Related Experiment Video
Updated: May 14, 2026

Resonance Fluorescence of an InGaAs Quantum Dot in a Planar Cavity Using Orthogonal Excitation and Detection
Published on: October 13, 2017
Photoinduced Charge Transfer and Vibronic Coherence in CdSe Quantum Dots with Methyl Viologen Acceptors
Nila Mohan T M1, Shanu A Shameem1, Chase H Leslie1
1Department of Chemistry, Michigan State University, 578 S. Shaw Lane, East Lansing, Michigan 48824 United States.
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.
Related Concept Videos
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
UV–Vis Spectroscopy: Molecular Electronic Transitions
UV–Vis Spectroscopy of Conjugated Systems
One of the factors influencing λmax is the extent of conjugation in the...
Molecular Spectroscopy: Absorption and Emission
π Electron Effects on Chemical Shift: Overview
Thermal and Photochemical Electrocyclic Reactions: Overview

