Please use this identifier to cite or link to this item: https://doi.org/10.1039/c7ta06817d
Title: Crystal structure and surface characteristics of Sr-doped GdBaCo 2 O6-: ? double perovskites: Oxygen evolution reaction and conductivity
Authors: Pramana, S.S
Cavallaro, A
Li, C
Handoko, A.D 
Chan, K.W
Walker, R.J
Regoutz, A
Herrin, J.S
Yeo, B.S 
Payne, D.J
Kilner, J.A
Ryan, M.P
Skinner, S.J
Keywords: Barium compounds
Catalysts
Gadolinium compounds
Iridium compounds
Oxygen
Perovskite
Alkaline-earth ions
Electrical conductivity
Electrochemical performance
Oxygen evolution activity
Oxygen evolution reaction
Reversible hydrogen electrodes
Surface characteristics
Sustainable energy systems
Crystal structure
Issue Date: 2018
Citation: Pramana, S.S, Cavallaro, A, Li, C, Handoko, A.D, Chan, K.W, Walker, R.J, Regoutz, A, Herrin, J.S, Yeo, B.S, Payne, D.J, Kilner, J.A, Ryan, M.P, Skinner, S.J (2018). Crystal structure and surface characteristics of Sr-doped GdBaCo 2 O6-: ? double perovskites: Oxygen evolution reaction and conductivity. Journal of Materials Chemistry A 6 (13) : 5335-5345. ScholarBank@NUS Repository. https://doi.org/10.1039/c7ta06817d
Abstract: A cheap and direct solution towards engineering better catalysts through identification of novel materials is required for a sustainable energy system. Perovskite oxides have emerged as potential candidates to replace the less economically attractive Pt and IrO 2 water splitting catalysts. In this work, excellent electrical conductivity (980 S cm -1 ) was found for the double perovskite of composition GdBa 0.6 Sr 0.4 Co 2 O 6-? which is consistent with a better oxygen evolution reaction activity with the onset polarisation of 1.51 V with respect to a reversible hydrogen electrode (RHE). GdBa 1-x Sr x Co 2 O 6-? with increasing Sr content was found to crystallise in the higher symmetry tetragonal P4/mmm space group in comparison with the undoped GdBaCo 2 O 6-? which is orthorhombic (Pmmm), and yields higher oxygen uptake, accompanied by higher Co oxidation states. This outstanding electrochemical performance is explained by the wider carrier bandwidth, which is a function of Co-O-Co buckling angles and Co-O bond lengths. Furthermore the higher oxygen evolution activity was observed despite the formation of non-lattice oxides (mainly hydroxide species) and enrichment of alkaline earth ions on the surface. © The Royal Society of Chemistry.
Source Title: Journal of Materials Chemistry A
URI: https://scholarbank.nus.edu.sg/handle/10635/175077
ISSN: 20507488
DOI: 10.1039/c7ta06817d
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