An efficient algorithm for finding the minimum energy path for cation migration in ionic materials

初始化 路径(计算) 插值(计算机图形学) 密度泛函理论 曲率 算法 分歧(语言学) 扩散 计算机科学 趋同(经济学) 计算物理学 统计物理学 物理 数学 化学 计算化学 几何学 量子力学 经济 哲学 计算机图形学(图像) 程序设计语言 语言学 动画 经济增长
作者
Ziqin Rong,Daniil A. Kitchaev,Pieremanuele Canepa,Wenxuan Huang,Gerbrand Ceder
出处
期刊:Journal of Chemical Physics [American Institute of Physics]
卷期号:145 (7) 被引量:73
标识
DOI:10.1063/1.4960790
摘要

The Nudged Elastic Band (NEB) is an established method for finding minimum-energy paths and energy barriers of ion migration in materials, but has been hampered in its general application by its significant computational expense when coupled with density functional theory (DFT) calculations. Typically, an NEB calculation is initialized from a linear interpolation of successive intermediate structures (also known as images) between known initial and final states. However, the linear interpolation introduces two problems: (1) slow convergence of the calculation, particularly in cases where the final path exhibits notable curvature; (2) divergence of the NEB calculations if any intermediate image comes too close to a non-diffusing species, causing instabilities in the ensuing calculation. In this work, we propose a new scheme to accelerate NEB calculations through an improved path initialization and associated energy estimation workflow. We demonstrate that for cation migration in an ionic framework, initializing the diffusion path as the minimum energy path through a static potential built upon the DFT charge density reproduces the true NEB path within a 0.2 Å deviation and yields up to a 25% improvement in typical NEB runtimes. Furthermore, we find that the locally relaxed energy barrier derived from this initialization yields a good approximation of the NEB barrier, with errors within 20 meV of the true NEB value, while reducing computational expense by up to a factor of 5. Finally, and of critical importance for the automation of migration path calculations in high-throughput studies, we find that the new approach significantly enhances the stability of the calculation by avoiding unphysical image initialization. Our algorithm promises to enable efficient calculations of diffusion pathways, resolving a long-standing obstacle to the computational screening of intercalation compounds for Li-ion and multivalent batteries.

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