A series samples of La0.6M0.4FeO3-δ (M = Ca, Sr, process (GNP). FTIR, TG-DSC, XRD and TEM techniques Ba) perovskite-type oxides were prepared by glycine nitrate were used to characterize the chemical constitution...A series samples of La0.6M0.4FeO3-δ (M = Ca, Sr, process (GNP). FTIR, TG-DSC, XRD and TEM techniques Ba) perovskite-type oxides were prepared by glycine nitrate were used to characterize the chemical constitution, thermal stability and phase structure. The electrical conductivity of the samples was investigated by four-probe technique. With the increase of substituted-ionic radius, the temperature of phase formation increases, and the solid solubility decreases gradually, respectively. The La0.6Ca0.4FeO3-δ(LCF)powder is pure cubic perovskite-type crystalline after fired at 850℃ for 2 h. The XRD patterns of La0.6Sr0.4FeO3-δ(LSF) powder shows a small quantity of SrO peaks sintered at 1050℃ for 2 h. The electrical conductivity of LCF and LSF at 500 - 800℃ is over 100 S·cm^ - 1, and the value of LCF is 1170 S·cm^ - 1 at 800℃, which indicate that LCF and LSF may be used as a profitable cathode for IT-SOFCs. The characteristic of La0.6 Ba0.4FeO3-δ(LBF) is poor, and the electrical conductivity at intermediate temperatures is 1/20 less than that of LSF.展开更多
Pr0.6-x NdxCa0.4 FeO3-δ ( x = 0.0, 0.2, 0.3, 0.4, 0.5, 0.6) were synthesized using Pechini method. A number of studies were conducted concerning composition, specific area, crystalline structure and microstructure ...Pr0.6-x NdxCa0.4 FeO3-δ ( x = 0.0, 0.2, 0.3, 0.4, 0.5, 0.6) were synthesized using Pechini method. A number of studies were conducted concerning composition, specific area, crystalline structure and microstructure of the samples by means of FT-IR, BET, XRD TG-DTA and SEM. The results show that all the samples with different doping amounts of Pr^3+ and Nd^3+ on A-site are fine dispersed, and mean particle size less than 100 nm. The powders have good sinterability, and the relative density is 95% after sintered at 1200 ℃ for 2 h. It is found that all specimens are entirely single phase solid solutions with orthorhombic perovskite structure, the stable perovskitetype phase is formed completely after calcination at 900 ℃.展开更多
基金Project Supported bythe Natural Science Foundation of Bureau Education Anhui Province (N2004kj326)
文摘A series samples of La0.6M0.4FeO3-δ (M = Ca, Sr, process (GNP). FTIR, TG-DSC, XRD and TEM techniques Ba) perovskite-type oxides were prepared by glycine nitrate were used to characterize the chemical constitution, thermal stability and phase structure. The electrical conductivity of the samples was investigated by four-probe technique. With the increase of substituted-ionic radius, the temperature of phase formation increases, and the solid solubility decreases gradually, respectively. The La0.6Ca0.4FeO3-δ(LCF)powder is pure cubic perovskite-type crystalline after fired at 850℃ for 2 h. The XRD patterns of La0.6Sr0.4FeO3-δ(LSF) powder shows a small quantity of SrO peaks sintered at 1050℃ for 2 h. The electrical conductivity of LCF and LSF at 500 - 800℃ is over 100 S·cm^ - 1, and the value of LCF is 1170 S·cm^ - 1 at 800℃, which indicate that LCF and LSF may be used as a profitable cathode for IT-SOFCs. The characteristic of La0.6 Ba0.4FeO3-δ(LBF) is poor, and the electrical conductivity at intermediate temperatures is 1/20 less than that of LSF.
文摘Pr0.6-x NdxCa0.4 FeO3-δ ( x = 0.0, 0.2, 0.3, 0.4, 0.5, 0.6) were synthesized using Pechini method. A number of studies were conducted concerning composition, specific area, crystalline structure and microstructure of the samples by means of FT-IR, BET, XRD TG-DTA and SEM. The results show that all the samples with different doping amounts of Pr^3+ and Nd^3+ on A-site are fine dispersed, and mean particle size less than 100 nm. The powders have good sinterability, and the relative density is 95% after sintered at 1200 ℃ for 2 h. It is found that all specimens are entirely single phase solid solutions with orthorhombic perovskite structure, the stable perovskitetype phase is formed completely after calcination at 900 ℃.