Loughborough University
Leicestershire, UK
LE11 3TU
+44 (0)1509 263171
Loughborough University

Loughborough University Institutional Repository

Please use this identifier to cite or link to this item: https://dspace.lboro.ac.uk/2134/28463

Title: Effect of mass transport on the electrochemical oxidation of alcohols over electrodeposited film and carbon-supported pt electrodes
Authors: Puthiyapura, V.K.
Lin, Wen-Feng
Russell, A.E.
Brett, Daniel J.L.
Hardacre, Christopher
Keywords: Direct alcohol fuel cells
Rotating disk electrode (RDE)
Issue Date: 2018
Publisher: © The Authors. Published by Springer
Citation: PUTHIYAPURA, V.K. ...et al., 2018. Effect of mass transport on the electrochemical oxidation of alcohols over electrodeposited film and carbon-supported pt electrodes. Topics in Catalysis, In Press.
Abstract: © 2018 The Author(s) Electrochemical oxidation of four different alcohol molecules (methanol, ethanol, n-butanol and 2-butanol) at electrodeposited Pt film and carbon-supported Pt catalyst film electrodes, as well as the effect of mass transport on the oxidation reaction, has been studied systematically using the rotating disk electrode (RDE) technique. It was shown that oxidation current decreased with an increase in the rotation rate (ω) for all alcohols studied over electrodeposited Pt film electrodes. In contrast, the oxidation current was found to increase with an increase in the ω for Pt/C in ethanol and n-butanol-containing solutions. The decrease was found to be nearly reversible for ethanol and n-butanol at the electrodeposited Pt film electrode ruling out the possibility of intermediate CO ads poisoning being the sole cause of the decrease and was attributed to the formation of soluble intermediate species which diffuse away from the electrode at higher ω. In contrast, an increase in the current with an increase in ω for the carbon supported catalyst may suggest that the increase in residence time of the soluble species within the catalyst layer, results in further oxidation of these species. Furthermore, the reversibility of the peak current on decreasing the ω could indicate that the surface state has not significantly changed due to the sluggish reaction kinetics of ethanol and n-butanol.
Description: This is an Open Access Article. It is published by Springer under the Creative Commons Attribution 4.0 Unported Licence (CC BY). Full details of this licence are available at: http://creativecommons.org/licenses/by/4.0/
Sponsor: This work was supported by EPSRC (Portfolio Grants. EP/K014706/2, EP/K014668/1, EP/K014854/1, EP/K014714/1 and EP/I019693/1).
Version: Published
DOI: 10.1007/s11244-018-0893-6
URI: https://dspace.lboro.ac.uk/2134/28463
Publisher Link: https://doi.org/10.1007/s11244-018-0893-6
ISSN: 1022-5528
Appears in Collections:Published Articles (Chemical Engineering)

Files associated with this item:

File Description SizeFormat
Topics in Catalysis 2018 1 19 online 10.1007_s11244-018-0893-6.pdfPublished version2.47 MBAdobe PDFView/Open


SFX Query

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