Mundy Washington 0250E 212

Total Page:16

File Type:pdf, Size:1020Kb

Mundy Washington 0250E 212 © Copyright 2020 Marja Elizabeth Mundy Aminophosphines as Precursors for Doped and Phase Pure Metal Phosphide Nanocrystals: Synthesis Beyond P(SiMe3)3 Marja Elizabeth Mundy A dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy University of Washington 2020 Reading Committee: Brandi M. Cossairt, Chair Daniel R. Gamelin D. Michael Heinekey Program Authorized to Offer Degree: Chemistry University of Washington Abstract Aminophosphines as Precursors for Doped and Phase Pure Metal Phosphide Nanocrystals: Synthesis Beyond P(SiMe3)3 Marja Elizabeth Mundy Chair of the Supervisory Committee: Associate Professor Brandi M. Cossairt Chemistry Colloidal metal phosphide nanocrystals represent attractive synthetic targets for researchers. They exemplify the diversity of emergent properties presented by nanomaterials, as the class encompasses both semiconductors and metals. When quantum confinement is accounted for, nanoscale semiconducting metal phosphides have optical properties that span the visible and NIR range of the spectrum, making them suitable for a wide range of applications. The metallic transition metal phosphides are consistently touted as earth-abundant alternatives for the hydrogen evolution reaction with competitive catalytic activity, particularly in the form of high surface area nanoparticles. Transition metal phosphides are plagued by synthetic challenges. The reactions are either multistep with low yields, require high temperatures and extended reaction times, or produce mixtures of crystalline phases. While high quality syntheses of several semiconducting metal phosphides exist, many are either capable of only producing nanocrystals in one size or rely on incomplete reactions for size tunability. Recent and exciting work synthesizing indium phosphide from aminophosphines demonstrated precursor-dependent size control based on the indium halide. Prior to the work discussed here, this reactivity was only known for indium phosphide. Chapter 2 discusses our efforts broadening the scope of aminophosphine-based nanocrystal synthesis to include II-V materials and transition metal phosphides. After establishing this versatile platform for the synthesis of phase-pure metal phosphides, Chapter 3 highlights research done establishing aminophosphine-derived InP as a substrate for copper doping and spectroscopic analysis of surface treated materials. TABLE OF CONTENTS List of Figures ................................................................................................................................ iii List of Tables ............................................................................................................................... viii Chapter 1. Introduction ................................................................................................................... 1 1.1 Colloidal nanocrystals and their applications ................................................................. 1 1.2 Metal phosphide nanocrystal synthesis ........................................................................... 2 1.3 Precursor-dependent size control in nanocrystal synthesis ............................................. 5 1.4 Cation doping in nanocrystals ......................................................................................... 6 1.5 References ..................................................................................................................... 10 Chapter 2. Aminophosphines as Versatile Precursors for the Synthesis of Metal Phosphide Nanocrystals .................................................................................................................................. 14 2.1 Note regarding collaborator contributions .................................................................... 14 2.2 Introduction ................................................................................................................... 14 2.3 Results and Discussion ................................................................................................. 15 2.3.1 Synthesis and Characterization of II-V materials ..................................................... 16 2.3.2 Synthesis and Characterization of Transition Metal Phosphides .............................. 21 2.3.3 Reactivity for HER and Proton Transfer .................................................................. 27 2.4 Conclusions ................................................................................................................... 30 2.5 Experimental methods .................................................................................................. 30 2.5.1 Synthentic methods and basic sample preparation ................................................... 31 2.5.2 X-ray absorption measurements ............................................................................... 32 i 2.5.3 Electrochemical characterization .............................................................................. 