Ultrathin Carbon-Shell-Encapsulated Cobalt Nanoparticles with Balanced Activity and Stability for Lithium-Sulfur Batteries

被引:15
作者
Zhang, Xinming [1 ]
Liu, Zichen [1 ]
Liu, Wen [1 ]
Han, Junwei [1 ]
Lv, Wei [1 ]
机构
[1] Tsinghua Univ, Shenzhen Geim Graphene Ctr, Tsinghua Shenzhen Int Grad Sch, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
lithium-sulfur batteries; transition-metal-based catalyst; carbon encapsulation; catalyst activity; catalyst stability; CONVERSION; POLYSULFIDES; GRAPHENE; CATHODE;
D O I
10.1021/acsami.3c01512
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
High-performance metal-based catalysts are pursued to improve the sluggish reaction kinetics in lithium-sulfur batteries. However, it is challenging to achieve high catalytic activity and stability simultaneously due to the inevitable passivation of the highly active metal nanoparticles by lithium polysulfides (LiPSs). Herein, we show a design with well-balanced activity and stability to solve the above problem, that is, the cobalt (Co) nanoparticles (NPs) encapsulated with ultrathin carbon shells prepared by the one-step pyrolysis of ZIF-67. With an ultrathin carbon coating (similar to 1 nm), the direct exposure of Co NPs to LiPSs is avoided, but it allows the fast electron transfer from the highly active Co NPs to LiPSs for their conversion to the solid products, ensuring the efficient suppression of shuttling in long cycling. As a result, the sulfur cathode with such a catalyst exhibited good cycling stability (0.073% capacity fading over 500 cycles) and high sulfur utilization (638 mAh g-1 after 180 cycles under a high sulfur mass loading of 7.37 mg cm-2 and a low electrolyte/sulfur ratio of 5 mu L mg-1). This work provides insights into the rational design of a protection layer on a metal-based catalyst to engineer both high catalytic activity and stability toward high-energy and long-life Li-S batteries.
引用
收藏
页码:19002 / 19010
页数:9
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