Multiple metallic dopants in nickel nanoparticles for electrocatalytic oxygen evolution
Developing efficient oxygen evolution reaction (OER) electrocatalysts is of great importance for sustainable energy conversion and storage. Ni-based catalysts have shown great potential as OER electrocatalysts, but their performance still needs to be improved. Herein, we report the multiple metal do...
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Veröffentlicht in: | Progress in natural science 2023-02, Vol.33 (1), p.67-73 |
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Sprache: | eng |
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Zusammenfassung: | Developing efficient oxygen evolution reaction (OER) electrocatalysts is of great importance for sustainable energy conversion and storage. Ni-based catalysts have shown great potential as OER electrocatalysts, but their performance still needs to be improved. Herein, we report the multiple metal doped nickel nanoparticles synthesized via a simple oil phase strategy as efficient OER catalysts. The FeMnMoV–Ni exhibits superior OER performance with an overpotential of 220 mV at 10 mA cm−2 and a long-term stability of 250 h in 1 M KOH solution. In situ Raman analysis shows that the NiOOH site works as the active center and multiple metallic dopants facilitate the formation of NiOOH. Mo and V dopants promote the formation of high-valence state of Ni sites, and Mn dopants increase the electrochemical active surface area and expose more active sites. This work provides a novel strategy for catalyst design, which is critical for developing multiple metal doped catalysts.
Based on Fe doped Ni catalysts (Fe–Ni nanoparticles), we introduce multiple metal dopants using a simple oil phase strategy in this study. The Fe–Ni nanoparticles, with other 3 dopants of Mn, Mo, and V, show an overpotential of 220 mV at 10 mA cm−2. [Display omitted]
•Multiple metal doped catalysts were synthesized via a simple oil phase strategy.•Mo and V dopants promote the formation of high-valence state of Ni sites.•Mn dopants increase the electrochemical active surface area and expose more active sites.•Multiple metal dopants promote the formation of active sites NiOOH. |
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ISSN: | 1002-0071 |
DOI: | 10.1016/j.pnsc.2023.03.002 |