Papers by Keyword: Mixed Conductivity

Abstract: La₂NiO_4+σ nanofibers exhibiting typical Ruddlesden–Popper structure (K₂NiO₄) were fabricated by a facile electrospinning method. X-ray diffraction, scanning electron microscopy and transmission electron microscopy were used to analyze the structure, morphology and crystal process of the La₂NiO_4+σ nanofibers. For electrical properties measurement, uniaxially aligned nanofibers were directly collected and assembled into electrode. In our research, La₂NiO_4+σ phase forms above 873K with no impurity phase emerges during the thermal treatments. The nanofibers are smooth and uniform throughout the entire length and the grain is growing as calcination temperature increases. Furthmore, the La₂NiO_4+σ nanofibers own high mixed conductivity at 773K, laying good foundation for intermediate temperature solid oxide fuel cells application.

Abstract: To develop novel cathode materials with high electrical performances for intermediate temperature solid oxide fuel cells (IT-SOFCs) and optimize the preparation process, perovskite-type oxides Pr_1-x-ySr_xCa_yCo_1-zFe_zO_3-δ (x=0.1, 0.2; y=0.1, 0.2; z=0.2, 0.3, 0.4; denoted as PSCCF-81182, PSCCF-72173 and PSCCF-62264) were prepared by solid state reaction. The formation process, phase structure and microstructure of the prepared samples were measured using TG-DTA, FT/IR, XRD and SEM techniques. The mixed conductivity of the samples was measured using DC four-terminal method in the range of 150-950 °C. Chemical state of the elements was measured by XPS experiments. The results show that the prepared samples PSCCF-81182, PSCCF-72173 and PSCCF-62264 exhibit a single phase with cubic perovskite structure after sintered at 1200 °C for 6 h. The mixed conductivity of the samples increases with temperature up to a maximum value, and then decreases. At lower temperature, the conductivity follows small polaron hopping mechanism. The negative temperature dependence occurring at higher temperature is due to the creation of oxygen vacancies for charge balance. At intermediate temperature (600-800 °C), the mixed conductivity values of the prepared samples are all much higher than 100 S•cm^-1，and can meet the demand of cathode materials for IT-SOFC. XPS tests show that Co and Fe elements in PSCCF-72173 are all of + 3 and + 4 valence. Absorbed oxygen can also be found from the XPS patterns, which is related to the concentration of oxygen vacancies in the perovskite-type oxides.

Abstract: Perovskite-type cathode materials La_0.6Sr_0.2Ca_0.2Co_1-yFe_yO_3-δ (0.2≤y≤0.5, marked as LSCCF62282, LSCCF62273, LSCCF62264 and LSCCF62255) for intermediate-temperature solid oxide fuel cells (IT-SOFCs) were prepared by solid state reaction. The establishment process and phase transformation were measured by TG-DTA, FT/IR and XRD techniques. Single hexagonal perovskite phase can be achieved after sintered at 1100 °C for 3 h. Mixed conductivity, thermal expansion behavior and chemical stability of sintered samples at 1100 °C for 3 h have been investigated. At intermediate temperature (600-800 °C), the mixed conductivity characterized by DC four-probe technique is higher than 100 S/cm. LSCCF62282 has the highest conductivity of 297.3 S/cm at 700 °C among the four samples. At lower temperatures, the conductivity follows small polaron hopping mechanism. Thermal expansion coefficients (TECs) of the samples from 50 °C to 850 °C exhibit a reducing tendency with increasing amount of doped Fe³⁺. Thermal expansion behavior can be improved by doping with Ca²⁺ and Fe³⁺ commonly. XRD pattern for LSCCF62282 and YSZ mixture sintered at 800 °C for 6h indicates that cathode material LSCCF62282 is chemically stable against YSZ electrolyte at operating temperature.

Abstract: The Y2O3-ZrO2 binary system ceramic is considered to be most developed in application to the ZrO2-based materials. A cubic fluorite structure is generally achieved, as the metal ion of the additive (Y) takes place of the Zr4+ and oxygen ion vacancies are produced in the lattice to maintain the charge balance. This leads to almost totally ionic conductivity. The introduction of changeable valued CeO2 can further improve the total electronic conductivity through the defect equilibrium reaction between tetravalent Ce4+ and trivalent Ce3+ at high temperature and reducing atmosphere. In this study, solid phase synthesis method was employed for the preparation of (YO1.5)x-(CeO2)0.08-(ZrO2)0.9-x and (YO1.5)0.05-(CeO2)y- (ZrO2)0.95-y ceramics, while four probe DC conductivity measurement method was also applied under the temperature between 300 to 800°C. The results prove that the concentration of Y3+ is the main contribution of the electrical conductivity at low temperature.

Abstract: Oxygen transport properties of perovskite-type SrCe1-xYxO3-δ (x = 0.05–0.10), exhibiting protonic transport in hydrogen-containing reducing atmospheres and mixed oxygen-ionic and ptype electronic conductivity at oxygen partial pressures close to atmospheric, were studied at 973– 1223 K under oxidizing conditions. The oxygen transference numbers of SrCe(Y)O3-δ in air vary in the range 0.37–0.80, decreasing when temperature increases. The oxygen permeability is significantly affected by the hole conduction, which influences both bulk ambipolar conductivity and surface exchange kinetics. The average thermal expansion coefficients of SrCe1-xYxO3-δ ceramics, calculated from dilatometric data in air, are (11.1–11.3)×10-6 K-1 at 373–1373 K.