<?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>2026-09-19T11:39:20Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/117947" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/117947</identifier><datestamp>2026-06-17T14:45:04Z</datestamp><setSpec>com_1721.1_7582</setSpec><setSpec>com_1721.1_7581</setSpec><setSpec>col_1721.1_131022</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">Christopher A. Schuh.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Xing, Wenting, Ph. D. Massachusetts Institute of Technology</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="other" lang="en_US">Massachusetts Institute of Technology. Department 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">2018-09-17T15:51:08Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2018-09-17T15:51:08Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="copyright" lang="en_US">2018</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2018</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/1721.1/117947</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">1051237336</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis: Ph. D., Massachusetts Institute of Technology, Department of Materials Science and Engineering, 2018.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Cataloged from PDF version of thesis.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Includes bibliographical references (pages 129-135).</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">The development of stable nanocrystalline binary alloys, which possess a large volume fraction of grain boundaries at elevated temperatures, is a promising route to high yield strength materials. Previous studies have focused on alloying by selecting solute elements that segregate at grain boundaries to stabilize the nanostructure. A selection criterion has been established for designing stable binary nanocrystalline materials. This thesis explores the extension of this concept to the design of multicomponent nanostructured systems. In contrast to the simplicity of a binary system where not many topological possibilities are accessible, multicomponent nanostructured systems are shown to occupy a vast space where the large majority of interesting configurations will be missed by a regular solution approximation. This thesis describes research to develop a conceptual basis for the thermodynamic properties of multicomponent nanocrystalline alloys, and to design interesting ternary configurations not accessible in binary systems. The conditions necessary to achieve the desired nanostructure configurations are developed in a model that takes solute interactions into consideration. Based on the model, we performed a systematic case study on one alloy system expected to exhibit nanocrystalline stability: Pt-Pd-Au. As a control, two binary systems (Pt-Au, Pt-Pd) were produced for comparison. While a uniform distribution of Pd is observed in binary Pt-Pd alloys at 400 °C, the results from scanning transmission electron microscopy (STEM) reveal that Pd segregation behavior was induced by the Au grain boundary segregation in the ternary system at 400 °C. Our work on induced co-segregation behavior of Pt-Pd-Au alloy is just a simple example of solute interaction in nanocrystalline alloys. Our approach more generally presents a new design framework to control the complex configurations possible in nanocrystalline materials by alloying element selection.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Wenting Xing.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree" lang="en_US">Ph.D.</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="extent" lang="en_US">135 pages</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">MIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written 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">Design of stable nanostructure configurations in ternary alloys</dim:field>
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   	&lt;Title>Design of stable nanostructure configurations in ternary alloys&lt;/Title>
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   	&lt;PublicationDate>2018&lt;/PublicationDate>
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    &lt;Keyword>Materials Science and Engineering.&lt;/Keyword>
   	&lt;Abstract>The development of stable nanocrystalline binary alloys, which possess a large volume fraction of grain boundaries at elevated temperatures, is a promising route to high yield strength materials. Previous studies have focused on alloying by selecting solute elements that segregate at grain boundaries to stabilize the nanostructure. A selection criterion has been established for designing stable binary nanocrystalline materials. This thesis explores the extension of this concept to the design of multicomponent nanostructured systems. In contrast to the simplicity of a binary system where not many topological possibilities are accessible, multicomponent nanostructured systems are shown to occupy a vast space where the large majority of interesting configurations will be missed by a regular solution approximation. This thesis describes research to develop a conceptual basis for the thermodynamic properties of multicomponent nanocrystalline alloys, and to design interesting ternary configurations not accessible in binary systems. The conditions necessary to achieve the desired nanostructure configurations are developed in a model that takes solute interactions into consideration. Based on the model, we performed a systematic case study on one alloy system expected to exhibit nanocrystalline stability: Pt-Pd-Au. As a control, two binary systems (Pt-Au, Pt-Pd) were produced for comparison. While a uniform distribution of Pd is observed in binary Pt-Pd alloys at 400 °C, the results from scanning transmission electron microscopy (STEM) reveal that Pd segregation behavior was induced by the Au grain boundary segregation in the ternary system at 400 °C. Our work on induced co-segregation behavior of Pt-Pd-Au alloy is just a simple example of solute interaction in nanocrystalline alloys. Our approach more generally presents a new design framework to control the complex configurations possible in nanocrystalline materials by alloying element selection.&lt;/Abstract>
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