Effect of deactivation and reactivation of palladium anode catalyst on performance of direct formic acid fuel cell (DFAFC)

Authors
Baik, S. M.Han, JongheeKim, JinsooKwon, Yongchai
Issue Date
2011-11
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, v.36, no.22, pp.14719 - 14724
Abstract
In the present study, degradation and recovery in cell performance of direct formic acid fuel cells (DFAFCs) are investigated. For DFAFC tests, palladium (Pd) and platinum (Pt) are used as anode and cathode catalysts, respectively, and are applied to a Nafion membrane by catalyst-coated membrane (CCM) spraying. As multiple repeated DFAFC operations are performed, the cell performance of DFAFC is steadily degraded. This behavior is ascribed to the electrooxidation of Pd into Pd-OH, which occurs between 0.1 and 0.55 V. To investigate the dependency of the cell performance on the Pd-OH and to evaluate how the cell performance is regenerated, cyclic voltammetry (CV) tests are executed. In CV experiments where the voltages applied to the DFAFC single cell are lower than 0.7 V vs. DHE, the cell performance is further deactivated due to continuous production of Pd-OH. Conversely, in CV experiments where the voltage is higher than 0.9 V vs. DHE, cell performance is reactivated due to redox reactions of Pd-OH into Pd-O and Pd-O into Pd. ATR-FTIR and XPS are used to confirm the transformations of Pd. Copyright (C) 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
Keywords
INFRARED-ABSORPTION SPECTROSCOPY; GOLD ELECTRODES; CARBON-MONOXIDE; ELECTROOXIDATION; METHANOL; PD; NANOPARTICLES; IMPEDANCE; OXIDATION; OXYGEN; INFRARED-ABSORPTION SPECTROSCOPY; GOLD ELECTRODES; CARBON-MONOXIDE; ELECTROOXIDATION; METHANOL; PD; NANOPARTICLES; IMPEDANCE; OXIDATION; OXYGEN; Direct formic acid fuel cell; Palladium deactivation; Palladium reactivation; Palladium electroredox reaction; ATR-FTIR
ISSN
0360-3199
URI
https://pubs.kist.re.kr/handle/201004/129853
DOI
10.1016/j.ijhydene.2011.04.181
Appears in Collections:
KIST Article > 2011
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