Triple phase boundary and power density enhancement in PEMFCs of a Pt/C electrode with double catalyst layers
- Authors
- Dung Van Dao; Adilbish, Ganpurev; Thanh Duc Le; Lee, In-Hwan; Yu, Yeon-Tae
- Issue Date
- 19-5월-2019
- Publisher
- ROYAL SOC CHEMISTRY
- Citation
- RSC ADVANCES, v.9, no.27, pp.15635 - 15641
- Indexed
- SCIE
SCOPUS
- Journal Title
- RSC ADVANCES
- Volume
- 9
- Number
- 27
- Start Page
- 15635
- End Page
- 15641
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/65397
- DOI
- 10.1039/c9ra01741k
- ISSN
- 2046-2069
- Abstract
- Exploring efficient approaches to design electrodes for proton exchange membrane fuel cells (PEMFCs) is of great advantage to overcome the current limitations of the standard platinum supported carbon (Pt/C) catalyst. Herein, a Pt/C electrode consisting of double catalyst layers (DCL) with low Pt loading of around 0.130 mg(Pt) cm(-2) is prepared using spray and electrophoresis (EPD) methods. The DCL electrode demonstrated a higher electrochemical surface area (ECSA-52.5 m(2) g(Pt)(-1)) and smaller internal resistance (133 ) as compared to single catalyst layer (SCL) sprayed (37.1 m(2) g(Pt)(-1) and 184 ) or EPD (42.4 m(2) g(Pt)(-1) and 170 ) electrodes. In addition, the corresponding DCL membrane electrode assembly (MEA), which consists of a Pt/C DCL electrode at the anode side and a Pt/C sprayed electrode at the cathode side, also showed improved PEMFC performance as compared to others. Specifically, the DCL MEA generated the highest power density of 4.9 W mg(Pt)(-1), whereas, the SCL MEAs only produced 3.1 and 3.8 W mg(Pt)(-1), respectively. The superior utilization of the Pt catalysts into the DCL MEA can originate from the enrichment of the triple phase boundary (TPB) presented on the Pt/C DCL electrode, which can strongly promote the adsorbed hydrogen intermediates' removal from the anode side, thus improving the overall PEMFC performance.
- Files in This Item
- There are no files associated with this item.
- Appears in
Collections - College of Engineering > Department of Materials Science and Engineering > 1. Journal Articles
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.