材料科学
超级电容器
纳米线
电解质
电化学
钴
锰
化学工程
电极
纳米颗粒
热分解
比表面积
无机化学
纳米技术
化学
冶金
物理化学
催化作用
有机化学
工程类
作者
Yanan Xu,Xiaofeng Wang,Cuihua An,Yijing Wang,Lifang Jiao,Huatang Yuan
出处
期刊:Journal of materials chemistry. A, Materials for energy and sustainability
[The Royal Society of Chemistry]
日期:2014-08-06
卷期号:2 (39): 16480-16488
被引量:297
摘要
Two types of porous cobalt manganese oxide nanowires (MnCo2O4 and CoMn2O4) with different structures have been successfully synthesized by thermal decomposition of organometallic compounds for the first time. Nitrilotriacetic acid (NA) was used as a chelating agent to coordinate Co(II) and Mn(II) ions in various molar ratios, in a hydrothermal condition. The microstructure of as-synthesized cobalt manganese oxides, composed of numerous nanoparticles, completely retains the 1D network structure of the Co–Mn–NA coordination precursors without structure collapse. Electrochemical properties of the cobalt manganese oxide materials have been tested for supercapacitors at room temperature. Both the MnCo2O4 and CoMn2O4 electrodes display the outstanding capacitive behaviors and superior electrochemical properties. The CoMn2O4 nanowire shows excellent capacitance and desirable rate performance (2108 F g−1 at 1 A g−1 and 1191 F g−1 at 20 A g−1) compared to that of the MnCo2O4 nanowire (1342 F g−1 at 1 A g−1 and 988 F g−1 at 20 A g−1). Electrochemical impedance spectra (EIS) results also reconfirm that the CoMn2O4 nanowires display more facile electrolyte diffusion and higher capacitor response frequency than MnCo2O4 nanowires. This can be ascribed to the facile electrolyte/OH− ion penetration and better Faradaic utilization of the electroactive surface sites that generated by the smaller particle size and higher surface area.
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