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Observation on sodium p-toluenesulfonate-doped polypyrrole cathode for sodium ion battery

机译:对甲苯磺酸钠掺杂聚吡咯钠离子电池正极的观察

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摘要

Sodium p-toluenesulfonate (TsONa)-doped polypyrrole (PPy) was synthesized as the cathode active material of sodium ion battery by way of facile one-step electrodeposition on iron (Fe) foil. The micro-morphology and micro-structure of assynthesized TsONa/PPy/iron cathode were characterized in terms of scanning electron microscopy, energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, X-ray diffraction; furthermore, the electrochemical Na-storage activity of TsONa/PPy/iron cathode was investigated by methods of, galvanostatic charge/discharge, cyclic voltammetry and alternating current impedance. As expected, the cauliflower-like TsONa-doped PPy particles tightly combined with the surface of the iron foil without any additional polymer binders; and also, the resultant TsONa/PPy/iron cathode delivered satisfactory electrochemical performances, mainly attributed to high Na-storage activity of PPy matrix and high electronic conductivity induced by doping of TsONa. For example, the reversible discharge capacity of TsONa/PPy/iron cathode remained about 98 mAh/g after at least 50 cycles and the corresponding coulombic efficiency was 92%, indicating high cyclic stability and reversibility of TsONa/PPy/iron cathode for sodium ion battery.
机译:通过在铁(Fe)箔上进行简单的一步电沉积,合成了对甲苯磺酸钠(TsONa)掺杂的聚吡咯(PPy)作为钠离子电池的阴极活性材料。通过扫描电子显微镜,能量色散X射线能谱,X射线光电子能谱,X射线衍射,对合成的TsONa / PPy /铁阴极的微观形貌和微观结构进行了表征。此外,通过恒电流充/放电,循环伏安法和交流阻抗方法研究了TsONa / PPy /铁阴极的电化学Na存储活性。正如预期的那样,花椰菜状的TsONa掺杂的PPy颗粒与铁箔的表面紧密结合,而没有任何其他的聚合物粘合剂。并且,所得的TsONa / PPy /铁阴极具有令人满意的电化学性能,这主要归因于PPy基体的高Na储藏活性和掺杂TsONa引起的高电导率。例如,在至少50次循环后,TsONa / PPy /铁阴极的可逆放电容量保持在约98 mAh / g,相应的库伦效率为92%,表明TsONa / PPy /铁阴极对钠离子的高循环稳定性和可逆性电池。

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  • 来源
    《Surface Innovations》 |2018年第2期|56-62|共7页
  • 作者单位

    Professor, Faculty of Material Science and Engineering, Kunming University of Science and Technology, Kunming, China;

    Faculty of Material Science and Engineering, Kunming University of Science and Technology, Kunming, China;

    Faculty of Material Science and Engineering, Kunming University of Science and Technology, Kunming, China;

    Faculty of Material Science and Engineering, Kunming University of Science and Technology, Kunming, China;

    Faculty of Material Science and Engineering, Kunming University of Science and Technology, Kunming, China;

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