可转让性
密度泛函理论
电子密度
高斯分布
高斯过程
缩放比例
统计物理学
协方差
计算机科学
可扩展性
计算化学
人工智能
机器学习
化学
物理
电子
数学
量子力学
统计
几何学
罗伊特
数据库
作者
Alberto Fabrizio,Ksenia R. Briling,Andrea Grisafi,Clémence Corminbœuf
出处
期刊:Chimia
[Swiss Chemical Society]
日期:2020-04-25
卷期号:74 (4): 232-232
被引量:14
标识
DOI:10.2533/chimia.2020.232
摘要
Machine-learning in quantum chemistry is currently booming, with reported applications spanning all molecular properties from simple atomization energies to complex mathematical objects such as the many-body wavefunction. Due to its central role in density functional theory, the electron density is a particularly compelling target for non-linear regression. Nevertheless, the scalability and the transferability of the existing machine-learning models of ρ(r) are limited by its complex rotational symmetries. Recently, in collaboration with Ceriotti and coworkers, we combined an efficient electron density decomposition scheme with a local regression framework based on symmetry-adapted Gaussian process regression able to accurately describe the covariance of the electron density spherical tensor components. The learning exercise is performed on local environments, allowing high transferability and linear-scaling of the prediction with respect to the number of atoms. Here, we review the main characteristics of the model and show its predictive power in a series of applications. The scalability and transferability of the trained model are demonstrated through the prediction of the electron density of Ubiquitin.
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