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Overcoming systematic softening in universal machine learning interatomic potentials by fine-tuning

arXiv 2405.07105 ↗First posted 11 May 2024cond-mat.mtrl-sci cs.AI cs.LGcited by 6

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Abstract (arXiv)

Machine learning interatomic potentials (MLIPs) have introduced a new paradigm for atomic simulations. Recent advancements have seen the emergence of universal MLIPs (uMLIPs) that are pre-trained on diverse materials datasets, providing opportunities for both ready-to-use universal force fields and robust foundations for downstream machine learning refinements. However, their performance in extrapolating to out-of-distribution complex atomic environments remains unclear. In this study, we highlight a consistent potential energy surface (PES) softening effect in three uMLIPs: M3GNet, CHGNet, and MACE-MP-0, which is characterized by energy and force under-prediction in a series of atomic-modeling benchmarks including surfaces, defects, solid-solution energetics, phonon vibration modes, ion migration barriers, and general high-energy states. We find that the PES softening behavior originates from a systematic underprediction error of the PES curvature, which derives from the biased sampling of near-equilibrium atomic arrangements in uMLIP pre-training datasets. We demonstrate that the PES softening issue can be effectively rectified by fine-tuning with a single additional data point. Our findings suggest that a considerable fraction of uMLIP errors are highly systematic, and can therefore be efficiently corrected. This result rationalizes the data-efficient fine-tuning performance boost commonly observed with foundational MLIPs. We argue for the importance of a comprehensive materials dataset with improved PES sampling for next-generation foundational MLIPs.

Key facts. Cited by 6 papers in the map (data through 14 Oct 2026). Builds on 10 of its 61 references that are in the map. First posted on arXiv 11 May 2024.

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10 of 61 references.

References · 10

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  6. 2024Enabling Efficient Equivariant Operations in the Fourier Basis via Gaunt Tensor Productscited by 36
  7. 2023Scaling the leading accuracy of deep equivariant models to biomolecular simulations of realistic sizecited by 33
  8. 2024Cartesian atomic cluster expansion for machine learning interatomic potentialscited by 31
  9. 2022DPA-1: Pretraining of Attention-based Deep Potential Model for Molecular Simulationcited by 15
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Cited by year (2026 to 14 Oct)

Citing papers per year: 2025: 5; 2026: 1.

6 papers.