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Foundation Models for Atomistic Simulation of Chemistry and Materials
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Given the power of large language and large vision models, it is of profound and fundamental interest to ask if a foundational model based on data and parameter scaling laws and pre-training strategies is possible for learned simulations of chemistry and materials. The scaling of large and diverse datasets and highly expressive architectures for chemical and materials sciences should result in a foundation model that is more efficient and broadly transferable, robust to out-of-distribution challenges, and easily fine-tuned to a variety of downstream observables, when compared to specific training from scratch on targeted applications in atomistic simulation. In this Perspective we aim to cover the rapidly advancing field of machine learned interatomic potentials (MLIP), and to illustrate a path to create chemistry and materials MLIP foundation models at larger scale.
Forward citations
Cited by 3 Pith papers
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From Evaluation to Design: Using Potential Energy Surface Smoothness Metrics to Guide Machine Learning Interatomic Potential Architectures
A bond-deformation benchmark plus a force-smoothness metric is proposed to detect PES artifacts and guide MLIP architecture design, with improvements shown on a new Transformer-style model.
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A universal augmentation framework for long-range electrostatics in machine learning interatomic potentials
LES augments short-range MLIPs with long-range electrostatics learned from energies and forces alone, improving accuracy and enabling Born effective charge and dipole prediction.
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Benchmarking foundation potentials against quantum chemistry methods for predicting molecular redox potentials
MACE-OMol foundation potential matches DFT accuracy for PCET redox potentials, but fails for multi-electron-transfer ions; a hybrid FP+DFT single-point workflow fixes this.
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