russell Sep 2001 B1
6291302 Yu Sep 2001 B1
6313901 Cacharelis Nov 2001 B1
6320296 Fujii et al. Nov 2001 B1
6327022 Nishi Dec 2001 B1
6331445 Janz et al. Dec 2001 B1
6331885 Nishi Dec 2001 B1
6340281 Haraguchi Jan 2002 B1
6372591 Mineji et al. Apr 2002 B1
6372611 Horikawa Apr 2002 B1
6379979 Connolly Apr 2002 B1
6420706 Lurie et al. Jul 2002 B1
6429036 Nixon et al. Aug 2002 B1
6429037 Wenham et al. Aug 2002 B1
6465860 Shigenaka et al. Oct 2002 B2
6475839 Zhang et al. Nov 2002 B2
6483116 Kozlowski et al. Nov 2002 B1
6483929 Marakami et al. Nov 2002 B1
6486522 Bishay et al. Nov 2002 B1
6493567 Krivitski et al. Dec 2002 B1
6498336 Tian et al. Dec 2002 B1
6500690 Yamagishi et al. Dec 2002 B1
6504178 Carlson et al. Jan 2003 B2
6580053 Voutsas Jun 2003 B1
6583936 Kaminsky et al. Jun 2003 B1
6597025 Lauter et al. Jul 2003 B2
6607927 Ramappa et al. Aug 2003 B2
6624049 Yamazaki Sep 2003 B1
6639253 Duane et al. Oct 2003 B2
6667528 Cohen et al. Dec 2003 B2
6677655 Fitzgerald Jan 2004 B2
6677656 François Jan 2004 B2
6683326 Iguchi et al. Jan 2004 B2
6689209 Falster et al. Feb 2004 B2
6753585 Kindt Jun 2004 B1
6759262 Theil et al. Jul 2004 B2
6790701 Shigenaka et al. Sep 2004 B2
6800541 Okumura Oct 2004 B2
6801799 Mendelson Oct 2004 B2
6803555 Parrish et al. Oct 2004 B1
6815685 Wany Nov 2004 B2
6818535 Lu et al. Nov 2004 B2
6822313 Matsushita Nov 2004 B2
6825057 Heyers et al. Nov 2004 B1
6864156 Conn Mar 2005 B1
6864190 Han et al. Mar 2005 B2
6867806 Lee et al. Mar 2005 B1
6900839 Kozlowski et al. May 2005 B1
6907135 Gifford Jun 2005 B2
6911375 Guarini et al. Jun 2005 B2
6919587 Ballon et al. Jul 2005 B2
6923625 Sparks Aug 2005 B2
6927432 Holm et al. Aug 2005 B2
6984816 Holm et al. Jan 2006 B2
7008854 Forbes Mar 2006 B2
7041525 Clevenger et al. May 2006 B2
7057256 Carey, III et al. Jun 2006 B2
7075079 Wood Jul 2006 B2
7091411 Falk et al. Aug 2006 B2
7109517 Zaidi Sep 2006 B2
7126212 Enquist et al. Oct 2006 B2
7132724 Merrill Nov 2006 B1
7202102 Yao Apr 2007 B2
7211501 Liu et al. May 2007 B2
7235812 Chu et al. Jun 2007 B2
7247527 Shimomura et al. Jul 2007 B2
7247812 Tsao Jul 2007 B2
7256102 Nakata et al. Aug 2007 B2
7271445 Forbes Sep 2007 B2
7271835 Iizuka et al. Sep 2007 B2
7285482 Ochi Oct 2007 B2
7314832 Kountz et al. Jan 2008 B2
7354792 Carey, III et al. Apr 2008 B2
7358498 Geng et al. Apr 2008 B2
7375378 Manivannan et al. May 2008 B2
7390689 Mazur et al. Jun 2008 B2
7432148 Li et al. Oct 2008 B2
7442629 Mazur et al. Oct 2008 B2
7446359 Lee et al. Nov 2008 B2
7446807 Hong Nov 2008 B2
7456452 Wells et al. Nov 2008 B2
7482532 Yi et al. Jan 2009 B2
7498650 Lauxtermann Mar 2009 B2
7504325 Koezuka et al. Mar 2009 B2
7504702 Mazur et al. Mar 2009 B2
7511750 Murakami Mar 2009 B2
7521737 Augusto Apr 2009 B2
7528463 Forbes May 2009 B2
7542085 Altice, Jr. et al. Jun 2009 B2
7547616 Fogel et al. Jun 2009 B2
7551059 Farrier Jun 2009 B2
7560750 Niira et al. Jul 2009 B2
7564631 Li et al. Jul 2009 B2
7582515 Choi et al. Sep 2009 B2
7592593 Kauffman et al. Sep 2009 B2
7595213 Kwon et al. Sep 2009 B2
7605397 Kindem et al. Oct 2009 B2
7615808 Pain et al. Nov 2009 B2
7618839 Rhodes Nov 2009 B2
7619269 Ohkawa Nov 2009 B2
7629582 Hoffman et al. Dec 2009 B2
7648851 Fu et al. Jan 2010 B2
7649156 Lee Jan 2010 B2
7705879 Kerr et al. Apr 2010 B2
7731665 Lee et al. Jun 2010 B2
7741666 Nozaki et al. Jun 2010 B2
7745901 McCaffrey et al. Jun 2010 B1
7763913 Fan et al. Jul 2010 B2
7772028 Adkisson et al. Aug 2010 B2
7781856 Mazur et al. Aug 2010 B2
7800192 Venezia Sep 2010 B2
7800684 Tatani Sep 2010 B2
7816220 Mazur et al. Oct 2010 B2
7828983 Weber et al. Nov 2010 B2
7847253 Carey et al. Dec 2010 B2
7847326 Park et al. Dec 2010 B2
7855406 Yamaguchi et al. Dec 2010 B2
7875498 Elbanhawy et al. Jan 2011 B2
7880168 Lenchenkov Feb 2011 B2
7884439 Mazur et al. Feb 2011 B2
7884446 Mazur et al. Feb 2011 B2
7897942 Bereket Mar 2011 B1
7910964 Kawahito et al. Mar 2011 B2
7923801 Tian et al. Apr 2011 B2
7968834 Veeder Jun 2011 B2
8008205 Fukushima et al. Aug 2011 B2
8013411 Cole Sep 2011 B2
8030726 Sumi Oct 2011 B2
8035343 Seman, Jr. Oct 2011 B2
8058615 McCaffrey Nov 2011 B2
8076746 McCarten et al. Dec 2011 B2
8080467 Carey et al. Dec 2011 B2
8088219 Knerer et al. Jan 2012 B2
8093559 Rajavel Jan 2012 B1
RE43169 Parker Feb 2012 E
8164126 Moon et al. Apr 2012 B2
8207051 Sickler et al. Jun 2012 B2
8247259 Grolier et al. Aug 2012 B2
8259293 Andreou et al. Sep 2012 B2
8288702 Veeder Oct 2012 B2
8470619 Bour Jun 2013 B2
8476681 Haddad et al. Jul 2013 B2
8564087 Yamamura et al. Oct 2013 B2
8603902 Mazer et al. Dec 2013 B2
8629485 Yammamura et al. Jan 2014 B2
8680591 Haddad Mar 2014 B2
