Vibronic Excitons and Conical Intersections in Semiconductor Quantum Dots
Surface defects and organic surface-capping ligands affect the photoluminescence properties of semiconductor quantum dots (QDs) by altering the rates of competing nonradiative relaxation processes. In this study, broadband two-dimensional electronic spectroscopy reveals that absorption of light by Q...
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Published in | The journal of physical chemistry letters Vol. 12; no. 39 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Chemical Society
30.09.2021
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Subjects | |
Online Access | Get full text |
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Summary: | Surface defects and organic surface-capping ligands affect the photoluminescence properties of semiconductor quantum dots (QDs) by altering the rates of competing nonradiative relaxation processes. In this study, broadband two-dimensional electronic spectroscopy reveals that absorption of light by QDs prepares vibronic excitons, excited states derived from quantum coherent mixing of the core electronic and ligand vibrational states. Rapidly damped coherent wavepacket motions of the ligands are observed during hot-carrier cooling, with vibronic coherence transferred to the photoluminescent state. These findings suggest a many-electron, molecular theory for the electronic structure of QDs, which is supported by calculations of the structures of conical intersections between the exciton potential surfaces of a small ammonia-passivated model CdSe nanoparticle. |
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Bibliography: | SC0021197; SC0010847; ACI-1548562 USDOE Office of Science (SC), Basic Energy Sciences (BES) National Science Foundation (NSF) |
ISSN: | 1948-7185 1948-7185 |