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六方稀土 - 铁混合氧化物(REFeO):晶体结构、合成及催化性能

Hexagonal Rare Earth-Iron Mixed Oxides (REFeO): Crystal Structure, Synthesis, and Catalytic Properties.

作者信息

Hosokawa Saburo

机构信息

Elements Strategy Initiative for Catalysts and Batteries, Kyoto University, Kyoto, Japan.

Department of Molecular Engineering, Graduate School of Engineering, Kyoto University, Kyoto, Japan.

出版信息

Front Chem. 2019 Jan 28;7:8. doi: 10.3389/fchem.2019.00008. eCollection 2019.

Abstract

The rare earth-iron mixed oxide (REFeO) is an attractive material in fields such as electronic, magnetic, and catalytic research. Generally, orthorhombic REFeO (-REFeO) with a perovskite structure is better known than hexagonal REFeO (-REFeO), because REFeO is thermodynamically stable for all RE elements. However, -REFeO has a very interesting crystal structure in which a RE and Fe layer are alternately stacked along the -axis in the unit cell; nevertheless, synthesis of the -REFeO belonging to metastable phase can be problematic. Fortunately, solution-based synthetic methods like solvothermal or coprecipitation synthesis have recently enabled the selective synthesis of -REFeO and -REFeO with comparative ease. Although the electronic and magnetic properties of -REFeO have typically been evaluated, recent research has also revealed excellent catalytic properties that enable environmental cleanup reactions such as hydrocarbon or CO oxidation. This mini-review introduces a synthetic method for controlling the crystal structure between orthorhombic and hexagonal REFeO and the catalytic performance of -REFeO-based materials.

摘要

稀土 - 铁混合氧化物(REFeO)是电子、磁性和催化研究等领域中一种具有吸引力的材料。一般来说,具有钙钛矿结构的正交晶系REFeO(-REFeO)比六方晶系REFeO(-REFeO)更为人所知,因为REFeO对于所有稀土元素来说在热力学上都是稳定的。然而,-REFeO具有一种非常有趣的晶体结构,其中在晶胞中稀土和铁层沿 - 轴交替堆叠;尽管如此,属于亚稳相的 -REFeO的合成可能存在问题。幸运的是,最近基于溶液的合成方法,如溶剂热合成或共沉淀合成,已经能够相对容易地选择性合成 -REFeO和 -REFeO。尽管 -REFeO的电子和磁性性质通常已经得到评估,但最近的研究还揭示了其优异的催化性能,能够实现烃类或CO氧化等环境净化反应。这篇小型综述介绍了一种控制正交晶系和六方晶系REFeO之间晶体结构的合成方法以及 -REFeO基材料的催化性能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5853/6360182/ab79048bf4bd/fchem-07-00008-g0001.jpg

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