Benchmarking Universal Machine Learning Force Fields for Crystal Structure Prediction of High-Energy Molecular Systems
TL;DR
This work tested the hypothesis that classical force-field pre-relaxation can provide a more suitable starting geometry for subsequent UMLIP relaxation on a large database of high energy molecular crystals, and revealed distinct trade-offs among the evaluated models.
Abstract
Recent developments of universal machine learning interatomic potentials (UMLIPs) offer a fast route for screening molecular crystals based on geometry relaxation and energy ranking, but their reliability across chemically diverse energetic materials remains elusive. In particular, it is unclear whether or not these UMLIPs are over-sensitive to break the desired molecular connectivity for relaxing the periodic crystals. Herein we tested the hypothesis that classical force-field pre-relaxation can provide a more suitable starting geometry for subsequent UMLIP relaxation on a large database of high energy molecular crystals. Three models (MACE, MACE-OFF and UMA) in conjunction with the General Amber Force Field (GAFF) were applied to test this hypothesis. Among them, direct MACE-OFF and UMA showed very high relaxation success and preserved the reference geometries most closely, but they still exhibit failures for some rare cases. Using GAFF pre-relaxation can systematically reduce the number of failed relaxations with lower computational costs. Our comparative failure and robustness analyses revealed distinct trade-offs among the evaluated models. Among them, MACE-OFF achieves a better compromise between potential energy surface smoothness, structural fidelity, and stress convergence, serving as a good choice to provide a reliable foundation for automated structural optimization.