Recyclable cobalt-molybdenum bimetallic carbide modified separator boosts the polysulfide adsorption-catalysis of lithium sulfur battery

SCIENCE CHINA-MATERIALS(2020)

引用 69|浏览98
暂无评分
摘要
The polysulfide shuttling and sluggish redox kinetics, due to the notorious adsorption-catalysis underperformance, are the ultimate obstacles of the practical application of lithium-sulfur (Li-S) batteries. Conventional carbon-based and transition metal compound-based material solutions generally suffer from poor catalysis and adsorption, respectively, despite the performance gain in terms of the other. Herein, we have enhanced polysulfide adsorption-catalytic capability and protected the Li anode using a complementary bimetallic carbide electrocatalyst, Co 3 Mo 3 C, modified commercial separator. With this demonstration, the potentials of bimetal compounds, which have been well recognized in other environmental catalysis, are also extended to Li-S batteries. Coupled with this modified separator, a simple cathode (S/Super P composite) can deliver high sulfur utilization, high rate performance, and excellent cycle stability with a low capacity decay rate of ∼0.034% per cycle at 1 C up to 1000 cycles. Even at a high S-loading of 8.0 mg cm −2 with electrolyte/sulfur ratio=6 mL g −1 , the cathode still exhibits high areal capacity of ∼6.8 mA h cm −2 . The experimental analysis and the first principles calculations proved that the bimetallic carbide Co 3 Mo 3 C provides more binding sites for adsorbing polysulfides and catalyzing the multiphase conversion of sulfur/polysulfide/sulfide than monometallic carbide Mo 2 C. Moreover, the modified separator can be reutilized with comparable electrochemical performance. We also showed other bimetallic carbides with similar catalytic effects on Li S batteries and this material family has great promise in different energy electrocatalytic systems.
更多
查看译文
关键词
lithium-sulfur batteries, bimetallic carbides, electrocatalysts, polysulfide adsorption-catalysis, modified separators
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要