薄膜
微晶
材料科学
钙钛矿(结构)
相(物质)
镧系元素
萤石
分析化学(期刊)
结晶学
化学
纳米技术
冶金
离子
有机化学
色谱法
作者
Kai Shen,Jian Chang,Rajeev Kumar,Ching‐Yu Wang,Eric A. Stach,Raymond J. Gorte,John M. Vohs
标识
DOI:10.1021/acs.jpcc.3c03240
摘要
The thermodynamic and structural properties of 1 nm thick films of CeVO4 and LaVO4 supported on γ-Al2O3 were examined and compared to the corresponding bulk rare-earth vanadates. The films were prepared by atomic layer deposition (ALD) on high-surface-area powders and then examined after either oxidation or reduction at 1073 K. Both CeVO4 and LaVO4 uniformly covered the γ-Al2O3 in the form of two-dimensional crystallites. Thin-film LaVO4 reversibly transitioned between a perovskite structure upon reduction to a monazite structure upon oxidation, similar to what is observed for the bulk material; however, coulometric titration (CT) showed that the P(O2) at which equilibrium is established between these two phases was 7 orders of magnitude higher for the thin-film material. Thin-film CeVO4 also formed a perovskite phase upon reduction but reversibly transitioned to a fluorite phase upon oxidation rather than the zircon phase, which is formed for bulk CeVO4. Multiple techniques showed that the oxidation states of both Ce and V in the thin-film CeVO4 were +4, which is also different from bulk CeVO4. Reasons for why the properties of the thin-film, rare-earth vanadates differ from their bulk counterparts are discussed.
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