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Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/12669

Title: Ab initio investigation of O2 adsorption on Ca-doped LaMnO3 cathodes in solid oxide fuel cells
Authors: Aniagyei, Albert
Dzade, Nelson Y.
Tia, Richard
Adei, Evans
Catlow, C. R. A.
et. al
Issue Date: 2018
Publisher: Royal Society of Chemistry
Citation: Aniagyei, Albert, Dzade, Nelson Y., Tia, Richard, Adei, Evans, Catlow, C. R. A. and de Leeuw,Nora H. 2018. Ab initio investigation of O2 adsorption on Ca-doped LaMnO3 cathodes in solidoxide fuel cells. Physical Chemistry Chemical Physics 20 (45) , p. 28685. 10.1039/C8CP02137F file
Abstract: We present a Hubbard-corrected density functional theory (DFT+U) study of the adsorption and reduction reactions of oxygen on the pure and 25% Ca-doped LaMnO3 (LCM25) {100} and {110} surfaces. The effect of oxygen vacancies on the adsorption characteristics and energetics has also been investigated. Our results show that the O2 adsorption/reduction process occurs through the formation of superoxide and peroxide intermediates, with the Mn sites found to be generally more active than the La sites. The LCM25{110} surface is found to be more efficient for O2 reduction than the LCM25{100} surface due to its stronger adsorption of O2, with the superoxide and peroxide intermediates shown to be energetically more favorable at the Mn sites than at the Ca sites. Moreover, oxygen vacancy defect sites on both the {100} and{110} surfaces are shown to be more efficient for O2 reduction, as reflected in the higher adsorption energies calculated on the defective surfaces compared to the perfect surfaces. We show from Lowdin population analysis that the O 2 adsorption on the pure and 25% Ca-doped ̈ LaMnO3 surfaces is characterized by charge transfer from the interacting surface species into the adsorbed oxygen pg orbital, which results in weakening of the O–O bonds and its subsequent reduction. The elongated O–O bonds were confirmed via vibrational frequency analysis.
Description: An article published by Royal Society of Chemistry and also available at http://dx.doi.org/10.1039/C8CP02137F
URI: http://hdl.handle.net/123456789/12669
Appears in Collections:College of Science

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