The precursors of La0.7Sr0.3-xCaxCo0.9Fe0.1O3-δ(LSCCF, x=0.05, 0.10, 0.15, 0.20) as the cathode materials for intermediate temperature solid oxide fuel cell (ITSOFC) were prepared by reverse titration co-precipitatio...The precursors of La0.7Sr0.3-xCaxCo0.9Fe0.1O3-δ(LSCCF, x=0.05, 0.10, 0.15, 0.20) as the cathode materials for intermediate temperature solid oxide fuel cell (ITSOFC) were prepared by reverse titration co-precipitation method with metal-nitrates as starting materials and mixed alkali (NaOH and Na2CO3) as a precipitating agent. The formation process of LSCCF from the precursors was monitored by TG-DSC, and the crystal structure and particles morphology of the precursors which were calcined at 600, 800, 1000 ℃ for 3 h were characterized using XRD, SEM technologies. Compared with the solid state reaction of constituent oxides, when the pH value of the precipitating solution was in the range of 9.1～9.5, the LSCCF powders from the precursors caclined at 800 ℃ for 3 h had high purity, homogeneous and single perovskite phase. The electrical conductivity of the LSCCF samples sintered at 1200 ℃ for 3 h, which was measured as a function of temperatures from 100 to 800 ℃ by DC four-probe method in air, decreased with x from 0.05 to 0.20. The value of electrical conductivity was almost equal because of Ca2+, Sr2+ co-dopant resulting in the 'mix effect' while x=0.10 or 0.15. The electrical conductivity of all doped samples was higher than 100 S·cm-1 at intermediate temperatures from 500 to 800 ℃, and there was good compatibility between the LSCCF cathode and Ce0.8Sm0.2O2 electrolyte.展开更多
Ce-doped Bi2O3 nanopowders were prepared by reverse titration chemical coprecipitation from Bi^3＋and Ce^（4＋）containing aqueous solution.Techniques of X-ray diffraction（XRD）,transmission electron microscopic（TEM...Ce-doped Bi2O3 nanopowders were prepared by reverse titration chemical coprecipitation from Bi^3＋and Ce^（4＋）containing aqueous solution.Techniques of X-ray diffraction（XRD）,transmission electron microscopic（TEM）and Fourier transform infrared spectroscopy（FTIR）were employed to characterize the as-synthesized materials.The XRD patterns indicated that the peaks can be easily indexed toβ-Bi2O3 and no diffraction peaks of Ce or other impurity phases were detected in the prepared samples.The calculated average crystalline size decreased from 31.72 to 11.96 nm when the Ce content increased from 1 wt%to 10 wt%.The morphology changed from flake-like into the spherical-like with increase in Ce content.The electric conductivity of Ce-doped Bi2O3 electrolyte was also investigated by two probe DC method.Conductivity analysis exhibited that the rate of conductivity increased with increasing Ce^2＋ratio,when the Ce concentration was up to 5 wt%,the as-synthesized Ce-doped Bi2O3 electrolyte showed the maximum value of conductivity（0.295 S？cm^（–1））.展开更多
基金the National High-Tech Development Plan (2006AA05Z417)the Natural Science Foundation of Lia-oning Province (20062145)the Education department of Liaoning Province (05L073)
文摘The precursors of La0.7Sr0.3-xCaxCo0.9Fe0.1O3-δ(LSCCF, x=0.05, 0.10, 0.15, 0.20) as the cathode materials for intermediate temperature solid oxide fuel cell (ITSOFC) were prepared by reverse titration co-precipitation method with metal-nitrates as starting materials and mixed alkali (NaOH and Na2CO3) as a precipitating agent. The formation process of LSCCF from the precursors was monitored by TG-DSC, and the crystal structure and particles morphology of the precursors which were calcined at 600, 800, 1000 ℃ for 3 h were characterized using XRD, SEM technologies. Compared with the solid state reaction of constituent oxides, when the pH value of the precipitating solution was in the range of 9.1～9.5, the LSCCF powders from the precursors caclined at 800 ℃ for 3 h had high purity, homogeneous and single perovskite phase. The electrical conductivity of the LSCCF samples sintered at 1200 ℃ for 3 h, which was measured as a function of temperatures from 100 to 800 ℃ by DC four-probe method in air, decreased with x from 0.05 to 0.20. The value of electrical conductivity was almost equal because of Ca2+, Sr2+ co-dopant resulting in the 'mix effect' while x=0.10 or 0.15. The electrical conductivity of all doped samples was higher than 100 S·cm-1 at intermediate temperatures from 500 to 800 ℃, and there was good compatibility between the LSCCF cathode and Ce0.8Sm0.2O2 electrolyte.
基金Funded by Changzhou Science and Technology Innovation Project(Nos.CC20140048,CC20130204)National Natural Science Foundation of China(No.51273027)2015 Research and Innovation Project for College Graduates of Jiangsu Province
文摘Ce-doped Bi2O3 nanopowders were prepared by reverse titration chemical coprecipitation from Bi^3＋and Ce^（4＋）containing aqueous solution.Techniques of X-ray diffraction（XRD）,transmission electron microscopic（TEM）and Fourier transform infrared spectroscopy（FTIR）were employed to characterize the as-synthesized materials.The XRD patterns indicated that the peaks can be easily indexed toβ-Bi2O3 and no diffraction peaks of Ce or other impurity phases were detected in the prepared samples.The calculated average crystalline size decreased from 31.72 to 11.96 nm when the Ce content increased from 1 wt%to 10 wt%.The morphology changed from flake-like into the spherical-like with increase in Ce content.The electric conductivity of Ce-doped Bi2O3 electrolyte was also investigated by two probe DC method.Conductivity analysis exhibited that the rate of conductivity increased with increasing Ce^2＋ratio,when the Ce concentration was up to 5 wt%,the as-synthesized Ce-doped Bi2O3 electrolyte showed the maximum value of conductivity（0.295 S？cm^（–1））.
