Method and apparatus for providing a charge blocking layer on an infrared up-conversion device

Abstract
Embodiments of the invention are directed to an improved device for sensing infrared (IR) radiation with up-conversion to provide an output of electromagnetic radiation having a shorter wavelength than the incident IR radiation, such as visible light. The device comprises an anode, a hole blocking layer to separate an IR sensing layer from the anode, an organic light emitting layer that is separated from the anode by the IR sensing layer, and a cathode. The hole blocking layer assures that when a potential is applied between the anode and the cathode the organic light emitting layer generates electromagnetic radiation only when the IR sensing layer is irradiated with IR radiation.
Description
BACKGROUND OF INVENTION

Infrared (IR)-to-visible light up-conversion devices have attracted a great deal of research interest due to the potential application 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. These devices consist of two parts in series: one part for photodetection and another for luminescence. The up-conversion devices are mainly distinguished by the method of photodetection. Up-conversion efficiencies of these devices are generally low. For example, one NIR-to-visible light up-conversion device that integrates a light-emitting diode (LED) with a semiconductor based photodetector exhibits a maximum external conversion efficiency of 0.3%. A hybrid organic/inorganic up-conversion device, having an inorganic InGaAs/InP photodetector integrated with an organic light-emitting diode (OLED), exhibits an external conversion efficiency of only 0.25%. Such inorganic and hybrid up-conversion devices are expensive to fabricate and processes and their fabrication is not compatible with large area applications.


Ni et al., Jpn. J. Appl. Phys. 2001, 40, L948 and Chikamatsu et al. Appl. Phys. Lett. 2002, 81, 769 disclose all organic up-conversion devices by coupling fluorescent OLEDs with a titanyl phthalocyanine (TiOPc) photosensitive hole injection layer to exhibited NIR-to-blue and red-to-green up-conversion, respectively. These all organic up-conversion devices display very low conversion efficiencies (less than 0.05%). The photodetectors used in the up-conversion devices have low quantum efficiencies, as the organic sensitizer yield photogenerated excitons having low charge-dissociation efficiency and the fluorescent OLEDs exhibit external quantum efficiencies (EQEs) of less than 5%, resulting in the low overall up-conversion efficiencies.


BRIEF SUMMARY

Embodiments of the invention are directed to a device for sensing infrared (IR) radiation and providing an output of higher energy electromagnetic radiation that includes an anode, a hole blocking layer (HBL) that separates the anode from an IR sensing layer, an organic light emitting layer that is separated from the anode by the IR sensing layer, and a cathode. Holes and electrons combine in the organic photon emitting layer to generate electromagnetic radiation, upon applying a potential between the anode and the cathode, when IR radiation strikes the IR sensing layer. In specific embodiments, one or both of the anode and cathode is transparent. In specific embodiments, the anode can be made from a material selected from the following: ITO, IZO, ATO, AZO, and carbon nanotubes, and the cathode can be made from a material selected from the following: LiF/Al, Ag, Ca:Mg, LiF/Al/ITO, Ag/ITO, CsCO3/ITO, and Ba/Al. The hole blocking layer can incorporate BCP, UGH2, BPhen, Alq3, mCP, C60, 3TPYMB, ZnO nanoparticles, and/or any combination thereof. The organic photon emitting layer can be made from a material selected from the following: MEH-PPV, Alqa, and FIrpic. The IR photodetecting layer can be made from an organic material, such as SnPc, SnPc:C60, AlPcCl, AlPcCl:C60, TiOPc, or TiOPc:C60, or it can be made from an inorganic material such as PbSe or PbS. In embodiments of the invention the device can include one or more charge transport layers made from materials such as TAPC, NPB, or TPD to transport holes, and/or 3TPYMB, BCP, BPhen, and Alq3 to transport electrons.





BRIEF DESCRIPTION OF DRAWINGS


FIGS. 1A-1B show a schematic energy diagram of a prior art infrared-to-green light up-conversion device without any charge blocking layer, where FIG. 1A shows the schematic energy band diagram under no applied voltage in the dark and FIG. 1B shows the schematic energy band diagram even under low applied voltage in the dark.



FIGS. 2A-2C show a schematic energy band diagram of an IR-to-green light up-conversion device with hole blocking layer according to an embodiment of the invention, where FIG. 2A shows the schematic energy band diagram under no applied voltage in the dark, FIG. 2B shows the schematic energy band diagram even under high applied voltage in the dark, and FIG. 2C shows the schematic energy band diagram under applied voltage in the IR irradiation.



FIGS. 3A-3B show (3A) I-V characteristics and (3B) L-V characteristics of IR-to-green light up-conversion devices with various organic hole blocking layers according to embodiments of the invention with BCP and UGH2 as hole blocking materials under dark and IR irradiation. FIGS. 4A-4B show (4A) I-V characteristics and (4B) L-V characteristics of IR-to-green light up-conversion devices with inorganic ZnO hole blocking layers according to embodiments of the invention compared with a device having an organic BCP hole blocking layer according to an embodiment of the invention under dark and IR irradiation.



