聚苯胺
材料科学
多硫化物
聚合
原位聚合
化学工程
复合材料
涂层
硫黄
电解质
电极
聚合物
化学
工程类
物理化学
冶金
作者
Feng Wu,Junzheng Chen,Li Li,Teng Zhao,Renjie Chen
摘要
Rapid in situ chemical oxidation polymerization of polyaniline was carried out to coat MWCNT-core/sulfur-shell structures. The S-coated-MWCNTs were obtained by ball-milling and thermal treatment. The polymerization was carried out by adding 2.6 g of dispersed S/MWCNT and 0.65 g of aniline hydrochloride to ethanol, and then mixing in a certain amount of ammonium peroxydisulfate dissolved in 0.2 M HCl. The addition of S/MWCNT reduced the polymerization time from 60 to 21 min. The composites were characterized by elemental analysis, FTIR, XRD, SEM, TEM, and electrochemical methods. A 70.0% sulfur, 20.2% emeraldine PANi salt and 9.8% MWCNT composite gave the typical two reduction peaks and two oxidation peaks; these are due to three polysulfide species. The initial discharge capacity was 1334.4 mAh g–1-S for the PANi-S/MWCNT electrode and the remaining capacity was 932.4 mAh g–1-S after 80 cycles. The columbic efficiency doubled to 92.4% compared to S-MWCNT-2. The rate of the reaction upon using PANi-S/MWCNT electrode was found to be almost twice that of the S/MWCNT composites. Because of the porous polymer, the diffusion distance of the lithium ion from the bulk liquid was reduced. The gel-like cathode composites and the higher conductivities improved the kinetics of the lithium sulfur redox reaction.
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