<?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>2026-09-21T12:49:29Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/127901" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/127901</identifier><datestamp>2026-06-16T18:52:12Z</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">Silvija Gradečak and Jing Kong.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Ke, Jian-An.</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" lang="en_US">Massachusetts Institute of Technology. Department of Materials Science and Engineering</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2020-10-08T21:29:31Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2020-10-08T21:29:31Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="copyright" lang="en_US">2020</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2020</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">https://hdl.handle.net/1721.1/127901</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">1197627222</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis: Ph. D., Massachusetts Institute of Technology, Department of Materials Science and Engineering, May, 2020</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Cataloged from the official PDF of thesis.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Includes bibliographical references (pages 114-129).</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">Two-dimensional (2D) transition metal dichalcogenides (TMDs) with engineered nanopores have been suggested as a promising materials system in membrane and catalysis applications in both the energy and environment fields. Because of its atomic thinness, 2DTMDs are promising candidates for osmosis energy harvesting membranes. Furthermore, the scalable nanopore preparation in MoS₂ crystals provides a more cost-efficient option replacing precious metal-based catalyst for hydrogen evolution reactions catalysis. As an emerging class of semiconductor materials, 2D-TMDs have also attracted attention in electronic and optoelectronic applications, which require lithography processes to define the desired device structure. However, conventional top-down patterning methods rely on temporarily coating a polymer-based resist, which has been found challenging to remove completely and as such is detrimental to 2D devices.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">Development of a resist-free, guided growth of TMDs is therefore desirable. We demonstrate the guided MoS₂ nanopore formation by engineering structural defects prior to the oxidative annealing process as a scalable and parallel process susceptible to large-scale applications. This process is based on our observation that the nanopore distribution is dramatically different in strained and unstrained MoS₂ crystals, which indicates that nanopore formation reflects distribution of the underlaying structural defects that act as nanopore nucleation sites. Our experimental observations indicate that dislocations in MoS₂ play a role in preferential nanopore nucleation. We further explore guided defect introduction by exposing MoS₂ crystals with electron and laser beams. By varying electron beam exposure dose prior to annealing MoS₂ in air, the nanopore formation density can be controlled.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">Laser beam exposure, as another beam-based treatment, is also observed to locally enhance the etching of mechanically exfoliated WS₂ under regular wet transferring protocol. Finally, we explored the guided growth on a laser exposed WS₂ template and on electron beam exposed dielectric substrates. We show that MoS₂ preferentially nucleates at laser exposed exfoliated WS₂ crystals, forming WS₂-MoS₂ heterostructure. We then further demonstrate that the MoS₂ growth can be guided to the customized pattern prepared by electron beam exposure on bare SiO₂ substrates. This thesis provides insights into the role of defects during nanopore formation, and new process approaches for guided TMD etching and growth, which serve as a concept generally applicable to other 2D materials systems.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Jian-An Ke.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree" lang="en_US">Ph.D.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="collection" lang="en_US">Ph.D. Massachusetts Institute of Technology, Department of Materials Science and Engineering</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="extent" lang="en_US">129 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 may be protected by copyright. Please reuse MIT thesis content according to the MIT Libraries Permissions Policy, which is available through the URL provided.</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">Guided etching and deposition of transition metal dichalcogenides</dim:field>
   <dim:field mdschema="dc" element="type" lang="en_US">Thesis</dim:field>
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   <dim:field mdschema="dspace" element="imported" lang="en_US">2020-10-08T21:29:30Z</dim:field>
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   <dim:field mdschema="mit" element="thesis" qualifier="degree" lang="en_US">Doctoral</dim:field>
   <dim:field mdschema="mit" element="thesis" qualifier="department" lang="en_US">MatSci</dim:field>
   <dim:field mdschema="others" element="access-status">unknown</dim:field>
   <dim:field mdschema="others" element="access-status">unknown</dim:field>
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   	&lt;Title>Guided etching and deposition of transition metal dichalcogenides&lt;/Title>
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   	&lt;PublicationDate>2020&lt;/PublicationDate>
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        	&lt;DisplayName>Ke, Jian-An.&lt;/DisplayName>
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    &lt;Keyword>Materials Science and Engineering.&lt;/Keyword>
   	&lt;Abstract>Two-dimensional (2D) transition metal dichalcogenides (TMDs) with engineered nanopores have been suggested as a promising materials system in membrane and catalysis applications in both the energy and environment fields. Because of its atomic thinness, 2DTMDs are promising candidates for osmosis energy harvesting membranes. Furthermore, the scalable nanopore preparation in MoS₂ crystals provides a more cost-efficient option replacing precious metal-based catalyst for hydrogen evolution reactions catalysis. As an emerging class of semiconductor materials, 2D-TMDs have also attracted attention in electronic and optoelectronic applications, which require lithography processes to define the desired device structure. However, conventional top-down patterning methods rely on temporarily coating a polymer-based resist, which has been found challenging to remove completely and as such is detrimental to 2D devices.&lt;/Abstract>
   	&lt;Abstract>Development of a resist-free, guided growth of TMDs is therefore desirable. We demonstrate the guided MoS₂ nanopore formation by engineering structural defects prior to the oxidative annealing process as a scalable and parallel process susceptible to large-scale applications. This process is based on our observation that the nanopore distribution is dramatically different in strained and unstrained MoS₂ crystals, which indicates that nanopore formation reflects distribution of the underlaying structural defects that act as nanopore nucleation sites. Our experimental observations indicate that dislocations in MoS₂ play a role in preferential nanopore nucleation. We further explore guided defect introduction by exposing MoS₂ crystals with electron and laser beams. By varying electron beam exposure dose prior to annealing MoS₂ in air, the nanopore formation density can be controlled.&lt;/Abstract>
   	&lt;Abstract>Laser beam exposure, as another beam-based treatment, is also observed to locally enhance the etching of mechanically exfoliated WS₂ under regular wet transferring protocol. Finally, we explored the guided growth on a laser exposed WS₂ template and on electron beam exposed dielectric substrates. We show that MoS₂ preferentially nucleates at laser exposed exfoliated WS₂ crystals, forming WS₂-MoS₂ heterostructure. We then further demonstrate that the MoS₂ growth can be guided to the customized pattern prepared by electron beam exposure on bare SiO₂ substrates. This thesis provides insights into the role of defects during nanopore formation, and new process approaches for guided TMD etching and growth, which serve as a concept generally applicable to other 2D materials systems.&lt;/Abstract>
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