材料科学
阳极
电解质
法拉第效率
阴极
电池(电)
电化学
成核
锂(药物)
电极
电镀(地质)
电镀
金属
化学工程
能量密度
电化学窗口
合金
集电器
电流密度
金属锂
纳米技术
冶金
离子电导率
化学
工程物理
功率(物理)
有机化学
物理化学
内分泌学
工程类
地质学
物理
图层(电子)
医学
量子力学
地球物理学
作者
Michael J. Wang,Eric A. Carmona,A. Gupta,Paul Albertus,Jeff Sakamoto
标识
DOI:10.1038/s41467-020-19004-4
摘要
Abstract The coupling of solid-state electrolytes with a Li-metal anode and state-of-the-art (SOA) cathode materials is a promising path to develop inherently safe batteries with high energy density (>1000 Wh L −1 ). However, integrating metallic Li with solid-electrolytes using scalable processes is not only challenging, but also adds extraneous volume since SOA cathodes are fully lithiated. Here we show the potential for “Li-free” battery manufacturing using the Li 7 La 3 Zr 2 O 12 (LLZO) electrolyte. We demonstrate that Li-metal anodes >20 μm can be electroplated onto a current collector in situ without LLZO degradation and we propose a model to relate electrochemical and nucleation behavior. A full cell consisting of in situ formed Li, LLZO, and NCA is demonstrated, which exhibits stable cycling over 50 cycles with high Coulombic efficiencies. These findings demonstrate the viability of “Li-free” configurations using LLZO which may guide the design and manufacturing of high energy density solid-state batteries.
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