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Analysis of a Permselective Membrane-Free Alkaline Direct Ethanol Fuel Cell

[+] Author Affiliations
Jing Huang, Hafez Bahrami, Amir Faghri

University of Connecticut, Storrs, CT

Paper No. IMECE2013-64988, pp. V06BT07A021; 11 pages
doi:10.1115/IMECE2013-64988
From:
  • ASME 2013 International Mechanical Engineering Congress and Exposition
  • Volume 6B: Energy
  • San Diego, California, USA, November 15–21, 2013
  • Conference Sponsors: ASME
  • ISBN: 978-0-7918-5629-1
  • Copyright © 2013 by ASME

abstract

A physical model is developed to study the coupled mass and charge transport in a permselective membrane-free alkaline direct ethanol fuel cell. This type of fuel cell is not only free of expensive ion exchange membranes and platinum based catalysts, but also features a facile oxygen reduction reaction due to the presence of alkaline electrolyte. The proposed model is first validated by comparing its predictions to the experimental results from literature and then used to predict the overall performance of the cell and reveal the details of ion transport, distribution of electrolyte potential and current density. It is found that: (i) KOH concentration lower than 1 M notably impairs cell performance due to low electrolyte conductivity; (ii) the concentration gradient and electrical field are equally important in driving ion transport in the electrolyte; (iii) the current density distributions in the anode and cathode catalyst layers keep non-uniform due to different reasons. In the anode, it is caused by the ethanol concentration gradient, while in the cathode it is because of the electrolyte potential gradient; and (iv) at low cell voltage, current density distribution in the catalyst layer shows stronger non-linearity in the anode than in the cathode.

Copyright © 2013 by ASME

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