Entropy Engineering-Modulated D-Band Center of Transition Metal Nitrides for Catalyzing Polysulfide Conversion in Lithium-Sulfur Batteries

被引:3
|
作者
Jiao, Jihuang [1 ]
Liu, Da [1 ]
He, Yufei [1 ]
Shen, Yinan [1 ]
Zhou, Jin [1 ]
Liang, Chu [2 ,3 ]
Pan, Hongge [4 ]
Wu, Renbing [1 ]
机构
[1] Fudan Univ, Dept Mat Sci, Shanghai 200433, Peoples R China
[2] Zhejiang Univ Technol, Zhejiang Carbon Neutral Innovat Inst, Hangzhou 310014, Peoples R China
[3] Zhejiang Univ Technol, Zhejiang Int Cooperat Base Sci & Technol Carbon Em, Hangzhou 310014, Peoples R China
[4] Xian Technol Univ, Inst Sci & Technol New Energy, Xian 710021, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
cathode; d-band center; entropy engineering; lithium-sulfur batteries; nitride;
D O I
10.1002/smll.202409740
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The sluggish sulfur redox kinetics and severe polysulfide shuttle effect seriously restrict the cycling stability and lower the sulfur utilization of lithium-sulfur (Li-S) batteries. Efficient catalytic conversion of polysulfides is deemed a crucial strategy to address these issues, but still suffers from an unclear electronic structure-activity relationship and a limited catalysis performance. Herein, entropy engineering-induced electronic state modulation of metal nitride nanoparticles embedded within hollow N-doped carbon (HNC) polyhedra are theoretically and experimentally constructed as a catalyst to accelerate the redox process of sulfur and suppress polysulfide migration in Li-S batteries. By introducing V, Cr, and Nb elements to engineer the entropy of TiN, the metal d-band center is optimized to approach the Fermi level, significantly facilitating the conversion of sulfur species. Accordingly, the TiVCrNbN@HNC catalyst enables Li-S batteries to achieve a high initial capacity (1299 mAh g-1 at 0.1 C) and excellent cycling stability with a low capacity decay rate of 0.086% per cycle after 500 cycles. This work may provide a new insight into entropy engineering in catalyst design for high-performance Li-S batteries.
引用
收藏
页数:10
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