Electrodeposition of the manganese-doped nickelphosphorus catalyst with enhanced hydrogen evolution reaction activity and durability
Abstract
Hydrogen technology is widely considered a novel clean energy source, and electrolysis is an effective method for hydrogen evolution. Therefore, efficient hydrogen evolution reaction (HER) catalysts are urgently needed to replace precious metal catalysts and meet ecological and environmental protection standards. Herein, Ni-Mn-P electrocatalysts are synthesized using facile electrodeposition technology. The influence of the Mn addition on the catalytic behavior is studied by the comprehensive analysis of catalytic performance and morphology of the catalysts. Among them, the Ni-Mn-P.01 catalyst exhibits small coral-like structures, greatly improving the adsorption and desorption of hydrogen ions and reducing the overpotential hydrogen evolution. Consequently, overpotential at 10 mA cm(-2) electric current density is 113 mV, and the value of the Tafel slope achieves 74 mV/dec. Furthermore, the NieMneP catalyst shows long-time (20 h) stability at current densities of 10 and 60 mA/cm(2). The results confirm that the synergistic effect of Ni, Mn, and P accelerates the electrochemical reaction. Meanwhile, the addition of manganese element can change the micromorphology of the catalyst, thereby exposing more active sites to participate in the reaction, enhancing water ionization, improving the catalytic performance. This study opens a new way toward improving the activity of the catalyst by adjusting Mn concentration during the electrodeposition process. (c) 2021 Hydrogen Energy Publications.Published by Elsevier Ltd. All rights reserved.
Más información
Título según WOS: | Electrodeposition of the manganese-doped nickelphosphorus catalyst with enhanced hydrogen evolution reaction activity and durability |
Título de la Revista: | INTERNATIONAL JOURNAL OF HYDROGEN ENERGY |
Volumen: | 47 |
Número: | 100 |
Editorial: | PERGAMON-ELSEVIER SCIENCE LTD |
Fecha de publicación: | 2022 |
Página de inicio: | 41994 |
Página final: | 42000 |
DOI: |
10.1016/j.ijhydene.2021.10.105 |
Notas: | ISI |