Lithiophilic interface dynamic engineering to inhibit Li dendrite growth for intrinsically safe Li-metal batteries

被引:11
|
作者
Jiang, Tingting [1 ]
Sun, Lingling [1 ]
Zhang, Yao [1 ]
Zhang, Xiaomin [1 ]
Lin, Huijuan [1 ]
Rui, Kun [1 ]
Zhu, Jixin [2 ]
机构
[1] Nanjing Tech Univ, Sch Flexible Elect Future Technol, Key Lab Flexible Elect KLOFE, 30 South Puzhu Rd, Nanjing 211816, Peoples R China
[2] Univ Sci & Technol China, State Key Lab Fire Sci, 443 Huangshan Rd, Hefei 230027, Peoples R China
基金
中国国家自然科学基金;
关键词
NiFe-LDH nanosheets; 3D self-supporting structure; Li metal anode; Long cycle life; OXYGEN EVOLUTION; LITHIUM; DEPOSITION; ANODES;
D O I
10.1016/j.cej.2023.142555
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Lithium (Li) metal is deemed as attractive anode due to its low electrochemical potential and high theoretical capacity. Nevertheless, the uncontrollable Li dendrite growth causes safety concern and battery failure, which severely impedes the commercialization of Li metal batteries (LMBs). Herein, 3D functional matrix comprising NiFe-layered-double-hydroxide nanosheet arrays (NiFe-LDH) evenly dispersed on acidified carbon cloth (NiFe-LDH@ACC) via hydrothermal method is designed to manipulate uniform Li electrodeposition morphology. Vertical NiFe-LDH nanosheets possess high accessible surface area to supply vast Li nucleation sites, thus effectively reducing the local current density and decreasing the nucleation energy barrier to suppress Li den-drites growth, which has been validated by simulation. Moreover, 3D structure of carbon cloth provides adequate space for storing Li metal, substantially abating volume fluctuation during repeated Li plating/stripping process. Consequently, the Li@NiFe-LDH@ACC electrode manifests ultra-long lifespan over 3500 h and low-voltage hysteresis in symmetric cells. Additionally, the full cell with limited Li@NiFe-LDH@ACC anode and commer-cial LiFePO4 cathode (mass loading: 8.35 mg cm-2) displays good rate capacity from 0.2 C to 5 C, and can steadily operate for 75 cycles at 2 C with a capacity of 131 mAh g- 1, revealing the practical feasibility of the surface modification strategy for constructing advanced Li metal anode with high safety and appealing durability.
引用
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页数:9
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