<?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>2026-09-19T23:46:29Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/17733" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/17733</identifier><datestamp>2022-01-13T07:54:21Z</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">Moungi G. Bawendi.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Chung, Inhee, 1976-</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="other" lang="en_US">Massachusetts Institute of Technology. Dept. of Chemistry.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department">Massachusetts Institute of Technology. Department of Chemistry</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2005-06-02T18:26:13Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2005-06-02T18:26:13Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="copyright" lang="en_US">2004</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2004</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/1721.1/17733</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">56474021</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2004.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Vita.</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">This thesis focuses on uncovering the photophysics of CdSe semiconductor quantum dots (QDs) at the single QD level, and correlating the phenomenological behavior observed at the single QD level to that observed at the ensemble level. Understanding the photophysics of QDs can potentially allow the specific optical properties of QDs to be applied in various ways. For example, through the study of the emission polarization of single QDs a 2D transition polarization property was discovered at room temperature. This enables us to monitor the 3D orientational dynamics of a target system by rigidly attaching a single QD to the system. Semiconductor QDs offer many advantages over other chromophores in a variety of applications because of their relatively narrow emission line width, an absorption spectrum that is well suited for multiplexed fluorescence detection, and their optical stability. However, fluorescence blinking phenomena in single colloidal QDs have been largely regarded as a undesirable optical properties. We have began to understand the phenomenology of the fluorescence blinking through a study of the statistics that are embedded in the fluorescence intensity time traces of collection of QDs. We have developed a statistical description of fluorescence blinking of single QDs and connected the blinking statistics to the fluorescence time traces of a collection of QDs. This study has shown that the fluorescence behavior of a collection of QDs is ergodic and moreover that it contains all the statistical information observed at the single QD level.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Inhee Chung.</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">129 leaves</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="extent">4123126 bytes</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="extent">4122936 bytes</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="mimetype">application/pdf</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="mimetype">application/pdf</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">Chemistry.</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">Understanding and engineering the photophysics of single CdSe nanocrystals</dim:field>
   <dim:field mdschema="dc" element="type" lang="en_US">Thesis</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="mimetype">application/pdf</dim:field>
   <dim:field mdschema="dspace" element="entity" qualifier="type">Publication</dim:field>
   <dim:field mdschema="others" element="access-status">unknown</dim:field>
   <dim:field mdschema="others" element="access-status">unknown</dim:field>
   <dim:field mdschema="cerif" element="openaire" authority="" confidence="-1">&lt;Publication xmlns="https://www.openaire.eu/cerif-profile/1.1/" id="5d747987-1ee7-460d-ac74-26a6852cf91a">
	&lt;Type xmlns="https://www.openaire.eu/cerif-profile/vocab/COAR_Publication_Types">http://purl.org/coar/resource_type/c_1843&lt;/Type>
	&lt;Language>eng&lt;/Language>
   	&lt;Title>Understanding and engineering the photophysics of single CdSe nanocrystals&lt;/Title>
   	&lt;PublishedIn>
    	&lt;Publication>
      	&lt;/Publication>
   	&lt;/PublishedIn>
   	&lt;PublicationDate>2004&lt;/PublicationDate>
   	&lt;Authors>
      	&lt;Author>
        	&lt;DisplayName>Chung, Inhee, 1976-&lt;/DisplayName>
         	&lt;Affiliation>
         		&lt;OrgUnit>
         		&lt;/OrgUnit>
         	&lt;/Affiliation>
      	&lt;/Author>
	&lt;/Authors>
   	&lt;Editors>
	&lt;/Editors>
    &lt;Publishers>
        &lt;Publisher>
            &lt;DisplayName>Massachusetts Institute of Technology&lt;/DisplayName>
            &lt;OrgUnit />
        &lt;/Publisher>
    &lt;/Publishers>
    &lt;License>http://dspace.mit.edu/handle/1721.1/7582&lt;/License>
    &lt;Keyword>Chemistry.&lt;/Keyword>
   	&lt;Abstract>This thesis focuses on uncovering the photophysics of CdSe semiconductor quantum dots (QDs) at the single QD level, and correlating the phenomenological behavior observed at the single QD level to that observed at the ensemble level. Understanding the photophysics of QDs can potentially allow the specific optical properties of QDs to be applied in various ways. For example, through the study of the emission polarization of single QDs a 2D transition polarization property was discovered at room temperature. This enables us to monitor the 3D orientational dynamics of a target system by rigidly attaching a single QD to the system. Semiconductor QDs offer many advantages over other chromophores in a variety of applications because of their relatively narrow emission line width, an absorption spectrum that is well suited for multiplexed fluorescence detection, and their optical stability. However, fluorescence blinking phenomena in single colloidal QDs have been largely regarded as a undesirable optical properties. We have began to understand the phenomenology of the fluorescence blinking through a study of the statistics that are embedded in the fluorescence intensity time traces of collection of QDs. We have developed a statistical description of fluorescence blinking of single QDs and connected the blinking statistics to the fluorescence time traces of a collection of QDs. This study has shown that the fluorescence behavior of a collection of QDs is ergodic and moreover that it contains all the statistical information observed at the single QD level.&lt;/Abstract>
	&lt;Access xmlns="http://purl.org/coar/access_right" 
    >
    &lt;/Access>
&lt;/Publication>
</dim:field>
</dim:dim>
</metadata></record></GetRecord></OAI-PMH>