Preparation of LSGM electrolyte via fast combustion method and analysis of electrical properties for ReSOC.

IF 1.7 4区 材料科学 Q2 MATERIALS SCIENCE, CERAMICS Journal of Electroceramics Pub Date : 2022-09-22 DOI:10.1007/s10832-022-00294-7
Erwin Sepúlveda, R. V. Mangalaraja, R. Udayabhaskar, Ramón Cobo, María Escudero Berzal, José Jiménez, Christopher Salvo, Carlos P. Camurri
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Abstract

In this work, we prepared La1 − xSrxGa1−yMgyO3 (LSGM) by the fast combustion method and assessed the electrical properties with respect to the composition and sintering temperature (1200, 1300, and 1400 °C by 6 h) as an electrolyte material for the reversible solid oxide cells (ReSOCs). For the preparation of samples, two different fuels, such as tartaric acid (TA) and citric acid (CA), with corresponding nitrate salts as precursors, were adopted for the fast combustion method (at 500 °C for 10 min). From the X-ray diffractograms, two main phases corresponding to LSGM orthorhombic (space group Imma) and LSGM-cubic (space group Pm-3 m) were identified. From the literature, both structures are reported as high oxygen ion conductive species, but normally they are not reported to appear together. Additionally, in some cases, an isolating (secondary) phase of LaSrGaO4 in a low concentration < 1.98% was observed. The scanning electron microscopy (SEM) studies on samples sintered at 1200 and 1300 °C revealed the smaller grain size and irregular morphology. The SEM micrographs depicted a well-defined superficial morphology with less porosity for the samples sintered at 1400 °C. For comparative analysis, the conductivity (S.cm− 1) was measured at varying temperatures (300–800 °C) for the samples sintered at 1300 and 1400 °C. Because of the large number of insulating phases produced by the incomplete sintering process, the samples sintered at 1300 °C had lower conductivities. A higher conductivity of 0.125 S.cm− 1 was observed for La0.80Sr0.20Ga0.80Mg0.20O3 (LSGM), which was obtained using the citric acid (sintered at 1400 °C), which is in the range of earlier reported similar studies. The observed variation in the conductivity with respect to different phases of LSGM, the influence of the secondary phase, and the wt% of the constituents of LSGM are discussed.

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快速燃烧法制备LSGM电解液及ReSOC电性能分析。
在这项工作中,我们采用快速燃烧方法制备了La1−xSrxGa1−yMgyO3 (LSGM),并评估了其作为可逆固体氧化物电池(ressoc)电解质材料的电学性能与组成和烧结温度(1200、1300和1400℃,烧结6 h)有关。制备样品时,采用酒石酸(TA)和柠檬酸(CA)两种不同的燃料,以相应的硝酸盐盐为前体,采用快速燃烧法(500℃,10 min)。从x射线衍射图中可以识别出LSGM正交相(空间群Imma)和LSGM立方相(空间群pm - 3m)两个主要相。从文献来看,这两种结构都被报道为高氧离子导电性物质,但通常它们不会一起出现。此外,在某些情况下,观察到低浓度(1.98%)的LaSrGaO4分离(次级)相。在1200°C和1300°C烧结的样品的扫描电镜(SEM)研究表明,晶粒尺寸较小,形貌不规则。在1400°C下烧结的样品,其表面形貌清晰,孔隙率较低。为了进行对比分析,在不同温度下(300-800°C)测量了1300和1400°C烧结样品的电导率(S.cm−1)。由于不完全烧结过程产生了大量的绝缘相,在1300℃下烧结的样品电导率较低。La0.80Sr0.20Ga0.80Mg0.20O3 (LSGM)的电导率较高,为0.125 S.cm−1,使用柠檬酸(在1400°C烧结)获得,这在早期报道的类似研究范围内。讨论了所观察到的电导率随不同相的变化,二次相的影响,以及lssgm成分的wt%。
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来源期刊
Journal of Electroceramics
Journal of Electroceramics 工程技术-材料科学:硅酸盐
CiteScore
2.80
自引率
5.90%
发文量
22
审稿时长
5.7 months
期刊介绍: While ceramics have traditionally been admired for their mechanical, chemical and thermal stability, their unique electrical, optical and magnetic properties have become of increasing importance in many key technologies including communications, energy conversion and storage, electronics and automation. Electroceramics benefit greatly from their versatility in properties including: -insulating to metallic and fast ion conductivity -piezo-, ferro-, and pyro-electricity -electro- and nonlinear optical properties -feromagnetism. When combined with thermal, mechanical, and chemical stability, these properties often render them the materials of choice. The Journal of Electroceramics is dedicated to providing a forum of discussion cutting across issues in electrical, optical, and magnetic ceramics. Driven by the need for miniaturization, cost, and enhanced functionality, the field of electroceramics is growing rapidly in many new directions. The Journal encourages discussions of resultant trends concerning silicon-electroceramic integration, nanotechnology, ceramic-polymer composites, grain boundary and defect engineering, etc.
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