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A Study of the Mechanism of the Hydrogen Evolution Reaction on Nickel by Surface Interrogation Scanning Electrochemical Microscopy

Liang, Zhenxing, Ahn, Hyun S., Bard, Allen J.·2017·Journal of the American Chemical Society

Abstract

The hydrogen evolution reaction (HER) on Ni in alkaline media was investigated by scanning electrochemical microscopy under two operating modes. First, the substrate generation/tip collection mode was employed to extract the "true" cathodic current associated with the HER from the total current in the polarization curve. Compared to metallic Ni, the electrocatalytic activity of the HER is improved in the presence of the low-valence-state oxide of Ni. This result is in agreement with a previous claim that the dissociative adsorption of water can be enhanced at the Ni/Ni oxide interface. Second, the surface-interrogation scanning electrochemical microscopy (SI-SECM) mode was used to directly measure the coverage of the adsorbed hydrogen on Ni at given potentials. Simulation indicates that the hydrogen coverage follows a Frumkin isotherm with respect to the applied potential. On the basis of the combined analysis of the Tafel slope and surface hydrogen coverage, the rate-determining step is suggested to be the adsorption of hydrogen (Volmer step) in the investigated potential window.

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Metadata

Authors
Liang, Z., Ahn, H. S., & Bard, A. J.
Venue
Journal of the American Chemical Society
Published
2017-03-22
Volume
139
Issue
13
Pages
4854-4858
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W2593787326
Cited by
159
References
1
FWCI
3.91
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: A Study of the Mechanism of the Hydrogen Evolution Reaction on Nickel by Surface Interrogation Scanning Electrochemical Microscopy. https://app.cochat.ai/papers/10.1021/jacs.7b00279
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Liang, Z., Ahn, H. S., & Bard, A. J. (2017). A Study of the Mechanism of the Hydrogen Evolution Reaction on Nickel by Surface Interrogation Scanning Electrochemical Microscopy. Journal of the American Chemical Society. https://doi.org/10.1021/jacs.7b00279

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