arXiv subjects

Suyeon Ju

Publications and source records attributed to Suyeon Ju.

5 recordsLinked to original sources

arXiv2026

A Robust Agentic Framework for Expert-Level Automation of Atomistic Simulations

Traditionally, atomistic simulation has been constrained by the computational scaling limits of ab initio methods and the parameterization overhead of empirical force fields. The recent emergence of universal machine learning interatomic potentials has significantly mitigated these bottlenecks, offering near-quantum accuracy and generalizability across diverse chemical spaces at a fraction of the computational cost. However, this shift has relocated the bottleneck to the human dimension: time-consuming mechanical processes, such as input preparation and data analysis, now dominate the research lifecycle. We introduce Paimon, a Platform for Agentic Integration in Materials Optimization and Nanoscale-simulations. Through hundreds of trials on an expert-level liquid electrolyte simulation, we show that Paimon substantially improves the reliability of agentic workflows by suppressing silent errors: plausible yet physically incorrect results. We further demonstrate that Paimon can cooperate with an external scientific agent and autonomously reproduce simulation methodologies from the literature. As an agent harness for atomistic simulations, Paimon affords researchers a continuous, science-centric workflow throughout the entire simulation lifecycle.

cond-mat.mtrl-sci↗

arXiv2025

Optimizing Cross-Domain Transfer for Universal Machine Learning Interatomic Potentials

Accurate yet transferable machine-learning interatomic potentials (MLIPs) are essential for accelerating materials and chemical discovery. However, most universal MLIPs overfit to narrow datasets or computational protocols, limiting their reliability across chemical and functional domains. We introduce a transferable multi-domain training strategy that jointly optimizes universal and task-specific parameters through selective regularization, coupled with a domain-bridging set (DBS) that aligns potential-energy surfaces across datasets. Systematic ablation experiments show that small DBS fractions (0.1%) and targeted regularization synergistically enhance out-of-distribution generalization while preserving in-domain fidelity. Trained on fifteen open databases spanning molecules, crystals, and surfaces, our model, SevenNet-Omni, achieves state-of-the-art cross-domain accuracy, including adsorption-energy errors below 0.06 eV on metallic surfaces and 0.1 eV on metal-organic frameworks. Despite containing only 0.5% r$^2$SCAN data, SevenNet-Omni reproduces high-fidelity r$^2$SCAN energetics, demonstrating effective cross-functional transfer from large PBE datasets. This framework offers a scalable route toward universal, transferable MLIPs that bridge quantum-mechanical fidelities and chemical domains.

cond-mat.mtrl-sci↗

arXiv2025

Application of pretrained universal machine-learning interatomic potential for physicochemical simulation of liquid electrolytes in Li-ion battery

Achieving higher operational voltages, faster charging, and broader temperature ranges for Li-ion batteries necessitates advancements in electrolyte engineering. However, the complexity of optimizing combinations of solvents, salts, and additives has limited the effectiveness of both experimental and computational screening methods for liquid electrolytes. Recently, pretrained universal machine-learning interatomic potentials (MLIPs) have emerged as promising tools for computational exploration of complex chemical spaces with high accuracy and efficiency. In this study, we evaluated the performance of the state-of-the-art equivariant pretrained MLIP, SevenNet-0, in predicting key properties of liquid electrolytes, including solvation behavior, density, and ion transport. To assess its suitability for extensive material screening, we considered a dataset comprising 20 solvents. Although SevenNet-0 was predominantly trained on inorganic compounds, its predictions for the properties of liquid electrolytes showed good agreement with experimental and $\textit{ab initio}$ data. However, systematic errors were identified, particularly in the predicted density of liquid electrolytes. To address this limitation, we fine-tuned SevenNet-0, achieving improved accuracy at a significantly reduced computational cost compared to developing bespoke models. Analysis of the training set suggested that the model achieved its accuracy by generalizing across the chemical space rather than memorizing specific configurations. This work highlights the potential of SevenNet-0 as a powerful tool for future engineering of liquid electrolyte systems.

cond-mat.mtrl-sci↗

arXiv2023

Disorder-dependent Li diffusion in $\mathrm{Li_6PS_5Cl}$ investigated by machine learning potential

Solid-state electrolytes with argyrodite structures, such as $\mathrm{Li_6PS_5Cl}$, have attracted considerable attention due to their superior safety compared to liquid electrolytes and higher ionic conductivity than other solid electrolytes. Although experimental efforts have been made to enhance conductivity by controlling the degree of disorder, the underlying diffusion mechanism is not yet fully understood. Moreover, existing theoretical analyses based on ab initio MD simulations have limitations in addressing various types of disorder at room temperature. In this study, we directly investigate Li-ion diffusion in $\mathrm{Li_6PS_5Cl}$ at 300 K using large-scale, long-term MD simulations empowered by machine learning potentials (MLPs). To ensure the convergence of conductivity values within an error range of 10%, we employ a 25 ns simulation using a $5\times5\times5$ supercell containing 6500 atoms. The computed Li-ion conductivity, activation energies, and equilibrium site occupancies align well with experimental observations. Notably, Li-ion conductivity peaks when Cl ions occupy 25% of the 4c sites, rather than at 50% where the disorder is maximized. This phenomenon is explained by the interplay between inter-cage and intra-cage jumps. By elucidating the key factors affecting Li-ion diffusion in $\mathrm{Li_6PS_5Cl}$, this work paves the way for optimizing ionic conductivity in the argyrodite family.

cond-mat.mtrl-sci↗

arXiv2020

Training machine-learning potentials for crystal structure prediction using disordered structures

Prediction of the stable crystal structure for multinary (ternary or higher) compounds with unexplored compositions demands fast and accurate evaluation of free energies in exploring the vast configurational space. The machine-learning potential such as the neural network potential (NNP) is poised to meet this requirement but a dearth of information on the crystal structure poses a challenge in choosing training sets. Herein we propose constructing the training set from densityfunctional-theory (DFT) based dynamical trajectories of liquid and quenched amorphous phases, which does not require any preceding information on material structures except for the chemical composition. To demonstrate suitability of the trained NNP in the crystal structure prediction, we compare NNP and DFT energies for Ba2AgSi3, Mg2SiO4, LiAlCl4, and InTe2O5F over experimental phases as well as low-energy crystal structures that are generated theoretically. For every material, we find strong correlations between DFT and NNP energies, ensuring that the NNPs can properly rank energies among low-energy crystalline structures. We also find that the evolutionary search using the NNPs can identify low-energy metastable phases more efficiently than the DFTbased approach. By proposing a way to developing reliable machine-learning potentials for the crystal structure prediction, this work will pave the way to identifying unexplored multinary phases efficiently.

physics.comp-ph↗