Published December 1, 2017 | Version v1
Journal article

Investigating Phase‐Change‐Induced Flow in Gas Diffusion Layers in Fuel Cells with X‐ray Computed Tomography

  • 1. Department of Mechanical Engineering, Tufts University, Medford, MA 02155 (United States)
  • 2. Advanced Light Source, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkleey, CA 94720 (United States)
  • 3. X-ray Science Division, Argonne National Laboratory, 9700 S. Class Avenue, Lemont, IL 60439 (United States)
  • 4. Energy Storage and Distributed Resources Division, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkleey, CA 94720 (United States)
  • 5. Dep Of Energy and Process Engineering, NTNU—The Norwegian Univ. of Sci. and Technol., NO-7491 Trondheim (Norway)

Description

The performance of polymer‐electrolyte fuel cells is heavily dependent on proper management of liquid water. One particular reason is that liquid water can collect in the gas diffusion layers (GDLs) blocking the reactant flow to the catalyst layer. This results in increased mass‐transport losses. At higher temperatures, evaporation of water becomes a dominant water‐removal mechanism and specifically phase‐change‐induced (PCI) flow is present due to thermal gradients. This study used synchrotron based micro X‐ray computed tomography (CT) to visualize and quantify the water distribution within gas diffusion layers subject to a thermal gradient. Plotting saturation as a function of through‐plane distance quantitatively shows water redistribution, where water evaporates at hotter locations and condenses in colder locations. The morphology of the GDLs on the micro‐scale, as well as evaporating water clusters, are resolved, indicating that the GDL voids are slightly prolate, whereas water clusters are oblate. From the mean radii of water distributions and visual inspection, it is observed that larger water clusters evaporate faster than smaller ones.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.electacta.2017.10.012

Additional details

Identifiers

DOI
10.1016/j.electacta.2017.10.012;
PII
S0013-4686(17)32070-4;

Publishing Information

Journal Title
Electrochimica Acta
Journal Volume
256
Journal Issue
Complete
Journal Page Range
p. 279-290
ISSN
0013-4686
CODEN
ELCAAV

Optional Information

Copyright
Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.