Hierarchically Porous Ti3C2 MXene with Tunable Active Edges and Unsaturated Coordination Bonds for Superior Lithium-Sulfur Batteries

被引:99
|
作者
Wang, Tong [1 ,2 ,3 ]
Luo, Dan [2 ,3 ,4 ]
Zhang, Yongguang [1 ,2 ,3 ]
Zhang, Zhen [4 ]
Wang, Jiayi [2 ,3 ]
Cui, Guoliang [2 ,3 ]
Wang, Xin [2 ,3 ]
Yu, Aiping [4 ]
Chen, Zhongwei [4 ]
机构
[1] Hebei Univ Technol, Sch Mat Sci & Engn, State Key Lab Reliabil & Intelligence Elect Equip, Tianjin 300130, Peoples R China
[2] South China Normal Univ, Sch Informat & Optoelect Sci & Engn, Guangzhou 510006, Peoples R China
[3] South China Normal Univ, Int Acad Optoelect Zhaoqing, Guangzhou 510006, Peoples R China
[4] Univ Waterloo, Dept Chem Engn, Waterloo, ON N2L 3G1, Canada
基金
中国博士后科学基金; 加拿大自然科学与工程研究理事会;
关键词
lithium-sulfur battery; MXene; coordination engineering; hierarchical pore; catalytic conversion; SITES;
D O I
10.1021/acsnano.1c06213
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lithium-sulfur (Li-S) batteries hold great promise for next-generation electronics owing to their high theoretical energy density, low cost, and eco-friendliness. Nevertheless, the practical implementation of Li-S batteries is hindered by the shuttle effect and sluggish reaction kinetics of polysulfides. Herein, the spray drying and chemical etching strategies are implemented to fabricate hierarchically porous MXene microspheres as a multifunctional sulfur electrocatalyst. The interconnected skeleton offers uniform sulfur distribution and prevents the restacking of MXene sheets, while the abundant edges endow the nanosheet-like Ti3C2 with rich active sites and regulated a d-band center of Ti atoms, leading to strong lithium polysulfide (UPS) adsorption. The unsaturated Ti on edge sites can further act as multifunctional sites for chemically anchoring LiPS and lowering Li-ion migration barriers, accelerating LiPS conversion. Owing to these structural advantages, excellent cycling and rate performances of the sulfur cathode can be obtained, even under a raised sulfur loading and lean electrolyte content.
引用
收藏
页码:19457 / 19467
页数:11
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