多硫化物
石墨烯
硫黄
材料科学
阴极
溶解
碳纤维
锂(药物)
纳米技术
石墨氮化碳
化学工程
催化作用
电极
化学
复合数
电解质
有机化学
复合材料
内分泌学
工程类
物理化学
冶金
医学
光催化
作者
Meng Wang,Qinghua Liang,Junwei Han,Ying Tao,Qiang Cai,Chen Zhang,Wei Lv,Quan‐Hong Yang
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2018-03-08
卷期号:11 (6): 3480-3489
被引量:106
标识
DOI:10.1007/s12274-018-2023-y
摘要
The practical application of lithium-sulfur batteries with a high energy density has been plagued by the poor cycling stability of the sulfur cathode, which is a result of the insulating nature of sulfur and the dissolution of polysulfides. Much work has been done to construct nanostructured or doped carbon as a porous or polar host for promising sulfur cathodes, although restricting the polysulfide shuttle effect by improving the redox reaction kinetics is more attractive. Herein, we present a well-designed strategy by introducing graphitic carbon nitride (g-C3N4) into a three-dimensional hierarchical porous graphene assembly to achieve a synergistic combination of confinement and catalyzation of polysulfides. The porous g-C3N4 nanosheets in situ formed inside the graphene network afford a highly accessible surface to catalyze the transformation of polysulfides, and the hierarchical porous graphene-assembled carbon can function as a conductive network and provide appropriate space for g-C3N4 catalysis in the sulfur cathode. Thus, this hybrid can effectively improve sulfur utilization and block the dissolution of polysulfides, achieving excellent cycling performance for sulfur cathodes in lithium-sulfur batteries.
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