4.8 Article

Accelerated Growth of Electrically Isolated Lithium Metal during Battery Cycling

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 30, 页码 35750-35758

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c08944

关键词

electrically isolated lithium; lithium-metal battery; lithium-loss rate; gas chromatography; photoacoustic imaging

资金

  1. Shanghai Sailing program [18YF1411100]

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The study systematically distinguishes and quantifies different rates of lithium loss during cycling of lithium-metal batteries, finding that the formation of electrically isolated lithium metal (dead Li) is accelerated upon cycling, dominating the total lithium loss, while much slower rates of loss are associated with galvanic corrosion and formation of the solid-electrolyte interphase. Photoacoustic imaging reveals the distinct three-dimensional spatial distribution of dead Li, different from that of freshly deposited lithium. The research highlights the importance of quantitative studies on conventional and solid-state lithium-metal batteries for optimizing lithium-metal electrochemistry.
Severe capacity loss during cycling of lithium-metal batteries is one of the most concerning obstacles hindering their practical application. As this capacity loss is related to the variety of side reactions occurring to lithium metal, identification and quantification of these lithium-loss processes are extremely important. In this work, we systematically distinguish and quantify the different rates of lithium loss associated with galvanic corrosion, the formation of a solid-electrolyte interphase, and the formation of electrically isolated lithium metal (i.e., dead lithium). We show that the formation of dead Li is accelerated upon cycling, dominating the total lithium loss, with much slower rates of lithium loss associated with galvanic corrosion and formation of the solid-electrolyte interphase. Furthermore, photoacoustic imaging reveals that the three-dimensional spatial distribution of dead Li is distinctly different from that of freshly deposited lithium. This quantification is further extended to a solid-state Li/Cu cell based on a Li10GeP2S12 solid-state electrolyte. The lithium loss in the solid-state cell is much severer than that of a conventional lithium-metal battery based on a liquid electrolyte. Our work highlights the importance of quantitative studies on conventional and solid-state lithium-metal batteries and provides a strong basis for the optimization of lithium-metal electrochemistry.

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