期刊
JOURNAL OF PHYSICAL CHEMISTRY LETTERS
卷 9, 期 17, 页码 4848-4851出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.8b02032
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资金
- Academy of Finland [290677, 289947]
- Academy of Finland (AKA) [289947, 290677, 290677, 289947] Funding Source: Academy of Finland (AKA)
When photoactive molecules interact strongly with confined light modes, new hybrid light matter states may form: the polaritons. These polaritons are coherent superpositions of excitations of the molecules and of the cavity photon. Recently, polaritons were shown to mediate energy transfer between chromophores at distances beyond the Forster limit. Here we explore the potential of strong coupling for light-harvesting applications by means of atomistic molecular dynamics simulations of mixtures of photoreactive and non-photo-reactive molecules strongly coupled to a single confined light mode. These molecules are spatially separated and present at different concentrations. Our simulations suggest that while the excitation is initially fully delocalized over all molecules and the confined light mode, it very rapidly localizes onto one of the photoreactive molecules, which then undergoes the reaction.
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