FIGS. 5A-5B show (5A) a schematic energy band diagram and (5B) L-I-V characteristics of a QD based IR-to-visible light up-conversion device without any charge blocking layer under dark and IR irradiation.



FIGS. 6A-6C show (6A) a schematic energy band diagram, (6B) I-V characteristics, and (6C) L-V characteristics of a QD based IR-to-visible light up-conversion device with ZnO hole blocking layer according to an embodiment of the invention under dark and IR irradiation.





DETAILED DISCLOSURE

High-efficiency organic light-emitting devices, such as organic light-emitting diodes (OLEDs) and high efficiency organic photodetectors, have been demonstrated and an all organic up-conversion device has been disclosed by the inventors where an OLED and an IR photodetector are integrated into one device. (see Kim et al., PCT Patent Application No. PCT/US2010/058015, filed Nov. 24, 2010 and Kim et al. Adv. Mater. 2010, 22, 2260-3, both of which are hereby incorporated by reference herein in their entirety and, in particular, are incorporated for their teachings of organic photodetectors and all organic up-conversion devices, for example, an organic light-emitting device, such as an OLED, and an IR photodetector integrated into one device). Because of their compatibility with lightweight rugged flexible plastic substrates, an all organic up-conversion device can permit applications unavailable to other more conventional technologies. Unfortunately, even in the absence of IR irradiation, an off state, organic up-conversion device can still give off visible light, due to the small difference between the work function of the anode and the highest occupied molecular orbit (HOMO) of the IR absorbing photodetector at low voltages.


Embodiments of the invention are directed to improved infrared imaging devices where emission results from the up-conversion of an IR photodetector coupled with an organic light-emitting device, such as an OLED, where emission of light occurs only under IR irradiation at a sufficiently high voltage. Other embodiments of the invention are directed to a method of fabrication that is relatively low in cost and yields lightweight, highly sensitive devices with high gain and image fidelity while consuming little power. Specific embodiments can incorporate one or more of the organic IR-to-green light up-conversion devices disclosed in Kim et al., PCT/US2010/058015, or Kim et al. Adv. Mater. 2010, 22, 2260-3, where, in an exemplary embodiment, a tin phthalocyanine: buckminsterfullerene (SnPc:C60) bulk heterostructure layer IR photodetector is connected in series with an fac-tris(2-phenylpyridine)iridium (Ir(ppy)3) based phosphorescent layer as a light emitting layer, where the structure can be generalized by the structure diagrammed in FIG. 1A, which is similar to a conventional OLED.


In an all-organic up-conversion device, it can be advantageous to have a poor hole transport IR-sensitizing layer such that the organic light-emitting device, such as an OLED, remains in the off state until IR irradiation occurs. Upon IR photo-excitation, holes are injected into the organic light emitting layer where the holes combine with electrons injected from the cathode to give off light of a shorter wavelength than the incident IR radiation, such as visible light. As in the case of a device with an indium-tin oxide (ITO) anode and IR detecting (absorbing) tin (II) phthalocyanine (SnPc) layer, due to the small difference between the anode's work function and the IR absorber's HOMO, hole injection from the anode occurs at low voltages, as illustrated in FIG. 1B. Hence, light can be generated, even with very little or no IR irradiation, with relatively low voltages applied to the electrodes.


In embodiments of the invention, the performance of an all organic up-conversion device is enhanced by inclusion of a charge blocking layer. In a specific embodiment, a hole blocking layer is placed between an ITO anode and a SnPc IR photodetecting layer, such that hole carriers from the ITO anode are efficiently blocked, suppressing visible luminance of the up-conversion device until a sufficiently high voltages and IR irradiation is applied, as shown in FIGS. 2A, 2B, and 2C. In addition to ITO, other materials that can be employed as an anode include, but are not limited to: Indium Zinc Oxide (IZO), Aluminum Tin Oxide (ATO), Aluminum Zinc Oxide (AZO), and carbon nanotube. In addition to SnPc:C60, other organic IR photodetector materials that can be employed include, but are not limited to: tin (II) phthalocyanine (SnPc), aluminum phthalocyanine chloride (AlPcCl), AlPcCl:C60, titanyl phthalocyanine (TiOPc), and TiOPc:C60. In addition to Ir(ppy)3, other electroluminescent organic light-emitting device, such as an OLED, materials that can be employed include, but are not limited to: poly-[2-methoxy, 5-(2′-ethyl-hexyloxy) phenylene vinylene] (MEH-PPV), tris-(8-hydroxy quinoline) aluminum (Alq3), and iridium (III) bis[(4,6-di-fluorophenyl)-pyridinate-N,C2′]picolinate (Flrpic). The cathode can be LiF/Al or can be any conductor with the appropriate work function including, but not limited to: Ag, Ca:Mg, LiF/Al/ITO, Ag/ITO, CsCO3/ITO, and Ba/Al. Materials that can be employed as electron transport layers include, but are not limited to: tris[3-(3-pyridyl)-mesityl ]borane(3TPYMB), 2,9-Dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP), 4,7-diphenyl-1,10-phenanthroline (BPhen), and tris-(8-hydroxy quinoline) aluminum (Alq3). Materials that can be employed as hole transport layers include, but are not limited to: 1,1-bis [(di-4-tolylamino)phenyl]cyclohexane (TAPC), N,N′-diphenyl-N,N′ (2-naphthyl)-(1,1′-phenyl)-4,4′ -diamine (NPB), and N,N′-diphenyl-N,N′-di(m-tolyl) benzidine (TPD). Those skilled in the art can readily identify appropriate combinations of anodes, cathodes, IR photodetectors, organic light-emitting device, such as OLED, materials, hole transport layers, and electron transport layers by their relative work functions, highest occupied molecular orbit (HOMO) and lowest unoccupied molecular orbit (LUMO) levels, layer compatibility, and the nature of any desired deposition methods used during their fabrication.