33 2.6 References ..................................................................................................................... 35 Chapter 3. Synthesis and Spectroscopy of Emissive, Surface-Modified, Copper-Doped Indium Phosphide Nanocrystals ................................................................................................................ 38 3.1 Note regarding collaborator contributions .................................................................... 38 3.2 Introduction ................................................................................................................... 38 3.3 Results and Discussion ................................................................................................. 40 3.3.1 Synthesis of Cu+:InP ................................................................................................. 41 3.3.2 Post-synthetic modifications of doped NCs .............................................................. 46 3.3.3 Photophysical characterizations ................................................................................ 53 3.4 Conclusions ................................................................................................................... 56 3.5 Experimental Details ..................................................................................................... 56 3.6 References ..................................................................................................................... 59 Appendix A: Attempts at the synthesis of InPZnE quaternary alloyed nanocrystals ................... 63 ii LIST OF FIGURES Figure 1.1. Model of a binary semiconducting nanocrystal surrounded by long-chain ligands stabilizing the surface. Reprinted from reference 5 with permission.5 ....................... 2 Figure 1.2. Proposed mechanism showing the formation of InP from aminophosphines and indium chloride. Figure modified from reference 17.17 .............................................. 4 Figure 1.3. Highly monodisperse PbS nanocrystals with size dictated by the reactivity of the thiourea. Reprinted with permission from reference 25.25 .......................................... 5 Figure 1.4. General schematics of synthetic approaches to nanocrystal doping with E 33 representing ion exchange within the previously formed lattice. ............................. 8 Figure 2.1. Standard reaction scheme for metal phosphide nanocrystal formation. ......... 16 Figure 2.2. A) TEM image (6.8 ± 0.5 nm), (B) UV-Vis spectrum, and (C) XRD pattern of Cd3P2 nanocrystals prepared at 250 °C from CdCl2 using a 1:3.6 ratio of Cd:P (Cd3P2 reference pattern PDF 01-070-3099 47-1443). D) TEM image of Cd3P2 prepared from CdCl2 at 250 °C using a 1:1.3 ratio of Cd:P (7.5 ± 0.3 nm). .......................................................... 17 Figure 2.3. (A) UV-Vis final traces of materials synthesized from CdX2 precursors. (B) XRD spectra of materials showing two populations of particles including one subset with a crystalline domain size >30 nm, consistent with mild heterogeneity observed in synthesis. TEM images of (C) CdBr2 (5.9 ± 0.7 nm) and (D) CdI2 (5.6 ± 0.5) products showing the expected trend towards smaller nanocrystals as the halide becomes a better leaving group. ................................................................................................................................... 18 Figure 2.4. Synthesis of Zn3P2 from ZnX2 (X = Cl, Br, I) and P(NEt2)3 at 250°C. (a) Representative UV-Vis absorbance spectra of the final products normalized at 400 nm. Inset: TEM of product from ZnCl2 and P(NEt2)3. (b) Air-free powder X-ray diffraction data of the purified products with Zn3P2 reference pattern (PDF 01-071-6507). ............. 20 31 Figure 2.5. 202.4 MHz P NMR of reaction aliquots in C6D6 with a triphenylphosphine internal standard: (A) Zn3P2 synthesis at 250°C. (B) Cd3P2 synthesis at 250°C. .................. 21 Figure 2.6. (A, B) TEM images (A: CoP 7.8 ± 0.7 nm; B: Co2P of various morphologies with widths/diameters of 6.5 ± 0.6 nm) and (C) XRD pattern of CoP and Co2P prepared at 250 iii °C and 200 °C, respectively. CoP (PDF 01-089-2598 29-497) and Co2P (PDF 01-070-8358) reference patterns. The inset in figure (A) shows a zoomed in image of a single CoP nanocrystal with the corresponding FFT. ................................................................. 22 Figure 2.7. Synthesis of cobalt phosphides from CoI2 at 250 °C. Powder X-ray diffraction data of products after different
Recommended publications
  • Aryl‑NHC Group 13 Trimethyl Complexes : Structural, Stability and Bonding Insights
