Please use this identifier to cite or link to this item: https://doi.org/10.1063/1.4960790
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dc.titleAn efficient algorithm for finding the minimum energy path for cation migration in ionic materials
dc.contributor.authorRong, Z
dc.contributor.authorKitchaev, D
dc.contributor.authorCanepa, P
dc.contributor.authorHuang, W
dc.contributor.authorCeder, G
dc.date.accessioned2020-10-23T08:02:17Z
dc.date.available2020-10-23T08:02:17Z
dc.date.issued2016
dc.identifier.citationRong, Z, Kitchaev, D, Canepa, P, Huang, W, Ceder, G (2016). An efficient algorithm for finding the minimum energy path for cation migration in ionic materials. Journal of Chemical Physics 145 (7) : 74112. ScholarBank@NUS Repository. https://doi.org/10.1063/1.4960790
dc.identifier.issn0021-9606
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/179608
dc.description.abstractThe 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. © 2016 Author(s).
dc.publisherAmerican Institute of Physics Inc.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectComputation theory
dc.subjectDensity functional theory
dc.subjectDiffusion barriers
dc.subjectEnergy barriers
dc.subjectIntercalation compounds
dc.subjectInterpolation
dc.subjectIons
dc.subjectLithium-ion batteries
dc.subjectPositive ions
dc.subjectReaction kinetics
dc.subjectComputational expense
dc.subjectGeneral applications
dc.subjectHigh throughput studies
dc.subjectIntermediate image
dc.subjectIntermediate structures
dc.subjectLinear Interpolation
dc.subjectMinimum energy paths
dc.subjectNudged elastic band
dc.subjectComputational efficiency
dc.typeArticle
dc.contributor.departmentMATERIALS SCIENCE AND ENGINEERING
dc.description.doi10.1063/1.4960790
dc.description.sourcetitleJournal of Chemical Physics
dc.description.volume145
dc.description.issue7
dc.description.page74112
dc.published.statePublished
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