4.7 Article

Hydrogen evolution reaction activities of electrodeposited nanocrystalline Ni-Mo thin films in alkaline baths

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 48, Issue 23, Pages 8409-8417

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2022.11.224

Keywords

Ni-Mo alloys; Electrodeposition; Nanocrystalline; Mixed phases; Electrocatalyst; Hydrogen evolution reaction

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The electrocatalytic activities of the hydrogen evolution reaction (HER) were evaluated and correlated with the composition, crystal structure, and crystallinity. Deposits with mixed phases exhibited the highest electro-chemically active surface area (ECSA), leading to enhanced exchange current density and overpotential. Low overpotentials were observed with specific Mo content. Tafel slope and exchange current density showed no dependence on Mo content, crystal phase, and grain size when normalized with ESCA. The metallic Ni-Mo thin films exhibited low mixed potential and overpotential at 10 mA/cm2.
The hydrogen evolution reaction (HER) electrocatalytic activities normalized to electro-chemically active surface area (ECSA) were systematically evaluated and correlated with its composition (i.e., Mo content up to 26 at. %), crystal structure (i.e., face-centered cubic (fcc) to orthorhombic phase and the mixed phases with different phase ratios), and crystallinity. The electrodeposited with mixed phases exhibited highest ECSA (up to 228 cm2 per 1 cm2 geometric surface area) compared to deposits with single phase, which serves as the dominant factor to enhance exchange current density and overpotential. Low over -potentials per ECSA were observed with Mo content of 5.16 at% (fcc) and 24.1 at% (mixed phases). After normalizing with ESCA, The Tafel slope and exchange current density were indifference with Mo content, crystal phase, and grain size. The metallic Ni-Mo thin films have low mixed potential and overpotential at 10 mA/cm2 of 20 mV and 120 mV, respectively.(c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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