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TR-499: Indium Phosphide (CASRN 22398-80-7) in F344/N Rats And
NTP TECHNICAL REPORT ON THE TOXICOLOGY AND CARCINOGENESIS STUDIES OF INDIUM PHOSPHIDE (CAS NO. 22398-80-7) IN F344/N RATS AND B6C3F1 MICE (INHALATION STUDIES) NATIONAL TOXICOLOGY PROGRAM P.O. Box 12233 Research Triangle Park, NC 27709 July 2001 NTP TR 499 NIH Publication No. 01-4433 U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES Public Health Service National Institutes of Health FOREWORD The National Toxicology Program (NTP) is made up of four charter agencies of the U.S. Department of Health and Human Services (DHHS): the National Cancer Institute (NCI), National Institutes of Health; the National Institute of Environmental Health Sciences (NIEHS), National Institutes of Health; the National Center for Toxicological Research (NCTR), Food and Drug Administration; and the National Institute for Occupational Safety and Health (NIOSH), Centers for Disease Control and Prevention. In July 1981, the Carcinogenesis Bioassay Testing Program, NCI, was transferred to the NIEHS. The NTP coordinates the relevant programs, staff, and resources from these Public Health Service agencies relating to basic and applied research and to biological assay development and validation. The NTP develops, evaluates, and disseminates scientific information about potentially toxic and hazardous chemicals. This knowledge is used for protecting the health of the American people and for the primary prevention of disease. The studies described in this Technical Report were performed under the direction of the NIEHS and were conducted in compliance with NTP laboratory health and safety requirements and must meet or exceed all applicable federal, state, and local health and safety regulations. Animal care and use were in accordance with the Public Health Service Policy on Humane Care and Use of Animals. -
Transition Metal Phosphides for the Catalytic Hydrodeoxygenation of Waste Oils Into Green Diesel
catalysts Review Transition Metal Phosphides for the Catalytic Hydrodeoxygenation of Waste Oils into Green Diesel M. Consuelo Alvarez-Galvan * , Jose M. Campos-Martin * and Jose L. G. Fierro * Energy and Sustainable Chemistry Group (EQS), Instituto de Catálisis y Petroleoquímica, CSIC, c/Marie Curie, 2 Cantoblanco, 28049 Madrid, Spain * Correspondence: [email protected] (M.C.A.-G.); [email protected] (J.M.C.-M.); jlgfi[email protected] (J.L.G.F.) Received: 28 February 2019; Accepted: 15 March 2019; Published: 22 March 2019 Abstract: Recently, catalysts based on transition metal phosphides (TMPs) have attracted increasing interest for their use in hydrodeoxygenation (HDO) processes destined to synthesize biofuels (green or renewable diesel) from waste vegetable oils and fats (known as hydrotreated vegetable oils (HVO)), or from bio-oils. This fossil-free diesel product is produced completely from renewable raw materials with exceptional quality. These efficient HDO catalysts present electronic properties similar to noble metals, are cost-efficient, and are more stable and resistant to the presence of water than other classical catalytic formulations used for hydrotreatment reactions based on transition metal sulfides, but they do not require the continuous supply of a sulfide source. TMPs develop a bifunctional character (metallic and acidic) and present tunable catalytic properties related to the metal type, phosphorous-metal ratio, support nature, texture properties, and so on. Here, the recent progress in TMP-based catalysts for HDO of waste oils is reviewed. First, the use of TMPs in catalysis is addressed; then, the general aspects of green diesel (from bio-oils or from waste vegetable oils and fats) production by HDO of nonedible oil compounds are presented; and, finally, we attempt to describe the main advances in the development of catalysts based on TMPs for HDO, with an emphasis on the influence of the nature of active phases and effects of phosphorous, promoters, and preparation methods on reactivity. -
Binary and Ternary Transition-Metal Phosphides As Hydrodenitrogenation Catalysts
