Interfaces-dominated Li2S nucleation behavior enabled by heterostructure catalyst for fast kinetics Li-S batteries

被引:103
作者
Cai, Da-Qian [1 ,2 ]
Yang, Jin-Lin [1 ]
Liu, Ting [3 ]
Zhao, Shi-Xi [1 ]
Cao, Guozhong [4 ]
机构
[1] Tsinghua Univ, Tsinghua Shenzhen Int Grad Sch, Shenzhen 518055, Peoples R China
[2] Tsinghua Univ, Sch Mat Sci & Engn, Beijing 100084, Peoples R China
[3] Foshan Southern China Inst New Mat, Foshan 528200, Peoples R China
[4] Univ Washington, Dept Mat Sci & Engn, Seattle, WA 98195 USA
关键词
Lithium-sulfur batteries; MoO2/alpha-MoC; Cathode additives; Catalytic effect; Li2S deposition; HYDROGEN EVOLUTION REACTION; SULFUR; CONVERSION; CARBON; PERFORMANCE; ELECTROCATALYSIS; POLYSULFIDES; GRAPHENE; STRATEGY; OXIDE;
D O I
10.1016/j.nanoen.2021.106452
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 (LSBs) have gained wide attention in the past decades for its high energy density and low cost. However, LSBs practical application is hindered by the severe shuttling of soluble intermediate lithium polysulfides (LiPSs), and the uncontrollable deposition of insulating Li2S, which limits the active species utilization and decelerates the redox kinetics. In this study, MoO2/alpha-MoC nanocomposite was investigated as a multifunctional electrocatalyst to address above problems. Not only does such electrocatalyst immobilizes LiPSs on its surface but also facilitate the subsequent conversion reaction, further enable the heterogeneous Li2S nucleation and induce three-dimensional precipitation of Li2S. MoO2/alpha-MoC-containing LSBs exhibit excellent rate performance, promising cycling stability, and a high specific capacity of 1177 mAh g(-1) at 0.2 C and 695 mAh g(-1) at 3 C with a low-capacity deterioration. Good cyclic stability was achieved at 0.5 C even with a high sulfur loading of 5 mg cm(-2) and a low E/S ratio of 6-7 mu L mg(-1) by employing a MoO2/alpha-MoC interlayer.
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页数:9
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