Identifying the Evolution of Selenium-Vacancy-Modulated MoSe2 Precatalyst in Lithium-Sulfur Chemistry

被引:160
|
作者
Wang, Menglei [1 ,2 ]
Sun, Zhongti [1 ,3 ]
Ci, Haina [1 ,2 ]
Shi, Zixiong [1 ]
Shen, Lin [1 ]
Wei, Chaohui [1 ]
Ding, Yifan [1 ]
Yang, Xianzhong [1 ]
Sun, Jingyu [1 ,2 ]
机构
[1] Soochow Univ, Coll Energy, Soochow Inst Energy & Mat Innovat SIEMIS, Jiangsu Prov Key Lab Adv Carbon Mat & Wearable En, Suzhou 215006, Peoples R China
[2] Beijing Graphene Inst BGI, Beijing 100095, Peoples R China
[3] Jiangsu Univ, Sch Mat Sci & Engn, Zhenjiang 212013, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
dynamic evolution; Li-S batteries; molybdenum; precatalyst; Se vacancies; POLYSULFIDE CONVERSION; LAYER; SPHERES; FILMS;
D O I
10.1002/anie.202109291
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Witnessing compositional evolution and identifying the catalytically active moiety of electrocatalysts is of paramount importance in Li-S chemistry. Nevertheless, this field remains elusive. We report the scalable salt-templated synthesis of Se-vacancy-incorporated MoSe2 architecture (SeVs-MoSe2) and reveal the phase evolution of the defective precatalyst in working Li-S batteries. The interaction between lithium polysulfides and SeVs-MoSe2 is probed to induce the transformation from SeVs-MoSe2 to MoSeS. Furthermore, operando Raman spectroscopy and ex situ X-ray diffraction measurements in combination with theoretical simulations verify that the effectual MoSeS catalyst could help promote conversion of Li2S2 to Li2S, thereby boosting the capacity performance. The Li-S battery accordingly exhibits a satisfactory rate and cycling capability even with and elevated sulfur loading and lean electrolyte conditions (7.67 mg cm(-2); 4.0 mu L mg(S)(-1)). This work elucidates the design strategies and catalytic mechanisms of efficient electrocatalysts bearing defects.
引用
收藏
页码:24558 / 24565
页数:8
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