Abstract
We show herein that photoinduced charge transfer from CdSe quantum dots (QDs) to surface-bound methyl viologen (MV2+) acceptors is mediated by a vibronically coherent, nonadiabatic mechanism. Broadband multidimensional electronic spectra and an analysis of coherences show that a mixed QD–MV charge-transfer (CT) state is populated on the <50 fs time scale after optical preparation of the X3 (1P3/2–1Pe) state, well prior to the appearance of the one-electron photoreduced ground state (MV+•). A partial redistribution of charge from the core of the QD to the acceptor is revealed by excited-state coherences of an out-of-plane vibrational mode local to MV2+ and of a low-frequency mode mixing a MV2+ mode with the longitudinal optical (LO) phonon of the QD core. The ultrafast damping of these coherences indicates that excited-state wavepackets travel from the optically prepared, Franck–Condon structure through a conical intersection to reach the CT state. These results suggest that vibronically coherent processes generating CT intermediates can be exploited to improve the efficiency of QD-based solar cells and photocatalysts.
| Original language | English |
|---|---|
| Pages (from-to) | 6580-6588 |
| Number of pages | 9 |
| Journal | Journal of Physical Chemistry C |
| Volume | 130 |
| Issue number | 18 |
| DOIs | |
| State | Published - May 7 2026 |
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