1. Understanding the oxophilic effect on the hydrogen electrode reaction through PtM nanostructures
- Author
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Nicolas Alonso-Vante and C.A. Campos-Roldán
- Subjects
Nanostructure ,Standard hydrogen electrode ,Dopant ,Chemistry ,Inorganic chemistry ,02 engineering and technology ,010402 general chemistry ,021001 nanoscience & nanotechnology ,Condensed Matter Physics ,Electrochemistry ,01 natural sciences ,Redox ,0104 chemical sciences ,Catalysis ,chemistry.chemical_compound ,General Materials Science ,Chemical route ,Electrical and Electronic Engineering ,0210 nano-technology ,Bifunctional - Abstract
Carbon-supported PtM nanostructured materials (M = Cr, Co, Ni, Cu, Mo, Y, Sm, Gd) were investigated for the hydrogen evolution/oxidation reactions (HER/HOR) in alkaline medium. All catalysts were synthesized by the carbonyl complex chemical route. Among PtM, Cr, Co, Ni, and Cu formed nanoalloys. M2O3 was generated with Y, Sm, and Gd, and Mo was found at a dopant concentration of Pt. The electrochemical results showed that the HER/HOR activities on PtNi/C and PtCo/C outperformed that of the Pt/C benchmark. The presence of OHads species, acting as a bifunctional mechanism, favored the HER/HOR activity on PtNi/C and PtCo/C. This process is concomitant with early DFT studies that concluded that the presence of OHads weakens the Hads and H2Oads energetics.
- Published
- 2020
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