    This document is downloaded from DR‑NTU (https://dr.ntu.edu.sg) Nanyang Technological University, Singapore. Aryl‑NHC group 13 trimethyl complexes : structural, stability and bonding insights Wu, Melissa Meiyi 2017 Wu, M. M. (2017). Aryl‑NHC group 13 trimethyl complexes : structural, stability and bonding insights. Doctoral thesis, Nanyang Technological University, Singapore. http://hdl.handle.net/10356/70204 https://doi.org/10.32657/10356/70204 Downloaded on 28 Sep 2021 13:14:06 SGT ATTENTION: The Singapore Copyright Act applies to the use of this document. Nanyang Technological University Library. NANYANG TECHNOLOGICAL UNIVERSITY DIVISION OF CHEMISTRY AND BIOLOGICAL CHEMISTRY SCHOOL OF PHYSICAL & MATHEMATICAL SCIENCES Aryl-NHC Group 13 Trimethyl Complexes: Structural, Stability and Bonding Insights Wu Meiyi Melissa G1102527F Supervisor: Asst Prof Felipe Garcia Contents Acknowledgements .............................................................................................................. iv Abbreviations ....................................................................................................................... v Abstract.............................................................................................................................. viii 1. Introduction 1.1. N-Heterocyclic Carbenes (NHC) ................................................................................. 1 1.1.1. Electronic Properties ............................................................................................ 1 1.1.2. Steric
    [Show full text]
  • Admission to AIM
    Admission to AIM THIS DOCUMENT IS IMPORTANT AND REQUIRES YOUR IMMEDIATE ATTENTION. If you are in doubt about the contents of this document, or as to the action you should take you are recommended immediately to seek your own personal financial advice from your stockbroker, accountant or other independent financial adviser authorised under the Financial Services and Markets Act 2000 who specialises in advising on the acquisition of shares and other securities. This document comprises an admission document prepared in accordance with the AIM Rules. This document does not constitute an offer to the public requiring an approved prospectus for the purposes of section 85 of FSMA; has not been prepared in accordance with the Prospectus Rules published by the Financial Services Authority; and has not been approved by or filed with the Financial Services Authority or by any other authority which could be a competent authority for the purposes of the Prospectus Directive. Copies of this document will be available free of charge to the public during normal business hours on any day (Saturdays, Sundays and public holidays excepted) at the offices of Evolutec Group plc at 7 Devonshire Square, London EC2M 4YH from the date of this document until one month from the date of Admission in accordance with Rule 3 of the AIM Rules. The Company, the Directors and Proposed Directors whose names appear on page 7 of this document, accept responsibility both individually and collectively for the information contained in this document. To the best of the knowledge and belief of the Company, the Directors and Proposed Directors (who have taken all reasonable care to ensure that such is the case), the information contained in this document is in accordance with the facts and does not omit anything likely to affect the import of such information.
    [Show full text]
  • Half Year Results Presentation
    HALF YEAR RESULTS PRESENTATION For the six months ended 31 January 2018 DISCLAIMER The following presentation is being made only to, and is only directed at, persons to whom such presentation may lawfully be communicated (“relevant persons”). Any person who is not a relevant person should not act or rely on this presentation or any of its contents. This presentation does not constitute an offering of securities or otherwise constitute an invitation or inducement to any person to underwrite, subscribe for or otherwise acquire securities in Nanoco Group PLC or any of its subsidiaries (“Nanoco”). It should be noted that past performance cannot be relied on as a guide to future performance. This presentation contains forward- looking statements with respect to Nanoco’s plans and objectives regarding its financial conditions, results of operations and businesses. The financial information referenced in this presentation does not contain sufficient detail to allow a full understanding of Nanoco’s results. For more detailed information, the entire text of the interim results announcement for the half year ending 31 January 2018, can be found on the Investor Relations section of the Nanoco website (www.nanocogroup.com). 1 HIGHLIGHTS – ENCOURAGING PROGRESS IN COMMERCIALISATION Momentum in current trading • Game changing Material Development and Supply Agreement with a large US-listed Corporation for advanced electronic devices • Increasing number of Nanoco equipped displays products moving through to commercial production with o First display products
    [Show full text]
  • Environmentally Friendly Quantum Dots for Display Applications
