材料科学
共价键
共价有机骨架
人工神经网络
原子间势
标杆管理
分子动力学
单体
化学物理
工作(物理)
纳米技术
集合(抽象数据类型)
航程(航空)
可扩展性
统计物理学
计算机科学
高保真
生物系统
多孔性
多孔介质
声子
分子
冷凝
忠诚
深度学习
可转让性
作者
Yunrui Yan,Somayeh Faraji,M Liu
标识
DOI:10.1021/acs.chemmater.6c00169
摘要
Covalent organic frameworks (COFs) are promising porous materials for a wide range of applications; however, first-principles simulations of COFs remain challenging due to their large unit cells compared with inorganic materials. Here, we present a machine learning interatomic potential (MLIP), named “COF-NN”, specifically developed for two-dimensional COFs composed of carbon, hydrogen, oxygen, and nitrogen. By combining a molecular-cluster training strategy, constructed from COF-relevant monomer condensation chemistry, with active learning and uncertainty quantification, this artificial neural network-based MLIP achieves both high efficiency and robust performance across a set of structurally diverse 2D COFs while retaining near–DFT accuracy. Benchmarking results show that COF-NN accurately reproduces equilibrium structures, elastic constants, and phonon frequencies, with performance comparable to that of two state-of-the-art universal MLIPs. Beyond COFs, our cluster-based active learning framework provides a general strategy for constructing interatomic potentials that transfer local chemical environments learned from molecular clusters to periodic, complex, low-symmetry porous materials. We believe this work enables scalable atomistic simulations and high-throughput discovery of COF materials with predictive fidelity that was previously inaccessible.
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