Abstract
The relationship between the binding of the reaction intermediates and oxygen reduction activity in alkaline media was experimentally explored. By introducing Cu into the 2nd surface layer of a Pt(111) single crystal, the surface reactivity was tuned. In both 0.1 m NaOH and 0.1 m KOH, the optimal catalyst should exhibit OH binding circa 0.1 eV weaker than Pt(111), via a Sabatier volcano; this observation suggests that the reaction is mediated via the same surface bound intermediates as in acid, in contrast to previous reports. In 0.1 m KOH, the alloy catalyst at the peak of the volcano exhibits a maximum activity of 101±8 mA cm2 at 0.9 V vs. a reversible hydrogen electrode (RHE). This activity constitutes a circa 60‐fold increase over Pt(111) in 0.1 m HClO4.
Original language | English |
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Journal | Angewandte Chemie |
Volume | 130 |
Issue number | 11 |
Pages (from-to) | 2850-2855 |
Number of pages | 6 |
ISSN | 0044-8249 |
DOIs | |
Publication status | Published - 2018 |
Keywords
- Electroanalysis
- Oxygen reduction
- Platinum
- Sabatier principle
- Surface chemistry