Tb-Er共掺Bi2O3固体电解质体系的合成与表征

BALCI, Murat
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引用次数: 0

摘要

在本研究中,采用固相反应制备Er-Tb共掺杂Bi2O3固体电解质体系。四点尖端技术(FPPT)、热重和差热分析(TG);采用差热分析(DTA)和x射线衍射(XRD)对生成的样品的结构、热性能和电导率进行表征。XRD数据表明,样品05Er05TbSB、05Er10TbSB和15Er05TbSB在室温下具有立方δ相稳定。由于掺杂离子比主体Bi3+阳离子要小,这些样品的晶格常数估计低于纯立方相的晶格常数。在研究温度范围内,样品被认为是热稳定的,因为热曲线没有显示吸热或放热峰的发展,表明潜在的相变。根据阿伦尼乌斯方程,随温度变化的电导率曲线呈现线性变化。电导率测量清楚地表明,掺杂率的增加导致电导率的突然下降。计算得到的活化能随掺杂比的增加而增加,从0.64 eV到1.12 eV不等。在700℃时,测定样品05Er05TbSB的电导率为0.128 S.cm-1,电导率最高,活化能最低。随着掺杂比的增加,电导率降低,活化能增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis and Characterization of Tb–Er Co–Doped Bi2O3 Solid Electrolyte Systems
In this study, solid state reactions were used to create Er–Tb co–doped Bi2O3 solid electrolyte systems. Four Point Tip Technique (FPPT), Thermo–gravimetric and Differential Thermal Analysis (TG & DTA), and X–Ray Diffraction (XRD) were used to characterize the generated samples' structural and thermal properties, and electrical conductivity. The samples 05Er05TbSB, 05Er10TbSB, and 15Er05TbSB stabilized with cubic δ–phase at room temperature, according to XRD data. Due to the smaller dopants ions compared to the host Bi3+ cation, the lattice constants estimated for these samples were lower than those of the pure cubic phase. The samples were thought to be thermally stable in the studied temperature range since the thermal curves did not show endothermic or exothermic peak development indicating a potential phase change. According to the Arrhenius equation, the temperature–dependent conductivity graphs displayed a linear change. The conductivity measurements clearly indicated that an increase in doping rate results in a sudden drop in electrical conductivity. The calculated activation energies increased with the doping ratio and varied from 0.64 eV to 1.12 eV. At 700 °C, it was determined to be 0.128 S.cm–1 for the sample 05Er05TbSB, which had the greatest conductivity and lowest activation energy among all samples. The conductivity was discovered to decrease and activation energy to increase when the doping ratio was gradually raised.
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