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Ultrafast dynamics in spatially confined photoisomerization: accelerated simulations through machine learning models.
- Source :
-
Physical chemistry chemical physics : PCCP [Phys Chem Chem Phys] 2024 Oct 17; Vol. 26 (40), pp. 25994-26003. Date of Electronic Publication: 2024 Oct 17. - Publication Year :
- 2024
-
Abstract
- This study sheds light on the exploration of photoresponsive host-guest systems, highlighting the intricate interplay between confined spaces and photosensitive guest molecules. Conducting nonadiabatic molecular dynamics (NAMD) simulations based on electronic structure calculations for such large systems remains a formidable challenge. By leveraging machine learning (ML) as an accelerator for NAMD simulations, we analytically constructed excited-state potential energy surfaces along relevant collective variables to investigate photoisomerization processes efficiently. Combining the quantum mechanics/molecular mechanics (QM/MM) methodology with ML-based NAMD simulations, we elucidated the reaction pathways and identified the key degrees of freedom as reaction coordinates leading to conical intersections. A machine learning-based nonadiabatic dynamics model has been developed to compare the excited-state dynamics of the guest molecule, benzopyran, in both the gas phase and its behavior within the confined space of cucurbit[5]uril. This comparative analysis was designed to determine the influence of the environment on the photoisomerization rate of the guest molecule. The results underscore the effectiveness of ML models in simulating trajectory evolution in a cost-effective manner. This research offers a practical approach to accelerate NAMD simulations in large-scale systems of photochemical reactions, with potential applications in other host-guest complex systems.
Details
- Language :
- English
- ISSN :
- 1463-9084
- Volume :
- 26
- Issue :
- 40
- Database :
- MEDLINE
- Journal :
- Physical chemistry chemical physics : PCCP
- Publication Type :
- Academic Journal
- Accession number :
- 39370956
- Full Text :
- https://doi.org/10.1039/d4cp01497a