材料科学
微乳液
阳极
多孔性
阴极
石墨烯
化学工程
硫黄
纳米技术
复合材料
物理化学
电极
肺表面活性物质
工程类
冶金
化学
作者
Juan Zhang,Jinyi Li,Wenpeng Wang,Xinghao Zhang,Xinghua Tan,Weiguo Chu,Yu‐Guo Guo
标识
DOI:10.1002/aenm.201702839
摘要
Abstract A 3D porous sulfur/graphene@g‐C 3 N 4 (S/GCN) hybrid sponge, which can be directly applied as a free‐standing cathode for Li–S batteries, is realized via a microemulsion assisted assembly approach. In this strategy, the interior oil emulsion droplets serve as soft templates to form pores to accommodate sulfur and the hydrophilic GCN stacks around oil droplets to assemble into a crosslinked 3D network. Through this microemulsion encapsulation route, S/GCN cathodes with a sulfur loading as high as 82 wt% can be achieved. Furthermore, the enriched N‐sites in GCN macropores offer numerous adhesion sites for polysulfides, realizing a “physical‐chemical” dual‐confinement for polysulfides from diffusion. Moreover, the robust and highly porous 3D graphene frameworks render efficient electron/Li + transport pathways for fast kinetics as well as good structure integrity. Consequently, in comparison to the conventional G‐sponge/Li 2 S n catholyte system, S/GCN delivers a higher specific capacity, superior high‐rate capability (612 mA h g −1 at 10 C), and alleviated anode corrosion issues. Particularly, an energy density as high as 1493 W h kg −1 (calculated on the total weight of the cathode) and an extremely low capacity fading rate of 0.017% per cycle over 800 cycles at 0.3 C are achieved.
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