In some embodiments of the invention the hole blocking layer can be an organic compound. FIG. 3A shows I-V characteristics, and FIG. 3B shows L-V characteristics, of IR-to-green light up-conversion devices according to embodiments of the invention fabricated with different organic hole blocking layers, 2,9-Dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP) and p-bis(triphenylsilyly)benzene (UGH2), under dark and IR irradiation. These hole blocking materials possess deep HOMO levels. Because these materials also have small LUMO energy, charge generation between the hole blocking layer and the IR sensitizing layer is negligible. As illustrated in FIGS. 3A and 3B, up-conversion devices with a hole blocking layer have higher turn-on voltage in the dark. In addition to BCP and UGH2, other organic hole blocking layers that can be employed in embodiments of the invention include, but are not limited to: 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 an inorganic hole blocking layer can be included in the up-conversion device. FIG. 4A shows the I-V characteristics and FIG. 4B shows the L-V characteristics of IR-to-green light up-conversion devices with differing thicknesses of ZnO hole blocking layers and, for comparison, a device with the organic BCP hole blocking layer under dark conditions and under IR irradiation. Devices with ZnO hole blocking layers display similar characteristics to that of BCP. In addition to ZnO, other inorganic hole blocking layers that can be employed in embodiments of the invention include, but are not limited to: TiO2, SiO, SiO2, Si3N4, and Al2O3. In some embodiments, the inorganic hole blocking layer can comprise a metal oxide. For example, in certain cases, the inorganic hole blocking layer can comprise an n-type semiconducting metal oxide. An n-type semiconducting metal oxide generally refers to a semiconducting metal oxide having a higher concentration of electrons than holes (e.g., the Fermi level lies closer to the conduction band than the valence band). Non-limiting examples of an n-type semiconducting metal oxide include ZnO and TiO2. In certain embodiments, the n-type semiconducting metal oxide can be present in the up-conversion device in the form of a thin film. The thin film can, for example, be synthesized using a sol-gel process. The thin film can also be formed by other methods, including chemical vapor deposition, electron beam evaporation, and/or ion sputtering.


In another embodiment of the invention, the IR photodetecting layer can be inorganic, for example quantum dots (QDs) and the hole blocking layer can be organic or inorganic. For an exemplary up-conversion device lacking a hole blocking layer, shown in FIG. 5A, a layer of PbSe QDs is employed as the IR sensitizer and MEH-PPV is employed as the electroluminescent organic light-emitting device, such as an OLED. The device of FIG. 5A displayed no hole blocking by the QD IR detecting layer, as shown in FIG. 5B where the L-I-V characteristics on the QD IR up-conversion device displays little difference between dark and IR irradiated current densities and luminance with applied voltage, with luminescence occurring at a low voltage. In contrast, a QD IR up-conversion device with a ZnO hole blocking layer, as shown in FIG. 6A, effectively blocks hole injection from the anode in the dark. This is shown by the I-V and L-V characteristics in FIGS. 6B and 6C for a QD IR up-conversion device with a ZnO hole blocking layer. In this embodiment, IR irradiation acts as an effective optical switch. In addition to PbSe, other QDs that can be employed include, but are not limited to: PbS. Other inorganic materials that can be employed as IR detectors include, but are not limited to: Si, Ge, and GaAs.


Embodiments of the invention pertain to methods and apparatus for detecting infrared (IR) radiation and providing an output having a shorter wavelength than the incident IR radiation, such as a visible light output. Because of their compatibility with lightweight rugged flexible plastic substrates, up-conversion devices in accordance with embodiments of the present invention can be used as a component, for example a pixel, for numerous applications including, but not limited to, night vision, range finding, security, and semiconductor wafer inspections.


All patents, patent applications, provisional applications, and publications referred to or cited herein are incorporated by reference in their entirety, including all figures and tables, to the extent they are not inconsistent with the explicit teachings of this specification.


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.

