<?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>2026-09-20T04:03:34Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/36216" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/36216</identifier><datestamp>2022-01-13T07:54:33Z</datestamp><setSpec>com_1721.1_7582</setSpec><setSpec>com_1721.1_7581</setSpec><setSpec>col_1721.1_131023</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">Mildred S. Dresselhaus and Jing Kong.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Steiner, Stephen Alan, III</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">2007-02-21T13:08:27Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2007-02-21T13:08:27Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="copyright" lang="en_US">2006</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2006</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/1721.1/36216</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">76906746</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2006.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Includes bibliographical references (leaves 219-233).</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">Carbon aerogels offer several unique advantages which make them ideal for evaluating a metal's ability to catalyze nanotube growth, including in situ carbothermic reduction of oxidized nanoparticles to their catalytic metallic phase as they form and production of a bulk quantity of nanoparticles which can be easily characterized. In this work, metal-doped carbon aerogels of seven transition metals were synthesized, characterized, and evaluated for their ability to catalyze growth of carbon nanotubes by thermal chemical vapor deposition (CVD). It was found that carbon aerogels doped with Fe, Rh, Re, Au, and Nb all catalyzed the formation of nanotubes in moderate to high yields, resulting in a direct growth of nanotubes on the exterior surfaces of aerogel monoliths. Ta was found to grow nanotubes only after thorough reduction of its oxides. Growth with W was inconclusive. CVD growth of nanotubes throughout the interior porosity of metal-doped carbon aerogels was also achieved by templating a network of interconnected macropores into the monoliths. Surface-based nanoparticles composed of rhenium, gold, and varying combinations of gold and rhenium were investigated for their ability to catalyze carbon nanotube growth.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">(cont.) Nanoparticles of these metals were nucleated onto silicon wafers from solutions of anhydrous ReCI5 and AuC13. After deposition, the nanoparticles were reduced under hydrogen for 10 min and then oxidized in air for 4 min. The samples were then processed by CVD employing hydrogen and ethanol-saturated Ar for 10 min. Nanoparticles deposited from metal chloride solutions with a 1:1 molar ratio of gold to rhenium or higher were found to result in high yields of single-walled nanotubes, where nanoparticles deposited from solutions with less than a 1:4 gold-to-rhenium ratio resulted in no nanotube growth. Lastly, a new low-pressure CVD system specialized for nanotube growth was developed. The objectives of the system are to provide a flexible architecture for developing new nanotube growth techniques and to lower the minimum temperature required for nanotube growth. The system features a separate sample heating plate for thermally activating nanoparticles and hot filament for carbon feedstock cracking. The system also features the ability to easily install or remove modules for electric field- and plasma-assisted growths.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Stephen Alan Steiner, III.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree" lang="en_US">S.M.</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="extent" lang="en_US">233 leaves</dim:field>
   <dim:field mdschema="dc" element="language" qualifier="iso" lang="en_US">eng</dim:field>
   <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>
   <dim:field mdschema="dc" element="rights" qualifier="uri">http://dspace.mit.edu/handle/1721.1/7582</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Materials Science and Engineering.</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">Engineering carbon nanostructures : development of novel aerogel-nanotube composites and optimization techniques for nanotube growth</dim:field>
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   	&lt;Title>Engineering carbon nanostructures : development of novel aerogel-nanotube composites and optimization techniques for nanotube growth&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 aerogels offer several unique advantages which make them ideal for evaluating a metal&amp;apos;s ability to catalyze nanotube growth, including in situ carbothermic reduction of oxidized nanoparticles to their catalytic metallic phase as they form and production of a bulk quantity of nanoparticles which can be easily characterized. In this work, metal-doped carbon aerogels of seven transition metals were synthesized, characterized, and evaluated for their ability to catalyze growth of carbon nanotubes by thermal chemical vapor deposition (CVD). It was found that carbon aerogels doped with Fe, Rh, Re, Au, and Nb all catalyzed the formation of nanotubes in moderate to high yields, resulting in a direct growth of nanotubes on the exterior surfaces of aerogel monoliths. Ta was found to grow nanotubes only after thorough reduction of its oxides. Growth with W was inconclusive. CVD growth of nanotubes throughout the interior porosity of metal-doped carbon aerogels was also achieved by templating a network of interconnected macropores into the monoliths. Surface-based nanoparticles composed of rhenium, gold, and varying combinations of gold and rhenium were investigated for their ability to catalyze carbon nanotube growth.&lt;/Abstract>
   	&lt;Abstract>(cont.) Nanoparticles of these metals were nucleated onto silicon wafers from solutions of anhydrous ReCI5 and AuC13. After deposition, the nanoparticles were reduced under hydrogen for 10 min and then oxidized in air for 4 min. The samples were then processed by CVD employing hydrogen and ethanol-saturated Ar for 10 min. Nanoparticles deposited from metal chloride solutions with a 1:1 molar ratio of gold to rhenium or higher were found to result in high yields of single-walled nanotubes, where nanoparticles deposited from solutions with less than a 1:4 gold-to-rhenium ratio resulted in no nanotube growth. Lastly, a new low-pressure CVD system specialized for nanotube growth was developed. The objectives of the system are to provide a flexible architecture for developing new nanotube growth techniques and to lower the minimum temperature required for nanotube growth. The system features a separate sample heating plate for thermally activating nanoparticles and hot filament for carbon feedstock cracking. The system also features the ability to easily install or remove modules for electric field- and plasma-assisted growths.&lt;/Abstract>
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