In this work, the anode current and power densities of alkaline fuel cells
using different Pd-based hydrogen diffusion anodes have been measured at 25
and 50 degrees C. A 25 mu m thick Pd foil submitted to different treatment
s and a Pt-catalyzed carbon-PTFE electrode were employed as anode and catho
de, respectively. The results have been discussed in the light of chronoamp
erometry, scanning electron microscopy, and energy dispersive spectroscopy
and Raman and X-ray photoelectron spectroscopy microanalyses. There was a s
trong tendency of the Pd foil to crease during the fuel cell operation and
thus, the current and power densities increased with rime. These fuel cell
characteristics appeared to be dramatically limited in the cast: of the use
of rigid joints which did not permit the Pd foil deformation. This limitat
ion was explained by a Gorsky effect. The PdO film produced on the Pd foil
by heating in a furnace was a good catalyst for the overall anodic process.
However, the cell performance decreased with time because of the oxide rem
oval. The highest cell parameters were obtained when Pt black was electrode
posited on Pd black. The marked effect of Pt was explained by its catalytic
activity on the interfacial reactions taking place at the gas side of the
Pd foil. (C) 2000 The Electrochemical Society. S0013-4651(99)04-010-0. All
rights reserved.