{"id":{"repo_id":"mit","oai_identifier":"oai:dspace.mit.edu:1721.1/58454"},"canonical_url":"https://search.dev.ndltd.org/etd/mit/oai:dspace.mit.edu:1721.1/58454","repository":{"repo_id":"mit","name":"MIT","base_url":"https://dspace.mit.edu/oai/request"},"display":{"title":"Electrical excitation of colloidally synthesized quantum dots in metal oxide structures","abstract":"This thesis develops methods for integrating colloidally synthesized quantum dots (QDs) and metal oxides in optoelectronic devices, presents three distinct light emitting devices (LEDs) with metal oxides surrounding a QD active layer, and uses these novel metal oxide based QD-LEDs to study mechanisms for electrical excitation of QDs. QD-LEDs have generated considerable interest for applications such as thin film displays with improved color saturation and white lighting with high color rendering index. This work demonstrates that air-stable metal oxides can be used to achieve QD-LEDs that have long shelf lives and operate at constant luminance in ambient conditions, unpackaged. Because metal oxides range from conductors to dielectrics, they can be used to develop a variety of different device architectures to explore mechanisms for electrical excitation of QDs. We report the first all-inorganic QD-LEDs with n- and p-type metal oxide charge transport layers and present design rules to enable systematic improvement of device efficiency. To shift away from direct charge injection as a means for electroluminescence (EL) in inorganic-based QD-LED structures, we develop a unipolar device architecture that presents the first evidence of field driven EL in QDs. To further explore this field driven excitation mechanism, we develop a structure that situates QDs between two insulating metal oxide layers. By eliminating the need for energy band alignment, these devices enable EL from QDs with emission peaks from 450 nm-1500 nm as well as from novel nanoparticles, such as phosphor doped-core/shell nanocrystals.","abstract_html":"This thesis develops methods for integrating colloidally synthesized quantum dots (QDs) and metal oxides in optoelectronic devices, presents three distinct light emitting devices (LEDs) with metal oxides surrounding a QD active layer, and uses these novel metal oxide based QD-LEDs to study mechanisms for electrical excitation of QDs. QD-LEDs have generated considerable interest for applications such as thin film displays with improved color saturation and white lighting with high color rendering index. This work demonstrates that air-stable metal oxides can be used to achieve QD-LEDs that have long shelf lives and operate at constant luminance in ambient conditions, unpackaged. Because metal oxides range from conductors to dielectrics, they can be used to develop a variety of different device architectures to explore mechanisms for electrical excitation of QDs. We report the first all-inorganic QD-LEDs with n- and p-type metal oxide charge transport layers and present design rules to enable systematic improvement of device efficiency. To shift away from direct charge injection as a means for electroluminescence (EL) in inorganic-based QD-LED structures, we develop a unipolar device architecture that presents the first evidence of field driven EL in QDs. To further explore this field driven excitation mechanism, we develop a structure that situates QDs between two insulating metal oxide layers. By eliminating the need for energy band alignment, these devices enable EL from QDs with emission peaks from 450 nm-1500 nm as well as from novel nanoparticles, such as phosphor doped-core/shell nanocrystals.","abstract_has_math":false,"creators":["Wood, Vanessa Claire"],"institution":"Massachusetts Institute of Technology","degree_name":null,"degree_level":null,"degree_discipline":null,"degree_department":"Massachusetts Institute of Technology. Dept. of Electrical Engineering and Computer Science.","school":null,"contributors":[],"advisors":["Vladimir Bulović."],"committee_chairs":[],"committee_members":[],"year":2010,"date_issued":"2010","date_published":"2010","updated_at":"2026-07-22T22:22:32Z","subjects":["Electrical Engineering and Computer Science."],"languages":["eng"],"rights":["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. 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Because metal oxides range from conductors to dielectrics, they can be used to develop a variety of different device architectures to explore mechanisms for electrical excitation of QDs. We report the first all-inorganic QD-LEDs with n- and p-type metal oxide charge transport layers and present design rules to enable systematic improvement of device efficiency. To shift away from direct charge injection as a means for electroluminescence (EL) in inorganic-based QD-LED structures, we develop a unipolar device architecture that presents the first evidence of field driven EL in QDs. To further explore this field driven excitation mechanism, we develop a structure that situates QDs between two insulating metal oxide layers. By eliminating the need for energy band alignment, these devices enable EL from QDs with emission peaks from 450 nm-1500 nm as well as from novel nanoparticles, such as phosphor doped-core/shell nanocrystals."]},{"key":"dc:description.degree","label":"Dc Description Degree","values":["Ph.D."]},{"key":"dc:title","label":"Title","values":["Electrical excitation of colloidally synthesized quantum dots in metal oxide structures"]}]}],"canonical_facts":{"dc:contributor.advisor":["Vladimir Bulović."],"dc:contributor.department":["Massachusetts Institute of Technology. Dept. of Electrical Engineering and Computer Science."],"dc:contributor.other":["Massachusetts Institute of Technology. Dept. of Electrical Engineering and Computer Science."],"dc:creator":["Wood, Vanessa Claire"],"dc:date.accessioned":["2010-09-03T18:55:10Z"],"dc:date.available":["2010-09-03T18:55:10Z"],"dc:date.issued":["2010"],"dc:description":["Thesis (Ph. 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Because metal oxides range from conductors to dielectrics, they can be used to develop a variety of different device architectures to explore mechanisms for electrical excitation of QDs. We report the first all-inorganic QD-LEDs with n- and p-type metal oxide charge transport layers and present design rules to enable systematic improvement of device efficiency. To shift away from direct charge injection as a means for electroluminescence (EL) in inorganic-based QD-LED structures, we develop a unipolar device architecture that presents the first evidence of field driven EL in QDs. To further explore this field driven excitation mechanism, we develop a structure that situates QDs between two insulating metal oxide layers. 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