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The universal mathematical form of machine-learning potentials (MLPs) shifts the core of development of interatomic potentials to collecting proper training data. Ideally, the training set should encompass diverse local atomic environments but the conventional approach is prone to sampling similar configurations repeatedly, mainly due to the Boltzmann statistics. As such, practitioners handpick a large pool of distinct configurations manually, stretching the development period significantly. Herein, we suggest a novel sampling method optimized for gathering diverse yet relevant configurations semi-automatically. This is achieved by applying the metadynamics with the descriptor for the local atomic environment as a collective variable. As a result, the simulation is automatically steered toward unvisited local environment space such that each atom experiences diverse chemical environments without redundancy. We apply the proposed metadynamics sampling to H:Pt(111), GeTe, and Si systems. Throughout the examples, a small number of metadynamics trajectories can provide reference structures necessary for training high-fidelity MLPs. By proposing a semi-automatic sampling method tuned for MLPs, the present work paves the way to wider applications of MLPs to many challenging applications.
Abstract Machine learning models, trained on data from ab initio quantum simulations, are yielding molecular dynamics potentials with unprecedented accuracy. One limiting factor is the quantity of available training data, which can be expensive to ob
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