纳米笼
硫黄
阴极
多硫化物
电化学
异质结
材料科学
化学工程
锂(药物)
纳米技术
化学
电极
催化作用
光电子学
冶金
电解质
物理化学
有机化学
工程类
内分泌学
医学
作者
Ji Zhou,Xin Chen,Wenbin Gong,Xiaodong Meng,Chao Chen,Xueqin Zhou,Manyun Wang,Kwun Nam Hui,Jianxin Geng
标识
DOI:10.1016/j.est.2023.109505
摘要
The intelligent design of electrocatalytic sulfur host materials is an essential step to achieving high-performance lithium−sulfur (LiS) batteries. Herein, we report double-shelled ZnS@CoS2 nanocages as sulfur hosts to electrocatalytically enhance sulfur cathode kinetics and suppress the shuttle effect of polysulfides. Combining theoretical calculations and experimental tests, we reveal that the built-in electric field formed at the ZnS@CoS2 heterojunction is uniquely suited to promoting sulfur cathode electrochemistry; the double-shelled ZnS@CoS2 nanocages facilitate Li+ transport while at the same time enabling the immobilization and rapid electrocatalytic conversion of key polysulfides. Consequently, LiS cells prepared from ZnS@CoS2 as sulfur host exhibit a high specific capacity (e.g., 1443 mA h g−1 at the current rate of 0.1 C) and an impressive cycling stability (e.g., an initial specific capacity of 801 mA h g−1 achieved at 2 C and 507 mA h g−1 retained after 650 cycles). Our new concept of designing a heterojunction to promote sulfur cathodic reactions can be potentially extended to other contemporary energy-storage systems.
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