Electrochemical Catalytic Behavior of Cu2O Catalyst for Oxygen Reduction Reaction in Molten Carbonate Fuel Cells

Authors
Song, Shin AeKim, KiyoungLim, Sung NamHan, JongheeYoon, Sung PilKang, Min-GooJang, Seong-Cheol
Issue Date
2018-09
Publisher
KOREAN ELECTROCHEMISTRY SOC
Citation
JOURNAL OF ELECTROCHEMICAL SCIENCE AND TECHNOLOGY, v.9, no.3, pp.195 - 201
Abstract
To enhance the performance of cathodes at low temperatures, a Cu-coated cathode is prepared, and its electrochemical performance is examined by testing its use in a single cell. At 620 degrees C and a current density of 150 mAcm(-2), a single cell containing the Cu-coated cathode has a significantly higher voltage (0.87 V) during the initial operation than does that with an uncoated cathode (0.79 V). According to EIS analysis, the high voltage of the cell with the Cu-coated cathode is due to the dramatic decrease in the high-frequency resistance related to electrochemical reactions. From XPS analysis, it is confirmed that the Cu is initially in the form of Cu2O and is converted into CuO after 150 h of operation, without any change in the state of the Ni or Li. Therefore, the high initial cell voltage is confirmed to be due to Cu2O. Because Cu2O is catalytically active toward O-2 adsorption and dissociation, Cu2O on a NiO cathode enhances cell performance and reduces cathode polarization. However, the cell with the Cu-coated cathode does not maintain its high voltage because Cu2O is oxidized to CuO, which demonstrates similar catalytic activity toward O-2 as NiO.
Keywords
LONG-TERM OPERATION; ELECTRODE PERFORMANCE; DIMETHYL CARBONATE; COATED CATHODE; OXIDATION; ANODE; NANOPARTICLES; TEMPERATURE; NICKEL; COPPER; LONG-TERM OPERATION; ELECTRODE PERFORMANCE; DIMETHYL CARBONATE; COATED CATHODE; OXIDATION; ANODE; NANOPARTICLES; TEMPERATURE; NICKEL; COPPER; Molten carbonate fuel cells; Copper-coated cathode; Catalytic activity; Lowering cathode polarization
ISSN
2093-8551
URI
https://pubs.kist.re.kr/handle/201004/120987
DOI
10.33961/JECST.2018.9.3.195
Appears in Collections:
KIST Article > 2018
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