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Selective electrochemical production of hydrogen peroxide at zigzag edges of exfoliated molybdenum telluride nanoflakes

The two-electron reduction of molecular oxygen represents an effective strategy to enable the green, mild and on-demand synthesis of hydrogen peroxide. Its practical viability, however, hinges on the development of advanced electrocatalysts, preferably composed of non-precious elements, to selective...

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Detalles Bibliográficos
Autores principales: Zhao, Xuan, Wang, Yu, Da, Yunli, Wang, Xinxia, Wang, Tingting, Xu, Mingquan, He, Xiaoyun, Zhou, Wu, Li, Yafei, Coleman, Jonathan N, Li, Yanguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8288933/
https://www.ncbi.nlm.nih.gov/pubmed/34692164
http://dx.doi.org/10.1093/nsr/nwaa084
Descripción
Sumario:The two-electron reduction of molecular oxygen represents an effective strategy to enable the green, mild and on-demand synthesis of hydrogen peroxide. Its practical viability, however, hinges on the development of advanced electrocatalysts, preferably composed of non-precious elements, to selectively expedite this reaction, particularly in acidic medium. Our study here introduces 2H-MoTe(2) for the first time as the efficient non-precious-metal-based electrocatalyst for the electrochemical production of hydrogen peroxide in acids. We show that exfoliated 2H-MoTe(2) nanoflakes have high activity (onset overpotential ∼140 mV and large mass activity of 27 A g(−1) at 0.4 V versus reversible hydrogen electrode), great selectivity (H(2)O(2) percentage up to 93%) and decent stability in 0.5 M H(2)SO(4). Theoretical simulations evidence that the high activity and selectivity of 2H-MoTe(2) arise from the proper binding energies of HOO(*) and O(*) at its zigzag edges that jointly favor the two-electron reduction instead of the four-electron reduction of molecular oxygen.