电解质
材料科学
快离子导体
电极
外延
固溶体
钙钛矿(结构)
纳米技术
结晶学
化学
冶金
图层(电子)
物理化学
作者
Fuzhen Li,Jingxuan Li,Feng Zhu,Ting Liu,Ben Xu,Tae‐Hoon Kim,M. J. Kramer,Cheng Ma,Lin Zhou,Ce‐Wen Nan
出处
期刊:Matter
[Elsevier]
日期:2019-08-21
卷期号:1 (4): 1001-1016
被引量:62
标识
DOI:10.1016/j.matt.2019.05.004
摘要
Solid electrolytes, as a promising replacement for the flammable liquid electrolyte in conventional Li-ion batteries, may greatly alleviate the safety issues and improve the energy density. However, mainstream electrodes are also solid. If solid electrolytes were employed, creating intimate electrode-electrolyte contact similar to that between solid and liquid would be quite difficult. Here we discovered that, by forming epitaxial interfaces, such a seamless solid-solid contact can happen between two widely studied systems: the Li-rich layered electrode and perovskite solid electrolyte. Atomic-resolution electron microscopy unambiguously demonstrated that the former can be epitaxially embedded into the latter. The solid-solid composite electrode formed this way exhibited a rate capability no lower than the one based on solid-liquid contact. With the periodic misfit dislocations reconciling structural differences, such epitaxy can tolerate large lattice mismatch, and thus may occur between many layered electrodes and perovskite solid electrolytes.
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