<?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>2026-09-20T09:06:46Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/122872" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/122872</identifier><datestamp>2026-06-16T18:54:37Z</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">Marc A. Baldo and Vladimir Bulović.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Wu, Mengfei,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 Electrical Engineering and Computer Science.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department" lang="en_US">Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2019-11-12T17:40:38Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2019-11-12T17:40:38Z</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">https://hdl.handle.net/1721.1/122872</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">1126650718</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis: Ph. D., Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science, 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 152-163).</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">Photon upconversion is a process where two or more low-energy photons are converted into a single higher-energy photon. Upconversion that turns infrared photons into visible ones is particularly useful, having potential applications in photovoltaics, infrared sensing, and biological imaging. In this thesis, I present a solid-state thin-film device that converts infrared photons with wavelength up to 1.1 [mu]m into visible wavelengths around [lambda] = 610 nm. The device consists of a monolayer of lead sulfide colloidal nanocrystals (NCs) and a thin film of rubrene mixed with emissive DBP molecules. Upconversion is realized via triplet-triplet annihilation (TTA) in rubrene sensitized by the NCs. We demonstrate that compared to the previous all-molecular upconverting systems, the use of inorganic NCs helps extend the excitation wavelength into the infrared and offers simple wavelength tunability.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">However, a monolayer of NCs has low infrared absorption, severely limiting the upconversion efficiency and necessitating a high excitation intensity. Here, by adding a silver back reflector with an optical spacer to the device structure, we achieve a five-fold increase in the NC absorption due to optical interference effects and an eleven-fold enhancement in the up-converted output. To extend the idea, we further introduce a distributed Bragg reflector at the front of the device. A resonant microcavity is formed with the NCs placed at the peak of a drastically enhanced optical field. The upconversion efficiency is improved by another order of magnitude, with threshold excitation intensity falling to 13 mW/cm² , which is below the available solar flux. At resonance, the device converts (0.06±0.01)% of incident photons at [lambda] = 980 nm into emitted higher-energy photons. In addition, we improve the upconversion efficiency by shortening the surface ligands on NCs.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">With faster triplet transfer, the upconverting device attains higher intrinsic efficiency, converting (7±l)% of the absorbed photons at [lambda] = 808 nm into higher-energy emissive excitons in rubrene. This thesis demonstrates the feasibility of NC-sensitized infrared-to-visible upconversion in solid thin films under low excitation intensities comparable to the solar flux, and paves the way toward the practical utilization of TTA-based upconversion in photovoltaics, imaging, and sensing technologies.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Mengfei Wu.</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 Electrical Engineering and Computer Science</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="extent" lang="en_US">163 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">Electrical Engineering and Computer Science.</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">Infrared-to-visible upconversion in hybrid thin films of colloidal nanocrystals and organic molecules</dim:field>
   <dim:field mdschema="dc" element="type" lang="en_US">Thesis</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">EECS</dim:field>
   <dim:field mdschema="others" element="access-status">unknown</dim:field>
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   	&lt;Title>Infrared-to-visible upconversion in hybrid thin films of colloidal nanocrystals and organic molecules&lt;/Title>
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   	&lt;PublicationDate>2018&lt;/PublicationDate>
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        	&lt;DisplayName>Wu, Mengfei,Ph.D.Massachusetts Institute of Technology.&lt;/DisplayName>
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    &lt;Keyword>Electrical Engineering and Computer Science.&lt;/Keyword>
   	&lt;Abstract>Photon upconversion is a process where two or more low-energy photons are converted into a single higher-energy photon. Upconversion that turns infrared photons into visible ones is particularly useful, having potential applications in photovoltaics, infrared sensing, and biological imaging. In this thesis, I present a solid-state thin-film device that converts infrared photons with wavelength up to 1.1 [mu]m into visible wavelengths around [lambda] = 610 nm. The device consists of a monolayer of lead sulfide colloidal nanocrystals (NCs) and a thin film of rubrene mixed with emissive DBP molecules. Upconversion is realized via triplet-triplet annihilation (TTA) in rubrene sensitized by the NCs. We demonstrate that compared to the previous all-molecular upconverting systems, the use of inorganic NCs helps extend the excitation wavelength into the infrared and offers simple wavelength tunability.&lt;/Abstract>
   	&lt;Abstract>However, a monolayer of NCs has low infrared absorption, severely limiting the upconversion efficiency and necessitating a high excitation intensity. Here, by adding a silver back reflector with an optical spacer to the device structure, we achieve a five-fold increase in the NC absorption due to optical interference effects and an eleven-fold enhancement in the up-converted output. To extend the idea, we further introduce a distributed Bragg reflector at the front of the device. A resonant microcavity is formed with the NCs placed at the peak of a drastically enhanced optical field. The upconversion efficiency is improved by another order of magnitude, with threshold excitation intensity falling to 13 mW/cm² , which is below the available solar flux. At resonance, the device converts (0.06±0.01)% of incident photons at [lambda] = 980 nm into emitted higher-energy photons. In addition, we improve the upconversion efficiency by shortening the surface ligands on NCs.&lt;/Abstract>
   	&lt;Abstract>With faster triplet transfer, the upconverting device attains higher intrinsic efficiency, converting (7±l)% of the absorbed photons at [lambda] = 808 nm into higher-energy emissive excitons in rubrene. This thesis demonstrates the feasibility of NC-sensitized infrared-to-visible upconversion in solid thin films under low excitation intensities comparable to the solar flux, and paves the way toward the practical utilization of TTA-based upconversion in photovoltaics, imaging, and sensing technologies.&lt;/Abstract>
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