Effect of the Interfacial Water Structure on the Hydrogen Evolution Reaction on Pt(111) Modified with Different Nickel Hydroxide Coverages in Alkaline Media

Please use this identifier to cite or link to this item: http://hdl.handle.net/10045/86872
Información del item - Informació de l'item - Item information
Title: Effect of the Interfacial Water Structure on the Hydrogen Evolution Reaction on Pt(111) Modified with Different Nickel Hydroxide Coverages in Alkaline Media
Authors: Sarabia, Francisco J. | Sebastián, Paula | Koper, Marc T.M. | Climent, Victor | Feliu, Juan M.
Research Group/s: Electroquímica de Superficies
Center, Department or Service: Universidad de Alicante. Departamento de Química Física | Universidad de Alicante. Instituto Universitario de Electroquímica
Keywords: Hydrogen evolution reaction | Platinum single crystal | Potential of zero charge | Potential of maximum entropy | Nickel adlayers | Interfacial water reorganization
Knowledge Area: Química Física
Issue Date: 12-Dec-2018
Publisher: American Chemical Society
Citation: ACS Applied Materials & Interfaces. 2019, 11(1): 613-623. doi:10.1021/acsami.8b15003
Abstract: The hydrogen evolution reaction (HER) constitutes one of the most important reactions in electrochemistry because of the value of hydrogen as a vector for energy storage and transport. Therefore, understanding the mechanism of this reaction in relation to its pH dependence is of crucial importance. While the HER on Pt(111) works efficiently in acid media, in alkaline media, the reaction is impeded and considerably larger applied overpotentials are necessary. The presence of Ni(OH)2 adsorbed on Pt(111) has been demonstrated to highly improve the rate of hydrogen evolution, decreasing the overpotential of this reaction in comparison to acid media. The way low coverages of Ni(OH)2 on the Pt surface improve HER is still under discussion. In this work, we have prepared different Ni(OH)2 coverages on Pt(111) to check how Ni(OH)2 deposited on Pt(111) influences the HER rate. To this end, the Ni(OH)2–Pt(111)|0.1 M NaOH interface was characterized with cyclic voltammetry, CO displacement technique, and Fourier transform infrared-reflection absorption spectroscopy. On the basis of the proposal made by Ledezma-Yanez et al. [Nature Energy 2017, 2, 17031] to explain the HER in alkaline media, we also studied the effect of the different Ni(OH)2 coverages on the electric field using the laser-induced temperature jump technique. This technique revealed that introduction of nickel adlayers on the surface decreases the ordering of the water network at the interphase, a fact that has relevant implications for the HER mechanism.
Sponsor: The authors thankfully acknowledge financial support from the MICINN (Spain) through project CTQ2016-76221-P. P. Sebastian acknowledges to MECD the award of a FPU grant. F.J.S. acknowledges to Ministerio de Economia, Industria y Competitividad (PEJ-2014-A-57942/PEJ-2014-P-00295).
URI: http://hdl.handle.net/10045/86872
ISSN: 1944-8244 (Print) | 1944-8252 (Online)
DOI: 10.1021/acsami.8b15003
Language: eng
Type: info:eu-repo/semantics/article
Rights: © 2018 American Chemical Society
Peer Review: si
Publisher version: https://doi.org/10.1021/acsami.8b15003
Appears in Collections:INV - EQSUP - Artículos de Revistas

Files in This Item:
Files in This Item:
File Description SizeFormat 
Thumbnail2019_Sarabia_etal_ACSApplMaterInterfaces_final.pdfVersión final (acceso restringido)2 MBAdobe PDFOpen    Request a copy
Thumbnail2019_Sarabia_etal_ACSApplMaterInterfaces_accepted.pdfEmbargo 12 meses (acceso abierto: 13 dic. 2019)1,08 MBAdobe PDFOpen    Request a copy


Items in RUA are protected by copyright, with all rights reserved, unless otherwise indicated.