Effects of platinum loading on performance of proton-exchange membrane fuel cells using surface-modified Nafion (R) membranes

Authors
Prasanna, M.Cho, E. A.Kim, H. -J.Lim, T. -H.Oh, I. -H.Hong, Sung-Ahn
Issue Date
2006-09-29
Publisher
ELSEVIER SCIENCE BV
Citation
JOURNAL OF POWER SOURCES, v.160, no.1, pp.90 - 96
Abstract
The interface between the electrolyte and electrode catalyst plays an important role in determining the performance of proton-exchange membrane fuel cells (PEMFCs) since the electrochemical reactions take place at the interface in contact with the reactant gases. To enhance catalyst activity by enlarging the interfacial area, the surface of a Nafion membrane is roughened by Ar+ ion beam bombardment that does not change the chemical structure of the membrane, as confirmed by FT-IR spectra. Among the membranes treated with ion dose densities of 0, 10(15), 10(6), 5 x 10(16) and 10(17) ions cm(-2) at ion energy of 1 keV, the membrane treated at ion dose density of 5 x 10(16) ions cm(-2) exhibits the highest performance. Using the untreated and the treated membrane with 5 x 10(16) ions cm(-2), the effects of platinum loading on cell performance are examined with Pt loadings of 01, 0.2, 0.3, 0.4 and 0.55 mg cm(-2). Except for a Pt loading of 0.55 mg cm(-2) where mass transport limits the cell performance, the single cell using a treated membrane gives a higher performance than that using an untreated membrane. This implies that the cell performance can be improved and the Pt loading can be reduced by ion beam bombardment. (c) 2006 Elsevier B.V. All rights reserved.
Keywords
WATER; SPECTROSCOPY; WATER; SPECTROSCOPY; ion beam treatment; surface morphology; proton exchange membrane fuel cells; platinum catalyst loading; interface; membrane characterization
ISSN
0378-7753
URI
https://pubs.kist.re.kr/handle/201004/135103
DOI
10.1016/j.jpowsour.2006.01.071
Appears in Collections:
KIST Article > 2006
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE