<?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>2026-09-20T02:19:44Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/101864" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/101864</identifier><datestamp>2026-06-17T14:47:41Z</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">W. Craig Carter, Yet-Ming Chiang, and John B. Vander Sande.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Ho, Bryan Y</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">2016-03-25T13:41:23Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2016-03-25T13:41:23Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="copyright" lang="en_US">2011</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2012</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/1721.1/101864</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">944029209</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis: Ph. D., Massachusetts Institute of Technology, Department of Materials Science and Engineering, February 2012.</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.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">A novel electrochemical energy storage device, the semi-solid flow cell (SSFC), has recently been demonstrated. The device features a complex fluid composite as its anode and cathode. Both electrodes incorporate particles of a lithium storage compound suspended in a carbon black electrolyte gel. This design of a mixed conductor gel host and electrochemically active filler allows for fluid electrodes to be pumped, from storage tanks, through reaction cells. The de-coupling of energy and power capacity in a high energy density device opens up new opportunities for low cost, high performance energy storage. This thesis explores the microstructure of these fluid composites and establishes links to macroscopic properties that determine the device's energy and power density, efficiency, and cycle life. The rapid agglomeration of colloidal carbon black aggregates leads to gelation by diffusion limited cluster aggregation. The low density, percolating network of carbon provides conduction paths for both ions and electrons. The gel's yield stress stably suspends density mismatched particles of lithium storage compounds, which can readily access the electrochemical reactants via the gel matrix. Application of shear reversibly destroys the gel network, allowing for flow. Flow-induced heterogeneities are also investigated and methods of maintaining macroscopic homogeneity are presented.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Bryan Y. Ho.</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">184 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">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">An experimental study on the structure-property relationship of composite fluid electrodes for use in high energy density semi-solid flow cells</dim:field>
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   	&lt;Title>An experimental study on the structure-property relationship of composite fluid electrodes for use in high energy density semi-solid flow cells&lt;/Title>
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   	&lt;PublicationDate>2012&lt;/PublicationDate>
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        	&lt;DisplayName>Ho, Bryan Y&lt;/DisplayName>
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            &lt;DisplayName>Massachusetts Institute of Technology&lt;/DisplayName>
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    &lt;Keyword>Materials Science and Engineering.&lt;/Keyword>
   	&lt;Abstract>A novel electrochemical energy storage device, the semi-solid flow cell (SSFC), has recently been demonstrated. The device features a complex fluid composite as its anode and cathode. Both electrodes incorporate particles of a lithium storage compound suspended in a carbon black electrolyte gel. This design of a mixed conductor gel host and electrochemically active filler allows for fluid electrodes to be pumped, from storage tanks, through reaction cells. The de-coupling of energy and power capacity in a high energy density device opens up new opportunities for low cost, high performance energy storage. This thesis explores the microstructure of these fluid composites and establishes links to macroscopic properties that determine the device&amp;apos;s energy and power density, efficiency, and cycle life. The rapid agglomeration of colloidal carbon black aggregates leads to gelation by diffusion limited cluster aggregation. The low density, percolating network of carbon provides conduction paths for both ions and electrons. The gel&amp;apos;s yield stress stably suspends density mismatched particles of lithium storage compounds, which can readily access the electrochemical reactants via the gel matrix. Application of shear reversibly destroys the gel network, allowing for flow. Flow-induced heterogeneities are also investigated and methods of maintaining macroscopic homogeneity are presented.&lt;/Abstract>
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