Enhancement of oxide ion and proton conductivity in Sr3-xCaxV2O8 palmierites through tuning of the crystal structure

IF 3.3 4区 材料科学 Q3 CHEMISTRY, PHYSICAL
Sophie G. Martin , Oscar J.B. Ballantyne , Clemens Ritter , Ying Zhou , Frazer N. Forrester , James A. Dawson , Abbie C. Mclaughlin
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引用次数: 0

Abstract

Sizeable oxide ion and proton conductivity have recently been reported in A3V2O8 (A = Ba, Sr) palmierites. The solid solution Sr3-xCaxV2O8 (x = 0.0–0.2) has been synthesised and investigated by electrochemical characterisation and atomistic modelling, revealing key insights into the design principles for enhancing oxide and proton conduction in palmierites. Neutron diffraction data shows that at 20 °C there is a reduction in crystal symmetry from R3¯m to C2/c for x ≥ 0.05. Upon heating to 600 °C, R3¯m symmetry is restored for all phases. An increase in both the oxide ion and proton conductivity are observed with Ca2+ doping. The oxide ion conductivity scales with the magnitude of displacement of the V5+ cation and VO2 bond length.
通过调整晶体结构增强Sr3-xCaxV2O8棕榈石中氧化离子和质子的电导率
最近报道了A3V2O8 (A = Ba, Sr)棕榈岩中较大的氧化物离子和质子电导率。合成了固溶体Sr3-xCaxV2O8 (x = 0.0-0.2),并通过电化学表征和原子建模对其进行了研究,揭示了增强棕榈石中氧化物和质子传导的设计原理。中子衍射数据表明,在20℃时,当x≥0.05时,晶体对称性从R3¯m降低到C2/ C。当加热到600°C时,所有相的R3¯m对称性恢复。钙离子掺杂后,氧化离子和质子电导率均有所提高。氧化离子的电导率与V5+阳离子的位移大小和VO2键的长度成正比。
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来源期刊
Solid State Ionics
Solid State Ionics 物理-物理:凝聚态物理
CiteScore
6.10
自引率
3.10%
发文量
152
审稿时长
58 days
期刊介绍: This interdisciplinary journal is devoted to the physics, chemistry and materials science of diffusion, mass transport, and reactivity of solids. The major part of each issue is devoted to articles on: (i) physics and chemistry of defects in solids; (ii) reactions in and on solids, e.g. intercalation, corrosion, oxidation, sintering; (iii) ion transport measurements, mechanisms and theory; (iv) solid state electrochemistry; (v) ionically-electronically mixed conducting solids. Related technological applications are also included, provided their characteristics are interpreted in terms of the basic solid state properties. Review papers and relevant symposium proceedings are welcome.
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