Mn-Mo-W Oxide Anodes for Oxygen Evolution in Seawater Electrolysis for Hydrogen Production

被引:31
作者
El-Moneim, A. A. [1 ]
Kumagai, N. [2 ]
Hashimoto, K. [3 ]
机构
[1] Natl Res Ctr, Adv Mat & Nanotechnol Grp, Cairo, Egypt
[2] Daiki Ataka Engn Co Ltd, Kashiwa, Chiba 2278515, Japan
[3] Tohoku Inst Technol, Sendai, Miyagi 9828577, Japan
关键词
oxygen evolution anode; oxide anode; seawater electrolysis; anodic deposition of oxide; electrical resistance of oxide; defect concentration; RAY PHOTOELECTRON-SPECTROSCOPY; MANGANESE OXIDE; CHLORATE ELECTROLYSIS; ELECTRODES; DIOXIDE; DEPOSITION;
D O I
10.2320/matertrans.M2009107
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
IrO2/Ti-supported gamma-MnO2-type Mn-Mo-W triple oxide anodes were prepared by anodic deposition in MnSO4-Na2MoO4-Na2WO4-H2SO4 solutions. The performance of anodes for oxygen evolution reaction during electrolysis of 0.5 kmol m(-3) NaCl solution was examined at 1000 Am-2. The stability, kinetics and physicochemical properties of the oxide deposit anodes were characterized by iR-corrected galvanostatic polarization, gravimetric, X-ray photoelectron spectroscopy and X-ray diffraction techniques. The addition of tungsten to the Mn-Mo oxide enhanced the oxygen evolution efficiency of anodes. The anode prepared in 0.2 kmol m(-3) Mn2+-0.003 kmol m(-3) Mo6+-0.006 kmol m(-3) W6+ electrolyte of pH 0 showed the best performance among anodes prepared in this work. The high performance was attributed to the formation of single phase triple oxide with optimum composition, thickness and defect concentration. Tungsten addition beneficially exerts its effect via increasing the electrical conductivity of oxide deposits. The deposition mechanism of the oxides was discussed in terms of stability and population of Mn3+ species at the anode/electrolyte interface. [doi: 10.2320/matertrans.M2009107]
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页码:1969 / 1977
页数:9
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