Graphene-Supported Platinum Catalyst-Based Membrane Electrode Assembly for Pem Fuel Cell

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Date

2016

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Volume Title

Publisher

Springer

Open Access Color

Green Open Access

No

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Abstract

The aim of this study is the preparation and characterization of a graphene-supported platinum (Pt) catalyst for proton exchange membrane fuel cell (PEMFC) applications. The graphene-supported Pt catalysts were prepared by chemical reduction of graphene and chloroplatinic acid (H2PtCl6) in ethylene glycol. X-ray powder diffraction, thermogravimetric analysis (TGA) and scanning electron microscopy have been used to analyze structure and surface morphology of the graphene-supported catalyst. The TGA results showed that the Pt loading of the graphene-supported catalyst was 31%. The proof of the Pt particles on the support surfaces was also verified by energy-dispersive x-ray spectroscopy analysis. The commercial carbon-supported catalyst and prepared Pt/graphene catalysts were used as both anode and cathode electrodes for PEMFC at ambient pressure and 70 degrees C. The maximum power density was obtained for the Pt/graphene-based membrane electrode assembly (MEA) with H-2/O-2 reactant gases as 0.925 W cm(2). The maximum current density of the Pt/graphene-based MEA can reach 1.267 and 0.43 A/cm(2) at 0.6 V with H-2/O-2 and H-2/air, respectively. The MEA prepared by the Pt/graphene catalyst shows good stability in long-term PEMFC durability tests. The PEMFC cell voltage was maintained at 0.6 V without apparent voltage drop when operated at 0.43 A/cm(2) constant current density and 70 degrees C for 400 h. As a result, PEMFC performance was found to be superlative for the graphene-supported Pt catalyst compared with the Pt/C commercial catalyst. The results indicate the graphene-supported Pt catalyst could be utilized as the electrocatalyst for PEMFC applications.

Description

DEVRIM, YILSER/0000-0001-8430-0702

Keywords

Hydrogen energy, fuel cell, PEM, membrane electrode assembly, graphene oxide, catalyst

Fields of Science

02 engineering and technology, 0210 nano-technology, 01 natural sciences, 0104 chemical sciences

Citation

WoS Q

Q2

Scopus Q

Q2
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OpenCitations Citation Count
49

Source

Journal of Electronic Materials

Volume

45

Issue

8

Start Page

3900

End Page

3907

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CrossRef : 7

Scopus : 50

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Mendeley Readers : 95

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52

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44

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4

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