Research Collection Doctoral Thesis Binary and ternary transition-metal phosphides as hydrodenitrogenation catalysts Author(s): Stinner, Christoph Publication Date: 2001 Permanent Link: https://doi.org/10.3929/ethz-a-004378279 Rights / License: In Copyright - Non-Commercial Use Permitted This page was generated automatically upon download from the ETH Zurich Research Collection. For more information please consult the Terms of use. ETH Library Diss. ETH No. 14422 Binary and Ternary Transition-Metal Phosphides as Hydrodenitrogenation Catalysts A dissertation submitted to the Swiss Federal Institute of Technology Zurich for the degree of Doctor of Natural Sciences Presented by Christoph Stinner Dipl.-Chem. University of Bonn born February 27, 1969 in Troisdorf (NRW), Germany Accepted on the recommendation of Prof. Dr. Roel Prins, examiner Prof. Dr. Reinhard Nesper, co-examiner Dr. Thomas Weber, co-examiner Zurich 2001 I Contents Zusammenfassung V Abstract IX 1 Introduction 1 1.1 Motivation 1 1.2 Phosphides 4 1.2.1 General 4 1.2.2 Classification 4 1.2.3 Preparation 5 1.2.4 Properties 12 1.2.5 Applications and Uses 13 1.3 Scope of the Thesis 14 1.4 References 16 2 Characterization Methods 1 2.1 FT Raman Spectroscopy 21 2.2 Thermogravimetric Analysis 24 2.3 Temperature-Programmed Reduction 25 2.4 X-Ray Powder Diffractometry 26 2.5 Nitrogen Adsorption 28 2.6 Solid State Nuclear Magnetic Resonance Spectroscopy 28 2.7 Catalytic Test 33 2.8 References 36 3 Formation, Structure, and HDN Activity of Unsupported Molybdenum Phosphide 37 3.1 Introduction -
Red-Light Leds for Next-Generation Displays 6 July 2020
Red-light LEDs for next-generation displays 6 July 2020 indium gallium nitride (InGaN) semiconductors. Integrating two material systems is difficult. "Creating RGB displays requires the mass transfer of the separate blue, green and red LEDs together," says KAUST researcher Zhe Zhuang. An easier solution would be to create different-colored LEDs all on a single semiconductor chip. Optimizing the geometry, fabrication and electrical contacts is vital to maximizing the efficiency of the LED. Credit: Zhuag et al. Novel red LEDs are more temperature stable than those made using the conventional semiconductor of choice. In efforts to optimize the performance of light- emitting diodes (LEDs), King Abdullah University of Science and Technology researchers are looking at every aspect of the design, fabrication and operation of these devices. Now, they have succeeded in fabricating red LEDs, based on the The team developed an InGaN red LED structure where naturally blue-emitting semiconductor indium the output power is more stable than that of InGaP red gallium nitride, that are as stable as those based LEDs. Credit: Zhe Zhuang on indium gallium phosphide. LEDs are optical sources made from semiconductors that offer improvements on Since InGaP semiconductors are unable to emit conventional visible-light sources in terms of blue or green light, the only solution to making energy saving, smaller size and longer lifetimes. monolithic RGB micro-LEDs is to use InGaN. This LEDs can emit across the spectrum, from the material has the potential to shift its emission from ultraviolet to blue (B), green (G), red (R) and into blue to green, yellow and red by introducing more the infrared. -
Chemical Vapor Deposition of Heteroepitaxial Boron Phosphide Thin Films
University of Tennessee, Knoxville TRACE: Tennessee Research and Creative Exchange Doctoral Dissertations Graduate School 12-2013 Chemical Vapor Deposition of Heteroepitaxial Boron Phosphide Thin Films John Daniel Brasfield University of Tennessee - Knoxville, [email protected] Follow this and additional works at: https://trace.tennessee.edu/utk_graddiss Part of the Semiconductor and Optical Materials Commons Recommended Citation Brasfield, John Daniel, "Chemical aporV Deposition of Heteroepitaxial Boron Phosphide Thin Films. " PhD diss., University of Tennessee, 2013. https://trace.tennessee.edu/utk_graddiss/2558 This Dissertation is brought to you for free and open access by the Graduate School at TRACE: Tennessee Research and Creative Exchange. It has been accepted for inclusion in Doctoral Dissertations by an authorized administrator of TRACE: Tennessee Research and Creative Exchange. For more information, please contact [email protected]. To the Graduate Council: I am submitting herewith a dissertation written by John Daniel Brasfield entitled "Chemical Vapor Deposition of Heteroepitaxial Boron Phosphide Thin Films." I have examined the final electronic copy of this dissertation for form and content and recommend that it be accepted in partial fulfillment of the equirr ements for the degree of Doctor of Philosophy, with a major in Chemistry. Charles S. Feigerle, Major Professor We have read this dissertation and recommend its acceptance: Laurence Miller, Frank Vogt, Ziling Xue Accepted for the Council: Carolyn R. Hodges Vice Provost and Dean of the Graduate School (Original signatures are on file with official studentecor r ds.) Chemical Vapor Deposition of Heteroepitaxial Boron Phosphide Thin Films A Dissertation Presented for the Doctor of Philosophy Degree The University of Tennessee, Knoxville John Daniel Brasfield December 2013 Copyright © 2013 by John Daniel Brasfield All rights reserved. -
