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Machine learning accelerated photodynamics simulations
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OA
AI
DOI：10.1063/5.0159247.png)
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Abstract
En 中文
Machine learning (ML) continues to revolutionize computational chemistry for accelerating predictions and simulations by training on experimental or accurate but expensive quantum mechanical (QM) calculations. Photodynamics simulations require hundreds of trajectories coupled with multiconfigurational QM calculations of excited-state potential energies surfaces that contribute to the prohibitive computational cost at long timescales and complex organic molecules. ML accelerates photodynamics simulations by combining nonadiabatic photodynamics simulations with an ML model trained with high-fidelity QM calculations of energies, forces, and non-adiabatic couplings. This approach has provided time-dependent molecular structural information for understanding photochemical reaction mechanisms of organic reactions in vacuum and complex environments (i.e., explicit solvation). This review focuses on the fundamentals of QM calculations and ML techniques. We, then, discuss the strategies to balance adequate training data and the computational cost of generating these training data. Finally, we demonstrate the power of applying these ML-photodynamics simulations to understand the origin of reactivities and selectivities of organic photochemical reactions, such as cis-trans isomerization, [2+2]-cycloaddition, 4 pi-electrostatic ring-closing, and hydrogen roaming mechanism.
Keywords:
NONADIABATIC MOLECULAR-DYNAMICS
DENSITY-FUNCTIONAL THEORY
SELF-CONSISTENT-FIELD
PARTICLE RANDOM-PHASE
QUANTUM MECHANICS/MOLECULAR MECHANICS
2ND-ORDER PERTURBATION-THEORY
APPROXIMATE COUPLED-CLUSTER
(1)PI-SIGMA-ASTERISK STATES
CONICAL INTERSECTIONS
CLASSICAL DYNAMICS
Journal
IF:
6.2
Papers:
192
Citations:
717