A tandem electrocatalyst with dense heterointerfaces enabling the stepwise conversion of polysulfide in lithium-sulfur batteries

被引:75
作者
Qin, Bin [1 ]
Zhao, Xiaomei [4 ]
Wang, Qun [3 ]
Yao, Weiqi [5 ]
Cai, Yifei [1 ]
Chen, Yuhan [6 ]
Wang, Pengcheng [1 ]
Zou, YongChun [7 ]
Cao, Jian [1 ]
Zheng, Xiaohang [2 ]
Qi, Junlei [1 ]
Cai, Wei [2 ]
机构
[1] Harbin Inst Technol, State Key Lab Adv Welding & Joining, Harbin 150001, Peoples R China
[2] Harbin Inst Technol, Sch Mat Sci & Engn, Harbin 150001, Peoples R China
[3] Taiyuan Univ Technol, Coll Chem & Chem Engn, Taiyuan 030024, Peoples R China
[4] Xiangtan Univ, Dept Chem, Key Lab Environmentally Friendly Chem Applicat, Key Lab Green Organ Synth & Applicat Hunan Prov,Mi, Xiangtan 411105, Peoples R China
[5] East China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
[6] City Univ Hong Kong, Dept Mech Engn, Hong Kong, Peoples R China
[7] Harbin Inst Technol, Ctr Anal Measurement & Comp, Harbin 150001, Peoples R China
关键词
Lithium -sulfur batteries; Heterostructures; Tandem catalysis; Synergistic effects; Stepwise conversion; PERFORMANCE;
D O I
10.1016/j.ensm.2022.12.014
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The complicated sulfur phase transformation and diversity kinetics of lithium polysulfide intermediates hinder the practical applications of Li-S batteries. Herein, we report that Mo-Ni bimetal sulfide nanosheets with dense heterointerfaces and defects can decouple the complicated reactions into well-controlled multi-steps in tandem. Specifically, the MoS2 in Mo-Ni tandem catalyst is more effective in catalyzing the phase transformation from Li2S8 to Li2S4, while NiS2 delivers higher catalytic activity toward both the Li2S4 to Li2S conversion and the Li2S dissociation steps, as indicated by density functional theory calculations and comprehensive experiments. This integrated system tends to selectively propel the stepwise conversion of sulfur and thereby enhancing the battery performance. As a result, the sulfur loaded cathode delivers a high initial capacity of 1481 mAh g-1 at 0.2 C, and a low capacity decay rate of 0.0236% per cycle over 1000 cycles at 2 C. This study demonstrates the feasibility of using tandem catalysis for regulating the smooth solid-liquid-solid multiphase transformation of polysulfides.
引用
收藏
页码:445 / 454
页数:10
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