The Common Intermediates of Oxygen Evolution and Dissolution Reactions during Water Electrolysis on Iridium

被引:402
|
作者
Kasian, Olga [1 ]
Grote, Jan-Philipp [1 ]
Geiger, Simon [1 ]
Cherevko, Serhiy [1 ,2 ]
Mayrhofer, Karl J. J. [1 ,2 ,3 ]
机构
[1] Max Planck Inst Eisenforsch GmbH, Max Planck Str 1, D-40237 Dusseldorf, Germany
[2] Forschungszentrum Julich, Helmholtz Inst Erlangen Nunberg Renewable Energy, Egerlandstr 3, D-91058 Erlangen, Germany
[3] Friedrich Alexander Univ Erlangen Nurnberg, Dept Chem & Biol Engn, Egerlandstr 3, D-91058 Erlangen, Germany
关键词
electrochemical mass spectrometry; iridium dissolution; oxygen evolution reaction; reaction mechanisms; water electrolysis; OXIDE-FILMS; ELECTRONIC-STRUCTURE; STABILITY; OXIDATION; CATALYST; ACTIVATION;
D O I
10.1002/anie.201709652
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Understanding the pathways of catalyst degradation during the oxygen evolution reaction is a cornerstone in the development of efficient and stable electrolyzers, since even for the most promising Ir based anodes the harsh reaction conditions are detrimental. The dissolution mechanism is complex and the correlation to the oxygen evolution reaction itself is still poorly understood. Here, by coupling a scanning flow cell with inductively coupled plasma and online electrochemical mass spectrometers, we monitor the oxygen evolution and degradation products of Ir and Ir oxides in situ. It is shown that at high anodic potentials several dissolution routes become possible, including formation of gaseous IrO3. On the basis of experimental data, possible pathways are proposed for the oxygen-evolution-triggered dissolution of Ir and the role of common intermediates for these reactions is discussed.
引用
收藏
页码:2488 / 2491
页数:4
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