Claims
  • 1. A device for sensing infrared (IR) radiation, comprising: an anode;a hole blocking layer comprising a metal oxide;an IR sensing layer separated from the anode by the hole blocking layer;an organic light emitting layer, separated from the anode by the IR sensing layer; anda cathode, wherein when a potential is applied between the anode and the cathode and IR radiation is incident on the IR sensing layer, electromagnetic radiation is generated in the organic light emitting layer.
  • 2. The device according to claim 1, wherein the metal oxide is TiO2.
  • 3. The device according to claim 1, wherein the metal oxide is ZnO.
  • 4. The device according to claim 1, wherein the organic light emitting layer only generates the electromagnetic radiation when IR radiation is incident on the inorganic IR sensing layer.
  • 5. The device according to claim 1, wherein the inorganic IR sensing layer comprises a material selected from the group consisting of: PbSe and PbS.
  • 6. The device according to claim 1, further comprising a hole transport layer, wherein the hole transport layer separates the organic light emitting layer from the inorganic IR sensing layer.
  • 7. The device according to claim 6, wherein the hole transport layer comprises a material selected from the group consisting of: TAPC, NPB, and TPD.
  • 8. The device according to claim 1, further comprising an electron transport layer, wherein the electron transport layer separates the organic light emitting layer from the cathode.
  • 9. The device of claim 8, wherein the electron transport layer comprises a material selected from the group consisting of: 3TPYMB, BCP, BPhen, and Alq3.
  • 10. The device according to claim 1, wherein the electromagnetic radiation is generated in the organic light emitting layer via electrons injected from the cathode combining with holes injected from the IR sensing layer.
  • 11. The device according to claim 10, wherein the electrons injected from the cathode travel through an electron transport layer from the cathode to the organic light emitting layer, and wherein the holes injected from the IR sensing layer travel through a hole transport layer from the IR sensing layer to the light emitting layer.
  • 12. The device according to claim 1, wherein the electromagnetic radiation is not generated until the potential reaches a threshold magnitude.
  • 13. The device according to claim 1, wherein charge generation between the hole blocking layer and the IR sensing layer is negligible.
  • 14. A method of detecting infrared (IR) radiation, comprising: applying a potential between an anode and a cathode of a device in a region of interest, the device comprising: the anode;a hole blocking layer comprising a metal oxide;an inorganic IR sensing layer separated from the anode by the hole blocking layer;an organic light emitting layer, separated from the anode by the inorganic IR sensing layer; andthe cathode;generating electromagnetic radiation in the organic light emitting layer in response to IR radiation incident on the inorganic IR sensing layer;: anddetermining that IR radiation is present in the region of interest when the electromagnetic radiation is detected.
  • 15. The method according to claim 14, wherein the metal oxide is TiO2.
  • 16. The method according to claim 14, wherein the metal oxide is ZnO.
  • 17. The method according to claim 14, wherein the organic light emitting layer only generates the electromagnetic radiation when IR radiation is incident on the IR sensing layer.
  • 18. The method according to claim 14, wherein the inorganic IR sensing layer comprises a material selected from the group consisting of: PbSe and PbS.
  • 19. The method according to claim 14, wherein the device further comprises a hole transport layer, wherein the hole transport layer separates the organic light emitting layer from the IR sensing layer.
  • 20. The method according to claim 19, wherein the hole transport layer comprises a material selected from the group consisting of: TAPC, NPB, and TPD.
  • 21. The method according to claim 14, wherein the device further comprises an electron transport layer, wherein the electron transport layer separates the organic light emitting layer from the cathode.
  • 22. The method of claim 21, wherein the electron transport layer comprises a material selected from the group consisting of: 3TPYMB, BCP, BPhen, and Alq3.
  • 23. The method according to claim 14, wherein the electromagnetic radiation is generated in the organic light emitting layer via electrons injected from the cathode combining with holes injected from the IR sensing layer.
  • 24. The method according to claim 23, wherein the electrons injected from the cathode travel through an electron transport layer from the cathode to the organic light emitting layer, and wherein the holes injected from the IR sensing layer travel through a hole transport layer from the IR sensing layer to the light emitting layer.
  • 25. The method according to claim 14, wherein the electromagnetic radiation is not generated until the potential reaches a threshold magnitude.
  • 26. The method according to claim 14, wherein charge generation between the hole blocking layer and the inorganic IR sensing layer is negligible.
CROSS-REFERENCE TO RELATED APPLICATION

The present application is a continuing application of U.S. patent application Ser. No. 13/114,896, filed May 24, 2011, which claims the benefit of U.S. Provisional Application Ser. No. 61/347,696, filed May 24, 2010, which is hereby incorporated by reference herein in its entirety, including any figures, tables, or drawings.

