{"title":"Convolutional Kernel-Embedded\n E\n (3)-Equivariant\nNetworks (KEN): Overcoming Architectural Rigidity in Machine Learning\nInteratomic Potentials","authors":"Jha Gautam","doi":"10.1021/acs.jctc.6c01109","DOIUrl":null,"url":null,"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.","PeriodicalId":45,"journal":{"name":"Journal of Chemical Theory and Computation","volume":"18 1","pages":""},"PeriodicalIF":5.8000,"publicationDate":"2026-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Theory and Computation","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.jctc.6c01109","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
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.
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.