8742528 Yamamura et al. Jun 2014 B2
8884226 Miyazaki et al. Nov 2014 B2
8906670 Gray Dec 2014 B2
8916945 Sakamoto et al. Dec 2014 B2
8994135 Yamamura et al. Mar 2015 B2
9184204 Hu Nov 2015 B2
9190551 Yamamura et al. Nov 2015 B2
9209345 Haddad Dec 2015 B2
9369641 Hu Jun 2016 B2
9419159 Sakamoto et al. Aug 2016 B2
9673250 Haddad Jun 2017 B2
20010017344 Aebi Aug 2001 A1
20010022768 Takahashi Sep 2001 A1
20010044175 Barret et al. Nov 2001 A1
20010044266 Katsuoka Nov 2001 A1
20020020893 Lhorte Feb 2002 A1
20020024618 Imai Feb 2002 A1
20020056845 Iguchi et al. May 2002 A1
20020060322 Tanabe et al. May 2002 A1
20020079290 Holdermann Jun 2002 A1
20020117699 Francois Aug 2002 A1
20020148964 Dausch et al. Oct 2002 A1
20020182769 Campbell Dec 2002 A1
20030029495 Mazur et al. Feb 2003 A1
20030030083 Lee et al. Feb 2003 A1
20030045092 Shin Mar 2003 A1
20030057357 Uppal et al. Mar 2003 A1
20030111106 Nagano et al. Jun 2003 A1
20030210332 Frame Nov 2003 A1
20030213515 Sano et al. Nov 2003 A1
20030214595 Mabuchi Nov 2003 A1
20030228883 Kusakari et al. Dec 2003 A1
20040014307 Shin et al. Jan 2004 A1
20040016886 Ringermacher et al. Jan 2004 A1
20040041168 Hembree et al. Mar 2004 A1
20040046224 Rossel et al. Mar 2004 A1
20040077117 Ding et al. Apr 2004 A1
20040080638 Lee Apr 2004 A1
20040130020 Kuwabara et al. Jul 2004 A1
20040161868 Hong Aug 2004 A1
20040222187 Lin Nov 2004 A1
20040252931 Belleville et al. Dec 2004 A1
20040256561 Buehler et al. Dec 2004 A1
20050040440 Murakami Feb 2005 A1
20050051822 Manning Mar 2005 A1
20050062041 Terakawa et al. Mar 2005 A1
20050088634 Kosugi Apr 2005 A1
20050093100 Chen May 2005 A1
20050101100 Kretchmer et al. May 2005 A1
20050101160 Garg et al. May 2005 A1
20050127401 Mazur et al. Jun 2005 A1
20050134698 Schroeder et al. Jun 2005 A1
20050150542 Madan Jul 2005 A1
20050158969 Binnis et al. Jul 2005 A1
20050211996 Krishna et al. Sep 2005 A1
20050227390 Shtein et al. Oct 2005 A1
20060006482 Rieve et al. Jan 2006 A1
20060011954 Ueda et al. Jan 2006 A1
20060011955 Baggenstoss Jan 2006 A1
20060060848 Chang et al. Mar 2006 A1
20060071254 Rhodes Apr 2006 A1
20060079062 Mazur et al. Apr 2006 A1
20060086956 Furukawa et al. Apr 2006 A1
20060097172 Park May 2006 A1
20060118781 Rhodes Jun 2006 A1
20060121680 Tanaka Jun 2006 A1
20060128087 Bamji et al. Jun 2006 A1
20060132633 Nam et al. Jun 2006 A1
20060138396 Lin et al. Jun 2006 A1
20060145148 Hirai et al. Jul 2006 A1
20060145176 Lee Jul 2006 A1
20060160343 Chong et al. Jul 2006 A1
20060166475 Mantl Jul 2006 A1
20060175529 Harmon et al. Aug 2006 A1
20060180885 Rhodes Aug 2006 A1
20060181627 Farrier Aug 2006 A1
20060210122 Cleveland Sep 2006 A1
20060214121 Schrey et al. Sep 2006 A1
20060228897 Timans Oct 2006 A1
20060231914 Carey et al. Oct 2006 A1
20060238632 Shah Oct 2006 A1
20060244090 Roy et al. Nov 2006 A1
20060255340 Manivannan et al. Nov 2006 A1
20060257140 Seger Nov 2006 A1
20070035849 Li Feb 2007 A1
20070035879 Hall et al. Feb 2007 A1
20070051876 Sumi et al. Mar 2007 A1
20070052050 Dierickx Mar 2007 A1
20070063219 Sa'ar et al. Mar 2007 A1
20070076481 Tennant Apr 2007 A1
20070103580 Noto May 2007 A1
20070115554 Breitung et al. May 2007 A1
20070123005 Hiura et al. May 2007 A1
20070125951 Snider et al. Jun 2007 A1
20070138590 Wells et al. Jun 2007 A1
20070145505 Kim et al. Jun 2007 A1
20070178672 Tanaka et al. Aug 2007 A1
20070187670 Hsu et al. Aug 2007 A1
20070194356 Moon et al. Aug 2007 A1
20070194401 Nagai et al. Aug 2007 A1
20070195056 Lloyd Aug 2007 A1
20070200940 Gruhlke et al. Aug 2007 A1
20070201859 Sarrat Aug 2007 A1
20070235827 Altice Oct 2007 A1
20070237504 Nakashiba Oct 2007 A1
20070247414 Roberts Oct 2007 A1
20070262366 Baek et al. Nov 2007 A1
20070290283 Park et al. Dec 2007 A1
20070296060 Tanabe et al. Dec 2007 A1
20080002863 Northcott Jan 2008 A1
20080020555 Shimomura et al. Jan 2008 A1
20080026550 Werner et al. Jan 2008 A1
20080036022 Hwang et al. Feb 2008 A1
20080044943 Mazur et al. Feb 2008 A1
20080076240 Veschtti et al. Mar 2008 A1
20080099804 Venezia May 2008 A1
20080121280 Carnel et al. May 2008 A1
20080121805 Tweet et al. May 2008 A1
20080142686 Konno et al. Jun 2008 A1
20080158398 Yaffe et al. Jul 2008 A1
20080170173 Park et al. Jul 2008 A1
20080173620 Grek Jul 2008 A1
20080174685 Shan et al. Jul 2008 A1
20080178932 Den Boer et al. Jul 2008 A1
20080179762 Cho et al. Jul 2008 A1
20080191310 Wu et al. Aug 2008 A1
20080192132 Bechtel et al. Aug 2008 A1
20080192133 Abiru et al. Aug 2008 A1
20080196761 Nakano et al. Aug 2008 A1
20080198251 Xu et al. Aug 2008 A1
20080202576 Hieslmair Aug 2008 A1
20080213936 Hatai Sep 2008 A1
20080223436 den Boer et al. Sep 2008 A1