    Environmentally Friendly Quantum Dots for Display Applications E. Jang SAIT, Samsung Electronics, Suwon, Korea, email: [email protected] Abstract— Ever since the physics of quantum dot (QD) was Color IQ technology, which was the glass tube optic using Cd- discovered, much research effort has been carried out for based QD. After that, TCL, Philips, BOE, Hisense and Konka more than 30 years, and lots of applications adopting QDs applied the same technology for their TV and monitor have been proposed. Especially, wide color gamut displays products. Nanosys has been very active in commercializing using QDs as active light emitting materials have drawn QD-film through the joint development with film-fabricating much attention. And, the QD-based consumer displays such companies such as 3M, LMS, Hitachi, and Nitto Denko. as LED TVs, tablets, and special monitors are now on the Starting from Amazon’s Kindle fire tablet, QD color market. They provide best color gamut, reasonable power converting film, which is called as QDEF, was adopted in the ASUS’s laptop and monitor, and TVs of Hisense, TCL, Vizio, efficiency, and affordable price showing superior competitive AUO. In China, Najing technology started to provide QDs to edge to OLED technology. However, still there are issues film makers such as Sangbo and Poly-OE, and work with TCL and argues using Cadmium containing materials in practical and Hisense to produce TVs. Nanoco is one of the pioneer consumer devices. In spite of the European RoHS companies to have developed the Cd-free QDs from the Exemptions, we need to be aware the environmental risk of beginning, and they have collaborated with Dow chemical and producing large quantity of Cd-containing materials and Merck for the mass-production.
    [Show full text]
  • Nanoco Group Plc
    NANOCO GROUP PLC NEEDHAM GROWTH CONFERENCE JANUARY 2019 DISCLAIMER The following presentation is being made only to, and is only directed at, persons to whom such presentation may lawfully be communicated (“relevant persons”). Any person who is not a relevant person should not act or rely on this presentation or any of its contents. This presentation does not constitute an offering of securities or otherwise constitute an invitation or inducement to any person to underwrite, subscribe for or otherwise acquire securities in Nanoco Group PLC or any of its subsidiaries (“Nanoco”). It should be noted that past performance cannot be relied on as a guide to future performance. This presentation contains forward-looking statements with respect to Nanoco’s plans and objectives regarding its financial conditions, results of operations and businesses. The financial information referenced in this presentation does not contain sufficient detail to allow a full understanding of Nanoco’s results. For more detailed information, the entire text of the preliminary results announcement for the full year ended 31 July 2018, can be found on the Investor Relations section of the Nanoco website (www.nanocogroup.com). COPYRIGHT NANOCO 1 PRESENTERS Dr Michael Edelman - Chief Executive Officer Nanoco has been led by Dr Michael Edelman since September 2004. Michael led the initial fundraising, spun Nanoco out of the University of Manchester, floated the Group on the London Stock Exchange in 2009 and grew Nanoco into the world-leading quantum dot player it is today. Prior to Nanoco, Michael held a number of executive roles, including having responsibility for licensing the technology developed by GE/Bayer joint venture Exatec LLP, Vice President and Managing Director at yet2.com, Commercial Director at Colloids Ltd and Business Manager at Brunner Mond & Co Ltd.
    [Show full text]
  • Advances-In-Inorganic-Chemistry-50
    Advances in INORGANIC CHEMISTRY Volume 50 ADVISORY BOARD I. Bertini J. Reedijk Universita´ degli Studi di Firenze Leiden University Florence, Italy Leiden, The Netherlands A. H. Cowley P. J. Sadler University of Edinburgh University of Texas Edinburgh, Scotland Austin, Texas, USA A. M. Sargeson H. B. Gray The Australian National University California Institute of Technology Canberrs, Australia Pasadena, California, USA Y. Sasaki M. L. H. Green Hokkaido University University of Oxford Sapporo, Japan Oxford, United Kingdom D. F. Shriver O. Kahn Northwestern University Evanston, Illinois, USA Institut de Chimie de la Matie`re Condense´e de Bordeaux Pessac, France R. van Eldik Universita¨t Erlangen-Nu¨mberg Andre´E. Merbach Erlangen, Germany Institut de Chimie Mine ´rale et Analytique K. Wieghardt Universite´ de Lausanne Max-Planck Institut Lausanne, Switzerland Mu¨lheim, Germany Advances in INORGANIC CHEMISTRY Main Group Chemistry EDITED BY A. G. Sykes Department of Chemistry The University of Newcastle Newcastle upon Tyne United Kingdom CO-EDITED BY Alan H. Cowley Department of Chemistry and Biochemistry The University of Texas at Austin Austin, Texas VOLUME 50 San Diego San Francisco New York Boston London Sydney Tokyo This book is printed on acid-free paper. ᭺ȍ Copyright 2000 by ACADEMIC PRESS All Rights Reserved. No part of this publication may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopy, recording, or any information storage and retrieval system, without permission in writing from the Publisher. The appearance of the code at the bottom of the first page of a chapter in this book indicates the Publisher’s consent that copies of the chapter may be made for personal or internal use of specific clients.
