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• W2415567315 abstract "We present a state-space-based path integral method to calculate the rate of electron transfer (ET) in multi-state, multi-electron condensed-phase processes. We employ an exact path integral in discrete electronic states and continuous Cartesian nuclear variables to obtain a transition state theory (TST) estimate to the rate. A dynamic recrossing correction to the TST rate is then obtained from real-time dynamics simulations using mean field ring polymer molecular dynamics. We employ two different reaction coordinates in our simulations and show that, despite the use of mean field dynamics, the use of an accurate dividing surface to compute TST rates allows us to achieve remarkable agreement with Fermi's golden rule rates for nonadiabatic ET in the normal regime of Marcus theory. Further, we show that using a reaction coordinate based on electronic state populations allows us to capture the turnover in rates for ET in the Marcus inverted regime." @default.
• W2415567315 created "2016-06-24" @default.
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• W2415567315 date "2016-06-04" @default.
• W2415567315 modified "2023-09-27" @default.
• W2415567315 title "State Space Path Integrals for Electronically Nonadiabatic Reaction Rates" @default.
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• W2415567315 hasPublicationYear "2016" @default.
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