US Referenced Citations (148)
Number Name Date Kind
4614958 Mikami et al. Sep 1986 A
4679063 White Jul 1987 A
4755674 Schaaf Jul 1988 A
4778692 Ishihara et al. Oct 1988 A
4885211 Tang et al. Dec 1989 A
5121398 Rao Jun 1992 A
5122905 Wheatley et al. Jun 1992 A
5270092 Griffith et al. Dec 1993 A
5315129 Forrest et al. May 1994 A
5336578 Nukada et al. Aug 1994 A
5389788 Grinberg et al. Feb 1995 A
5438198 Ebitani et al. Aug 1995 A
5619039 Montanari Apr 1997 A
5710428 Ko Jan 1998 A
5811834 Tamano et al. Sep 1998 A
6140646 Busta et al. Oct 2000 A
6509574 Yuan et al. Jan 2003 B2
6579629 Raychaudhuri et al. Jun 2003 B1
6734452 Gunapala et al. May 2004 B2
6777961 Hamamoto et al. Aug 2004 B2
6906326 Koch et al. Jun 2005 B2
6914315 Lai et al. Jul 2005 B2
6972431 Forrest et al. Dec 2005 B2
7247850 Laou et al. Jul 2007 B2
7270586 Tokailin et al. Sep 2007 B2
7279705 Iou Oct 2007 B2
7300731 Wang Nov 2007 B2
7381953 Kaufman Jun 2008 B1
8304728 So Nov 2012 B2
8405028 So Mar 2013 B2
8441187 Hunze et al. May 2013 B2
8507865 Boberl et al. Aug 2013 B2
8592801 So et al. Nov 2013 B2
8716701 So et al. May 2014 B2
8796699 So et al. Aug 2014 B2
8829498 So et al. Sep 2014 B2
9006752 So et al. Apr 2015 B2
9196661 So et al. Nov 2015 B2
9214502 So et al. Dec 2015 B2
9276048 So Mar 2016 B2
20020027206 Yuan et al. Mar 2002 A1
20020066904 Yuan et al. Jun 2002 A1
20020130248 Bretschneider et al. Sep 2002 A1
20030122749 Booth et al. Jul 2003 A1
20030168599 Liddiard Sep 2003 A1
20030218166 Tsutsui Nov 2003 A1
20040016923 Yu et al. Jan 2004 A1
20040027059 Tsutsui Feb 2004 A1
20040031965 Forrest et al. Feb 2004 A1
20040135222 Alfano et al. Jul 2004 A1
20040222306 Fajarillo Nov 2004 A1
20040253759 Garber et al. Dec 2004 A1
20050077539 Lipson Apr 2005 A1
20050088079 Daniels Apr 2005 A1
20050088365 Yamazaki et al. Apr 2005 A1
20050110007 Forrest et al. May 2005 A1
20050137301 Wu et al. Jun 2005 A1
20050155641 Fafard Jul 2005 A1
20050156609 Pfaff et al. Jul 2005 A1
20050161703 Costello Jul 2005 A1
20050168137 Adamovich et al. Aug 2005 A1
20040818923 Barnes et al. Oct 2005
20050236556 Sargent et al. Oct 2005 A1
20060011927 Ko Jan 2006 A1
20060024526 Thompson et al. Feb 2006 A1
20060032528 Wang Feb 2006 A1
20060043361 Lee et al. Mar 2006 A1
20060081840 Mori et al. Apr 2006 A1
20060084347 Tutt Apr 2006 A1
20060097247 Kim et al. May 2006 A1
20060157806 Rhodes Jul 2006 A1
20060180197 Gui et al. Aug 2006 A1
20060186803 Lim et al. Aug 2006 A1
20060192125 Yoganandan et al. Aug 2006 A1
20060222979 Ishida et al. Oct 2006 A1
20060227531 Iou Oct 2006 A1
20060266998 Vega et al. Nov 2006 A1
20060290270 Kim et al. Dec 2006 A1
20070029482 Laou et al. Feb 2007 A1
20070048548 Kim Mar 2007 A1
20070062576 Duerr et al. Mar 2007 A1
20070096085 Rand et al. May 2007 A1
20070116983 Kanno et al. May 2007 A1
20070129545 Inoue et al. Jun 2007 A1
20070176541 Son et al. Aug 2007 A1
20070215868 Forrest et al. Sep 2007 A1
20070216985 Woodall et al. Sep 2007 A1
20070221888 Sakata Sep 2007 A1
20070235753 Debucquoy et al. Oct 2007 A1
20080041447 Tseng et al. Feb 2008 A1
20080110499 Chen et al. May 2008 A1
20080138797 Hunt et al. Jun 2008 A1
20080142075 Reddy et al. Jun 2008 A1
20080223445 Marks et al. Sep 2008 A1
20080272713 Kang et al. Nov 2008 A1
20090045728 Murano et al. Feb 2009 A1
20090115310 Yamamoto May 2009 A1
20090140238 Brabec et al. Jun 2009 A1
20090152664 Klem et al. Jun 2009 A1
20090206237 Shannon et al. Aug 2009 A1
20090206745 Hwang et al. Aug 2009 A1
20090208776 Liu et al. Aug 2009 A1
20090214967 Iwanaga et al. Aug 2009 A1
20090217967 Hovel et al. Sep 2009 A1
20090223566 Mitsui et al. Sep 2009 A1
20090286338 Coe-Sullivan et al. Nov 2009 A1
20090301556 Kawano et al. Dec 2009 A1
20090321726 Thompson Dec 2009 A1
20100025662 Cho et al. Feb 2010 A1
20100044676 Sargent et al. Feb 2010 A1
20100044767 Chaudhry et al. Feb 2010 A1
20100059097 McDonald et al. Mar 2010 A1
