Please use this identifier to cite or link to this item: https://apo.ansto.gov.au/dspace/handle/10238/11757
Title: Expanded chemistry and proton conductivity in vanadium-substituted variants of γ-Ba4Nb2O9
Authors: Brown, AJ
Schwaighofer, B
Avdeev, M
Johannessen, B
Evans, IR
Ling, CD
Keywords: X-ray diffration
Transition elements
Electric conductivity
Thermal gravimetric analysis
Absorption
Neutron diffraction
Perovskite
Issue Date: 9-Sep-2021
Publisher: American Chemical Society
Citation: Brown, A. J., Schwaighofer, B., Avdeev, M., Johannessen, B., Evans, I. R., & Ling, C. D. (2021). Expanded chemistry and proton conductivity in vanadium-substituted variants of γ-Ba4Nb2O9. Chemistry of Materials. doi:10.1021/acs.chemmater.1c02340
Abstract: We have substantially expanded the chemical phase space of the hitherto unique γ-Ba4Nb2O9 type structure by designing and synthesizing stoichiometric ordered analogues γ-Ba4V1/3Ta5/3O9 and γ-Ba4V1/3Nb5/3O9 and exploring the solid-solution series γ-Ba4VxTa2–xO9 and γ-Ba4VxNb2–xO9. Undoped Ba4Ta2O9 forms a 6H-perovskite type phase, but with sufficient V doping the γ-type phase is thermodynamically preferred and possibly more stable than γ-Ba4Nb2O9, forming at a 200 °C lower synthesis temperature. This is explained by the fact that Nb5+ ions in γ-Ba4Nb2O9 simultaneously occupy 4-, 5-, and 6-coordinate sites in the oxide sublattice, which is less stable than allowing smaller V5+ to occupy the former two and larger Ta5+ to occupy the latter. The x = 1/3 phase γ-Ba4V1/3Ta5/3O9 shows greatly improved ionic conduction compared to the x = 0 phase 6H-Ba4Ta2O9. We characterized the structures of the new phases using a combination of X-ray and neutron powder diffraction. All compositions hydrate rapidly and extensively (up to 1/3 H2O per formula unit) in ambient conditions, like the parent γ-Ba4Nb2O9 phase. At lower temperatures, the ionic conduction is predominately protonic, while at higher temperatures it is likely other charge carriers make increasing contributions.© 2021 American Chemical Society
URI: https://doi.org/10.1021/acs.chemmater.1c02340
https://apo.ansto.gov.au/dspace/handle/10238/11757
ISSN: 1520-5002
Appears in Collections:Journal Articles

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