期刊
CERAMICS INTERNATIONAL
卷 49, 期 8, 页码 12805-12813出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.ceramint.2022.12.146
关键词
Hydrogen separation membrane; Lanthanide molybdate; Polymorphism; Mixed ionic-electronic conductor
In this study, ceramics with composition Ln(5.4)MoO(11.1) (Ln = Nd, Sm and Gd) were prepared and their polymorphic forms were investigated by sintering at different rates. X-ray diffraction studies confirmed single-phase materials, with a simple cubic fluorite structure for the quenching-cooled samples. Electron diffraction studies indicated the formation of domains with superstructure ordering. XPS analysis showed the presence of mixed Mo6+ and Mo5+ for all compositions, explaining the electronic conduction in an oxidizing atmosphere.
Mixed proton-electronic conductors are of great interest for high temperature electrochemical devices, such as hydrogen separation membranes. In this contribution, ceramics with composition Ln(5.4)MoO(11.1) (Ln = Nd, Sm and Gd) were prepared by a freeze-drying precursor method. The resulting powders were sintered at 1500 degrees C and cooled down at different rates to investigate the different polymorphic forms: quenching (rapid cooling), 5 and 0.5 degrees C min(-1). The ceramics were characterized by different techniques: X-ray diffraction, scanning and trans-mission electron microscopies and X-ray photoelectron and impedance spectroscopies. X-ray diffraction studies confirmed that all materials are single phase regardless of the cooling rate used. Those cooled by quenching present a simple cubic fluorite structure. At lower rates, 5 and 0.5 degrees C min(-1), the cubic symmetry is stabilized as the size of the lanthanide decreases. However, electron diffraction studies indicated the formation of domains with superstructure ordering. Furthermore, XPS analysis showed the presence of mixed Mo6+ and Mo5+ for all compositions, which explains the electronic conduction in an oxidizing atmosphere. All materials are stable in reducing atmosphere and the ionic and electronic conductivities show opposite trends as the ionic radii of the lanthanide element becomes smaller, where the former decreases and the latter increases.
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