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In relation to this article, we declare that there is no conflict of interest.
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Received March 31, 2020
Accepted May 11, 2020
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Colloidal synthetic methods of amorphous molybdenum phosphide nanoparticles for hydrogen evolution reaction catalysts

School of Integrative Engineering, Chung-Ang University, Seoul 06974, Korea 1Chuncheon Center, Korea Basic Science Institute, Chuncheon 24341, Korea 2Western Seoul Center, Korea Basic Science Institute, Seoul 03579, Korea
dhha@cau.ac.kr
Korean Journal of Chemical Engineering, August 2020, 37(8), 1419-1426(8), 10.1007/s11814-020-0576-4
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Abstract

Transition metal phosphides (TMPs) have recently emerged as promising hydrogen evolution reaction (HER) catalytic alternatives to platinum. Among them, molybdenum phosphide (MoP) has attracted extensive attention due to its high electrical conductivity, good stability, and Pt-like electronic structure; however, there is no systematic comparison of its different colloidal synthetic routes. This study systematically compares two colloidal synthetic methods, one-pot and two-step, for amorphous MoP and the associated morphological changes during their reaction time. The amorphous MoP nanoparticles synthesized via the two-step method within 4 h exhibited the highest HER performance with an overpotential of 177 mV in 0.50 M H2SO4 for a current density of -10 mA cm 2; this might be due to their highly developed Mo-P bondings revealed by X-ray photoelectron spectroscopy analysis. Thus, this work demonstrates that the HER catalytic performance of MoP can be significantly influenced by its synthetic method and reaction time.

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