New Insights into the Oxygen Reduction Reaction Mechanism on Pt(111): A Detailed Electrochemical Study

被引:63
作者
Gomez-Marin, Ana M. [1 ]
Feliu, Juan M. [1 ]
机构
[1] Univ Alicante, Univ Inst Electrochem, E-03080 Alicante, Spain
关键词
electrochemistry; oxygen; platinum; radicals; surface chemistry; SINGLE-CRYSTAL SURFACES; ROTATING-DISK HMRD; SCANNING-TUNNELING-MICROSCOPY; PLATINUM STEPPED SURFACES; PERCHLORIC-ACID SOLUTIONS; DENSITY-FUNCTIONAL THEORY; OXIDE-FREE PLATINUM; HYDROGEN-PEROXIDE; REVERSIBLE POTENTIALS; ACTIVATION-ENERGIES;
D O I
10.1002/cssc.201200847
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The oxygen reduction reaction (ORR) is undoubtedly the most important fuel-cell cathodic reaction. In this work, a detailed electrochemical analysis of the ORR on Pt(111) in nonadsorbing electrolytes was performed, which included the high-potential region Eup=1.15V while ensuring the electrode surface structure stability. Our results suggest that the reduction of a soluble intermediate species formed during the ORR is the rate-determining step in the whole reaction mechanism. This species does not undergo any other electrochemical reaction at E>0.9V and may accumulate close to the electrode surface. Together with dissolved O2, this intermediate may modify the oxide-growth dynamics on Pt(111). Hence, both species interact with the electrode surface through complex catalytic networks. Under certain experimental conditions, oxygenated species from the oxidation of Pt(111) may enhance the overall ORR current. These results propose an alternative to explain the current state of the art for this fundamental process.
引用
收藏
页码:1091 / 1100
页数:10
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