用机器学习预测单粒子密度矩阵

IF 5.5 1区 化学 Q2 CHEMISTRY, PHYSICAL
S. Hazra, U. Patil and S. Sanvito*, 
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引用次数: 0

摘要

哈特里-福克(Hartree-Fock)密度泛函理论和科恩-沙姆(Kohn-Sham)密度泛函理论是两种应用最广泛的电子结构理论方法,它们都需要迭代求解一组类似薛定谔的方程。这一过程的收敛速度取决于所研究系统的复杂程度、所采用的自洽场算法以及对密度矩阵的初始猜测。如果初始密度矩阵接近基态矩阵,就能有效地省去许多实现收敛所需的自洽步骤。在这里,我们通过构建一个只使用原子位置信息的神经网络来预测 Kohn-Sham 密度泛函理论的密度矩阵。这种神经网络提供的密度矩阵初始猜测远优于其他任何可用的方法。此外,这种神经网络密度矩阵的质量足以评估原子间作用力。这使我们能够运行加速的自洽分子动力学,几乎不需要自洽步骤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Predicting the One-Particle Density Matrix with Machine Learning

Predicting the One-Particle Density Matrix with Machine Learning

Predicting the One-Particle Density Matrix with Machine Learning

Two of the most widely used electronic-structure theory methods, namely, Hartree–Fock and Kohn–Sham density functional theory, require the iterative solution of a set of Schrödinger-like equations. The speed of convergence of such a process depends on the complexity of the system under investigation, the self-consistent-field algorithm employed, and the initial guess for the density matrix. An initial density matrix close to the ground-state matrix will effectively allow one to cut out many of the self-consistent steps necessary to achieve convergence. Here, we predict the density matrix of Kohn–Sham density functional theory by constructing a neural network that uses only the atomic positions as information. Such a neural network provides an initial guess for the density matrix far superior to that of any other recipes available. Furthermore, the quality of such a neural-network density matrix is good enough for the evaluation of interatomic forces. This allows us to run accelerated ab initio molecular dynamics with little to no self-consistent steps.

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来源期刊
Journal of Chemical Theory and Computation
Journal of Chemical Theory and Computation 化学-物理:原子、分子和化学物理
CiteScore
9.90
自引率
16.40%
发文量
568
审稿时长
1 months
期刊介绍: The Journal of Chemical Theory and Computation invites new and original contributions with the understanding that, if accepted, they will not be published elsewhere. Papers reporting new theories, methodology, and/or important applications in quantum electronic structure, molecular dynamics, and statistical mechanics are appropriate for submission to this Journal. Specific topics include advances in or applications of ab initio quantum mechanics, density functional theory, design and properties of new materials, surface science, Monte Carlo simulations, solvation models, QM/MM calculations, biomolecular structure prediction, and molecular dynamics in the broadest sense including gas-phase dynamics, ab initio dynamics, biomolecular dynamics, and protein folding. The Journal does not consider papers that are straightforward applications of known methods including DFT and molecular dynamics. The Journal favors submissions that include advances in theory or methodology with applications to compelling problems.
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