Plasma Surface Modification of Carbon Electrodes for Polymer Electrolyte Fuel Cells (EFC 2005-86319)

[+] Author and Article Information
K.-F. Chiu1

Department of Materials Science and Engineering,  Feng Chia University, 100 Wen Hwa Rd., Taichung 407, Taiwankfchiu@fcu.edu.tw

M. Y. Hsieh

Department of Materials Science and Engineering,  Feng Chia University, 100 Wen Hwa Rd., Taichung 407, Taiwan


Corresponding author.

J. Fuel Cell Sci. Technol 3(3), 322-326 (Jan 04, 2006) (5 pages) doi:10.1115/1.2211638 History: Received November 29, 2005; Revised January 04, 2006

Carbon electrodes are one of the key materials in polymer electrolyte fuel cells (PEFC), or proton exchange membrane fuel cells (PEMFC). The electrodes should allow water or water vapor, which is produced by the redox reactions, to flow out of the cells efficiently. In the meantime, the catalysis reactions are not interfered. In this study, the carbon electrodes for PEMFC have been modified in terms of the hydrophobic and hydrophilic properties by plasma irradiation. The process utilized inductively coupled plasma (ICP) driven by applying radio frequency (rf) power on an induction coil. A pure Ar, O2, and ArO2 gas mixture were used as the plasma gas. Only one side of the sample has been treated. The material properties of the plasma treated and untreated carbon electrodes were investigated by Raman spectroscopy, Fourier transformed infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). FTIR results show the plasma treatments effectively modified the functional groups on the carbon surface, and therefore the hydrophilic and hydrophobic properties of the surface. SEM and Raman spectra data suggested that the ion bombardment during plasma treatments alters the surface morphology and carbon bonding structures of the samples, which also result in a hydrophilic surface. The treated carbon electrodes were used as cathodes and have been packed with commercial carbon anodes and catalyst coated membrane to form 5cm×5cm fuel cells. The current-voltage polarization curves of these fuel cells were measured and compared. The test results show the feasibility of improving the cell performance by plasma treated electrodes. The feasibility of altering the hydrophobic and hydrophilic properties by plasma treatment has been demonstrated. The capillary effect due to the unbalanced hydrophilicity between the treated and untreated electrode surfaces may be responsible for the improved cell performance.

Copyright © 2006 by American Society of Mechanical Engineers
Your Session has timed out. Please sign back in to continue.



Grahic Jump Location
Figure 2

Currents measured on the substrate holder as a function of the rf coil power different plasma

Grahic Jump Location
Figure 1

Apparatus of the inductively coupled plasma system

Grahic Jump Location
Figure 3

Water drop contact angles as a function of applied rf coil power on the top surfaces of the samples (a) immediately after treatment, (b) five days after treatment, and (c) on the backsides of samples five days after treatment

Grahic Jump Location
Figure 4

Surface morphologies of (a) untreated, (b) Ar plasma, (c) Ar∕O2 plasma, and (d) O2 plasma treated samples (1min, 120W)

Grahic Jump Location
Figure 5

Raman spectra of (a) untreated, (b) Ar∕O2 plasma treated, (c) Ar plasma treated, and (d) O2 plasma treated samples. The ID∕IG ratios are also indicated.

Grahic Jump Location
Figure 6

FTIR spectra of Ar∕O2, Ar, and O2 plasma treated and untreated samples

Grahic Jump Location
Figure 7

(a) Polarization curves of cells using different cathodes, and (b) powers as a function of operating currents for treated and untreated cathodes. A cell using untreated commercial E-TEK (B-1∕A) electrodes is measured for comparison.



Some tools below are only available to our subscribers or users with an online account.

Related Content

Customize your page view by dragging and repositioning the boxes below.

Related Journal Articles
Related eBook Content
Topic Collections

Sorry! You do not have access to this content. For assistance or to subscribe, please contact us:

  • TELEPHONE: 1-800-843-2763 (Toll-free in the USA)
  • EMAIL: asmedigitalcollection@asme.org
Sign In