Yizhi Zhu

Evan Dramko, Yizhi Zhu, Aleksandar Krivokapic et al.

Vital to the creation of advanced materials is performing structural relaxations. Traditional approaches built on physics-derived first-principles calculations are computationally expensive, motivating the creation of machine-learning interatomic potentials (MLIPs). Traditional approaches to training MLIPs for structural relaxations involves training models to faithfully reproduce first-principles computed forces. We propose a fine-tuning method to be used on a pretrained MLIP in which we create a fully-differentiable end-to-end simulation loop that optimizes the predicted final structures directly. Trajectories are unrolled and gradients are tracked through the entire relaxation. We show that this method achieves substantial performance gains when applied to pretrained models, leading to a nearly $50\%$ reduction in test error across the sample datasets. Interestingly, we show the process is robust to substantial variation in the relaxation setup, achieving negligibly different results across varied hyperparameter and procedural modifications. Experimental results indicate this is due to a ``preference'' of BPTT to modify the MLIP rather than the other trainable parameters. Of particular interest to practitioners is that this approach lowers the data requirements for producing an effective domain-specific MLIP, addressing a common bottleneck in practical deployment.

Evan Dramko, Yihuang Xiong, Yizhi Zhu et al.

Point defects play a central role in driving the properties of materials. First-principles methods are widely used to compute defect energetics and structures, including at scale for high-throughput defect databases. However, these methods are computationally expensive, making machine-learning force fields (MLFFs) an attractive alternative for accelerating structural relaxations. Most existing MLFFs are based on graph neural networks (GNNs), which can suffer from oversmoothing and poor representation of long-range interactions. Both of these issues are especially of concern when modeling point defects. To address these challenges, we introduce the Accelerated Deep Atomic Potential Transformer (ADAPT), an MLFF that replaces graph representations with a direct coordinates-in-space formulation and explicitly considers all pairwise atomic interactions. Atoms are treated as tokens, with a Transformer encoder modeling their interactions. Applied to a dataset of silicon point defects, ADAPT achieves a roughly 33 percent reduction in both force and energy prediction errors relative to a state-of-the-art GNN-based model, while requiring only a fraction of the computational cost.