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The role of arginine as nitrogen doping and carbon source for enhanced oxygen reduction reaction

Authors
Kim, Do-HyoungKwak, Da-HeeHan, Sang-BeomPark, Hyun-SukPark, Jin-YoungWon, Ji-EunMa, Kyeng-BaeYun, Seok-HyeonKwon, Suk-HuiKoh, Moon HyunPark, Kyung-Won
Issue Date
Jan-2018
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
Doped carbon nanostructure; Arginine; Non-precious metal catalyst; Oxygen reduction reaction
Citation
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, v.43, no.3, pp.1479 - 1488
Journal Title
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume
43
Number
3
Start Page
1479
End Page
1488
URI
http://scholarworks.bwise.kr/ssu/handle/2018.sw.ssu/32111
DOI
10.1016/j.ijhydene.2017.11.173
ISSN
0360-3199
Abstract
Doped carbon nanostructures as non-precious metal (NPM) catalysts for oxygen reduction reaction (ORR) in acid medium are mainly synthesized using 5, 10, 15, 20-tetrakis (4methoxyphenyl)-porphyrin-Fe (III) chloride (Fe-TMPP) as doping and carbon sources. In this study, the doped carbon nanostructures used as cathode NPM catalysts for ORR are prepared using a mixture of iron phthalocyanine (FePc) and arginine as doping and carbon sources. The morphology and composition of the as-prepared samples are characterized using field-emission scanning electron microscopy, field-emission transmission electron microscopy, and energy dispersive X-ray (EDX) spectroscopy. The crystal and pore structures are analyzed using X-ray diffraction method, Raman spectroscopy, and nitrogen adsorption/desorption method. The sample prepared using a precursor mixture with a proper ratio of FePc and arginine exhibits significantly superior ORR performance, i.e. high specific activity, enhanced half-wave potential, and improved stability in an acid medium, as even compared to a commercial Pt/C. The improved ORR properties is mainly attributed to high portion of pyridinic N state with a relatively high specific surface area, which can result from the FePc precursor surrounded by the fused arginine. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
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