Reducing Bow of Ingap on Silicon Wafers
94 Technology focus: III-Vs on silicon Reducing bow of InGaP on silicon wafers Researchers use strain engineering without impacting dislocation density. esearchers based in Singapore and the USA have been working to control the wafer bow of Rindium gallium phosphide (InGaP) epitaxial lay- ers on 200mm silicon (Si) wafers [Bing Wang et al, Semicond. Sci. Technol., vol32, p125013, 2017]. “Based on these Wafer bow is caused by observations, we can stress arising mainly conclude that the from mismatches of threading dislocation coefficients of thermal expansion between densities of the InGaP InGaP, or other III-V wafers are not compound semiconduc- affected by the lattice tors, and silicon. The mismatch. Our Ge bow (more than 200µm buffers have similar in one recent report of gallium arsenide on threading dislocation 300mm silicon wafer) is density of 3x107/cm2. introduced when the The hetero-epitaxy of material cools after high- GaAs buffers and temperature epitaxial Figure 1. Epitaxial layer structure of three InGaP/Si deposition. Bowing InGaP films did not wafers. adversely affects wafer- increase the scale processing, partic- threading dislocation was by metal-organic chemical vapor deposition ularly for large-diameter density, which (MOCVD). The germanium on silicon template layer substrates. Wafer-scale was prepared separately in a two-step low/high-tem- indicates very good equipment typically perature process, using germane (GeH4) precursor. restricts the permitted epitaxy quality.” Plan-view transmission electron microscopy (PV-TEM) bow to less than 50µm. The team believes and etch pit density (EPD) analysis gave an estimate of 7 2 The team from the that the technique dislocation density of the order 3x10 /cm . -
Supporting Information For: Solution Phase Synthesis of Indium Gallium Phosphide Alloy Nanowires Nikolay Kornienko , Desiré D
Supporting Information for: Solution Phase Synthesis of Indium Gallium Phosphide Alloy Nanowires Nikolay Kornienko1, Desiré D. Whitmore1, Yi Yu1, Stephen R. Leone1,2,4, Peidong Yang*1,3,5,6 1Department of Chemistry, 2Department of Physics and 3Department of Materials Science Engineering, University of California, Berkeley 94720, United States 4Chemical Sciences Division and 5Materials Sciences Division, Lawrence Berkeley National Lab, Berkeley CA 94720, United States 6Kavli Energy Nanosciences Institute, Berkeley, California 94720, United States * Correspondence to: [email protected] Table of Contents: Figure S1. TEM In/Ga growth seeds ............................................................................................................................. 2 Figure S2. TEM of InP and GaP NWs ............................................................................................................................. 2 Figure S3. Composition and diameter control ......................................................................................................... 3 Figure S4. XRD of InxGa1‐xP NWs .................................................................................................................................. 4 Figure S5. Electron diffraction of InxGa1‐xP NWs ................................................................................................... 5 Figure S6. Raman spectra of InP and GaP .................................................................................................................. 6 -
Arxiv:1010.1610V1 [Physics.Ins-Det] 8 Oct 2010 Ai Mouneyrac, David Emndtetm Osat O H Rpigadde- and Illumination
