计算机科学
势能面
量子
网格
卷积神经网络
离散化
深度学习
化学空间
滤波器(信号处理)
不变(物理)
水准点(测量)
量子动力学
可微函数
人工智能
理论计算机科学
统计物理学
分子
物理
量子力学
化学
数学
计算机视觉
几何学
地理
大地测量学
生物化学
数学分析
药物发现
作者
Kristof T. Schütt,Pieter-Jan Kindermans,Huziel E. Sauceda,Stefan Chmiela,Alexandre Tkatchenko,Klaus‐Robert Müller
出处
期刊:University of Luxembourg - Open Repository and Bibliography
[University of Luxembourg]
日期:2017-06-26
卷期号:30: 992-1002
被引量:464
标识
DOI:10.48550/arxiv.1706.08566
摘要
Deep learning has the potential to revolutionize quantum chemistry as it is ideally suited to learn representations for structured data and speed up the exploration of chemical space. While convolutional neural networks have proven to be the first choice for images, audio and video data, the atoms in molecules are not restricted to a grid. Instead, their precise locations contain essential physical information, that would get lost if discretized. Thus, we propose to use continuous-filter convolutional layers to be able to model local correlations without requiring the data to lie on a grid. We apply those layers in SchNet: a novel deep learning architecture modeling quantum interactions in molecules. We obtain a joint model for the total energy and interatomic forces that follows fundamental quantum-chemical principles. This includes rotationally invariant energy predictions and a smooth, differentiable potential energy surface. Our architecture achieves state-of-the-art performance for benchmarks of equilibrium molecules and molecular dynamics trajectories. Finally, we introduce a more challenging benchmark with chemical and structural variations that suggests the path for further work.
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