    [Show full text]
  • 8 Chemistry Title of Case Study
    Impact case study (REF3b) Institution: Imperial College London Unit of Assessment: 8 Chemistry Title of case study: C6 - Nanoco: a successful quantum dot nanotechnology company 1. Summary of the impact (indicative maximum 100 words) The research on the use of single source precursors in quantum dot synthesis undertaken by Professor Paul O’Brien in the Department of Chemistry at Imperial College between 1994 and 1999 resulted in papers and a patent which led to the formation of Nanoco Group PLC, currently a world-leader in the supply of quantum dots (QDs). Quantum dots have applications in backlighting for LCD displays, LED general lighting and thin film solar cells. Nanoco was listed on AIM on the London Stock Exchange in 2009 and by January 2013 Nanoco employed 78 people, had annual revenue of £3 million, and had signed agreements with several major companies in the US and Japan including Dow Chemical, Osram and Tokyo Electron. 2. Underpinning research (indicative maximum 500 words) The underpinning research on single source precursors, the key technology on which the company Nanoco Group PLC was based, was developed at Imperial College London by Professor Paul O’Brien during the period 1994 -1999. Specifically, Tito Trindade carried out the key seminal work on the use of group 2 and group 4 metal diselenocarbamates and dithiocarbamates as precursors for the organometallic synthesis of quantum dots [1,2]. Prior to this work, the only published and available precursor system for the preparation of high quality semiconductor nanoparticles were metal alkyls, silylated chalcogens and phosphorus-chalcogen compounds. This limited the synthesis of quantum dots to expert organometallic chemistry laboratories, and the yield of the reactions using these precursors was often extremely low.
    [Show full text]
  • The Study of Coupling in Ingaas Quantum Rings Grown by Droplet Epitaxy
    The Study of Coupling in InGaAs Quantum Rings Grown by Droplet Epitaxy A thesis presented to the faculty of the College of Arts and Sciences of Ohio University In partial fulfillment of the requirements for the degree Master of Science Samar M. Alsolamy May 2013 © 2013 Samar M. Alsolamy. All Rights Reserved. 2 This thesis titled The Study of Coupling in InGaAs Quantum Rings Grown by Droplet Epitaxy by SAMAR M. ALSOLAMY has been approved for the Department of Physics and Astronomy and the College of Arts and Sciences by Eric A. Stinaff Associate Professor of Physics and Astronomy Robert Frank Dean, College of Arts and Sciences 3 ABSTRACT ALSOLAMY, SAMAR, M., M.S., May 2013, Physics and Astronomy The Study of Coupling in InGaAs Quantum Rings Grown by Droplet Epitaxy Director ofThesis: Eric A. Stinaff The use of metal droplet epitaxy may provide a novel method of growing laterally coupled nanostructures. We will present optical studies of InAs/GaAs nanostructures which result in twin quantum dots (QD) formed on a single quantum ring (QR). Previous studies have investigated the coupling between vertically grown quantum dot pairs. In this thesis, we have used photoluminescence (PL) and photoluminescence excitation (PLE) to examine the possibility of energy transfer and coupling between quantum dot pairs in a single InGaAs quantum ring grown by droplet epitaxy. Power dependent photoluminescence spectra reveal a few peaks at low power, which are identified with emission from the ground state of the individual dots. As the power is increased we observe multi-exciton and excited state emission. We then perform PLE, tuning the excitation laser energy continuously from the high energy ring emission down to the individual dot states.