20080242005 Dozen et al. Oct 2008 A1
20080257409 Li et al. Oct 2008 A1
20080258604 Mazur et al. Oct 2008 A1
20080266434 Sugawa et al. Oct 2008 A1
20080266435 Agranov et al. Oct 2008 A1
20080281174 Dietiker Nov 2008 A1
20080284884 Makino et al. Nov 2008 A1
20080309913 Fallon Dec 2008 A1
20090002528 Manabe et al. Jan 2009 A1
20090009596 Kerr et al. Jan 2009 A1
20090014056 Hockaday Jan 2009 A1
20090027640 Shibazaki Jan 2009 A1
20090038669 Atanackovic Feb 2009 A1
20090039397 Chao Feb 2009 A1
20090050944 Hong Feb 2009 A1
20090056797 Barnett et al. Mar 2009 A1
20090057536 Hirose Mar 2009 A1
20090065051 Chan et al. Mar 2009 A1
20090078316 Khazeni et al. Mar 2009 A1
20090095887 Saveliev Apr 2009 A1
20090097290 Chandrasekaran Apr 2009 A1
20090101197 Morikawa Apr 2009 A1
20090109305 Dai et al. Apr 2009 A1
20090114630 Hawryluk May 2009 A1
20090142879 Isaka et al. Jun 2009 A1
20090146240 Carey, III et al. Jun 2009 A1
20090160983 Lenchenkov Jun 2009 A1
20090174026 Carey et al. Jul 2009 A1
20090180010 Adikisson et al. Jul 2009 A1
20090194671 Nozaki et al. Aug 2009 A1
20090200454 Barbier et al. Aug 2009 A1
20090200586 Mao et al. Aug 2009 A1
20090200626 Qian et al. Aug 2009 A1
20090200631 Tai et al. Aug 2009 A1
20090206237 Shannon et al. Aug 2009 A1
20090211627 Meier et al. Aug 2009 A1
20090213883 Mazur et al. Aug 2009 A1
20090218493 McCaffrey et al. Sep 2009 A1
20090223561 Kim et al. Sep 2009 A1
20090227061 Bateman et al. Sep 2009 A1
20090242019 Ramamoorthy et al. Oct 2009 A1
20090242032 Yamazaki et al. Oct 2009 A1
20090242933 Hu et al. Oct 2009 A1
20090256156 Hsieh Oct 2009 A1
20090256226 Tatani Oct 2009 A1
20090261255 Nakamura et al. Oct 2009 A1
20090283807 Adkisson et al. Nov 2009 A1
20090294787 Nakaji et al. Dec 2009 A1
20090308450 Adibi et al. Dec 2009 A1
20090308457 Smith Dec 2009 A1
20100000597 Cousins Jan 2010 A1
20100013036 Carey Jan 2010 A1
20100013039 Qian et al. Jan 2010 A1
20100013593 Luckhardt Jan 2010 A1
20100024871 Oh et al. Feb 2010 A1
20100032008 Adekore Feb 2010 A1
20100037952 Lin Feb 2010 A1
20100038523 Venezia et al. Feb 2010 A1
20100038542 Carey et al. Feb 2010 A1
20100040981 Kiesel et al. Feb 2010 A1
20100044552 Chen Feb 2010 A1
20100051809 Onat et al. Mar 2010 A1
20100052088 Carey Mar 2010 A1
20100053382 Kuniba Mar 2010 A1
20100055887 Piwczyk Mar 2010 A1
20100059385 Li Mar 2010 A1
20100059803 Gidon et al. Mar 2010 A1
20100072349 Veeder Mar 2010 A1
20100074396 Schmand et al. Mar 2010 A1
20100083997 Hovel Apr 2010 A1
20100084009 Carlson et al. Apr 2010 A1
20100096718 Hynecek et al. Apr 2010 A1
20100097609 Jaeger et al. Apr 2010 A1
20100102206 Cazaux et al. Apr 2010 A1
20100102366 Lee et al. Apr 2010 A1
20100109060 Mao et al. May 2010 A1
20100116312 Peumans et al. May 2010 A1
20100117181 Kim et al. May 2010 A1
20100118172 McCarten et al. May 2010 A1
20100128937 Yoo et al. May 2010 A1
20100133635 Lee et al. Jun 2010 A1
20100140733 Lee et al. Jun 2010 A1
20100140768 Zafiropoulo Jun 2010 A1
20100143744 Gupta Jun 2010 A1
20100147383 Carey et al. Jun 2010 A1
20100200658 Olmstead et al. Aug 2010 A1
20100219506 Gupta Sep 2010 A1
20100224229 Pralle et al. Sep 2010 A1
20100240169 Petti et al. Sep 2010 A1
20100245647 Honda et al. Sep 2010 A1
20100258176 Kang et al. Oct 2010 A1
20100264473 Adkisson et al. Oct 2010 A1
20100289885 Lu et al. Nov 2010 A1
20100290668 Friedman et al. Nov 2010 A1
20100300505 Chen Dec 2010 A1
20100300507 Heng et al. Dec 2010 A1
20100313932 Kroll et al. Dec 2010 A1
20110003424 DeCeuster et al. Jan 2011 A1
20110019050 Yamashita Jan 2011 A1
20110056544 Ji et al. Mar 2011 A1
20110073976 Vaillant Mar 2011 A1
20110095387 Carey et al. Apr 2011 A1
20110104850 Weidman et al. May 2011 A1
20110127567 Seong Jun 2011 A1
20110140221 Venezia et al. Jun 2011 A1
20110194100 Thiel et al. Aug 2011 A1
20110220971 Haddad Sep 2011 A1
20110227138 Haddad Sep 2011 A1
20110251478 Wieczorek Oct 2011 A1
20110260059 Jiang et al. Oct 2011 A1
20110266644 Yamamura et al. Nov 2011 A1
20110292380 Bamji Dec 2011 A1
20110303999 Sakamoto et al. Dec 2011 A1
20120024363 Dimer et al. Feb 2012 A1
20120024364 Carey, III et al. Feb 2012 A1
20120038811 Ellis-monaghan et al. Feb 2012 A1
20120043637 King et al. Feb 2012 A1
20120049242 Atanackovic et al. Mar 2012 A1
20120080733 Doan et al. Apr 2012 A1
20120111396 Saylor et al. May 2012 A1
20120171804 Moslehi et al. Jul 2012 A1
20120187190 Wang et al. Jul 2012 A1
20120222396 Clemen Sep 2012 A1
20120274744 Wan Nov 2012 A1
20120291859 Vineis et al. Nov 2012 A1
20120300037 Laudo Nov 2012 A1
20120305063 Moslehi et al. Dec 2012 A1
20120312304 Lynch et al. Dec 2012 A1
20120313204 Haddad et al. Dec 2012 A1
