用户名: 密码: 验证码:
Silica Doped Nanopolyaniline with Endured Electrochemical Energy Storage and the Magnetic Field Effects
详细信息    查看全文
文摘
Phosphoric acid doped conductive polyainiline (PANI)/silica nanocomposites used as supercapacitor electrodes are tested in this article. The nanocomposites with 10.0, 20.0, 40.0, and 60.0 wt % silica nanoparticle loadings were synthesized via a facile surface initiated polymerization method. The morphology and chemical structure of the nanocomposites were characterized by scanning electron microscopy and Fourier transform infrared spectroscopy. The electrochemical performances of the nanocomposites were evaluated by cyclic voltammetry, galvanostatic charge鈥揹ischarge measurement, and electrochemical impedance spectroscopy techniques. The nanocomposites with a loading of 10.0 wt % silica nanoparticles displayed an optimum supercapacitive performances with a maximum gravimetric capacitance of 344.1 F/g at a scan rate of 5.0 mV/s (280.3 F/g for PANI nanoparticles) when normalized to the mass of PANI. Meanwhile, a maximum energy density of 37.4 Wh/kg (34.7 for pure PANI nanoparticles) at a power density of 430 W/kg (415 W/kg for pure PANI) is obtained from the charge鈥揹ischarge measurement at a current density of 1.0 A/g. The effect of electrolytes on the electrochemical performances was also studied by using sulfuric acid and sodium sulfate in aqueous solution, respectively. A pseudocapacitance contribution was observed arising from PANI in the acid H2SO4 electrolyte medium whereas most of the capacitance came from the electric double layer capacitance in the neutral Na2SO4 electrolyte. In addition, external magnetic field was applied onto the nanocomposite electrode, which showed reduced capacitances due to the induced positive magnetoresistance. The cyclic stability studies revealed a much more superior stability of the nanocomposites than that of pure PANI after 500 charge鈥揹ischarge cycles.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700