    [Show full text]
  • Indium(III) Chloride – Catalyzed Michael Addition of Thiols to Chalcones : a Remarkable Solvent Effect
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Publications of the IAS Fellows Issue in Honor of Dr. Rama Rao ARKIVOC 2005 (iii) 44-50 Indium(III) chloride – catalyzed Michael addition of thiols to chalcones : a remarkable solvent effect Brindaban C. Ranu,* Suvendu S. Dey, and Sampak Samanta Department of Organic Chemistry, Indian Association for the Cultivation of Science, Jadavpur, Calcutta – 700 032, India E-mail: [email protected] Dedicated to Dr. A. V. Rama Rao on the occasion of his 70th birthday (received 28 Aug 04; accepted 23 Sep 04; published on the web 26 Sep 04) Abstract Indium(III) chloride in methanol efficiently catalyzes Michael addition of aromatic and aliphatic thiols to chalcones and related compounds. This reaction is remarkably solvent selective and it does not proceed in conventional solvents such as tetrahydrofuran, methylene chloride and water. Keywords: Michael addition, thiol, chalcone, indium(III) chloride, solvent effect Introduction The Michael addition of thiols to electron deficient alkenes is a very useful process for making carbon-sulfur bond. This addition to chalcone derivatives is very interesting and challenging as it is less facile compared to the addition to aliphatic acyclic enones and thus it is not always satisfactory with the conventional reagents used for general 1,4-addition. Recently, a number of 1a procedures involving a variety of catalysts such as synthetic diphosphate Na2CaP2O7, natural 1b 1c 1d phosphate, InBr3, fluorapatite, have been reported. Indium halides, particularly indium(III) chloride have emerged as a potent Lewis acid for various organic transformations in recent times.2 As a part of our interest in indium(III) chloride 3 catalyzed reactions we discovered that although InCl3 has been used in the Michael addition of silylenol ethers,4a amines,4b pyrroles4c and indoles4d to electron-deficient alkenes no report has been found demonstrating the use of InCl3 for addition of thiols to chalcones and related systems.
    [Show full text]
  • Download (7Mb)
    A Thesis Submitted for the Degree of PhD at the University of Warwick Permanent WRAP URL: http://wrap.warwick.ac.uk/90802 Copyright and reuse: This thesis is made available online and is protected by original copyright. Please scroll down to view the document itself. Please refer to the repository record for this item for information to help you to cite it. Our policy information is available from the repository home page. For more information, please contact the WRAP Team at: [email protected] warwick.ac.uk/lib-publications Reactions and Co-ordination Chemistry of Indium Trialkyls and Trihalides. Ian Alan Degnan A thesis submitted for the degree of Doctor of Philosophy. University of Warwick, Department of Chemistry. Septem ber 1989 To Mam and Dad -for making this possible. Contents. Page. Chapter 1: Introduction. Group 13 Elements. 4 Co-ordination Chemistry of the Indium Trihalides. 9 Mono-Complexes of Indium Trihalides. 10 Bis-Complexes of Indium Trihalides. 12 Tris-Complexes of Indium Trihalides. 17 Unusual Indium Trihalide Complexes. 20 Phosphine Complexes of Indium Triiodide. 22 Metathetical Reactions of Indium Trihalides. 30 Organometallic Derivatives of Indium. 33 Organoindium Halides. 33 Organoindium Compounds. 37 Reactions of Organoindium Compounds. 39 Control of Oligomerisation in Indium Compounds. 55 Chapter 2. Phosphine Complexes of Indium Trihalides. 58 Introduction. 59 Mono-Phosphine Complexes of Indium Triiodide. 60 X-ray Diffraction Study of InCI3(PMe3)2. 83 Indium Triiodide Complexes of Diphos. 86 Chapter 3. Metathetical Reactions of Indium Trihalides. 94 Introduction. 95 Reaction of Indium Triiodide Phosphine Complexes with Methyllithium. 96 Reaction of Indium Triiodide Triphenylphosphine Complex with Methyllithium.
