Durability Of Pt Catalysts Supported On Ordered Mesoporous ...
© 2013 ECS - The Electrochemical Society ECS Transactions, Volume 58, Number 1Citation Nam-In Kim et al 2013 ECS Trans. 58 1277DOI 10.1149/05801.1277ecst
AuthorsNam-In Kim
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Sejong University
Jinhae Seong
AFFILIATIONS
Sejong University
Min-Ji Yang
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Sejong University
Sung-Hwa Cho
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Sejong University
Jun-Young Park
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Sejong University
Hanshin CHOI
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Korea Institute of Industrial Technology, Incheon 406-840, South Korea
Sang Hoon Joo
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UNIST
Kyungjung Kwon
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Sejong University
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Open scienceAuthorsNam-In Kim
AFFILIATIONS
Sejong University
Jinhae Seong
AFFILIATIONS
Sejong University
Min-Ji Yang
AFFILIATIONS
Sejong University
Sung-Hwa Cho
AFFILIATIONS
Sejong University
Jun-Young Park
AFFILIATIONS
Sejong University
Hanshin CHOI
AFFILIATIONS
Korea Institute of Industrial Technology, Incheon 406-840, South Korea
Sang Hoon Joo
AFFILIATIONS
UNIST
Kyungjung Kwon
AFFILIATIONS
Sejong University
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Article information 1938-5862/58/1/1277Abstract
Ordered mesoporous carbons (OMCs) are investigated as support materials of Pt catalyst in proton exchange membrane fuel cells. Four types of Pt/OMC catalysts are prepared and their electrochemical performances and durability are evaluated by cyclic voltammetry and linear sweep voltammetry using a rotating disk electrode system. Pt nanoparticles of 2-3 nm seem to be uniformly dispersed on the supports regardless of the kind of OMC. The different pore structure between CMK-3 and CMK-5 affects the surface areas of carbon supports and the resulting Pt nanoparticles with indicating that larger surface area accompanies higher oxygen reduction reaction (ORR) activity. Although the graphitization of carbon support from CMK-3 to CMK-3G reduces the surface area of carbon support, the surface area and the ORR activity of Pt nanoparticles on CMK-3G are increased. In general, the reductions in electrochemical surface area (ECSA) and ORR activity become more noticeable in proportion to the initial ECSA and ORR of Pt/OMC after accelerated durability test.
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