Existing night vision goggles are complex electro-optical devices that intensify existing light instead of relying on their own light source. In a typical configuration, a conventional lens, called the objective lens, captures ambient light and some near-infrared light. The gathered light is then sent to an image-intensifier tube. The image-intensifier tube uses a photo cathode to collect photons of light energy for the generation of electrons. As the electrons pass through the tube, more electrons can be released from atoms in the tube, multiplying the original number of electrons by a factor of thousands, often accomplished using a micro channel plate (MCP). The image-intensifier tube can be positioned such that a cascade of electrons hits a screen coated with phosphors at the end of the tube with the electrons retaining the position of the channel through which they passed. The energy of the electrons causes the phosphors to reach an excited state and release photons, which create a green image on the screen and characterize state of the art night vision. The green phosphor image can be viewed through an ocular lens where the image is magnified and focused.
Recently, light up-conversion devices have attracted a great deal of research interest because of their potential applications in night vision, range finding, security, and semiconductor wafer inspections. Early near infrared (NIR) up-conversion devices were mostly based on the heterojunction structure of inorganic semiconductors, where a photodetecting and a luminescent section are in series. The up-conversion devices are mainly distinguished by the method of photodetection. Currently inorganic and hybrid up-conversion devices are expensive to fabricate and the processes used for fabricating these devices are not compatible with large area applications. Efforts are being made to achieve low cost up-conversion devices that have higher conversion efficiencies. Unfortunately, none have been identified to allow sufficient detectivity at low drive voltages, generally because of a high dark current density that leads to insufficient contrast in the photodetector. Hence, there remains a need to achieve high contrast in an up-conversion device and an IR photodetector with high detectivity while requiring low drive voltages, for example, about 10V.
Embodiments of the invention are directed to infrared (IR) photodetectors comprising an IR sensitizing layer separating an electron blocking layer (EBL) and a hole blocking layer (HBL), wherein the IR photodetector has high detectivity. The IR photodetectors can be used at voltages below 20V. IR sensitizing layers of perylene-3,4,9,10-tetracarboxylic-3,4,9,10-dianhydride (PCTDA), tin (II) phthalocyanine (SnPc), SnPc:C60, aluminum phthalocyanine chloride (AlPcCl), AlPcCl:C60, titanyl phthalocyanine (TiOPc), TiOPc:C60 PbSe quantum dots (QDs), PbS QDs, PbSe thin films, PbS thin films, InAs, InGaAs, Si, Ge, or GaAs can be used. The EBL can be poly(9,9-dioctyl-fluorene-co-N-(4-butylphenyl)diphenylamine) (TFB), Poly-N,N-bis-4-butylphenyl-N,N-bis-phenylbenzidine (poly-TPD), or polystyrene-N,N-diphenyl-N,N-bis(4-n-butylphenyl)-(1,10-biphenyl)-4,4-diamine-perfluorocyclobutane (PS-TPD-PFCB) and the HBL can be 2,9-Dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP), p-bis(triphenylsilyl)benzene (UGH2), 4,7-diphenyl-1,10-phenanthroline (BPhen), tris-(8-hydroxy quinoline) aluminum (Alq3), 3,5′-N,N′-dicarbazole-benzene (mCP), C60, tris[3-(3-pyridyl)-mesityl]borane (3TPYMB), ZnO thin films, ZnO nanoparticles, TiO2 thin films, or TiO2 nanoparticles.
Embodiments of the invention are directed to an infrared photodetector with high detectivity for use as a sensor and for use in an up-conversion device. When the dark current is the dominant noise factor, detectivity can be expressed as the following equation (1).
D*=R(2qJd)1/2 (1)
where R is the responsivity, Jd is the dark current density, and q is the elementary charge (1.6×10−19 C). To achieve a photodetector with an optimal detectivity, a very low dark current density is required. The photodetectors, according to embodiments of the invention, comprise a hole blocking layer (HBL) with a deep highest occupied molecule orbital (HOMO) and an electron blocking layer (EBL) with a high lowest unoccupied molecule orbital (LUMO), where the EBL is situated on the anode facing surface and the HBL is situated on the cathode facing surface of an IR photosensitive layer, as shown in
In embodiments of the invention, the IR photosensitive layer can be an organic or organometallic comprising material or an inorganic material. In some embodiments of the invention, the material absorbs through a large portion of the IR, extending beyond the near IR (700 to 1400 nm), for example, to wavelengths up to 1800 nm or greater. Exemplary organic or organometallic comprising materials include: perylene-3,4,9,10-tetracarboxylic-3,4,9,10-dianhydride (PCTDA); tin (II) phthalocyanine (SnPc); SnPc:C60; aluminum phthalocyanine chloride (AlPcCl); AlPcCl:C60; titanyl phthalocyanine (TiOPc); and TiOPc:C60. Inorganic materials for use as photosensitive layers include: PbSe quantum dots (QDs); PbS QDs; PbSe thin films; PbS thin films; InAs; InGaAs; Si; Ge; and GaAs.
In embodiments of the invention, the HBL can be an organic or organometallic comprising material including, but not limited to: 2,9-Dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP); p-bis(triphenylsilyl)benzene (UGH2); 4,7-diphenyl-1,10-phenanthroline (BPhen); tris-(8-hydroxy quinoline) aluminum (Alq3); 3,5′-N,N′-dicarbazole-benzene (mCP); C60; and tris[3-(3-pyridyl)-mesityl]borane (3TPYMB). In other embodiments of the invention, the HBL can be an inorganic material including, but not limited to, thin films or nanoparticles of ZnO or TiO2.
In embodiments of the invention, the EBL can be an organic material, including, but not limited to: poly(9,9-dioctyl-fluorene-co-N-(4-butylphenyl)diphenylamine) (TFB); 1,1-bis[(di-4-tolylamino)phenyl]cyclohexane (TAPC); N,N′-diphenyl-N,N′(2-naphthyl)-(1,1′-phenyl)-4,4′-diamine (NPB); N,N′-diphenyl-N,N′-di(m-tolyl) benzidine (TPD); poly-N,N′-bis-4-butylphenyl-N,N′-bis-phenylbenzidine (poly-TPD); or polystyrene-N,N-diphenyl-N,N-bis(4-n-butylphenyl)-(1,10-biphenyl)-4,4-diamine-perfluorocyclobutane (PS-TPD-PFCB).
Photodetectors were prepared having no blocking layer, poly-TPD as an EBL, ZnO nanoparticles as a HBL, and with poly-TPD and ZnO nanoparticles as an EBL and a HBL, respectively, as shown in
Inorganic nanoparticle photodetectors were also constructed having no blocking layers and with EBL and HBL layers. The photodetector, as schematically illustrated in
It should be understood that the examples and embodiments described herein are for illustrative purposes only and that various modifications or changes in light thereof will be suggested to persons skilled in the art and are to be included within the spirit and purview of this application.
The present application claims the benefit of U.S. Provisional Application Ser. No. 61/416,630, filed Nov. 23, 2010, which is hereby incorporated by reference herein in its entirety, including any figures, tables, or drawings.
Number | Date | Country | |
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61416630 | Nov 2010 | US |