20120313205 Haddad et al. Dec 2012 A1
20120326008 Mckee et al. Dec 2012 A1
20130001553 Vineis et al. Jan 2013 A1
20130082343 Fudaba et al. Apr 2013 A1
20130135439 Kakuko et al. May 2013 A1
20130168792 Haddad et al. Jul 2013 A1
20130168803 Haddad et al. Jul 2013 A1
20130200251 Velichko Aug 2013 A1
20130207214 Haddad et al. Aug 2013 A1
20130285130 Ting Oct 2013 A1
20140198240 Rhoads Jul 2014 A1
20140247378 Sharma et al. Sep 2014 A1
20140352779 Smirnov Dec 2014 A1
20150076468 Yamaguchi et al. Mar 2015 A1
Foreign Referenced Citations (86)
Number Date Country
3666484 Jun 1985 AU
101404307 Apr 2009 CN
19838439 Apr 2000 DE
0473439 Mar 1992 EP
0566156 Oct 1993 EP
1630871 Jan 2006 EP
1873840 Jan 2008 EP
2073270 May 2012 EP
2509107 Oct 2012 EP
2827707 Jan 2003 FR
2030766 Apr 1980 GB
S5771188 May 1982 JP
S57173966 Oct 1982 JP
S63116421 May 1988 JP
H02152226 Jun 1990 JP
H02237026 Sep 1990 JP
H03183037 Aug 1991 JP
H04318970 Nov 1992 JP
H06104414 Apr 1994 JP
H06244444 Sep 1994 JP
H06267868 Sep 1994 JP
H06275641 Sep 1994 JP
H07235658 May 1995 JP
2007183484 Jul 1995 JP
9148594 Jun 1997 JP
H09298308 Nov 1997 JP
11077348 Mar 1999 JP
11097724 Apr 1999 JP
2000164914 Jun 2000 JP
2001007381 Jan 2001 JP
2001024936 Jan 2001 JP
2001189478 Jul 2001 JP
2001257927 Sep 2001 JP
2001339057 Dec 2001 JP
2002043594 Feb 2002 JP
2002134640 May 2002 JP
2003163360 Jun 2003 JP
2003242125 Aug 2003 JP
2003258285 Sep 2003 JP
2003308130 Oct 2003 JP
2004047682 Feb 2004 JP
2004273886 Sep 2004 JP
2004273887 Sep 2004 JP
2005339425 Dec 2005 JP
2006033493 Feb 2006 JP
2006147991 Jun 2006 JP
2006173381 Jun 2006 JP
2006255430 Sep 2006 JP
2006261372 Sep 2006 JP
2007165909 Jun 2007 JP
2007180642 Jul 2007 JP
2007180643 Jul 2007 JP
2007305675 Nov 2007 JP
2008187003 Aug 2008 JP
2006210701 Aug 2008 JP
2008187003 Aug 2008 JP
2008283219 Nov 2008 JP
2009021479 Jan 2009 JP
2009152569 Jul 2009 JP
2010278472 Dec 2010 JP
2011091128 May 2011 JP
20010061058 Apr 2001 KR
2005039273 Apr 2005 KR
100825808 Apr 2008 KR
20090077274 Jul 2009 KR
20100118864 Nov 2010 KR
20060052278 May 2016 KR
200627675 Aug 2006 TW
200818529 Apr 2008 TW
WO 9114284 Sep 1991 WO
0031679 Jun 2000 WO
WO 0241363 May 2002 WO
WO 03059390 Jul 2003 WO
WO 2006086014 Aug 2006 WO
WO 2008091242 Jul 2008 WO
WO 2008099524 Aug 2008 WO
WO 2008145097 Dec 2008 WO
2009016846 Feb 2009 WO
WO 2009100023 Aug 2009 WO
2009147085 Dec 2009 WO
WO 2009147085 Dec 2009 WO
WO 2010033127 Mar 2010 WO
WO 2011003871 Jan 2011 WO
WO 2011035188 Mar 2011 WO
WO 2011119618 Mar 2011 WO
2012174752 Dec 2012 WO
Non-Patent Literature Citations (154)
Entry
Berger, Michael; Moth Eyes Inspire Self-Cleaning Antireflection Nanotechnology Coatings; 2008; 3 pages; Nanowerk LLC.
Boden, S.A. et al.; Nanoimprinting for Antireflective Moth-Eye Surfaces; 4 pages; 2008.
Buttgen, B.; “Demodulation Pixel Based on Static Drift Fields”; IEEE Transactions on Electron Devices, vol. 53, No. 11, Nov. 2006.
Carey et al., “Femtosecond-Laser-Assisted Microstructuring of Silicon Surfaces”, Optics and Photonics News, 2003. 14, 32-36.
Carey, et al. “Femtosecond Laser-Assisted Microstructuring of Silicon for Novel Detector, Sensing and Display Technologies”, LEOS 2003, 481-482, Tuscon, AR.
Carey, et al. “Femtosecond Laser-Assisted Microstructuring of Silicon for Novel Detector, Sensing and Display Technologies”, LEOS; 2002, 97-98, Glasgos, Scotland, 2002.
Carey, et al., “Fabrication of Micrometer-Sized Conical Field Emitters Using Femtosecond Laser-Assisted Etching of Silicon,” Proc. IVMC 2001, 75-76, UC Davis, Davis, CA.
Carey, et al., “Field Emission from Silicon. Microstructures Formed by Femtosecond Laser Assisted Etching,” Proc. CLEO 2001 (Baltimore, MD 2001) 555-557.
Carey, et al., “High Sensitivity Silicon-Based VIS/NIR Photodetectors”, Optical Society of America (2003) 1-2.
Carey, III; “Femtosecond-laser Microstructuring of Silicon for Novel Optoelectronic Devices”; Harvard University, Jul. 2004; (Thesis).
Chen, Q. et al.; Broadband moth-eye antireflection coatings fabricated by low-cost nanoimprinting; Applied Physics Letters 94; pp. 263118-1-263118-3; 2009; American Institute of Physics.
Chien et al, “Pulse Width Effect in Ultrafast Laser Processing of Materials,” Applied Physics A, 2005, 1257-1263, 81, Springer Berlin, Heidelberg, Germany.
Cmosis; “Global Shutter Image Sensors for Machine Vision Application”; Image Sensors Europe 2010, Mar. 23-25, 2010; .COPYRGT. copyright 2010.
Cotter, Jeffrey E.; Optical intensity of light in layers of silicon with rear diffuse reflectors; Journal of Applied Physics; Jul. 1, 1998; pp. 618-624; vol. 84, No. 1; American Institute of Physics.
