posted on 2014-08-20, 10:19authored bySamuel Cruz-Manzo, Rui Chen
In this study the mass transport resistance in the cathode catalyst layer (CCL) of a polymer electrolyte fuel
cell (PEFC) is estimated using electrochemical impedance spectroscopy (EIS) measurements. Experimental
impedance measurements were carried out in a 6 cm2 PEFC operated with two different relative
humidity (RH) values in the cathode and different partial pressures of oxygen in He/O2 and N2/O2 gas
mixtures. A mathematical model predicting the CCL impedance response, derived in the authors’ previous
study, is applied to EIS measurements to calculate the CCL mass transport resistance. The experimental
results show the presence of an overlapped second semicircle at low frequencies which is attributed to an
increase in the time constant to diffuse oxygen through the CCL when the PEFC is operated at low oxygen
partial pressures, p(O2) 6 20%, in He/O2 or N2/O2 gas mixtures. The results also show that oxygen diluted
with nitrogen can reduce the steady state oxygen concentration in the CCL-gas diffusion layer (GDL)
interface and can increase CCL mass transport resistance. It is possible, as such, to harness capabilities
from both modelling and real-world EIS data in a complementary manner.
Funding
The authors thank the Mexican
National Council for Science and Technology (CONACYT) for
the sponsorship of the Ph.D research study of S. Cruz-Manzo (Grant No. 183195).
History
School
Aeronautical, Automotive, Chemical and Materials Engineering
Department
Aeronautical and Automotive Engineering
Published in
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
Volume
702
Pages
45 - 48 (4)
Citation
CRUZ-MANZO, S. and CHEN, R., 2013. Electrochemical impedance study on estimating the mass transport resistance in the polymer electrolyte fuel cell cathode catalyst layer. Journal of Electroanalytical Chemistry, 702, pp.45-48.
This work is made available according to the conditions of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) licence. Full details of this licence are available at: https://creativecommons.org/licenses/by-nc-nd/4.0/
Publication date
2013
Notes
NOTICE: this is the author’s version of a work that was accepted for publication in Journal of Electroanalytical Chemistry. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published at: http://dx.doi.org/10.1016/j.jelechem.2013.05.008