Detrapping and retrapping of free carriers in nominally pure single crystal GaP, GaAs and 4H-SiC semiconductors under light illumination at cryogenic temperatures David Mouneyrac,1,2 John G. Hartnett,1 Jean-Michel Le Floch,1 Michael E. Tobar,1 Dominique Cros,2 Jerzy Krupka3∗ 1School of Physics, University of Western Australia 35 Stirling Hwy, Crawley 6009 WA Australia 2Xlim, UMR CNRS 6172, 123 av. Albert Thomas, 87060 Limoges Cedex - France 3Institute of Microelectronics and Optoelectronics Department of Electronics, Warsaw University of Technology, Warsaw, Poland (Dated: October 27, 2018) We report on extremely sensitive measurements of changes in the microwave properties of high purity non-intentionally-doped single-crystal semiconductor samples of gallium phosphide, gallium arsenide and 4H-silicon carbide when illuminated with light of different wavelengths at cryogenic temperatures. Whispering gallery modes were excited in the semiconductors whilst they were cooled on the coldfinger of a single-stage cryocooler and their frequencies and Q-factors measured under light and dark conditions. With these materials, the whispering gallery mode technique is able to resolve changes of a few parts per million in the permittivity and the microwave losses as compared with those measured in darkness. A phenomenological model is proposed to explain the observed changes, which result not from direct valence to conduction band transitions but from detrapping and retrapping of carriers from impurity/defect sites with ionization energies that lay in the semicon- ductor band gap. Detrapping and retrapping relaxation times have been evaluated from comparison with measured data. PACS numbers: 72.20.Jv 71.20.Nr 77.22.-d I. -
Subject Index
SUBJECT INDEX Vol. 1: 1–698, Vol. 2: 699–1395, Vol. 3: 1397–2111, Vol. 4: 2113–2798, Vol. 5: 2799–3440. Page numbers suffixed by t and f refer to Tables and Figures respectively. Absorption spectra in aqueous solution, 752–770 of americium, 1364–1368 compounds of, 721–752 americium (III), 1364–1365, 1365f coordination complexes in solution, americium (IV), 1365 771–782 americium (V), 1366, 1367f history of, 699–700 americium (VI), 1366, 1367f isotope production, 702–703 americium (VII), 1367–1368, 1368f metallic state of, 717–721 of liquid plutonium, 963 in nature, 703–704 of neptunium, 763–766, 763f, 786–787 nuclear properties of, 700–702 neptunium (VII) ternary oxides, 729 separation and purification, 704–717 of plutonium plutonium hexafluoride, 1088, 1089f atomic properties of, 857–862 ions, 1113–1117, 1116t compounds of, 987–1108 plutonium (IV), 849 metal and intermetallic compounds of, polymerization, 1151, 1151f 862–987 tetrachloride, 1093–1094, 1094f natural occurrence of, 822–824 tribromide, 1099t, 1100 nuclear properties of, 815–822 trichloride, 1099, 1099t separation and purification of, 826–857 Accelerator mass spectrometry (AMS), of solution chemistry of, 1108–1203 neptunium, 790 Actinide elements Acetates atomic volumes of, 922–923, 923f of americium, 1322, 1323t extraction of of plutonium, 1177, 1180 DIDPA, 1276 Acetone, derived compounds, of americium, HDEHP, 1275 1322, 1323t, 1324 organophosphorus and Acids carbamoylphosphonate reagents, for Purex process, 711 1276–1278 for solvent extraction, 839 stripping of, 1280–1281 Actinide -
Basic Light Emitting Diodes
The following is for information purposes only and comes with no warranty. See http://www.bristolwatch.com/ Light Emitting Diodes Light Emitting Diodes are made from compound type semiconductor materials such as Gallium Arsenide (GaAs), Gallium Phosphide (GaP), Gallium Arsenide Phosphide (GaAsP), Silicon Carbide (SiC) or Gallium Indium Nitride (GaInN). The exact choice of the semiconductor material used will determine the overall wavelength of the photon light emissions and therefore the resulting color of the light emitted, as in the case of the visible light colored LEDs, (RED, AMBER, GREEN etc). Before a light emitting diode can "emit" any form of light it needs a current to flow through it, as it is a current dependent device. As the LED is to be connected in a forward bias condition across a power supply it should be Current Limited using a series resistor to protect it from excessive current flow. From the table above we can see that each LED has its own forward voltage drop across the PN junction and this parameter which is determined by the semiconductor material used is the forward voltage drop for a given amount of forward conduction current, typically for a forward current of 20mA. In most cases LEDs are operated from a low voltage DC supply, with a series resistor to limit the forward current to a suitable value from say 5mA for a simple LED indicator to 30mA or more where a high brightness light output is needed. Typical LED Characteristics Semiconductor Material Wavelength Color voltage at 20mA GaAs 850-940nm Infra-Red 1.2v GaAsP 630-660nm Red 1.8v GaAsP 605-620nm Amber 2.0v GaAsP:N 585-595nm Yellow 2.2v GaP 550-570nm Green 3.5v SiC 430-505nm Blue 3.6v GaInN 450nm White 4.0v 1 Multi-LEDs LEDs are available in a wide range of shapes, colors and various sizes with different light output intensities available, with the most common (and cheapest to produce) being the standard 5mm Red LED. -