Crouch et al., “Comparison of Structure and Properties of Femtosecond and Nanosecond Laser-Structured Silicon” Appl. Phys. Lett., 2004, 84,1850-1852.
Crouch et al., “Infrared Absorption by Sulfur-Doped Silicon Formed by Femtosecond Laser Irradiation”, Appl. Phys. A, 2004, 79, 1635-1641.
Despeisse, et al.; “Thin Film Silicon Solar Cell on Highly Textured Substrates for High Conversion Efficiency”; 2004.
Dewan, Rahul et al.; Light Trapping in Thin-Film Silicon Solar Cells with Submicron Surface Texture; Optics Express; vol. 17, No. 25; Dec. 7, 2009; Optical Society of America.
Deych et al.; Advances in Computed Tomography and Digital Mammography; Power Point; Nov. 18, 2008; Analogic Corp.; Peabody, MA.
Dobie, et al.; “Minimization of reflected light in photovoltaic modules”; Mar. 1, 2009.
Dobrzanski, L.A. et al.; Laser Surface Treatment of Multicrystalline Silicon for Enhancing Optical Properties; Journal of Materials Processing Technology; p. 291-296; 2007; Elsevier B.V.
Dolgaev et al., “Formation of Conical Microstructures Upon Laser Evaporation of Solids”, Appl. Phys. A, 2001, 73, 177-181.
Duerinckx, et al.; “Optical Path Length Enhancement for >13% Screenprinted Thin Film Silicon Solar Cells”; 2006.
Dulinski, Wojciech et al.; Tests of backside illumincated monolithic CMOS pixel sensor in an HPD set-up; Nuclear Instruments and methods in Physics Research; Apr. 19, 2005; pp. 274-280; Elsevier B.V.
EP Search Report dated May 19, 2014 in EP App. No. 10817938.3 (5 pages).
Forbes; “Texturing, reflectivity, diffuse scattering and light trapping in silicon solar cells”; 2012.
Forbes, L. and M.Y. Louie, “Backside Nanoscale Texturing to Improve IR Response of Silicon Photodetectors and Solar Cells,” Nanotech, vol. 2, pp. 9-12, Jun. 2010.
Fowlkes et al., “Surface Microstructuring and Long-Range Ordering of Silicon Nanoparticles”, Appl. Phys. Lett., 2002, 80 (20), 3799-3801.
Gjessing, J. et al.; 2D back-side diffraction grating for impored light trapping in thin silicon solar cells; Optics Express; vol. 18, No. 6; pp. 5481-5495; Mar. 15, 2010; Optical Society of America.
Goetzberger, et al.; “Solar Energy Materials & Solar Cells”; vol. 92 (2008) pp. 1570-1578.
Haug, et al.; “Light Trapping effects in thin film silicon solar cells”; 2009.
Her et al., “Microstructuring of Silicon with Femtosecond Laser Pulses,” Applied Physics Letters, 1998, 1673-1675, vol. 73, No. 12, American Institute of Physics.
Her et al., “Novel Conical Microstructures Created in Silicon With Femtosecond Laser Pulses”, CLEO 1998, 511-512, San Francisco, CA.
Her, et al., “Femtosecond laser-induced formation of spikes on silicon,” Applied Physics A, 2000, 70, 383-385.
Hermann, S. et al.; Impact of Surface Topography and Laser Pulse Duration for Laser Ablation of Solar Cell Front Side Passivating SiNx Layers; Journal of Applied Physics; vol. 108, No. 11; pp. 114514-1-114514-8; 2010; American Institute of Physics.
High-Performance Technologies for Advanced Biomedical Applications; .COPYRGT. 2004Brochure; pp. 1-46; PerkinElmerOptoelectronics.
Hu et al., “Solar Cells from Basic to Advanced Systems,” McGraw Hill Book Co., 1983, 39, New York, New York.
Huang, et al.; “Microstructured silicon photodetector”; Applied Physics Letters 89, 033506; 2006 American Institute of Physics; 2000.
Hüpkes, J. et al.; Light Scattering and Trapping in Different Thin Film Photovoltaic Devices; 24th European Photovoltaic Solar Energy Conference, Hamburg, Germany (Sep. 21-25, 2009); pp. 2766-2769.
International Search Report of the International Searching Authority dated Mar. 28, 2013, in PCT/US2012/060291 filed Oct. 15, 2012.
Joy, T. et al.; Development of a Production-Ready, Back-Illuminated CMOS Image Sensor with Small Pixels; Electron Devices Meeting; pp. 1007-1010; 2007; IEEE.
Juntunen et al.; Advanced Photodiode Detector for Medical CT Imaging: Design and Performance; 2007; pp. 2730-2735; IEEE.
Kim et al.; “Strong Sub-Band-Gap Infrared Absorption in Silicon Supersaturated with Sulfur”; 2006 Appl. Phys. Lett. 88, 241902-1-241902-3.
Kray, D. et al.; Laser-doped Silicon Soalr Cells by Laser Chemical Processing (LCP) exceeding 20% Efficiency; 33rd IEEE Photovoltaic Specialist Conference; 3 pages; May 2008; IEEE.
Kroning et al.; X-ray Imaging Systems for NDT and General Applications; 2002; Fraunhofer Institute for Nondestructive Testing; Saarbrucken and Dresden, Germany.
Li, “Design and Simulation of an Uncooled Double-Cantilever Microbolometer with the Potential for .about.mK NETD,” 2004, Sensors and Actuators A, 351-359, vol. 112, Elsevier B.V.
Li, Hongsong et al.; An experimental study of the correlation between surface roughness and light scattering for rough metallic surfaces; Advanced Characterization Techniques for Optics, Semiconductors, and Nanotechnologies II; 2005; pp. 25780V-1-25780V-15; vol. 5878; SPIE Bellingham, WA.
Lin, A. et al.; Optimization of Random Diffraction Gratings in Thin-Film Solar Cells Using Genetic Algorithms; 2007; 1 page; SSEL Annual Report.
Madzhaov, et al.; “Light trapping in thin-firm silicon solar cells for superstrate and substrate configuration” Abstract #1614, 218.sup.th ECS Meeting .COPYRGT. 2010 the Electrochemical Society.
Mateus; C.F.R. et al.; Ultrabroadband Mirror Using Low-Index Cladded Subwavelength Grating; Photonics Technology Letters; vol. 16, Issue No. 2; pp. 518-520; Feb. 2004; IEEE.
Matsuno, Shigeru et al.; Advanced Technologies for High Efficiency Photovoltaic Systems; Mitsubishi Electric Advance; vol. 122; pp. 17-19; Jun. 2008.
Moloney, A.M. et al.; Novel Black Silicon PIN Photodiodes; 8 pages; Jan. 25, 2006; SPIE.
