Bifunctional effect of laser-induced nucleation-preferable microchannels andin situformed LiF SEI in MXenes for stable lithium-metal batteries

被引:39
|
作者
Xiong, Cheng [1 ]
Wang, Zhenyu [1 ]
Peng, Xudong [1 ]
Guo, Yang [2 ]
Xu, Shaolin [2 ]
Zhao, Tianshou [1 ]
机构
[1] Hong Kong Univ Sci & Technol, Dept Mech & Aerosp Engn, Kowloon, Clear Water Bay, Hong Kong, Peoples R China
[2] Southern Univ Sci & Technol, Dept Mech & Energy Engn, Shenzhen, Peoples R China
关键词
RECHARGEABLE BATTERIES; CURRENT COLLECTOR; DENDRITE GROWTH; ANODE; CARBON; ELECTROLYTES; PROTECTION; NETWORK; COPPER; LAYER;
D O I
10.1039/d0ta04302h
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 (Li) metal is considered to be the ultimate choice of anode for high energy density lithium-based batteries. However, the uncontrollable dendrite growth, in particular at large current rates, hinders its practical applications. Herein, a novel MXene/TiO(2)membrane with aligned microchannels as the lithium host is fabricated using a femtosecond laser, with numerous lithiophilic sites (TiO2) spatial-precisely synthesized on the channel walls. Benefiting from the exposed nanometer-scale edges of the MXene, a favorable Li(+)ion migration into the channels is achieved by the well-manipulated electric field, thus resulting in preferential Li deposition inside the microchannels. Moreover, a lithium fluoride (LiF) reinforced SEI is generated on the top surface of the host upon electrochemical cycling thanks to the built-in fluorine terminals in the MXene. As a result, a long lifespan of 750 cycles (1500 hours) with a coulombic efficiency of 98.8% is achieved at 1 mA cm(-2). Even at an ultrahigh current density of 20 mA cm(-2), a lifespan of 500 cycles with a coulombic efficiency of 95.9% is still delivered.
引用
收藏
页码:14114 / 14125
页数:12
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