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SIAM International Conference on Data Mining

Development of Accelerated Quantum Chemical Molecular Dynamics Method for the Dynamics Calculations under the Electric Fields and Its Application

Momoji Kubo, Naoyuki Isoda, Katsumi Sasata, Hitoshi Kurokawa, Akira Endou, Akira Imamura, Akira Miyamoto

Published Oct 21, 2003• 0 citations
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The quantum rotor in external fields such as static electric, magnetic, and time-dependent fields is one of the most studied research problems due to its applicability in chemical physics, molecular dynamics, and many other related areas. The problem finds applications in quantum chaos and nonlinear dynamics as well. In this work, we present a Machine learning (ML) approach to model a one-dimensional quantum rotor in an external electric field. Our approach is to develop a surrogate model, keeping in mind the inherent smoothness of the eigenenergies of the dressed rotor and the directional parameters such as orientation, i.e., expectation value of cosϕ , and the alignment parameter ( 〈 cos 2 ϕ 〉 ) with the applied static field. The model we developed is very efficient, achieving microsecond-scale predictions with high accuracy. The model we developed is as follows: first, we train it on the basis of data generated from numerical calculations taking rotor-static field interaction into account and expanding the wavefunction as a finite basis. The model gives an excellent performance with R2 values exceeding 0.9999 for all predicted quantities. We further explore the physics of the system and the data generation, the details of the ML model, and its uses in designing an inverse model. The work shows that ML can be used to speed up computational time in related areas such as molecular physics and may be used to optimize the experimental parameters. This approach is directly extensible to three-dimensional rotors, time-dependent fields, and multi-parameter optimization, with potential applications in quantum control, molecular alignment, and spectroscopic fitting.
In the study of non-adiabatic chemical processes such as photocatalysis and photosynthesis, non-adiabatic molecular dynamics (NAMD) is an indispensable theoretical tool, which requires precise potential energy surfaces (PESs) of ground and excited states. Quantum computing offers promising potential for calculating PESs that are intractable for classical computers. However, its realistic application poses significant challenges to the development of quantum algorithms that are sufficiently general to enable efficient and precise PES calculations across chemical systems with diverse properties, as well as to seamlessly adapt existing NAMD theories to quantum computing. In this work, we introduce a quantum-adapted extension to the Landau-Zener-Surface-Hopping (LZSH) NAMD. This extension incorporates curvature-driven hopping corrections that protect the population evolution while maintaining the efficiency gained from avoiding the computation of non-adiabatic couplings (NACs), as well as preserving the trajectory independence that enables parallelization. Furthermore, to ensure the high-precision PESs required for surface hopping dynamics, we develop a sub-microhartree-accurate PES calculation protocol. This protocol supports active space selection, enables parallel acceleration either on quantum or classical clusters, and demonstrates adaptability to diverse chemical systems - including the charged H3+ ion and the C2H4 molecule, a prototypical multi-reference benchmark. This work paves the way for practical application of quantum computing in NAMD, showcasing the potential of parallel simulation on quantum-classical heterogeneous clusters for ab-initio computational chemistry.