<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-19T21:11:34Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/35072" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/35072</identifier><datestamp>2022-01-13T07:54:33Z</datestamp><setSpec>com_1721.1_7582</setSpec><setSpec>com_1721.1_7581</setSpec><setSpec>col_1721.1_131024</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="advisor" lang="en_US">Donald R. Sadoway.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Cooper, Benjamin D</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="other" lang="en_US">Massachusetts Institute of Technology. Dept. of Materials Science and Engineering.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department">Massachusetts Institute of Technology. Department of Materials Science and Engineering</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2006-12-18T20:02:17Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2006-12-18T20:02:17Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2006</dim:field>
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   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">71231057</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis (S.B.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, June 2006.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">"May 2006."</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Includes bibliographical references (leaves 35-36).</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">Carbon, tungsten, platinum, and iridium were examined as candidate anode materials for an electrolytic cell. The materials were pre-selected to endure high process temperatures and were characterized for inertness and high current density during electrolysis using voltammometric techniques. Inertness is viewable through current discrepancies dependent on voltage scan direction at low voltage, consumption of current by metal oxide formation, and ease of surface oxide electro-stripping. Conductivity during electrolytic oxidation is observable as current density maximization at high voltages. While carbon, tungsten, and platinum formed surface oxides, iridium remained quite inert. In addition, the voltage hold-time was found to affect the leading current density, as platinum performed best during cyclic voltammometry, but iridium performed best during potentiostatic electrolysis. The intermediate potentiodynamic scan-rate displays the transition from platinum to iridium dominated current density.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Benjamin D. Cooper.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree" lang="en_US">S.B.</dim:field>
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   <dim:field mdschema="dc" element="publisher" lang="en_US">Massachusetts Institute of Technology</dim:field>
   <dim:field mdschema="dc" element="rights" lang="en_US">M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.</dim:field>
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   <dim:field mdschema="dc" element="subject" lang="en_US">Materials Science and Engineering.</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">Electrode materials for the electrolysis of metal oxides</dim:field>
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   	&lt;Title>Electrode materials for the electrolysis of metal oxides&lt;/Title>
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   	&lt;PublicationDate>2006&lt;/PublicationDate>
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    &lt;Keyword>Materials Science and Engineering.&lt;/Keyword>
   	&lt;Abstract>Carbon, tungsten, platinum, and iridium were examined as candidate anode materials for an electrolytic cell. The materials were pre-selected to endure high process temperatures and were characterized for inertness and high current density during electrolysis using voltammometric techniques. Inertness is viewable through current discrepancies dependent on voltage scan direction at low voltage, consumption of current by metal oxide formation, and ease of surface oxide electro-stripping. Conductivity during electrolytic oxidation is observable as current density maximization at high voltages. While carbon, tungsten, and platinum formed surface oxides, iridium remained quite inert. In addition, the voltage hold-time was found to affect the leading current density, as platinum performed best during cyclic voltammometry, but iridium performed best during potentiostatic electrolysis. The intermediate potentiodynamic scan-rate displays the transition from platinum to iridium dominated current density.&lt;/Abstract>
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