Charge-Density-Wave Phase Transitions in Monolayer 1T-TaS2 from Universal Machine Learning Molecular Dynamics

Abstract

Charge-density-wave (CDW) phases in 1T transition-metal dichalcogenides arise from strong electron-phonon coupling and accompanying lattice instabilities. Capturing their temperature-dependent structural evolution using conventional first-principles molecular dynamics (MD) remains challenging because of the large supercells and extensive finite-temperature sampling required. Here, we combine density functional theory (DFT), universal machine-learning interatomic potentials (MLIPs), MD, and temperature-dependent effective potential phonon calculations to investigate the structural and vibrational signatures of CDW transitions in monolayer 1T-TaS2. Benchmarking against DFT displacement energies identifies UMA-s-1p1 universal machine learning potentials with sufficient accuracy for subsequent finite-temperature simulations. Our results show that large-scale MD simulations reproduce the experimentally observed phase transition sequence from the low-temperature Star-of-David (SoD) distorted structure to the high-temperature primitive hexagonal structure, as quantified by the number of Ta atoms attributed to SoDs. Heating-cooling cycles exhibit thermal hysteresis, and upon cooling, the system freezes into a multi-domain state in which {\alpha} and \b{eta} CDW chiralities nucleate independently and persist to the lowest temperatures. These findings demonstrate that carefully benchmarked universal MLIPs can provide a scalable framework for finite-temperature studies of CDW materials.