Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Fuel cell cathode studies in aqueous K sub 2 CO sub 3 and KOH

Journal Article · · Journal of the Electrochemical Society; (United States)
DOI:https://doi.org/10.1149/1.2086222· OSTI ID:5556747
; ;  [1]
  1. Applied Science Div., Lawrence Berkeley Lab., Dept. of Chemical Engineering, Univ. of California, Berkeley, CA (US)

This paper reports on the galvanostatic steady-state performance of PTFE-bonded Pt-on-carbon gas diffusion electrodes (GDEs) has been measured with variable oxygen partial pressures in 2 to 11 {ital M} KOH and 2 to 5.5 {ital M} K{sub 2}CO{sub 3}. The catalyst in the porous electrodes was characterized with cyclic voltammetry in a special cell with low uncompensated solution resistance. Cyclic voltammograms yielded measurements of the wetted areas of carbon and Pt and the local electrolyte composition. Conditions for differences in the area of Pt wetted by the KOHG electrolyte collapsed oxygen reduction (OR) performance curves for several different electrodes into a single curve of log-specific current density vs. potential. Comparisons with kinetic results suggest that OR on carbon contributes to the high current densities in 6.9 {ital M} KOH at high overpotentials. In K{sub 2}CO{sub 3} electrolyte, current density was found to be proportional to the square root of both wetted Pt area and O{sub 2} pressure, indicating that mass-transfer rates were not limited by O{sub 2} transport.

OSTI ID:
5556747
Journal Information:
Journal of the Electrochemical Society; (United States), Journal Name: Journal of the Electrochemical Society; (United States) Vol. 137:11; ISSN 0013-4651; ISSN JESOA
Country of Publication:
United States
Language:
English