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Quantum Coherence in Ultrafast Photo-driven Charge Separation


Coherent interactions are prevalent in numerous photodriven processes, ranging from photosynthetic energy transfer to superexchange-mediated electron transfer, resulting in numerous studies aimed towards identifying and understanding these interactions. A key motivator of this interest is the non-statistical scaling laws that result from coherently traversing multiple pathways due to quantum interference. To that end, we employed ultrafast transient absorption spectroscopy to measure electron transfer in two donor-acceptor molecular systems comprising a p-(9-anthryl)-N,N-dimethylaniline chromophore/electron donor and either one or two equivalent naphthalene-1,8:4,5-bis(dicarboximide) electron acceptors at both ambient and cryogenic temperatures. The two-acceptor compound shows a statistical factor of 2.1  0.2 rate enhancement at room temperature and a non-statistical factor of 2.6  0.2 rate enhancement at cryogenic temperatures, suggesting correlated interactions between the two acceptors with the donor and with the bath modes. Comparing the charge recombination rates indicates that the electron is delocalized over both acceptors at low temperature but localized on a single acceptor at room temperature. These results highlight the importance of shielding the system from bath fluctuations to preserve and ultimately exploit the coherent interactions.

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Publication details

The article was accepted on 08 Jan 2019 and first published on 08 Jan 2019

Article type: Paper
DOI: 10.1039/C8FD00218E
Citation: Faraday Discuss., 2019, Accepted Manuscript

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    Quantum Coherence in Ultrafast Photo-driven Charge Separation

    B. T. Phelan, J. Schultz, J. Zhang, G. Huang, R. M. Young and M. R. Wasielewski, Faraday Discuss., 2019, Accepted Manuscript , DOI: 10.1039/C8FD00218E

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