Abstract
We present a rare event sampling scheme applicable to coupled electronic excited states. In particular, we extend the forward flux sampling (FFS) method for rare event sampling to a nonadiabatic version (NAFFS) that uses the trajectory surface hopping (TSH) method for nonadiabatic dynamics. NAFFS is applied to two dynamically relevant excited-state models that feature an avoided crossing and a conical intersection with tunable parameters. We investigate how nonadiabatic couplings, temperature, and reaction barriers affect transition rate constants in regimes that cannot be otherwise obtained with plain, traditional TSH. The comparison with reference brute-force TSH simulations for limiting cases of rareness shows that NAFFS can be several orders of magnitude cheaper than conventional TSH and thus represents a conceptually novel tool to extend excited-state dynamics to time scales that are able to capture rare nonadiabatic events.
| Original language | English |
|---|---|
| Pages (from-to) | 1657–1671 |
| Number of pages | 15 |
| Journal | Journal of Chemical Theory and Computation |
| Volume | 19 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - 28 Mar 2023 |
Funding
The authors thank the University of Vienna for continuous support, in particular that provided in the framework of the research platform ViRAPID. M.X.T. and L.G. appreciate additional support provided by the Austrian Science Fund, W 1232 (MolTag). The computational results presented have been achieved (in part) using the Vienna Scientific Cluster (VSC). The authors thank the SHARC development team and the ViRAPID members for insightful discussions. We thank Barbara Wagner for her contributions to some NAFFS calculations.
Austrian Fields of Science 2012
- 103006 Chemical physics
- 104022 Theoretical chemistry
- 102009 Computer simulation
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