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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...

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Detalles Bibliográficos
Autores principales: Zhang, Zhiqi, Liu, Jiapeng, Wang, Jian, Wang, Qi, Wang, Yuhao, Wang, Kai, Wang, Zheng, Gu, Meng, Tang, Zhenghua, Lim, Jongwoo, Zhao, Tianshou, Ciucci, Francesco
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
Descripción
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.