材料科学
法拉第效率
相间
阳极
电解质
成核
阴极
化学工程
电镀(地质)
纳米技术
电极
物理化学
有机化学
地质学
地球物理学
化学
工程类
生物
遗传学
作者
Qifan Yang,Jiulin Hu,Zhenguo Yao,Jianjun Liu,Chilin Li
标识
DOI:10.1002/adfm.202206778
摘要
Abstract Lithium metal batteries (LMBs) are becoming the promising candidate of high‐energy storage systems. However, the fragile natural solid electrolyte interphase (SEI) cannot retard the Li dendrite growth at anode, which will cause the low coulombic efficiency (CE) of Li plating/stripping and safety hazards in LMBs. Here, an in situ construction strategy of novel artificial SEI consisting of Li 2 CN 2 ionic conductor wired by carbon nanodomains via dicyandiamide solution reaction method on Li metal surface is proposed. This lithiophilic Li 2 CN 2 has the higher anti‐reduction stability and longer critical length for Li dendrite, showing the excellent dendrite suppressing ability. The wired carbon domains promote the electron connection and charge homogenization in SEI, leading to the uniform Li nucleation around Li 2 CN 2 /C grains with enhanced interface kinetics and reduced polarization. This dual conductive Li 2 CN 2 /C network enables the durable preservation of high CE and low voltage hysteresis during Li plating/stripping, endowing LiNi 0.8 Mn 0.1 Co 0.1 O 2 /Li cells with ultralong cycling life exceeding 1000 cycles at high rate. The cycling stabilization effect is also remarkable even under thin Li anode and high‐loading cathode conditions. This study provides a solution to robust SEI configuration of high conductivity via in situ interface lithiation reaction for high‐performance LMBs.
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