β-Mo2C Nanoparticles Produced by Carburization of Molybdenum Oxides with Carbon Black under Microwave Irradiation for Electrocatalytic Hydrogen Evolution Reaction

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Abstract

The synthesis of electrochemically active β-Mo2C nanoparticles for hydrogen production was achieved by a fast and energy-efficient microwave-assisted carburization process from molybdenum oxides and carbon black. With the use of microwave-based production methods, we aim to reduce the long-time high-temperature treatments and the use of hazardous gases often seen in traditional molybdenum carbide synthesis processes. In our process, carbon black not only serves as a carbon source but also as a susceptor (microwave absorber) and conductive substrate. The irradiation power, reaction time, and Mo:C ratio were optimized to achieve the highest electrocatalytic performance toward hydrogen production in an acidic electrolyte. A complete transformation of MoO3 to β-Mo2C nanoparticles and an additional graphitization of the carbon black matrix were achieved at 1000 W, 600 s, and Mo:C ratio above 1:7.5. Under these conditions, the optimized composite exhibited an excellent HER performance (η10 = 156 mV, Tafel slope of 53 mV·dec-1) and large turnover frequency per active site (3.09 H2·s-1 at an overpotential of 200 mV), making it among the most efficient non-noble-metal catalysts. The excellent activity was achieved thanks to the abundance of β-Mo2C nanoparticles, the intimate nanoparticle-substrate interface, and enhanced electron transport toward the carbon black matrix. We also investigated the flexibility of the synthesis method by adding additional Fe or V as secondary transition metals, as well as the effect of the substrate.

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Fan, J., Wu, X., Piñeiro-García, A., Boulanger, N., Panecatl-Bernal, Y., Ashok, A., … Gracia-Espino, E. (2021). β-Mo2C Nanoparticles Produced by Carburization of Molybdenum Oxides with Carbon Black under Microwave Irradiation for Electrocatalytic Hydrogen Evolution Reaction. ACS Applied Nano Materials, 4(11), 12270–12277. https://doi.org/10.1021/acsanm.1c02770

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