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김귀용

Kim, Kwiyong
Redox and electrochemistry advancing clean technologies Lab.
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Carbon supported bimetallic Pd-Co catalysts for alkaline sulfide oxidation in direct alkaline sulfide fuel cell

Author(s)
Kim, KwiyongHan, Jong-In
Issued Date
2015-04
DOI
10.1016/j.ijhydene.2015.02.009
URI
https://scholarworks.unist.ac.kr/handle/201301/62125
Citation
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, v.40, no.13, pp.4567 - 4572
Abstract
In this study, carbon supported Pd and Pd-Co alloys were synthesized and investigated as anode catalysts for the practical application of a promising sulfide-fed fuel cell, named direct alkaline sulfide fuel cell (DASFC). Physical and electrochemical properties of the Pd/C and Pd-Co/C catalysts were evaluated using X-ray diffraction (XRD), transmission electron microscope (TEM), energy dispersive X-ray (EDX), inductively coupled plasma optical emission spectroscopy (ICP-OES), cyclic voltammetry (CV), linear sweep voltammetry (LSV), I-V analysis and electrochemical impedance spectroscopy (EIS). Among all the Pd-based catalysts tested, Pd8Co2/C showed the highest sulfide oxidation activity in terms of the lowest onset potential and the highest current density, mass activity, and specific activity at -0.2 V (vs. Ag/AgCl). The maximum power density of DASFC with Pd8Co2/C anode catalyst was 46.82 mW cm(-2) at 70 degrees C, which is 26% higher than that with Pd/C. It is speculated that the incorporation of Co into Pd facilitated the adsorption of OHads at a lower potential, and Pd8Co2/C provided the optimal coverage of OHads that played a catalytic role and thus led to the highest performance. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
ISSN
0360-3199
Keyword (Author)
Hydrogen sulfideDirect alkaline sulfide fuel cellPd-Co catalystsOHads adsorption
Keyword
OXYGEN REDUCTION REACTIONHYDROGEN-SULFIDEAEROBIC OXIDATIONANODE CATALYSTSPERFORMANCEELECTROLYTESULFURELECTROCATALYSTSDECOMPOSITIONNANOPARTICLES

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