Nanoreactors Encapsulating Built-in Electric Field as a "Bridge" for Li-S Batteries: Directional Migration and Rapid Conversion of Polysulfides

被引:104
作者
Li, Junhao [1 ,2 ]
Wang, Zhengyi [1 ]
Shi, Kaixiang [1 ,3 ,4 ]
Wu, Yujie [1 ]
Huang, Wenzhi [1 ]
Min, Yonggang [5 ]
Liu, Quanbing [1 ,3 ]
Liang, Zhenxing [2 ,4 ]
机构
[1] Guangdong Univ Technol, Sch Chem Engn & Light Ind, Guangzhou Key Lab Clean Transportat Energy Chem, Guangdong Prov Key Lab Plant Resources Biorefinery, Guangzhou 510006, Peoples R China
[2] South China Univ Technol, Sch Chem & Chem Engn, Guangzhou 510641, Peoples R China
[3] Jieyang Branch Chem & Chem Engn, Guangdong Lab, Rongjiang Lab, Jieyang 515200, Peoples R China
[4] Guangdong Prov Key Lab Fuel Cell Technol, Guangzhou 510641, Peoples R China
[5] Guangdong Univ Technol, Sch Mat & Energy, Guangzhou 510006, Peoples R China
基金
中国国家自然科学基金;
关键词
built-in electric field; directional migration; heterostructure; lithium-sulfur batteries; shuttle effect; LITHIUM; HETEROSTRUCTURE; PERFORMANCE;
D O I
10.1002/aenm.202303546
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
Lithium-sulfur batteries (Li-S) are recognized as the next generation of secondary batteries due to their satisfactory theoretical specific capacity and energy density. However, a series of problems such as disordered migration behavior, sluggish redox kinetics, and serious shuttle effect of lithium polysulfides (LiPSs) greatly limit the commercial application. Herein, nanoreactors encapsulate heterostructure to guarantee sulfur conversion in the hosts where the heterostructure consists of FeP with moderate adsorption ability, excellent catalytic active and low work function, and Fe3O4 with strong adsorption ability and high work function. This rational configuration of heterostructure controls the direction of the interface built-in electric field (BIEF) between catalyst and adsorbent, realizing the successive "trapping-directional migration-conversion" reaction mechanism to sulfur species. Thanks to BIEF as a bridge to connect the trapping site and catalytic site, Fe3O4/FeP@CS cathode delivers an ultrahigh initial specific capacity of 1402 mAh g-1 at 0.1 C and remains more than 450 mAh g-1 at 5 C after 350 cycles. Even with a sulfur loading of 5.20 mg cm-2, it displayed the initial specific capacity of 970 mAh g-1. This work provided an effective strategy to design high-performance electrocatalysts for commercial Li-S batteries. Controlling the direction of interface built-in electric field between catalyst and adsorbent to realize a successive "trapping-directional migration-conversion" reaction mechanism to sulfur species.image
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页数:12
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