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Top-down preparation of Ni-Pd-P@graphitic carbon core-shell nanostructure as a non-Pt catalyst for enhanced electrocatalytic reactions

Authors
Park, Deok-HyeKim, Yo-SeobHan, Sang-BeomLee, Woo-JunLee, Hak-JooLee, Yong-SooMoon, Sang-HyunPark, Kyung-Won
Issue Date
23-Jun-2021
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
Bimetal phosphide; Electrocatalyst; Oxygen evolution reaction; Oxygen reduction reaction; Methanol oxidation reaction
Citation
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, v.46, no.43, pp.22499 - 22507
Journal Title
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume
46
Number
43
Start Page
22499
End Page
22507
URI
http://scholarworks.bwise.kr/ssu/handle/2018.sw.ssu/41239
DOI
10.1016/j.ijhydene.2021.04.079
ISSN
0360-3199
Abstract
Electrochemical reactions such as the oxygen evolution reaction (OER), oxygen reduction reaction (ORR), and methanol oxidation reaction (MOR) are essential for energy conversion applications such as water electrolysis and fuel cells. Furthermore, Pt or Ir-related materials have been extensively utilized as electrocatalysts for the OER, ORR, and MOR. To reduce the utilization of precious metals, innovative catalyst structures should be proposed. Herein, we report a bi-metallic phosphide (Ni2P and PdP2) structure surrounded by graphitic carbon (Ni-Pd-P/C) with an enhanced electrochemical activity as compared to conventional electrocatalysts. Despite the low Pd content of 3 at%, Ni-Pd-P/C exhibits a low overpotential of 330 mV at 10 mA cm(-2) in the OER, high specific activity (2.82 mA cm(-2) at 0.8 V) for the ORR, and a high current density of 1.101 A mg(-1) for the MOR. The superior electrochemical performance of Ni-Pd-P/C may be attributed to the synergistic effect of the bi-metallic phosphide structure and core-shell structure formed by graphitic carbon. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
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