20100133418 Sargent et al. Jun 2010 A1
20100133434 Meng et al. Jun 2010 A1
20100133522 Pieh et al. Jun 2010 A1
20100141122 Begley et al. Jun 2010 A1
20100181552 So Jul 2010 A1
20100229921 Farris et al. Sep 2010 A1
20100233842 Grein et al. Sep 2010 A1
20100243053 Coe-Sullivan et al. Sep 2010 A1
20100282309 Pschirer et al. Nov 2010 A1
20100294936 Boeberl et al. Nov 2010 A1
20100302419 Den Boer et al. Dec 2010 A1
20100326506 Lifshitz et al. Dec 2010 A1
20110012091 Forrest Jan 2011 A1
20110031399 So Feb 2011 A1
20110031403 So Feb 2011 A1
20110049489 Forrest et al. Mar 2011 A1
20110068330 Akimoto et al. Mar 2011 A1
20110079706 Michalewicz Apr 2011 A1
20110114921 Yang et al. May 2011 A1
20110140075 Zhou et al. Jun 2011 A1
20110248249 Forrest et al. Oct 2011 A1
20110303906 Goldman Dec 2011 A1
20120068140 Greenham et al. Mar 2012 A1
20120126204 So et al. May 2012 A1
20120187295 So et al. Jul 2012 A1
20120193689 Park et al. Aug 2012 A1
20120241723 Klem et al. Sep 2012 A1
20120286296 So et al. Nov 2012 A1
20130044250 Senda et al. Feb 2013 A1
20130206988 So Aug 2013 A1
20140060613 So et al. Mar 2014 A1
20140111652 So et al. Apr 2014 A1
20140217284 So et al. Aug 2014 A1
20140353502 So et al. Dec 2014 A1
20150001395 So et al. Jan 2015 A1
20150372046 Kim et al. Dec 2015 A1
Foreign Referenced Citations (93)
Number Date Country
1532959 Sep 2004 CN
1637628 Jul 2005 CN
1773732 May 2006 CN
1806343 Jul 2006 CN
1856888 Nov 2006 CN
101340749 Jan 2009 CN
101405888 Apr 2009 CN
101421664 Apr 2009 CN
101558348 Oct 2009 CN
101794834 Aug 2010 CN
101872793 Oct 2010 CN
102725616 Oct 2012 CN
0508970 Oct 1992 EP
0 848 433 Jun 1998 EP
0569257 Jun 2002 EP
1 351 558 Oct 2003 EP
1 498 960 Jan 2005 EP
S60-030163 Feb 1985 JP
S61-149831 Jul 1986 JP
S63-088872 Apr 1988 JP
S64-012583 Jan 1989 JP
H02-016421 Jan 1990 JP
H03-079693 Apr 1991 JP
H07-122762 May 1995 JP
H07-175420 Jul 1995 JP
H08-007096 Jan 1996 JP
H08-007096 Jan 1996 JP
10-065200 Mar 1998 JP
H10-242493 Sep 1998 JP
11-329736 Nov 1999 JP
2002-523904 Jul 2000 JP
2000-277265 Oct 2000 JP
2000-349365 Dec 2000 JP
2001-006876 Jan 2001 JP
2001-076882 Mar 2001 JP
2002-340668 Nov 2002 JP
2003-083809 Mar 2003 JP
2003-178887 Jun 2003 JP
2004-511911 Apr 2004 JP
2005-522005 Jul 2005 JP
2005-266537 Sep 2005 JP
2005-277113 Oct 2005 JP
2006-013103 Jan 2006 JP
2006-066395 Mar 2006 JP
2006-128437 May 2006 JP
2006-518110 Aug 2006 JP
2006-251555 Sep 2006 JP
2007-519237 Jul 2007 JP
2008-016831 Jan 2008 JP
2008-053736 Mar 2008 JP
2008-523615 Jul 2008 JP
2009-509129 Mar 2009 JP
2009-520358 May 2009 JP
2009-527108 Jul 2009 JP
2009-192919 Aug 2009 JP
2009-531837 Sep 2009 JP
2009-253173 Oct 2009 JP
2009-272528 Nov 2009 JP
2010-506386 Feb 2010 JP
2010-067802 Mar 2010 JP
2010-087205 Apr 2010 JP
2010-192931 Sep 2010 JP
2010-263030 Nov 2010 JP
2010-534409 Nov 2010 JP
2011-098948 May 2011 JP
2012-524991 Oct 2012 JP
2013-512439 Apr 2013 JP
200637425 Oct 2006 TW
200847449 Dec 2008 TW
201041203 Nov 2010 TW
WO 02099896 Dec 2002 WO
WO 03084292 Oct 2003 WO
WO 2004073082 Aug 2004 WO
WO 2005069387 Jul 2005 WO
WO 2005101530 Oct 2005 WO
WO 2006130717 Dec 2006 WO
WO 2007017475 Feb 2007 WO
WO 2007095386 Aug 2007 WO
WO 2007102051 Sep 2007 WO
WO 2007131126 Nov 2007 WO
WO 2008042859 Apr 2008 WO
WO 2008054845 May 2008 WO
WO 2008140601 Nov 2008 WO
WO 2009074993 Jun 2009 WO
WO 2009116511 Sep 2009 WO
WO 2010070563 Jun 2010 WO
WO 2010120393 Oct 2010 WO
WO 2010142947 Dec 2010 WO
WO 2011033974 Mar 2011 WO
WO 2011066396 Jun 2011 WO
WO 2012170457 Dec 2012 WO
WO 2012178071 Dec 2012 WO
WO 2013003850 Jan 2013 WO
Non-Patent Literature Citations (69)
Entry
International Search Report and Written Opinion dated Jan. 4, 2012, in connection with Application No. PCT/US2011/037772.
International Preliminary Report on Patentability dated Dec. 6, 2012, in connection with Application No. PCT/US2011/037772.
