Chemical Recognition of Active Oxygen Species on the Surface of Oxygen Evolution Reaction Electrocatalysts

被引:219
作者
Yang, Chunzhen [1 ]
Fontaine, Olivier [2 ,3 ]
Tarascon, Jean-Marie [1 ,3 ,4 ,5 ]
Grimaud, Alexis [1 ,3 ]
机构
[1] Coll France, UMR 8260, Chim Solide & Energie, F-75231 Paris 05, France
[2] Univ Montpellier, UMR 5253, Inst Charles Gerhardt Montpellier, Pl Eugene Bataillon, F-34095 Montpellier, France
[3] CNRS, FR3459, RS2E, 33 Rue St Leu, F-80039 Amiens, France
[4] UPMC, Dept Chem, 4 Pl Jussieu, F-75005 Paris, France
[5] FR CNRS 3104, ALISTORE European Res Inst, F-80039 Amiens, France
基金
欧洲研究理事会;
关键词
deprotonation; isotopic effect; nickel oxyhydroxide; oxygen evolution reaction; ELECTROCHEMICAL WATER OXIDATION; OXIDE CATALYSTS; METAL-OXIDES; REDOX; PH; ELECTROLYSIS; ELECTRODES; MECHANISM; DESIGN; SITES;
D O I
10.1002/anie.201701984
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Owing to the transient nature of the intermediates formed during the oxygen evolution reaction (OER) on the surface of transition metal oxides, their nature remains largely elusive by the means of simple techniques. The use of chemical probes is proposed, which, owing to their specific affinities towards different oxygen species, unravel the role played by these species on the OER mechanism. For that, tetraalkylammonium (TAA) cations, previously known for their surfactant properties, are introduced, which interact with the active oxygen sites and modify the hydrogen bond network on the surface of OER catalysts. Combining chemical probes with isotopic and pH-dependent measurements, it is further demonstrated that the introduction of iron into amorphous Ni oxyhydroxide films used as model catalysts deeply modifies the proton exchange properties, and therefore the OER mechanism and activity.
引用
收藏
页码:8652 / 8656
页数:5
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