TY - JOUR
T1 - Defect Diffusion Graph Neural Networks for Materials Discovery in High-Temperature Energy Applications
AU - Way, Lauren
AU - Spataru, Catalin D.
AU - Jones, Reese E.
AU - Trinkle, Dallas R.
AU - Rowberg, Andrew J.E.
AU - Varley, Joel B.
AU - Wexler, Robert B.
AU - Smyth, Christopher M.
AU - Douglas, Tyra C.
AU - Bishop, Sean R.
AU - Fuller, Elliot J.
AU - McDaniel, Anthony H.
AU - Lany, Stephan
AU - Witman, Matthew D.
N1 - Publisher Copyright:
© 2025 American Chemical Society
PY - 2025/9/9
Y1 - 2025/9/9
N2 - The migration of crystallographic defects dictates material properties and performance for a plethora of technological applications. Density functional theory (DFT)-based nudged elastic band (NEB) calculations are a powerful computational technique for predicting defect migration activation energy barriers, yet they become prohibitively expensive for high-throughput screening of defect diffusivities. Without introducing hand-crafted (i.e., chemistry- or structure-specific) descriptors, we propose a generalized deep learning approach to train surrogate models for NEB energies of vacancy migration by hybridizing graph neural networks with transformer encoders and simply using pristine host structures as input. With sufficient training data, computationally efficient and simultaneous inference of vacancy defect thermodynamics and migration activation energies can be obtained to compute temperature-dependent vacancy diffusivities and to down-select candidates for more thorough DFT analysis or experiments. Thus, as we specifically demonstrate for potential water-splitting materials, candidates with desired defect thermodynamics, kinetics, and host stability properties can be more rapidly targeted from open-source databases of experimentally validated or hypothetical materials.
AB - The migration of crystallographic defects dictates material properties and performance for a plethora of technological applications. Density functional theory (DFT)-based nudged elastic band (NEB) calculations are a powerful computational technique for predicting defect migration activation energy barriers, yet they become prohibitively expensive for high-throughput screening of defect diffusivities. Without introducing hand-crafted (i.e., chemistry- or structure-specific) descriptors, we propose a generalized deep learning approach to train surrogate models for NEB energies of vacancy migration by hybridizing graph neural networks with transformer encoders and simply using pristine host structures as input. With sufficient training data, computationally efficient and simultaneous inference of vacancy defect thermodynamics and migration activation energies can be obtained to compute temperature-dependent vacancy diffusivities and to down-select candidates for more thorough DFT analysis or experiments. Thus, as we specifically demonstrate for potential water-splitting materials, candidates with desired defect thermodynamics, kinetics, and host stability properties can be more rapidly targeted from open-source databases of experimentally validated or hypothetical materials.
UR - https://www.scopus.com/pages/publications/105015541241
U2 - 10.1021/acs.chemmater.5c00021
DO - 10.1021/acs.chemmater.5c00021
M3 - Article
AN - SCOPUS:105015541241
SN - 0897-4756
VL - 37
SP - 6473
EP - 6484
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 17
ER -