锂(药物)
材料科学
法拉第效率
阳极
电解质
化学工程
金属
分析化学(期刊)
透射电子显微镜
扫描电子显微镜
化学物理
纳米技术
电极
化学
复合材料
物理化学
冶金
有机化学
内分泌学
工程类
医学
作者
Shuo Zhang,Jun‐Fan Ding,Rui Xu,Ye Xiao,Chong Yan,Jia‐Qi Huang
标识
DOI:10.1002/aenm.202303726
摘要
Abstract Lithium (Li) metal has been strongly regarded as the ultimate anode option for next‐generation high‐energy‐density batteries. Nevertheless, the insufficient Coulombic efficiency induced by the extensive active Li loss largely hinders the practical operation of Li metal batteries under wide temperature range. Herein, the temperature‐mediated dynamic growth of inactive Li from −20 to 60°C via titration gas chromatograph measurements is quantitatively decoupled. Combined X‐ray photoelectronic spectroscopy, cryo‐transmission electronic microscopy, and scanning electronic microscopy methods depicted that both solid electrolyte interphase (SEI) characteristics and Li deposition compactness can be profoundly manipulated by working temperature. The elevation of temperature is found to fundamentally aggravate the parasitic reactions and deteriorate the spatial uniformity of SEI, yet promote the lateral growth of Li by kinetic reason. The opposite effects of temperature on SEI properties and Li deposition compactness can properly explain the intricate temperature‐dependent growth rates of SEI‐Li + and dead Li 0 capacity loss observed under titration gas chromatograph measurements. Design implications towards more stable Li metal anodes with higher reversibility can thus be yielded.
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