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无序和有序稀土氧化物稳定氧化铋离子导体的能量学。

Energetics of disordered and ordered rare earth oxide-stabilized bismuth oxide ionic conductors.

机构信息

Peter A. Rock Thermochemistry Laboratory and NEAT ORU, University of California, Davis, CA 95616, USA.

出版信息

Phys Chem Chem Phys. 2014 Feb 14;16(6):2331-7. doi: 10.1039/c3cp54553a.

Abstract

Rare-earth stabilized bismuth oxides are known for their excellent ionic conductivity at intermediate temperatures. However, previous studies have shown that their conductivity deteriorates during extended heat treatments at 500-600 °C, although the fluorite phase is maintained. In this study, the enthalpies of formation of quenched and aged ytterbia- and dysprosia-stabilized bismuth oxides were measured using high-temperature oxide melt solution calorimetry in 3Na2O-4MoO3 solvent at 702 °C. While a modest energy difference (-2 to -3 kJ mol(-1)) drives the kinetically slow aging transformation in the ytterbia-stabilized system at moderate dopant contents, no energetic driving force is detectable in the dysprosia-stabilized system. Although the small magnitude of the exothermic ordering energy suggests extensive short range ordering in both the quenched and aged samples, the anion configuration specific to the aged samples is nevertheless responsible for the significant decrease in conductivity.

摘要

稀土稳定的氧化铋在中温下具有优异的离子导电性。然而,先前的研究表明,尽管保持萤石相,它们的电导率在 500-600°C 的长时间热处理过程中会恶化。在这项研究中,使用高温氧化物熔体溶液量热法在 702°C 的 3Na2O-4MoO3 溶剂中测量了淬火和时效的掺镱和掺镝稳定氧化铋的生成焓。虽然在中等掺杂含量下,在动力学上缓慢的老化转变中,较小的能量差(-2 至-3 kJ mol(-1)) 会驱动,但在掺镝稳定体系中,没有可检测到的能量驱动力。尽管放热有序能的幅度较小表明在淬火和时效样品中都存在广泛的短程有序,但对于时效样品来说,阴离子构型的特异性仍然是导致电导率显著下降的原因。

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