多硫化物
材料科学
阴极
硫黄
氧化还原
化学工程
介孔材料
电化学
动力学
电池(电)
碳纤维
吸附
多孔性
电化学动力学
锂硫电池
电导率
纳米技术
催化作用
储能
无机化学
电极
氧化物
作者
YingHua Li,Mengtian Zhang,Z Xu,Zhilin Liu,Mingyan Chuai,Xiao Xiao,Xiaodong Guo,Guangmin Zhou,Yiyong Mai,Fugui Xu,Hong Li
摘要
ABSTRACT The electrochemical performance of lithium‐sulfur batteries is hindered by the shuttle effect of lithium polysulfides, the poor electrical conductivity of sulfur, and sluggish redox kinetics of sulfur species. By mimicking the high‐efficiency mass transport, excellent nutriment capture capability, and rapid catalytic conversion properties of marine sponges, a multifunctional bicontinuous mesoporous carbonaceous sulfur host incorporated with Co single atoms (denoted as bimeso‐CoNC) is constructed as a cathode material for Li‐S batteries. The 3D interconnected mesochannels in bimeso‐CoNC enhance the Li + transport and sulfur loading, while the incorporated Co single atoms exhibit strong polysulfide adsorption and accelerate the kinetics of polysulfide conversion. Remarkably, the bimeso‐CoNC/S‐based cathode delivers a high capability of 570.0 mAh g −1 at 6 C, a high areal capacity of 11.6 mAh cm −2 at an ultrahigh sulfur loading of 13.5 mg cm −2 , and remarkable long‐term stability (over 1200 cycles with 0.039% capacity decay per cycle). The comprehensive performance ranks among the best of the reported carbon‐based cathode materials for Li‐S batteries. This study presents a pore engineering strategy to improve the loading and adsorption of sulfur as well as accelerate the sulfur redox kinetics in Li‐S batteries, which remarkably suppresses the shuttling effect and thus enhances the performance of Li‐S batteries.
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