Moses; Nuclear Medical Imaging—Techniques and Challenges; Power Point; Feb. 9, 2005; Lawrence Berkeley National Laboratory Department of Functional Imaging.
Munday, J.N. et al.; Large Integrated Absorption Enhancement in Plasmonic Solar Cells by Combining Metallic Gratings and Antireflection Coatings; Nano Letters; vol. 11, No. 6; pp. 2195-2201; Oct. 14, 2010; American Chemical Society.
Nayak et al, “Semiconductor Laesr Crystallization of a--Si:H,” SPIE Digital Library, 2003, 277-380, vol. 4977, Bellingham, Washington. 2003.
Nayak et al, “Ultrafast-Laser-Assisted Chemical Restructuring of Silicon and Germanium Surfaces,” Applied Surface Science, 2007, 6580-6583, vol. 253, Issue 15, Elsevier B.V.
Nayak et al, “Semiconductor Laser Crystallization of a--Si:H on Conducting Tin-Oxide-Coated Glass for Solar Cell and Display Applications,” Applied Physics A, 2005, 1077-1080, 80, Springer Berlin, Heidelberg, Germany.
Nayak, B.K. et al.; Ultrafast Laser Textured Silicon Solar Cells; Mater. Res. Soc. Symp. Proc.; vol. 1123; 6 pages; 2009; Materials Research Society.
Oden, et al.; “Optical and Infrared Detection Using Microcantilevers;” SPIE Digital Library on Oct. 13, 2010; vol. 2744; 10 pages.
Pain, Bedabrata; Backside Illumination Technology for SOI-CMOS Image Sensors; 2009 IISW Symposium on Backside Illujination of Solid-State Image Sensors, Bergen Norway; Jun. 25, 2009; pp. 1-23.
Pain, Bedabrata; “A Back-Illuminated Megapixel CMOS Image Sensor”; http://hdl.handle.net/2014/39312; May 1, 2005.
Payne, D.N.R. et al.; Characterization of Experimental Textured ZnO:Al Films for Thin Film Solar Cell Applications and Comparison with Commercial and Plasmonic Alternatives; Photovoltaic Specialists Conference (PVSC); pp. 1560-1564; 2010; IEEE.
International Search Report mailed Apr. 28, 2011 in PCT Application PCT/US2010/049375 filed Sep. 17, 2010 (3 pages).
International Report on Patentability and Written Opinion mailed Mar. 20, 2012 in PCT/US2010/049375 filed Sep. 17, 2010 (5 pages).
PCT/US2011/066602; filed Dec. 21, 2011; SiOnyx, Inc. et al.; international search report dated Sep. 7, 2012.
PCT/US2013/033554; filed Mar. 22, 2013; Sionyx, Inc., international search report dated Jul. 24, 2013.
Pedraza et al., “Silicon Microcolumn Arrays Grown by Nanosecond Pulsed-Excimer Laser Irradiation”, Appl. Phys. Lett., 1999, 74 (16), 2322-2324, American Institute of Physics.
Pedraza et al., “Surface Nanostructuring of Silicon”, Appl. Phys. A, 2003, 77, 277-284.
Russell, et al.; “Nanosecond Eximer Laser Processing for Novel Microelectronic Fabrication”; Nanosecond Excimer Laser Processing; 6 pages; 1989.
Russell, Ramirez and Kelley, “Nanosecond Excimer Laser Processing for Novel Microelectronic Devices,” US Navy, SPAWAR, San Diego, Techical Report, 2003.
Russell, Ramirez, Kelley, “Nanosecond Excimer Laser Processing for Novel Microelectronic Fabrication,” SSC Pacific Technical Reports , pp. 228-233, 2003, vol. 4, US Navy.
Sai, H. et al.; Enhancement of Light Trapping in Thin-Film Hydrogenated Microcrystalline Si Solar Cells Using Back Reflectors with Self-Ordered Dimple Pattern; Applied Physics Letters; vol. 93; 2008; American Institute of Physics.
Sanchez et al., “Whiskerlike Structure Growth on Silicon Exposed to ArF Excimer Laser Irradiation”, Appl. Phys. Lett., 1996, 69 (5), 620-622.
Sanchez et al., “Dynamics of the Hydrodynamical Growth of Columns on Silicon Exposed to ArF Excimer-Laser Irradiation”, Appl. Phys. A, 1998, 66, 83-86.
Sarnet et al.; “Femtosecond laser for black silicon and photovoltaic cells”; Feb. 21, 2008, Proc. of SPIE; vol. 6881; pags 1-15.
Senoussaoui, N. et al.; Thin-Film Solar Cells with Periodic Grating Coupler; Thin Solid Films; pp. 397-401; 2003; Elsevier B.V.
Serpenguzel et al., “Temperature Dependence of Photluminescence in Non-Crystalline Silicon”, Photonics West (San Jose, CA, 2004) 454-462.
Shen et al., “Formation of Regular Arrays of Silicon Micorspikes by Femotsecond Laser Irradiation Through a Mask”, Appl. Phys. Lett., 82, 1715-1717 (2003).
Solar Energy Research Institute, “Basic Photovoltaic Principles and Methods,” Van Nostrand Reinhold Co., NY 1984, pp. 45-47 and 138-142.
Stone et al.; The X-ray Sensitivity of Amorphous Selenium for Mammography;.Am. Assoc. Phys. Med.; Mar. 2002; pp. 319-324; vol. 29 No. 3; Am. Assoc. Phys. Med.
Szlufcik, J. et al.; Simple Integral Screenprinting process for selective emitter polycrystalline silicon solar cells; Applied Physics Letters; vol. 59, No. 13; Sep. 23, 1991; American Institute of Physics.
Tabbal et al., “Formation of Single Crystal Sulfur Supersaturated Silicon Based Junctions by Pulsed Laser Melting”. 2007, J. Vac. Sci. Technol. B25(6), 1847-1852.
Takayanagi, et al.; “A 600.times.600 Pixel, 500, fps CMOS Image Sensor with a 4.4 jum Pinned Photodiode 5-Transistor Global Shutter Pixel”; 2007 International Image Sensor Workshop; Jun. 6-10, 2007.
Tower, John R. et al.; Large Format Backside Illuminated CCD Imager for Space Surveillance; IEEE Transactions on Electron Devices, vol. 50, No. 1; Jan. 2003; pp. 218-224.
Tull; “Femtosecond Laser Ablation of Silicon: Nanoparticles, Doping and Photovotaics”; Harvard University, Jun. 2007 (Thesis).
Wilson, “Depth Distributions of Sulfur Implanted Into Silicon as a Function of Ion energy, Ion Fluence, and Anneal Temperature,” 1984, Appl. Phys. 55(10, 3490-3494.
Winderbaum, S. et al.; Reactive ion etching (RIE) as a method for texturing polycrystalline silicon solar cells; Solar Energy Materials and Solar Cells; 1997; pp. 239-248; Elsevier Science B.V.
