The influence of membrane electrode assembly water content on the performance of a polymer electrolyte membrane fuel cell as investigated by 1H NMR microscopy

Phys Chem Chem Phys. 2007 Apr 21;9(15):1850-7. doi: 10.1039/b617551a. Epub 2007 Feb 7.

Abstract

The relation between the performance of a self-humidifying H(2)/O(2) polymer electrolyte membrane fuel cell and the amount and distribution of water as observed using (1)H NMR microscopy was investigated. The integrated (1)H NMR image signal intensity (proportional to water content) from the region of the polymer electrolyte membrane between the catalyst layers was found to correlate well with the power output of the fuel cell. Several examples are provided which demonstrate the sensitivity of the (1)H NMR image intensity to the operating conditions of the fuel cell. Changes in the O(2)(g) flow rate cause predictable trends in both the power density and the image intensity. Higher power densities, achieved by decreasing the resistance of the external circuit, were found to increase the water in the PEM. An observed plateau of both the power density and the integrated (1)H NMR image signal intensity from the membrane electrode assembly and subsequent decline of the power density is postulated to result from the accumulation of H(2)O(l) in the gas diffusion layer and cathode flow field. The potential of using (1)H NMR microscopy to obtain the absolute water content of the polymer electrolyte membrane is discussed and several recommendations for future research are provided.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Electric Power Supplies*
  • Electrochemistry / instrumentation*
  • Electrochemistry / methods
  • Electrodes*
  • Electrolytes / chemistry*
  • Equipment Design
  • Equipment Failure Analysis
  • Magnetic Resonance Spectroscopy / methods*
  • Materials Testing / methods
  • Membranes, Artificial
  • Polymers / chemistry*
  • Protons
  • Water / chemistry*

Substances

  • Electrolytes
  • Membranes, Artificial
  • Polymers
  • Protons
  • Water