The Nature of Quantum States Created by One Photon Absorption: Pulsed Coherent vs. Pulsed Incoherent Light
arXiv:1211.5794 · doi:10.1021/jp4023986
Abstract
We analyze electronically excited nuclear wave functions and their coherence when subjecting a molecule to the action of natural, pulsed incoherent solar-like light, and to that of ultrashort coherent light assumed to have the same center frequencies and spectral bandwidths. Specifically, we compute the spatio-temporal dependence of the excited wave packets and their electronic coherence for these two types of light sources, on different electronic potential energy surfaces. The resultant excited state wave functions are shown to be qualitatively different, reflecting the light source from which they originated. In addition, electronic coherence is found to decay significantly faster for incoherent light than for coherent ultrafast excitation, for both continuum and bound wave packets. These results confirm that the dynamics observed in studies using ultrashort coherent pulses are not relevant to naturally occurring solar-induced processes such as photosynthesis and vision.
7 pages, 3 figures
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Cited by in corpus (8)
- Single-photon absorption by single photosynthetic light-harvesting complexes
- Long-range coherent energy transport in Photosystem II
- Open System Perspective on Incoherent Excitation of Light Harvesting Systems
- Dynamic Coherence in Excitonic Molecular Complexes under Various Excitation Conditions
- Transform-Limited-Pulse Representation of Excitation with Natural Incoherent Light
- Transient Quantum Coherent Response to a Partially Coherent Radiation Field
- Coherent quantum dynamics launched by incoherent relaxation in a quantum circuit simulator of a light-harvesting complex
- Photochemical dynamics under incoherent illumination: light harvesting in self-assembled molecular J-aggregates