Kinetics of Oxygen Evolution Reaction on Ti/IrO2+MnO2 Electrode Form Acid Solution
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作者:
Zhou Jian
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机构:
Lanzhou Jiaotong Univ, Lanzhou 730070, Peoples R China
Key Lab Yellow River Water Environm Gansu Prov, Lanzhou 730070, Peoples R ChinaLanzhou Jiaotong Univ, Lanzhou 730070, Peoples R China
Zhou Jian
[1
,2
]
Jia Yu
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h-index: 0
机构:
Lanzhou Jiaotong Univ, Lanzhou 730070, Peoples R China
Key Lab Yellow River Water Environm Gansu Prov, Lanzhou 730070, Peoples R ChinaLanzhou Jiaotong Univ, Lanzhou 730070, Peoples R China
Jia Yu
[1
,2
]
Song Xiaosan
论文数: 0引用数: 0
h-index: 0
机构:
Lanzhou Jiaotong Univ, Lanzhou 730070, Peoples R China
Key Lab Yellow River Water Environm Gansu Prov, Lanzhou 730070, Peoples R ChinaLanzhou Jiaotong Univ, Lanzhou 730070, Peoples R China
Song Xiaosan
[1
,2
]
机构:
[1] Lanzhou Jiaotong Univ, Lanzhou 730070, Peoples R China
[2] Key Lab Yellow River Water Environm Gansu Prov, Lanzhou 730070, Peoples R China
Ti/IrO2+MnO2 composite electrodes were prepared by thermal decomposition. The kinetics of oxygen evolution reaction on Ti/IrO2+MnO2 electrodes were studied deeply with quasi-stationary polarization curve recorded by slow linear potential sweep voltammetry. The related kinetics parameters, reaction process and rate determining steps were obtained. Tafel linear regions with double slopes are explained well by analyzing the Ohmic voltage drop corrected Tafel curves. Kinetics equations based on the proposed oxygen evolution reaction mechanism are deduced mathematically, which are in good agreement with the experimental results. The reaction order of hydrogen ion is close to 0, the one of apparent activation energy of 30.31 kJ/mol in the low potential region and the other of 13.64 kJ/mol in the high potential region, which further proves the correctness of above mathematical model.