Convolutional Kernel-Embedded E (3)-Equivariant Networks (KEN): Overcoming Architectural Rigidity in Machine Learning Interatomic Potentials

IF 5.8 1区 化学 Q2 CHEMISTRY, PHYSICAL
Jha Gautam
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引用次数: 0

Abstract

Abstract Machine learning interatomic potentials (MLIPs) have emerged as scalable alternatives to first-principles methods such as density functional theory (DFT). Among them, E(3)-equivariant graph neural networks (GNNs) like PACE and MACE are highly accurate but structurally rigid, limiting the incorporation of rich, multichannel electronic descriptors. We introduce convolutional kernel-embedded E(3)-equivariant networks (KEN), a hybrid architecture that combines the local environmental extraction of 2D convolutional kernels with the many-body expressivity of an E(3)-equivariant GNN backbone. This design preserves symmetry while enabling flexible, multimodal input features without increasing training data requirements. Trained and tested on heavy element 26 (HE26) dataset, KEN was compared with MACE-osaka26 model. Further validation on lattice parameter prediction through Birch–Murnaghan equation of state, magnetic moment prediction, and comparison with CHGNet framework, and microcanonical molecular dynamics confirms robust energy conservation and accurate reproduction of the forces, and thus, demonstrates a viable pathway to overcoming architectural rigidity in state-of-the-art MLIPs.
卷积核嵌入E(3)-等变网络(KEN):克服机器学习中的架构刚性
机器学习原子间势(MLIPs)已经成为密度泛函理论(DFT)等第一性原理方法的可扩展替代品。其中,像PACE和MACE这样的E(3)-等变图神经网络(gnn)精度很高,但结构僵化,限制了丰富的多通道电子描述符的加入。我们介绍了卷积核嵌入E(3)-等变网络(KEN),这是一种混合架构,将2D卷积核的局部环境提取与E(3)-等变GNN主干的多体表达性相结合。这种设计保持了对称性,同时在不增加训练数据要求的情况下实现了灵活的多模态输入功能。KEN模型在HE26数据集上进行训练和测试,并与MACE-osaka26模型进行了比较。通过Birch-Murnaghan状态方程、磁矩预测以及与CHGNet框架和微正则分子动力学的比较,进一步验证了晶格参数预测,证实了强大的能量守恒和准确的力再现,从而证明了克服最先进mlip结构刚性的可行途径。
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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Theory and Computation invites new and original contributions with the understanding that, if accepted, they will not be published elsewhere.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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