Effects of ionomer content on Pt catalyst/ordered mesoporous carbon support in polymer electrolyte membrane fuel cells
Cited 7 times in
Cited 0 times in
- Title
- Effects of ionomer content on Pt catalyst/ordered mesoporous carbon support in polymer electrolyte membrane fuel cells
- Author
- Ahn, Chi-Yeong; Cheon, Jae-Yeong; Joo, Sang-Hoon; Kim, Junbom
- Issue Date
- 2013-01
- Publisher
- ELSEVIER SCIENCE BV
- Citation
- JOURNAL OF POWER SOURCES, v.222, pp.477 - 482
- Abstract
- In this paper, the optimum Nafion ionomer content in platinum (Pt) dispersed on ordered mesoporous carbon (OMC) catalyst is investigated. The ionomer content can affect catalytic activity, ionic conductivity and mass transfer characteristics. A nano-replication method using ordered mesoporous silicas (OMS) is applied to prepare OMCs, and Pt/OMC with high loading are synthesized by the incipient wetness method for polymer electrolyte membrane fuel cells (PEMFCs). Catalyst characteristics have been analyzed using TGA, XRD, TEM and BET. Cathode electrodes have different ionomer loadings (in the range of 5-30 wt. %) with Pt/OMCs. Commercial Pt/C catalyst is used in anode. All membrane electrode assemblies (MEAs) fabricated by the decal transfer method show about 0.4 mg cm(-2) Pt loading. The PEMFC performances have been measured by electrochemical methods such as polarization curves, electrochemical impedance spectroscopy (EIS), and cyclic voltammetry (CV). The performances is different at low and high current density regions, and the optimum content of ionomer is 10 wt. % in the catalyst, due to unique structure of OMCs.
- URI
- https://scholarworks.unist.ac.kr/handle/201301/3169
- URL
- http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84866696148
- DOI
- 10.1016/j.jpowsour.2012.09.012
- ISSN
- 0378-7753
- Appears in Collections:
- CHM_Journal Papers
- Files in This Item:
- There are no files associated with this item.
can give you direct access to the published full text of this article. (UNISTARs only)
Show full item record
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.