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Analysis of Capacitive Properties of Ti/Mn(0.8-x)SnxIr0.2O2 Electrodes
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College of Materials Science and Engineering,Fuzhou University,College of Materials Science and Engineering,Fuzhou University,College of Materials Science and Engineering,Fuzhou University,College of Materials Science and Engineering,Xiamen University of Technology,College of Materials Science and Engineering,Fuzhou University

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    Abstract:

    An experimental set-up was designed for measuring the self-field losses of Bi2223/Ag HTS tapes using a transport current method. Ti/Mn(0.8-x)SnxIr0.2O2 ternary oxide electrode materials were obtained by Pechini sol-gel method. The organizational structure and electrochemical performance of Ti/Mn(0.8-x)SnxIr0.2O2 electrodeswas investigated by Scanning electron microscope (SEM), X ray diffraction (XRD), cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The results showed that: SnO2 has a great influence on the organization structure of coating. With the content of SnO2 increasing, affirmative structure of Mn3O4 phase in Ti/Mn (0.8-x) SnxIr0.2O2 electrodes oxide coating is gradually reduced, but affirmative structure of SnO2 phase increased. Compared with the Mn-Ir-based binary oxides, the addition of SnO2 can significantly improve the current response of electrodes in the range of 0~0.5V and enhance activity of manganese oxide, but suppress activity of iridium oxide. Impedance analysis indicated that the charge transfer resistance,the relaxation time constant and the capacity of different frequency response of electrode materials were changed after addition of SnO2. In contrast, the Ti/Ir0.2Mn0.6Sn0.2O2 electrode with better capacitance response and higher activity in the low frequency range (≤ 1Hz), demonstrates the highest specific capacitance.

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[YI Zhaoyu, Cheng Zhijie, SHAO Yanqun, ZHU Junqiu, TANG Dian. Analysis of Capacitive Properties of Ti/Mn(0.8-x)SnxIr0.2O2 Electrodes[J]. Rare Metal Materials and Engineering,2018,47(2):546~552.]
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History
  • Received:December 03,2015
  • Revised:April 27,2016
  • Adopted:May 18,2016
  • Online: March 15,2018
  • Published: