Nanoscale observation of the solid electrolyte interface and lithium dendrite nucleation-growth process during the initial lithium electrodeposition

被引:25
|
作者
Wang, Shuwei [1 ,2 ]
Yin, Xiaoguang [1 ,3 ]
Liu, Dongqing [1 ,4 ]
Liu, Yuanming [1 ]
Qin, Xianying [1 ]
Wang, Wei [1 ,2 ]
Zhao, Rui [1 ,2 ]
Zeng, Xiaojie [1 ,2 ]
Li, Baohua [1 ]
机构
[1] Tsinghua Shenzhen Int Grad Sch, Shenzhen Geim Graphene Ctr, Shenzhen Key Lab Power Battery Safety Res, Shenzhen 518055, Peoples R China
[2] Tsinghua Univ, Lab Adv Mat, Sch Mat Sci & Engn, Beijing 100084, Peoples R China
[3] Southern Univ Sci & Technol, Sch Environm Sci & Engn, Shenzhen 518055, Peoples R China
[4] Shenzhen Univ, coll Mechatron & Control Engn, Shenzhen 518060, Peoples R China
基金
中国国家自然科学基金;
关键词
ATOMIC-FORCE MICROSCOPY; INTERPHASE LAYER; LI DEPOSITION; METAL ANODE; LI4TI5O12;
D O I
10.1039/d0ta06141g
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Lithium metal is one of the most promising anode materials for next-generation batteries. However, the growth of lithium dendrites and the high reactivity of lithium cause serious safety and cyclability problems. A comprehensive understanding of the lithium deposition behavior, especially during the initial deposition stages, is critical for its performance improvement. The influences of current density and capacity on the nucleation size, site distribution, and growth pattern were discussedvia in situelectrochemical AFM (EC-AFM) and COMSOL simulation, suggesting that lithium deposition initially follows reaction- and then transport-limited mechanisms. In addition, the solid electrolyte interface (SEI) during lithium deposition was systematically analyzed by conductive-AFM, AFM force probing and X-ray photoelectron spectroscopy (XPS) depth profiling to give a comprehensive picture of the electronic, mechanical and chemical properties of SEI film under realistic conditions.
引用
收藏
页码:18348 / 18357
页数:10
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