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LiOCl玻璃电解质中的多离子传导

Multi-ion Conduction in LiOCl Glass Electrolytes.

作者信息

Heenen Hendrik H, Voss Johannes, Scheurer Christoph, Reuter Karsten, Luntz Alan C

机构信息

Chair for Theoretical Chemistry and Catalysis Research Center , Technische Universität München , Lichtenbergstr. 4 , D-85747 Garching , Germany.

SUNCAT Center for Interface Science and Catalysis , SLAC National Accelerator Laboratory , 2575 Sand Hill Road , Menlo Park , California 94025 , United States.

出版信息

J Phys Chem Lett. 2019 May 2;10(9):2264-2269. doi: 10.1021/acs.jpclett.9b00500. Epub 2019 Apr 23.

Abstract

Antiperovskite glasses such as LiOCl and doped analogues have been proposed as excellent electrolytes for all-solid-state Li ion batteries (ASSB). Incorporating these electrolytes in ASSBs results in puzzling properties. This Letter describes a theoretical LiOCl glass created by conventional melt-quench procedures. The ion conductivities are calculated using molecular dynamics based on a polarizable force field that is fitted to an extensive set of density functional theory-based energies, forces, and stresses for a wide range of nonequilibrium structures encompassing crystal, glass, and melt. We find high Li ion conductivity in good agreement with experiments. However, we also find that the Cl ion is mobile as well so that the LiOCl glass is not a single-ion conductor, with a transference number t ≈ 0.84. This has important implications for its use as an electrolyte for all-solid-state batteries because the Cl could react irreversibly with the electrodes and/or produce glass decomposition during discharge-charge.

摘要

反钙钛矿玻璃,如LiOCl及其掺杂类似物,已被提议作为全固态锂离子电池(ASSB)的优良电解质。将这些电解质应用于全固态锂离子电池会产生令人困惑的特性。本文描述了一种通过传统熔体淬火工艺制备的理论LiOCl玻璃。离子电导率是使用基于极化力场的分子动力学计算得出的,该极化力场是根据广泛的基于密度泛函理论的能量、力和应力拟合而成的,适用于包括晶体、玻璃和熔体在内的各种非平衡结构。我们发现锂离子电导率很高,与实验结果吻合良好。然而,我们还发现Cl离子也具有迁移性,因此LiOCl玻璃不是单离子导体,迁移数t≈0.84。这对其作为全固态电池电解质的应用具有重要意义,因为Cl在充放电过程中可能会与电极发生不可逆反应和/或导致玻璃分解。

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