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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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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 |
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. |
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