<?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>2026-09-20T11:33:10Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/43207" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/43207</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">Francesco Stellacci.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Stefanescu, Cristina F</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">2008-11-07T19:15:57Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2008-11-07T19:15:57Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="copyright" lang="en_US">2008</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2008</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/1721.1/43207</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">259121530</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis (S.B.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2008.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Includes bibliographical references (p. 45).</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">The application of rippled gold nanoparticles with bi-ligand surface morphology as a catalyst was tested. The hydrolysis of 2,4-dinitrophenyl acetate (DNPA) served as the catalytic reaction being analyzed and the bi-ligand composition used was 16-mercaptohexadecanoic acid to imidazole thiol (MHA to IT). The influence of temperature on catalytic reaction of DNPA with the MHA: IT system was tested for ligand rations of 2:1, 1:2, and 1:1 by monitoring the catalytic system on a UV-VIS spectrometer. Catalytic rate constants were obtained and found to increase with increased temperature. The measured catalytic rate constants were greatest overall for the 1:1 system, followed by the 1:2 system, and lastly the 2:1 system. The activation energy for each ligand-ratio system was measured and found to be 22.17 kJ/mol for the 2:1 system, 14.7 kJ/mol for the 1:2 system, and 26.52 for the 1:1 system. The 2:1 and 1:2 systems followed the trend of lower activation energy values for systems with faster rates; however the 1:1 system did not fit this trend as it resulted in the highest activation energy value as well as the fastest reaction rates.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Cristina F. Stefanescu.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree" lang="en_US">S.B.</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="extent" lang="en_US">45 p.</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" lang="en_US">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">Exploration of catalysis activation emergency as a function of gold nanoparticle surface morphology</dim:field>
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   	&lt;Title>Exploration of catalysis activation emergency as a function of gold nanoparticle surface morphology&lt;/Title>
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   	&lt;PublicationDate>2008&lt;/PublicationDate>
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        	&lt;DisplayName>Stefanescu, Cristina F&lt;/DisplayName>
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    &lt;Keyword>Materials Science and Engineering.&lt;/Keyword>
   	&lt;Abstract>The application of rippled gold nanoparticles with bi-ligand surface morphology as a catalyst was tested. The hydrolysis of 2,4-dinitrophenyl acetate (DNPA) served as the catalytic reaction being analyzed and the bi-ligand composition used was 16-mercaptohexadecanoic acid to imidazole thiol (MHA to IT). The influence of temperature on catalytic reaction of DNPA with the MHA: IT system was tested for ligand rations of 2:1, 1:2, and 1:1 by monitoring the catalytic system on a UV-VIS spectrometer. Catalytic rate constants were obtained and found to increase with increased temperature. The measured catalytic rate constants were greatest overall for the 1:1 system, followed by the 1:2 system, and lastly the 2:1 system. The activation energy for each ligand-ratio system was measured and found to be 22.17 kJ/mol for the 2:1 system, 14.7 kJ/mol for the 1:2 system, and 26.52 for the 1:1 system. The 2:1 and 1:2 systems followed the trend of lower activation energy values for systems with faster rates; however the 1:1 system did not fit this trend as it resulted in the highest activation energy value as well as the fastest reaction rates.&lt;/Abstract>
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