材料科学
电解质
金属锂
接触电阻
石墨氮化碳
金属
锂(药物)
电极
氮化物
石墨烯
纳米技术
碳纤维
化学
复合材料
催化作用
图层(电子)
冶金
物理化学
内分泌学
复合数
医学
光催化
生物化学
作者
Ying Huang,Bo Chen,Jian Duan,Fei Yang,Tengrui Wang,Zheng‐Feng Wang,Wenjuan Yang,Chenchen Hu,Wei Luo,Yunhui Huang
标识
DOI:10.1002/anie.201914417
摘要
Abstract Solid‐state Li metal batteries (SSLMBs) have attracted considerable interests due to their promising energy density as well as high safety. However, the realization of a well‐matched Li metal/solid‐state electrolyte (SSE) interface remains challenging. Herein, we report g‐C 3 N 4 as a new interface enabler. We discover that introducing g‐C 3 N 4 into Li metal can not only convert the Li metal/garnet‐type SSE interface from point contact to intimate contact but also greatly enhance the capability to suppress the dendritic Li formation because of the greatly enhanced viscosity, decreased surface tension of molten Li, and the in situ formation of Li 3 N at the interface. Thus, the resulting Li‐C 3 N 4 |SSE|Li‐C 3 N 4 symmetric cell gives a significantly low interfacial resistance of 11 Ω cm 2 and a high critical current density (CCD) of 1500 μA cm −2 . In contrast, the same symmetric cell configuration with pristine Li metal electrodes has a much larger interfacial resistance (428 Ω cm 2 ) and a much lower CCD (50 μA cm −2 ).
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