多硫化物
材料科学
钴
介孔材料
硫黄
纳米技术
锂(药物)
碳纤维
阴极
掺杂剂
电化学
硫化钴
化学工程
催化作用
兴奋剂
电极
化学
有机化学
复合数
物理化学
复合材料
内分泌学
冶金
工程类
医学
电解质
光电子学
作者
Jin Xie,Bo‐Quan Li,Hong‐Jie Peng,Yun‐Wei Song,Meng Zhao,Xiao Chen,Qiang Zhang,Jia‐Qi Huang
标识
DOI:10.1002/adma.201903813
摘要
Lithium-sulfur (Li-S) batteries hold great promise to serve as next-generation energy storage devices. However, the practical performances of Li-S batteries are severely limited by the sulfur cathode regarding its low conductivity, huge volume change, and the polysulfide shuttle effect. The first two issues have been well addressed by introducing mesoporous carbon hosts to the sulfur cathode. Unfortunately, the nonpolar nature of carbon materials renders poor affinity to polar polysulfides, leaving the shuttling issue unaddressed. In this contribution, atomic cobalt is implanted within the skeleton of mesoporous carbon via a supramolecular self-templating strategy, which simultaneously improves the interaction with polysulfides and maintains the mesoporous structure. Moreover, the atomic cobalt dopants serve as active sites to improve the kinetics of the sulfur redox reactions. With the atomic-cobalt-decorated mesoporous carbon host, a high capacity of 1130 mAh gS-1 at 0.5 C and a high stability with a retention of 74.1% after 300 cycles are realized. Implanting atomic metal in mesoporous carbon demonstrates a feasible strategy to endow nanomaterials with targeted functions for Li-S batteries and broad applications.
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