Promotion of Hydrogen Desorption from Palladium Surfaces by Fluoropolymer Coating

Journal Article (2016)
Author(s)

Renaud Delmelle (Swiss Federal Laboratories for Materials Science and Technology (Empa))

Peter Ngene (TU Delft - Applied Sciences)

Bernard Dam (TU Delft - Applied Sciences)

Davide Bleiner (Swiss Federal Laboratories for Materials Science and Technology (Empa))

Andreas Borgschulte (Swiss Federal Laboratories for Materials Science and Technology (Empa))

Research Group
ChemE/Materials for Energy Conversion and Storage
DOI related publication
https://doi.org/10.1002/cctc.201600168 Final published version
More Info
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Publication Year
2016
Language
English
Research Group
ChemE/Materials for Energy Conversion and Storage
Issue number
9
Volume number
8
Pages (from-to)
1646-1650
Downloads counter
187

Abstract

The catalytic activity of Pd surfaces towards hydrogen desorption was significantly improved by a nanometer-thin polytetrafluoroethylene (PTFE) layer, as shown by an enhancement in the permeability of a Pd membrane coated on the permeate side. The origin of this effect was found to be due to a lowering of the barrier for hydrogen desorption, as evidenced by a change in the rate-limiting mechanism of hydrogen permeation through the membrane from desorption (un-coated) to diffusion controlled. In situ X-ray photoelectron spectroscopy (XPS) revealed the electronic structure of the sputtered PTFE. Apart from C-Fn subunits (n=1, 2, 3), we found that nonsaturated carbon atoms became hydrogenated during hydrogen permeation, which was indicative of an interaction between Pd and PTFE. This interaction was weak; no Pd-F bonds were formed. We thus attributed the effect to an increase in the hydrophobicity of the surface by the porous PTFE layer and to a promoter effect of hydrogen desorption as a result of electrostatic interactions between chemisorbed hydrogen and physisorbed PTFE.