材料科学
硅烷化
电解质
阳极
阴极
金属锂
金属
化学工程
电化学
比能量
电极
成核
锂(药物)
纳米技术
复合材料
冶金
化学
有机化学
医学
物理
工程类
内分泌学
物理化学
量子力学
作者
Yuliang Gao,Manyi Guo,Kai Yuan,Chao Shen,Zengying Ren,Kun Zhang,Hui Zhao,Fahong Qiao,Jinlei Gu,Yaqin Qi,Keyu Xie,Bingqing Wei
标识
DOI:10.1002/aenm.201903362
摘要
Abstract Lithium (Li) metal has attracted unprecedented attention as the ultimate anode material for future rechargeable batteries, but the electrochemical behavior (such as Li dendrites and gassing problems) in real Li metal pouch cells has received little attention. To achieve realistic high‐energy Li metal batteries, the designed solid electrolyte interface to suppress both Li dendrites and catastrophic gassing problems is urgently needed at cell level. Here, an efficient multifunctional silanization interface (MSI) is proposed for high‐energy Li metal pouch cells. Such an MSI not only guides uniform nucleation and growth of Li metal but also suppresses interfacial parasitic reactions between Li metal and electrolyte. As a result, under harsh conditions (negative to positive electrode capacity ratio of 2.96 and electrolyte weight to cathode capacity ratio of 2.7 g Ah −1 ), a long‐running lifespan (over 160 cycles with a capacity retention of 96% at 1 C), and low‐gassing behavior of realistic high‐energy Li metal pouch cell (1 Ah, 300 Wh kg −1 ) is achieved. This work opens a promising avenue toward the commercial applications of high‐energy Li metal batteries.
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