Cargando…
Single-atom catalyst for high-performance methanol oxidation
Single-atom catalysts have been widely investigated for several electrocatalytic reactions except electrochemical alcohol oxidation. Herein, we synthesize atomically dispersed platinum on ruthenium oxide (Pt(1)/RuO(2)) using a simple impregnation-adsorption method. We find that Pt(1)/RuO(2) has good...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413426/ https://www.ncbi.nlm.nih.gov/pubmed/34475400 http://dx.doi.org/10.1038/s41467-021-25562-y |
Sumario: | Single-atom catalysts have been widely investigated for several electrocatalytic reactions except electrochemical alcohol oxidation. Herein, we synthesize atomically dispersed platinum on ruthenium oxide (Pt(1)/RuO(2)) using a simple impregnation-adsorption method. We find that Pt(1)/RuO(2) has good electrocatalytic activity towards methanol oxidation in an alkaline media with a mass activity that is 15.3-times higher than that of commercial Pt/C (6766 vs. 441 mA mg(‒1)(Pt)). In contrast, single atom Pt on carbon black is inert. Further, the mass activity of Pt(1)/RuO(2) is superior to that of most Pt-based catalysts previously developed. Moreover, Pt(1)/RuO(2) has a high tolerance towards CO poisoning, resulting in excellent catalytic stability. Ab initio simulations and experiments reveal that the presence of Pt‒O(3f) (3-fold coordinatively bonded O)‒Ru(cus) (coordinatively unsaturated Ru) bonds with the undercoordinated bridging O in Pt(1)/RuO(2) favors the electrochemical dehydrogenation of methanol with lower energy barriers and onset potential than those encountered for Pt‒C and Pt‒Ru. |
---|