多硫化物
材料科学
聚丙烯腈
介孔材料
化学工程
纳米纤维
阴极
静电纺丝
碳纳米纤维
碳纤维
硫黄
电解质
复合材料
聚合物
电极
有机化学
碳纳米管
复合数
化学
催化作用
冶金
物理化学
工程类
作者
Snatika Sarkar,Jong Sung Won,Meichun An,Rui Zhang,Jin Hong Lee,Seung‐Goo Lee,Yong Lak Joo
出处
期刊:Polymers
[Multidisciplinary Digital Publishing Institute]
日期:2022-03-25
卷期号:14 (7): 1342-1342
被引量:4
标识
DOI:10.3390/polym14071342
摘要
In the current work, we combined different physical and chemical modifications of carbon nanofibers through the creation of micro-, meso-, and macro-pores as well as the incorporation of nitrogen groups in cyclic polyacrylonitrile (CPAN) using gas-assisted electrospinning and air-controlled electrospray processes. We incorporated them into electrode and interlayer in Li-Sulfur batteries. First, we controlled pore size and distributions in mesoporous carbon fibers (mpCNF) via adding polymethyl methacrylate as a sacrificial polymer to the polyacrylonitrile carbon precursor, followed by varying activation conditions. Secondly, nitrogen groups were introduced via cyclization of PAN on mesoporous carbon nanofibers (mpCPAN). We compared the synergistic effects of all these features in cathode substrate and interlayer on the performance Li-Sulfur batteries and used various characterization tools to understand them. Our results revealed that coating CPAN on both mesoporous carbon cathode and interlayer greatly enhanced the rate capability and capacity retention, leading to the capacity of 1000 mAh/g at 2 C and 1200 mAh/g at 0.5 C with the capability retention of 88% after 100 cycles. The presence of nitrogen groups and mesopores in both cathodes and interlayers resulted in more effective polysulfide confinement and also show more promise for higher loading systems.
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