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|a 10.1021/acs.chemmater.2c03001
|2 doi
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|a pubmed24n1171.xml
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|a (DE-627)NLM351551085
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|a (NLM)36644215
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|a DE-627
|b ger
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|e rakwb
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|a eng
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|a Yue, Yajun
|e verfasserin
|4 aut
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|a Local Structure in α-BIMEVOXes (ME = Ge, Sn)
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|c 2023
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|a Text
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|a ƒaComputermedien
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|2 rdamedia
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|a ƒa Online-Ressource
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|a Date Revised 17.01.2023
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|a published: Electronic-eCollection
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|a Citation Status PubMed-not-MEDLINE
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|a © 2022 The Authors. Published by American Chemical Society.
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|a The BIMEVOXes are among the best oxide ion conductors at low and intermediate temperatures. Their high conductivity is associated with local defect structure. In this work, the local structures of two BIMEVOX compositions, Bi2V0.9Ge0.1O5.45 and Bi2V0.95Sn0.05O5.475, are examined using total neutron and X-ray scattering methods, with both compositions exhibiting the ordered α-phase at 25 °C and the disordered γ-phase at 700 °C. While the diffraction data for the α-phase do not allow for the polar (C2) and nonpolar (C2/m) structures to be readily distinguished, measurements of dielectric permittivity suggest the α-phase is weakly ferroelectric in character, consistent with calculations of spontaneous polarization based on a combination of density functional calculations and machine learning methodology. Reverse Monte Carlo (RMC) analysis of total scattering data reveals Ge preferentially adopts tetrahedral geometry at both temperatures, while Sn is found to predominantly adopt octahedral coordination in the α-phase and tetrahedral coordination in the γ-phase. In all cases, V polyhedra are found to consist of tetrahedral, pentacoordinate, and octahedral geometries, as also predicted by the crystallographic analysis and confirmed by 51V solid state NMR spectroscopy. Although similar long-range structures are observed at room temperature, the oxide ion vacancy distributions were found to be quite different between the two studied compositions, with a nonrandom deficiency in vacancy pairs in the second-nearest shell along the ⟨100⟩ tetragonal direction for BIGEVOX10, compared with a long-distance (>8.0 Å) ordering of equatorial vacancies for BISNVOX05. This is attributed to the differences in the preferred coordination geometries of the substituent cations in the two systems. Impedance spectroscopy measurements reveal both compositions show high conductivity in the order of 10-1 S cm-1 at 600 °C
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|a Journal Article
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|a Dzięgielewska, Aleksandra
|e verfasserin
|4 aut
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|a Zhang, Man
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|a Hull, Stephen
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|a Krok, Franciszek
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|a Whiteley, Richard M
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|4 aut
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|a Toms, Harold
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|a Malys, Marcin
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|4 aut
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|a Huang, Xuankai
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|4 aut
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|a Krynski, Marcin
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|4 aut
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|a Miao, Ping
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|a Yan, Haixue
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|a Abrahams, Isaac
|e verfasserin
|4 aut
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| 773 |
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|i Enthalten in
|t Chemistry of materials : a publication of the American Chemical Society
|d 1998
|g 35(2023), 1 vom: 10. Jan., Seite 189-206
|w (DE-627)NLM098194763
|x 0897-4756
|7 nnns
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| 773 |
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|g volume:35
|g year:2023
|g number:1
|g day:10
|g month:01
|g pages:189-206
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|u http://dx.doi.org/10.1021/acs.chemmater.2c03001
|3 Volltext
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