    [Show full text]
  • Thermochemical Modelling and Experimental Validation of in Situ Indium Volatilization by Released Halides During Pyrolysis of Smartphone Displays
    metals Article Thermochemical Modelling and Experimental Validation of In Situ Indium Volatilization by Released Halides during Pyrolysis of Smartphone Displays Benedikt Flerus 1,2,*, Thomas Swiontek 1, Katrin Bokelmann 2, Rudolf Stauber 2 and Bernd Friedrich 1 1 Institute of Process Metallurgy and Metal Recycling IME, RWTH Aachen University, Intzestraße 3, 52056 Aachen, Germany; [email protected] (T.S.); [email protected] (B.F.) 2 Project Group, Materials Recycling and Resource Strategies IWKS, Fraunhofer Institute for Silicate Research ISC, Brentanostraße 2, 63755 Alzenau, Germany; [email protected] (K.B.); [email protected] (R.S.) * Correspondence: bfl[email protected]; Tel.: +49-(0)241-80-95856 Received: 22 November 2018; Accepted: 5 December 2018; Published: 8 December 2018 Abstract: The present study focuses on the pyrolysis of discarded smartphone displays in order to investigate if a halogenation and volatilization of indium is possible without a supplementary halogenation agent. After the conduction of several pyrolysis experiments it was found that the indium evaporation is highly temperature-dependent. At temperatures of 750 ◦C or higher the indium concentration in the pyrolysis residue was pushed below the detection limit of 20 ppm, which proved that a complete indium volatilization by using only the halides originating from the plastic fraction of the displays is possible. A continuous analysis of the pyrolysis gas via FTIR showed that the amounts of HBr, HCl and CO increase strongly at elevated temperatures. The subsequent thermodynamic consideration by means of FactSage confirmed the synergetic effect of CO on the halogenation of indium oxide. Furthermore, HBr is predicted to be a stronger halogenation agent compared to HCl.
    [Show full text]
  • Stabilization and Reactivity of Low Oxidation State Indium Compounds
    University of Windsor Scholarship at UWindsor Electronic Theses and Dissertations Theses, Dissertations, and Major Papers 2013 Stabilization and Reactivity of Low Oxidation State Indium Compounds Christopher Allan University of Windsor Follow this and additional works at: https://scholar.uwindsor.ca/etd Recommended Citation Allan, Christopher, "Stabilization and Reactivity of Low Oxidation State Indium Compounds" (2013). Electronic Theses and Dissertations. 4939. https://scholar.uwindsor.ca/etd/4939 This online database contains the full-text of PhD dissertations and Masters’ theses of University of Windsor students from 1954 forward. These documents are made available for personal study and research purposes only, in accordance with the Canadian Copyright Act and the Creative Commons license—CC BY-NC-ND (Attribution, Non-Commercial, No Derivative Works). Under this license, works must always be attributed to the copyright holder (original author), cannot be used for any commercial purposes, and may not be altered. Any other use would require the permission of the copyright holder. Students may inquire about withdrawing their dissertation and/or thesis from this database. For additional inquiries, please contact the repository administrator via email ([email protected]) or by telephone at 519-253-3000ext. 3208. STABILIZATION AND REACTIVITY OF LOW OXIDATION STATE INDIUM COMPOUNDS By Christopher J. Allan A Dissertation Submitted to the Faculty of Graduate Studies Through Chemistry and Biochemistry In Partial Fulfillment of the Requirements for The Degree of Doctor of Philosophy at the University of Windsor Windsor, Ontario, Canada 2013 ©2013 Christopher J. Allan Declaration of Co-Authorship / Previous Publications I. Declaration of Co-Authorship This thesis incorporates the outcome of joint research undertaken in collaboration with Hugh Cowley under the supervision of Jeremy Rawson.
    [Show full text]