Abstract

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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