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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 |
Appears in Collections: | Elements Staff Publications |
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