Li metal deposition and stripping in a solid-state battery via Coble creep

过电位 电解质 锂(药物) 材料科学 离子键合 电化学 蠕动 化学工程 复合材料 电极 化学 离子 物理化学 有机化学 内分泌学 工程类 医学
作者
Yuming Chen,Ziqiang Wang,Xiaoyan Li,Xiahui Yao,Chao Wang,Yutao Li,Weijiang Xue,Daiwei Yu,So Yeon Kim,Fei Yang,Akihiro Kushima,Guoge Zhang,Haitao Huang,Nan Wu,Yiu‐Wing Mai,John B. Goodenough,Ju Li
出处
期刊:Nature [Nature Portfolio]
卷期号:578 (7794): 251-255 被引量:498
标识
DOI:10.1038/s41586-020-1972-y
摘要

Solid-state lithium metal batteries require accommodation of electrochemically generated mechanical stress inside the lithium: this stress can be1,2 up to 1 gigapascal for an overpotential of 135 millivolts. Maintaining the mechanical and electrochemical stability of the solid structure despite physical contact with moving corrosive lithium metal is a demanding requirement. Using in situ transmission electron microscopy, we investigated the deposition and stripping of metallic lithium or sodium held within a large number of parallel hollow tubules made of a mixed ionic-electronic conductor (MIEC). Here we show that these alkali metals—as single crystals—can grow out of and retract inside the tubules via mainly diffusional Coble creep along the MIEC/metal phase boundary. Unlike solid electrolytes, many MIECs are electrochemically stable in contact with lithium (that is, there is a direct tie-line to metallic lithium on the equilibrium phase diagram), so this Coble creep mechanism can effectively relieve stress, maintain electronic and ionic contacts, eliminate solid-electrolyte interphase debris, and allow the reversible deposition/stripping of lithium across a distance of 10 micrometres for 100 cycles. A centimetre-wide full cell—consisting of approximately 1010 MIEC cylinders/solid electrolyte/LiFePO4—shows a high capacity of about 164 milliampere hours per gram of LiFePO4, and almost no degradation for over 50 cycles, starting with a 1× excess of Li. Modelling shows that the design is insensitive to MIEC material choice with channels about 100 nanometres wide and 10–100 micrometres deep. The behaviour of lithium metal within the MIEC channels suggests that the chemical and mechanical stability issues with the metal–electrolyte interface in solid-state lithium metal batteries can be overcome using this architecture. By containing lithium metal within oriented tubes of a mixed ionic-electronic conductor, a 3D anode for lithium metal batteries is produced that overcomes  chemomechanical stability issues at the electrolyte interface.
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