Liquid Water Visualization in the Pt-Loading Catalyst Layers of Polymer Electrolyte Fuel Cells Using Operando Synchrotron X-ray Radiography

17 April 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Water management is important for addressing the challenges posed by next-generation fuel cell electric vehicles. Although X-ray imaging techniques are useful for probing the mechanism of water transport in the gas diffusion layer of polymer electrolyte fuel cells, they cannot be easily applied to the Pt-loading catalyst layer because of its low X-ray transmittance due to the high absorption coefficient of Pt. Herein, we propose a method to realize the high-resolution X-ray imaging of the cathode catalyst layer in polymer electrolyte fuel cells using synchrotron X-ray radiography, thus bridging the above gap. The results of operando synchrotron X-ray radiography measurements reveal that water accumulation in the cathode catalyst layer depends on the cell temperature, feed gas humidity, and cell voltage, while time-slice analysis shows that the water accumulation rate in the cathode catalyst layer is approximately four times that in the cathode gas diffusion layer. The proposed imaging method can be used to evaluate the water uptake capability of the catalyst layer and thus deepen our understanding of flooding phenomena and cold-start behavior at subzero temperatures.

Keywords

polymer electrolyte fuel cell
catalyst layer
X-ray radiography
liquid water
water management

Supplementary materials

Title
Description
Actions
Title
Supporting Information
Description
Experimental details
Actions
Title
Movie S1
Description
Movie of transient liquid water behavior in a polymer electrolyte fuel cell
Actions

Comments

Comments are not moderated before they are posted, but they can be removed by the site moderators if they are found to be in contravention of our Commenting Policy [opens in a new tab] - please read this policy before you post. Comments should be used for scholarly discussion of the content in question. You can find more information about how to use the commenting feature here [opens in a new tab] .
This site is protected by reCAPTCHA and the Google Privacy Policy [opens in a new tab] and Terms of Service [opens in a new tab] apply.