Chikamatsu et al., Light up-conversion from near-infrared to blue using a photoresponsive organic light-emitting device. Appl Phys Lett. 2002;81(4):769.
Kim et al., Organic infrared upconversion device. Adv Mater. May 25, 2010;22(20):2260-3. doi: 10.1002/adma.200903312.
Ni et al., Organic light-emitting diode with TiOPc layer—A new multifunctional optoelectronic device. Jpn J Appl Phys. 2001;40:L948-51. doi:10.1143/JJAP.40.L948.
U.S. Appl. No. 11/865,505, filed Oct. 1, 2007, So.
U.S. Appl. No. 14/763,394, filed Jul. 24, 2015, Kim et al.
U.S. Appl. No. 13/272,995, filed Oct. 13, 2011, So et al.
U.S. Appl. No. 14/124,136, filed Dec. 5, 2013, So et al.
U.S. Appl. No. 14/129,225, filed Mar. 27, 2014, So et al.
U.S. Appl. No. 14/009,945, filed Nov. 18, 2013, So et al.
PCT/US2007/080104, Jun. 25, 2008, International Search Report.
EP 10833930.0, Jul. 19, 2016, Extended European Search Report.
PCT/US2010/058015, Jul. 29, 2011, International Search Report and Written Opinion.
EP 14791448.5, Jul. 25, 2016, Extended European Search Report.
PCT/US2014/012722, Nov. 24, 2014, International Search Report and Written Opinion.
PCT/US2014/012722, Feb. 12, 2015, Third Party Observation.
EP 11843638.5, Nov. 3, 2014, Extended European Search Report.
PCT/US2011/056180, Mar. 6, 2012, International Search Report and Written Opinion.
EP 12797523.3, Apr. 20, 2015, Extended European Search Report.
PCT/US2012/040980, Jan. 29, 2013, International Search Report and Written Opinion.
EP 12804913.7, Feb. 4, 2015, Extended European Search Report.
PCT/US2012/045272, Jan. 7, 2013, International Search Report and Written Opinion.
PCT/US2011/056178, Mar. 19, 2012, International Search Report and Written Opinion.
PCT/US2012/026920, Nov. 23, 2012, International Search Report and Written Opinion.
EP 1276466.1, Sep. 8, 2014, Extended European Search Report.
PCT/US2012/031988, Oct. 31, 2012, International Search Report and Written Opinion.
Extended European Search Report mailed May 27, 2016 for Application No. EP 11787262.2.
International Search Report mailed Jun. 25, 2008 in connection with Application No. PCT/US2007/080104.
Extended European Search Report mailed Jul. 19, 2016 in connection with Application No. EP 10833930.0.
International Search Report and Written Opinion mailed Jul. 29, 2011 in connection with Application No. PCT/US2010/058015.
Extended European Search Report mailed Jul. 25, 2016 in connection with Application No. EP 14791448.5.
International Search Report and Written Opinion mailed Nov. 24, 2014 in connection with Application No. PCT/US2014/012722.
Third Party Observation mailed Feb. 12, 2015 in connection with Application No. PCT/US2014/012722.
Extended European Search Report mailed Nov. 3, 2014 in connection with Application No. EP 11843638.5.
International Search Report and Written Opinion mailed Mar. 6, 2012 in connection with Application No. PCT/US2011/056180.
Extended European Search Report mailed Apr. 20, 2015 in connection with Application No. EP 12797523.3.
International Search Report and Written Opinion mailed Jan. 29, 2013 in connection with Application No. PCT/US2012/040980.
Extended European Search Report mailed Feb. 4, 2015 in connection with Application No. EP 12804913.7.
International Search Report and Written Opinion mailed Jan. 7, 2013 in connection with Application No. PCT/US2012/045272.
International Search Report and Written Opinion mailed Mar. 19, 2012 in connection with Application No. PCT/US2011/056178.
International Search Report and Written Opinion mailed Nov. 23, 2012 in connection with Application No. PCT/US2012/026920.
Extended European Search Report mailed Sep. 8, 2014 in connection with Application No. EP 1276466.1.
International Search Report and Written Opinion mailed Oct. 31, 2012 in connection with Application No. PCT/US2012/031988.
