阳极
材料科学
电解质
纳米片
电化学
化学工程
锂(药物)
氮化硼
极化(电化学)
金属
纳米技术
电极
无机化学
化学
物理化学
冶金
工程类
内分泌学
医学
作者
Zhiyu Wang,Si Qin,Fangfang Chen,Shasha Chen,Dan Liú,Degang Jiang,Peng Zhang,Pablo Mota‐Santiago,Dylan Hegh,Peter A. Lynch,Abdulrahman S. Alotabi,Gunther G. Andersson,Patrick C. Howlett,Maria Forsyth,Weiwei Lei,Joselito M. Razal
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-01-18
卷期号:18 (4): 3531-3541
被引量:12
标识
DOI:10.1021/acsnano.3c11135
摘要
Metallic lithium (Li) is the most attractive anode for Li batteries because it holds the highest theoretical specific capacity (3860 mA h g–1) and the lowest redox potential (−3.040 V vs SHE). However, the poor interface stability of the Li anode, which is caused by the high reactivity and dendrite formation of metallic Li upon cycling, leads to undesired electrochemical performance and safety issues. While two-dimensional boron nitride (BN) nanosheets have been utilized as an interfacial layer, the mechanism on how they stabilize the Li–electrolyte interface remains elusive. Here, we show how BN nanosheet interlayers suppress Li dendrite formation, enhance Li ion transport kinetics, facilitate Li deposition, and reduce electrolyte decomposition. We show through both simulation and experimental data that the desolvation process of a solvated Li ion within the interlayer nanochannels kinetically favors Li deposition. This process enables long cycling stability, reduced voltage polarization, improved interface stability, and negligible volume expansion. Their application as an interfacial layer in symmetric cells and full cells that display significantly improved electrochemical properties is also demonstrated. The knowledge gained in this study provides both critical insights and practical guidelines for designing a Li metal anode with significantly improved performance.
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