Built-in Electric Field Within CoSe2-FeSe2 Heterostructure for Enhanced Sulfur Reduction Reaction in Li-S Batteries

被引:0
|
作者
Luo, Ruijian [1 ]
Zhao, Junzhe [1 ]
Zheng, Ming [1 ]
Wang, Zichen [1 ]
Zhang, Shunqiang [1 ]
Zhang, Jiancan [1 ]
Xiao, Yong [1 ]
Jiang, Yinghui [1 ]
Cai, Zhixiong [1 ]
Cheng, Niancai [1 ]
机构
[1] Fuzhou Univ, Coll Mat Sci & Engn, Fuzhou 350108, Peoples R China
基金
中国国家自然科学基金;
关键词
heterostructures; liquid-solid conversion; lithium-sulfur batteries; modified separator; PRUSSIAN BLUE; LITHIUM; DERIVATIVES; ANALOGS; HOLLOW;
D O I
10.1002/smll.202406415
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The conversion of Li2S4 to Li2S is the most important and slowest rate-limiting step in the complex sulfur reduction reaction (SRR) for Li-S batteries, the adjustment of which can effectively inhibit the notorious "shuttle effect". Herein, a CoSe2-FeSe2 heterostructure embedded in 3D N-doped nanocage as a modified layer on commercial separator is designed (CoSe2-FeSe2@NC//PP). The CoSe2-FeSe2 heterostructure forms a built-in electric field at the two-phase interface, which leads to the optimized adsorption force on polysulfides and the accelerated reaction kinetics for Li2S4-Li2S evolution. Density functional theory (DFT) calculations and experimental results combine to show that the liquid-solid reaction (Li2S4-Li2S2/Li2S) is significantly enhanced in terms of thermodynamics and electrodynamics. Consequently, the batteries assembled with CoSe2-FeSe2@NC//PP delivered an excellent rate capability (606 mAh g(-1) under 8.0 C) and a long cycling lifespan (only 0.056% at 1.0 C after 1000 cycles). In addition, the cells can provide high initial capacity of 887 mAh g(-1) at sulfur loading of 5.8 mg cm(-2) and 0.1 C. This work would provide valuable insights into binary metal selenide heterostructures for liquid-solid conversion in Li-S batteries.
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页数:10
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