Wu et al., “Black Silicon: A New Light Absorber,” APS Centennial Meeting (Mar. 23, 1999).
Wu et al., “Femtosecond laser-gas-solid interactions,” Thesis presented to the Department of Physics at Harvard University, pp. 1-113, 126-136, Aug. 2000.
Wu et al., “Visible Luminescence From Silicon Surfaces Microstructured in Air”. Appl. Phys. Lett., vol. 81, No. 11, 1999-2001 (2002).
Wu, et al “Near-Unity Below-Band-Gap Absorption by Microstructured Silicon,” 2001, Applied Physics Letters, 1850-1852, vol. 78, No. 13, American Institute of Physics.
Xu, Y., et al, “Infrared Detection Using Thermally Isolated Diode,” Sensors and Actuators A, Elsevier Sequoia S.A., 1993, vol. 36, 209-217, Lausanne, Switzerland.
Yablonovitch, et al.; “Intensity Enhancement in Textured Optical Sheets for Solar Cells”; .COPYRGT. 1982 IEEE.
Yamamoto, K. et al.; NIR Sensitivity Enhancement by Laser Treatment for Si Detectors; Nuclear Instruments and Methods in Physics Research A; pp. 520-523; Mar. 31, 2010; Elsevier.
Yan, B.; Light Trapping Effect from Randomized Textures of Ag/ZnO Back Reflector on Hyrdrogenated Amorphous and Nanocrystalline Silicon Based Solar Cells; Thin Film Solar Technology II; vol. 7771; 2010; SPIE.
Yasutomi, et al.; “Two-Stage Charge Transfer Pixel Using Pinned Diodes for Low-Noise Global Shutter Imaging”; 2009 International Image Sensor Workshop; Mar. 28, 2009.
Younkin et al., “Infrared Absorption by Conical Silicon Microstructures Made in a Variety of Background Gases Using Femtosecond-Laser Pulses”, J. Appl. Phys., 93, 2626-2629 (2003).
Younkin, “Surface Studies and Microstructure Fabrication Using Femtosecond Laser Pulses,” Thesis presented to the Division of Engineering & Applied sciences at Harvard University (Aug. 2001).
Yuan, et al.; “Efficient black silicon solar cell with a density-graded nanoporous surface: Optical properties, performance limitations, and design rules”; American Institute of Physics; Applied Physics Letters 95. 1230501 (2009) 3 pages.
Zaidi, S.H. et al.; Diffraction Grating Structures in Solar Cells; Photovoltaic Specialists Conference, 2000; 4 pages; Sep. 2000; IEEE.
A. Arndt, J.F. Allison, J.G. Haynos, and A. Meulenberg, Jr., “Optical Properties of the COMSAT Non-reflective Cell,” 11th IEEE Photovoltaic Spec. Conf., p. 40, 1975.
Asom et al., Interstitial Defect Reactions in Silicon; Appl. Phys. Lett.; Jul. 27, 1987; pp. 256-258; vol. 51(4); American Institute of Physics.
Berger, O., Inns, D. and Aberle, A.E. “Commercial White Paint as Back Surface Reflector for Thin-Film Solar Cells”, Solar Energy Materials & Solar Cells, vol. 91, pp. 1215-1221,2007.
Betta et al.; Si-PIN X-Ray Detector Technology; Nuclear Instruments and Methods in Physics Research; 1997; pp. 344-348; vol. A, No. 395; Elsevier Science B.V.
Bogue: “From bolometers to beetles: the development of the thermal imaging sensors;” sensor Review; 2007; pp. 278-281; Emerald Group Publishing Limited (ISSN 0260-2288).
Borghesi et al.; “Oxygen Precipitation in Silicon,” J. Appl. Phys., v. 77(9), pp. 4169-4244 (May 1, 1995).
Brieger,S., O.Dubbers, S.Fricker, A.Manzke, C.Pfahler, A.Plettl, and P.Zlemann, “An Approach for the Fabrication of Hexagonally Ordered Arrays of Cylindrical Nanoholes in Crystalline and Amorphous Silicon Based on the Self-Organization of Polymer Micelles”, Nanotechnology, vol. 17, pp. 4991-4994, 2006, doi:10.1088/0957-4884/17/19/036.
Chang, S.W., V.P.Chuang, S.T.Boles, and C.V.Thompson, “Metal-Catalyzed Etching of Vertically Aligned Polysilicon and Amorphous Silicon Nanowire Arrays by Etching Direction Confinement”, Advanced Functional Materials, vol. 20, No. 24, pp. 4364-4370, 2010.
Chiang, Wen Jen Et al., “Silicon Nanocrystal-Based Photosensor on Low-Temperature Polycrystalline-Silicone Panels”, Applied Physics Letters, 2007, 51120-1-51120-3, Ltt. 91, American Inst. of Physics, Melville, NY.
Cilingiroglu et al., “An evaluation of MOS Interface-Trap Charge Pump as and Ultralow Constant-Current Generator,” IEEE Journal of Solid-State Circuit, 2003, vol. 38, No. 1, Jan. 2003, 71-83.
Detection of X-ray and Gamma-ray Photons Using Silicon Diodes; Dec. 2000; Detection Technology, Inc.; Micropolis, Finland.
Gjessing, J. et al.; 2D blazed grating for light trapping in thin silicon solar cells; 3 pages; 2010; Optical Society of America.
Gloeckler et al. Band-Gap Grading in CU(In,GA)Se2 Solar Cells, Journal of Physics and Chemistry of Solids; 2005; pp. 189-194; vol. 66.
Han et al., “Evaluation of a Small Negative Transfer Gate Bias on the Performance of 4T CMOS Image Sensor Pixels,” 2007 International Image Sensor Workshop, 238-240, Ogunquit, Maine.
Holland; Fabrication of Detectors and Transistors on High-Resistivity Silicon; Nuclear Instruments and Methods in Physics Research, vol. A275, pp. 537-541 (1989).
Hong et al., “Cryogenic processed metal-semiconductor-metal (MSM) photodetectors on MBE grown ZnSe,”, 1999, IEEE Transactions on Electron Devices, vol. 46, No. 6, pp. 1127-1134.
Hsieh et al., “Focal-Plane-Arrays and CMOS Readout Techniques of Infrared Imaging Systems,” IEE Transactions on Circuits and Systems for Video Technology, 1997, vol. 7, No. 4, Aug. 1997, 594-605.
Igalson et al. Defect States in the CIGS Solar cells by Photocapacitance and Deep Level Optical Spectroscopy; Bulletin of the Polish Academy of Sciences Technical Sciences; 2005; pp. 157-161; vol. 53(2).
“Infrared Absorption by Sulfur-Doped Silicon formed by Femtosecond Laser Irradiation”; Springer Berline/Heidelberg, vol. 79, Nov. 2004.