[No Author Listed] OLED Display for Thermal Imaging Helmet, Military and Aerospace Electronics. Oct. 7, 2003. http://www.militaryaerospace.com/articles/2003/10/oled-display-for-thermal-imagin-helmut [last accessed Dec. 8, 2014]. 2 pages.
Ban et al., Near-infrared to visible light optical upconversion by direct tandem integration of organic light-emitting diode and inorganic photodetector. Appl Phys Lett. Feb. 27, 2007;90(9):93108.1-3.
Carlson et al., Amorphous silicon solar cell. Appl Phys Lett. 1976;28:671-3.
Chen et al., Near-infrared inorganic/organic optical upconverter with an external power efficiency of >100%. Adv Mater. Nov. 16, 2010;22(43):4900-4. doi: 10.1002/adma.201001946.
Chen et al., Near-infrared optical upconverter based on i-In0.53Ga0.47As/C60 photovoltaic heterojunction. Electron Lett. Jul. 2009;45(14):753-5.
Chikamatsu et al., Photoresponsive organic electroluminescent devices. J Photochem Photobiol A: Chem. Jun. 1, 2003;158(2-3):215-8.
Gong et al., High-Detectivity Polymer Photodetectors with Special Response from 300 nm to 1450 nm. Sci. Sep. 25, 2009;325:1665-7.
Gong et al., Semiconducting Polymer Photodetectors with Electron and Hole Blocking Layers: High Detectivity in the Near-Infrared. Sensors. Jul. 1, 2010;10:6488-96.
Im et al., Near-infrared photodetection based on PbS colloidal quantum dots/organic hole conductor. Org Electron. Jan. 4, 2010;11(4):696-9.
Kim et al., PbSe nanocrystal-based infrared-to-visible up-conversion device. Nano Lett. May 11, 2011;11(5):2109-13. doi: 10.1021/n1200704h. Epub Apr. 19, 2011. 5 pages.
Kim, Organic Photovoltaic Cells and Organic Up-Convertion Devices. University of Florida. Thesis. May 31, 2009. 84 pages.
Konstantatos et al., Solution-Processed Quantum Dot Photodetectors. Proc IEEE. Oct. 2009;97(10):1666-83.
Konstantatos, Sensitive solution-processed quantum dot photodetectors. PhD Thesis Graduate Dept of Electrical and Computer Engineering. University of Toronto. 2008:133 pages.
Lepnev et al., Two-diode organic light amplifiers/converters and peculiarities of photocurrent multiplaction. Synth Met. Apr. 5, 2006;156(7-8):624-32.
Luo et al., Optical upconverter with integrated heterojunction phototransistor and light-emitting diode. Appl Phys Lett. Feb. 2006;88(7):73501.1-3.
McDonald et al., Solution-processed PbS quantum dot infrared photodetectors and photovoltaics. Nat Mater. Feb. 2005;4:138-43. Supplementary Figure. 1 page.
Mustafa et al., Solution processed nickel oxide anodes for organic photovoltaic devices. Appl Phys Lett. 2014;104(6):e063302.1-5.
Overton, Detectors: Near-IR image uses quantum-dot-sensitized photodiodes. Laser Focus World. Sep. 2009:25-8.
Sarasqueta et al., Organic and inorganic blocking layers for solution-processed colloidal PbSe nanocrystal infrared photodetectors. Adv Funct Mater. 2011;21(1):167-71.
Sargent, Infrared Quantum Dots. Adv Mater. Mar. 8, 2005;17(5):515-22.
Wagner et al., Change of electrochemical impedance spectra (EIS) with time during CO-poisoning of the Pt-anode in a membrane fuel cell. J Power Science. Mar. 10, 2004;127(1-2):341-7.
Wang et al., Correlation between mechanical stress and optical properties of SiO2/Ta2O5 multilayer UV narrow-bandpass filters deposited by plasma ion-assisted deposition. Proc of SPIE. Aug. 2005;5870:58700e.1-9.
Xie et al., InAs/InP/ZnSe Core/Shell/Shell Quantum Dots as Near-Infrared Emitters: Bright, Narrow-Band, Non-Cadmium Containing, and Biocompatible. Nano Res. 2008;1:457-64.
Yang et al., Semiconductor infrared up-conversion devices. Prog Quant Electr. 2011;35:77-108.
Yase et al., Organic Light-emitting Devices with Photoresponsive Layer. Pacific Rim Conference on Lasers and Electro-Optics. Tokyo, Japan. Jul. 11-15, 2005;569-70.
Related Publications (1)
Number Date Country
20140367572 A1 Dec 2014 US
Provisional Applications (1)
Number Date Country
61347696 May 2010 US
Continuations (1)
Number Date Country
Parent 13114896 May 2011 US
Child 14247130 US