Organometallic Pnictogen Chemistry
Institut für Anorganische Chemie 2014 Fakultät für Chemie und Pharmazie | Sabine Reisinger aus Regensburg, geb. Scheuermayer am 15.07.1983 Studium: Chemie, Universität Regensburg Abschluss: Diplom Promotion: Prof. Dr. Manfred Scheer, Institut für Anorganische Chemie Sabine Reisinger Die vorliegende Arbeit enthält drei Kapitel zu unterschiedlichen Aspekten der metallorganischen Phosphor- und Arsen-Chemie. Zunächst werden Beiträge zur supramolekularen Chemie mit 5 Pn-Ligandkomplexen basierend auf [Cp*Fe(η -P5)] und 5 i [Cp*Fe(η - Pr3C3P2)] gezeigt, gefolgt von der Eisen-vermittelten Organometallic Pnictogen Aktivierung von P4, die zu einer selektiven C–P-Bindungsknüpfung führt, während das dritte Kapitel die Verwendung von Phosphor Chemistry – Three Aspects und Arsen als Donoratome in mehrkernigen Komplexen mit paramagnetischen Metallionen behandelt. Sabine Reisinger 2014 Alumniverein Chemie der Universität Regensburg E.V. [email protected] http://www.alumnichemie-uniregensburg.de Aspects Three – Chemistry Pnictogen Organometallic Fakultät für Chemie und Pharmazie ISBN 978-3-86845-118-4 Universität Regensburg Universitätsstraße 31 93053 Regensburg www.uni-regensburg.de 9 783868 451184 4 Sabine Reisinger Organometallic Pnictogen Chemistry – Three Aspects Organometallic Pnictogen Chemistry – Three Aspects Dissertation zur Erlangung des Doktorgrades der Naturwissenschaften (Dr. rer. nat.) der Fakultät für Chemie und Pharmazie der Universität Regensburg vorgelegt von Sabine Reisinger, geb. Scheuermayer Regensburg 2014 Die Arbeit wurde von Prof. Dr. Manfred Scheer angeleitet. Das Promotionsgesuch wurde am 20.06.2014 eingereicht. Das Kolloquium fand am 11.07.2014 statt. Prüfungsausschuss: Vorsitzender: Prof. Dr. Helmut Motschmann 1. Gutachter: Prof. Dr. Manfred Scheer 2. Gutachter: Prof. Dr. Henri Brunner weiterer Prüfer: Prof. Dr. Bernhard Dick Dissertationsreihe der Fakultät für Chemie und Pharmazie der Universität Regensburg, Band 4 Herausgegeben vom Alumniverein Chemie der Universität Regensburg e.V. -
Nonlinear Properties of III-V Semiconductor Nanowaveguides
Nonlinear Properties of III-V Semiconductor Nanowaveguides ELEONORA DE LUCA Doctoral Thesis in Physics School of Engineering Sciences KTH Royal Institute of Technology Stockholm, Sweden 2019 Akademisk avhandling som med tillstånd av Kungliga Tekniska högskolan fram- lägges till offentlig granskning för avläggande av teknologie doktorsexamen i fysik onsdag den 23 oktober 2019 klockan 10:00 i sal FA32, AlbaNova Universitetscent- rum, Kungliga Tekniska Högskolan, Roslagstullsbacken 21, Stockholm. TRITA-SCI-FOU 2019:45 • ISBN 978-91-7873-318-7 "O frati," dissi, "che per cento milia perigli siete giunti a l’occidente, a questa tanto picciola vigilia d’i nostri sensi ch’é del rimanente non vogliate negar l’esperïenza, di retro al sol, del mondo sanza gente. Considerate la vostra semenza: fatti non foste a viver come bruti, ma per seguir virtute e canoscenza". Dante Alighieri. Commedia. Inferno – Canto XXVI. "O brothers, who amid a hundred thousand Perils," I said, "have come unto the West, To this so inconsiderable vigil Which is remaining of your senses still, Be ye unwilling to deny the knowledge, Following the sun, of the unpeopled world. Consider ye the seed from which ye sprang; Ye were not made to live like unto brutes, But for pursuit of virtue and of knowledge" Dante Alighieri. Commedia. Inferno – Canto XXVI. Translated by Henry Wadsworth Longfellow. Abstract Nonlinear optics (NLO) plays a major role in the modern world: nonlin- ear optical phenomena have been observed in a wavelength range going from the deep infrared to the extreme ultraviolet, to THz radiation. The optical nonlinearities can be found in crystals, amorphous materials, polymers, liquid crystals, liquids, organic materials, and even gases and plasmas.