Paving the Way to The Integration of Smart Nanostructures: Part II: Nanostructured Microdispersed Hydrated Metal Oxides for Electrochemical Energy Conversion and Storage Applications

被引:0
|
作者
Rebouillat, Serge [1 ]
Lyons, Michael E. G. [2 ]
Brandon, Michael P. [2 ]
Doyle, Richard L. [2 ]
机构
[1] DuPont Int SA, CH-1218 Geneva, Switzerland
[2] Univ Dublin, Trinity Coll, Sch Chem, Phys & Mat Electrochem Lab, Dublin 2, Ireland
来源
INTERNATIONAL JOURNAL OF ELECTROCHEMICAL SCIENCE | 2011年 / 6卷 / 11期
基金
爱尔兰科学基金会;
关键词
oxygen evolution electrocatalysis; oxidized iron; nickel and cobalt electrodes; transition metal electrochemistry; oxygen evolution mechanisms; OXYGEN EVOLUTION REACTION; QUARTZ-CRYSTAL MICROBALANCE; NICKEL-HYDROXIDE ELECTRODES; PROBE BEAM DEFLECTION; POTENTIAL CYCLING CONDITIONS; GLASSY-CARBON ELECTRODES; RING-DISK ELECTRODE; SURFACE REDOX CATALYSIS; LI-DOPED CO3O4; ALKALINE-SOLUTIONS;
D O I
暂无
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The use of hydrogen gas produced by the electrolysis of water is the basis of a long term energy conversion and storage option that has been and still continues to be the subject of considerable research. Alkaline water electrolysis, using electricity generated by renewable sources has been proposed as an environmentally inoffensive route to the production of the large volumes of hydrogen gas required by a possible hydrogen economy. The electrochemistry of oxygen has proved to be of perennial interest both from a fundamental and an applied perspective, especially in the important areas of energy conversion and storage. Despite the recent renewal in interest in the oxygen evolution reaction (OER) at transition metal oxide based electrodes in alkaline solution, the details of the mechanism remain controversial. In the present extended essay, the redox, charge storage and electrocatalytic behavior with respect to the OER of oxidized Ni, Fe and Co oxides in alkaline solution is discussed, the acid/base properties of the oxide is emphasized, and a plausible general reaction pathway involving the rate determining formation of a superoxy (-OOH) intermediate is proposed.
引用
收藏
页码:5830 / 5917
页数:88
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