Job et al., “Doping of Oxidized Float Zone Silincon by Thermal Donors—A low Thermal Budget Doping Method for Device Applications?” Mat. Res. Soc. Symp. Pro.; v. 719, F9.5.1-F9.5.6 (2002).
Kolasinski et al., “Laser Assisted and Wet Chemical Etching of Silicon Nanostructures,” J. Vac. Sci. Technol., A 24(4), Jul./Aug. 2006, 1474-1479.
Konstantatos et al., “Engineering the Temproal Response of Photoconductive Photodetectors via Selective Introduction of Surface Trap States,” Nano Letters, v. 8(5), pp. 1446-1450 (Apr. 2, 2008).
Konstantatos et al., “PbS Colloidal Quantum Dot Photoconductive Photodetectors: Transport, Traps, and Gain,” Appl. Phys. Lett., v. 91, pp. 173505-1-173505-3 (Oct. 23, 2007).
Kryski; A High Speed 4 Megapixel Digital CMOS Sensor; 2007 International Image Sensor Workshop; Jun. 6-10, 2007.
Li et al., “Gettering in High Resistive Float Zone Silicon Wafers,” Transaction on Nuclear Science, vol. 36(1), pp. 290-294 (Feb. 1, 1989).
Low Dose Technologies; Power Point.
“Masimo Rainbow SET Pulse CO-Oximetry,” 2010, Masimo Corporation, Irvine, California, http://www.masimo.com/Rainbow/about.htm.
Meynants, et al.; “Backside illuminated global shutter COMOS image sensors”; 2011 International Image Sensor Workshop; Jun. 11, 2011.
Moon et al. Selective emitter using porous silicon for crystalline silicon solar cells. Solar Energy Materials & Solar Cells, v. 93, pp. 846-850 (2009).
Murkin, JM and Arangol, M, “Near Infrared spectroscopy as an index of rain and tissue oxygenation,” Bri. J. of Anathesia (BJA/PGA Supplement):13-il3 (2009).
Nauka et al., Intrinsic Gettering in Oxygen-Free Silicon; App. Phys. Lett., vol. 46(7), Apr. 4, 1985.
Nauka et al., “New Intrinsic Gettering Process in Silicon Based on Interactions of Silicon Interstitials,” J. App. Phys., vol. 60(2), pp. 615-621, Jul. 15, 1986.
Nayak, et al.; “Efficient light trapping in silicon solar cells by ultrafast-laser-induced self-assembled micro/nano structures”; Progress in Photovoltaics: Research and Applications; 2011.
Palm et al. CIGSSe Thin Film PB Modules: From Fundamental Investigators to Advanced Performance and Stability; Thin Solid Films; 2004; pp. 544-551; vol. 451-2.
Rashkeev et al., “Hydrogen passivation and Activation of Oxygen Complexes in Silicon,” American Institute of Physics, vol. 78(11), pp. 1571-1573 (Mar. 12, 2001).
Solhusvik, J. et al. “A 1280x960 3.75um pixel CMOS imager with Triple Exposure HDR,” Proc. of 2009 International Image Sensor Workshop, Bergen, Norway, Jun. 22-28, 2009.
Uehara et al., “A High-Sensitive Digital Photosensor Using MOS Interface-Trap Charge Pumping,” IEICE Electronics Express, 2004, vol. 1, No. 18, 556-561.
Zhang et al, “Ultra-Shallow P+—Junction Formation in Silicon by Excimer Laser Doping: a Heat and Mass Transfer Perspective,” Int. J. Heat Mass Transfer, 1996, 3835-3844, vol. 39, No. 18, Elsevier Science Ltd., Great Britain.
Zhu et al., “Evolution of Silicon Surface Microstructures by Picosecond and Femtosecond Laser Irradiations,” Applied Surface Science, 2005, 102-108, Elsevie, Amsterdam, NL.Ultra-Shallow P+—Junction Formation in Silicon by Excimer Laser Doping: a Heat and Mass Transfer Perspective, Int. J. Heat Mass Transfer, 1996, 3835-3844, vol. 39, No. 18, Elsevier Science Ltd., Great Britain.
Bernhard, C.G., “Structural and Functional Adaptation in a Visual System” Endevor vol. 26, pp. 79-84, May 1967.
Chichkiv, B.N. et al, “Femtosecond, picosecond and nanosecond laser ablation of solids” Appl. Phys. A 63, 109-115; 1996.
Clapham, P.B. et al, “Reduction of Lens Reflexion by the Moth Eye Principle” Nature, vol. 244. Aug. 1973, pp. 281-282.
Huang, et al.; “Key Technique for texturing a uniform pyramid structure with a layer of silicon nitride on monocrystalline silicon wafer” Applied Surface Science; 2013 pp. 245-249.
Jansen, H. et al., “The Black Silicon Method: a universal method for determining the parameter setting of a flourine-based reactive ion etcher in deep silicon trench etching with profile control”,J. Micromech. Microeng. vol. 5, 1995 pp. 115-120.
Koh et al., “Simple nanostructuring on silicon surfaceby means of focused beam patterning and wet etching”, Applied Surface Science, 2000 pp. 599-603.
Myers, Richard et al., “Enhancing Near-IR Avalanche Photodiodes Performance by Femtosecond Laser Microstructuring” Harvard Dept. of Physics.
Wu et al., “Black Silicon” Harvard UPS 1999.
Zhong, S. et al. “Excellent Light Trapping in Ultrathin Solar Cells,” AFM-Journal, May 2016 pp. 1-11.
Born, M. and E.Wolf, “Princip les of Optics, 7th Ed.”, Cambridge University Press, 1999, pp. 246-255.
Carey, P.G. et al., “In-situ Doping of Silicon Using Gas Immersion Laser Doping (GILD) Process,” Appl. Surf. Sci. 43, 325-332 (1989).
Gibbons, J., “Ion Implantation in Semiconductors-Part II; Damage Production and Annealing”, proceedings of the IEEE vol. 60, No. 9 pp. 1062-1096. Jun. 1972.
Ziou et al., “Depth from defocus using the hermite transform”, Image Processing, 1998. ICIP 98. Intl. Conference on Chicago, IL. Oct. 1998 pp. 958-962.
Campbell, Stephen A., “The Science and Engineering of Microeletronic Fabrication, 2nd Ed.”, Oxford University Press, 2001, pp. 406-411.
Ohring, Milton., “The Materials Science of Thin Films”, Academic Press, 1992, pp. 176-179.
Related Publications (2)
Number Date Country
20150270306 A1 Sep 2015 US
20170309669 A9 Oct 2017 US
Provisional Applications (3)
Number Date Country
61243434 Sep 2009 US
61311004 Mar 2010 US
61311107 Mar 2010 US
Continuations (1)
Number Date Country
Parent 12885158 Sep 2010 US
Child 14223938 US