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Localized concentration reversal of lithium during intercalation into nanoparticles

Nanoparticulate electrodes, such as Li(x)FePO(4), have unique advantages over their microparticulate counterparts for the applications in Li-ion batteries because of the shortened diffusion path and access to nonequilibrium routes for fast Li incorporation, thus radically boosting power density of t...

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Detalles Bibliográficos
Autores principales: Zhang, Wei, Yu, Hui-Chia, Wu, Lijun, Liu, Hao, Abdellahi, Aziz, Qiu, Bao, Bai, Jianming, Orvananos, Bernardo, Strobridge, Fiona C., Zhou, Xufeng, Liu, Zhaoping, Ceder, Gerbrand, Zhu, Yimei, Thornton, Katsuyo, Grey, Clare P., Wang, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5766330/
https://www.ncbi.nlm.nih.gov/pubmed/29340302
http://dx.doi.org/10.1126/sciadv.aao2608
Descripción
Sumario:Nanoparticulate electrodes, such as Li(x)FePO(4), have unique advantages over their microparticulate counterparts for the applications in Li-ion batteries because of the shortened diffusion path and access to nonequilibrium routes for fast Li incorporation, thus radically boosting power density of the electrodes. However, how Li intercalation occurs locally in a single nanoparticle of such materials remains unresolved because real-time observation at such a fine scale is still lacking. We report visualization of local Li intercalation via solid-solution transformation in individual Li(x)FePO(4) nanoparticles, enabled by probing sub-angstrom changes in the lattice spacing in situ. The real-time observation reveals inhomogeneous intercalation, accompanied with an unexpected reversal of Li concentration at the nanometer scale. The origin of the reversal phenomenon is elucidated through phase-field simulations, and it is attributed to the presence of structurally different regions that have distinct chemical potential functions. The findings from this study provide a new perspective on the local intercalation dynamics in battery electrodes.