杂原子
材料科学
多硫化物
硫黄
碳纤维
法拉第效率
钴
化学工程
氧化还原
阴极
金属
锂(药物)
无机化学
阳极
电解质
电极
化学
有机化学
冶金
复合材料
戒指(化学)
物理化学
内分泌学
工程类
复合数
医学
作者
Shaohong Liu,Jia Li,Yan Xue,Quanfei Su,Yuheng Lu,Jieshan Qiu,Zhiyu Wang,Xidong Lin,Junlong Huang,Ruliang Liu,Bingna Zheng,Luyi Chen,Ruowen Fu,Dingcai Wu
标识
DOI:10.1002/adma.201706895
摘要
Lithium-sulfur (Li-S) batteries, based on the redox reaction between elemental sulfur and lithium metal, have attracted great interest because of their inherently high theoretical energy density. However, the severe polysulfide shuttle effect and sluggish reaction kinetics in sulfur cathodes, as well as dendrite growth in lithium-metal anodes are great obstacles for their practical application. Herein, a two-in-one approach with superhierarchical cobalt-embedded nitrogen-doped porous carbon nanosheets (Co/N-PCNSs) as stable hosts for both elemental sulfur and metallic lithium to improve their performance simultaneously is reported. Experimental and theoretical results reveal that stable Co nanoparticles, elaborately encapsulated by N-doped graphitic carbon, can work synergistically with N heteroatoms to reserve the soluble polysulfides and promote the redox reaction kinetics of sulfur cathodes. Moreover, the high-surface-area pore structure and the Co-enhanced lithiophilic N heteroatoms in Co/N-PCNSs can regulate metallic lithium plating and successfully suppress lithium dendrite growth in the anodes. As a result, a full lithium-sulfur cell constructed with Co/N-PCNSs as two-in-one hosts demonstrates excellent capacity retention with stable Coulombic efficiency.
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