期刊
RSC ADVANCES
卷 5, 期 17, 页码 13046-13051出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4ra14820g
关键词
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资金
- NSFC [21305041, 21275052]
- Scientific Research Fund of Hunan Provincial Education Department [13B063]
- Start-Up Fund for Young Teachers in Hunan Normal University
Direct carbonization and simultaneous chemical activation of a cobalt ion-impregnated sulfonic acid ion exchange resin is found to be an efficient approach to the large-scale synthesis of sulfur-doped porous carbon nanosheets (S-PCNS) for supercapacitors with high specific energy and excellent rate capability. The as-prepared S-PCNS showed a three-dimensional interconnected structure, high graphitization degree, high C/O atomic ratio (22.9:1), high-level sulfur doping (9.6 wt%), high specific surface area (2005 m(2) g(-1)), and good porosity. The S-PCNS serving as an electrode material for supercapacitors exhibited a specific capacitance as high as 312 F g(-1) at 0.5 A g(-1), excellent rate capability (78% of capacitance retention at 50 A g(-1)), high energy density (11.0 W h kg(-1) at 0.5 A g(-1)), and outstanding cycling stability (similar to 97% of its initial capacitance after 10 000 cycles at 2 A g(-1)) in 6.0 M aqueous KOH electrolyte. Due to the unique structure of S-PCNS, the specific capacitance of S-PCNS is higher than that of sulfur-doped activated carbon. The excellent capacitance performance coupled with the facile synthesis of S-PCNS indicates a potential electrode material for supercapacitors.
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