Nonadiabatic transition path sampling

被引:4
|
作者
Sherman, M. C. [1 ]
Corcelli, S. A. [1 ]
机构
[1] Univ Notre Dame, Dept Chem & Biochem, Notre Dame, IN 46556 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2016年 / 145卷 / 03期
关键词
MOLECULAR-DYNAMICS SIMULATION; ELECTRON-TRANSFER REACTIONS; PROTON-TRANSFER; ISOMERIZATION DYNAMICS; CHEMICAL-REACTIONS; RATE CONSTANTS; STATE THEORY; MODEL; DECOHERENCE; MECHANICS;
D O I
10.1063/1.4959038
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Fewest-switches surface hopping (FSSH) is combined with transition path sampling (TPS) to produce a new method called nonadiabatic path sampling (NAPS). The NAPS method is validated on a model electron transfer system coupled to a Langevin bath. Numerically exact rate constants are computed using the reactive flux (RF) method over a broad range of solvent frictions that span from the energy diffusion (low friction) regime to the spatial diffusion (high friction) regime. The NAPS method is shown to quantitatively reproduce the RF benchmark rate constants over the full range of solvent friction. Integrating FSSH within the TPS framework expands the applicability of both approaches and creates a new method that will be helpful in determining detailed mechanisms for nonadiabatic reactions in the condensed-phase. Published by AIP Publishing.
引用
收藏
页数:8
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