Single-phase perovskite La0.6Sr0.4Co0.8Fe0.2O3-δ has been successfully prepared by using citrate-EDTA complexation method at relatively low calcination temperature. The structure and thermal decomposition process of ...Single-phase perovskite La0.6Sr0.4Co0.8Fe0.2O3-δ has been successfully prepared by using citrate-EDTA complexation method at relatively low calcination temperature. The structure and thermal decomposition process of the complex precursor have been investigated by means of differential scanning calorimetry-thermal gravimetric analysis （DSC/TGA）, X-ray diffraction （XRD）, and Fourier transform infrared spectroscopic （FT-IR） measurements. The precursor decomposed completely and started to form perovskite-type oxide above 420 ℃ according to the differential scanning calorimetry （DSC） and thermal gravimetric analysis （TGA） results. Single-phase perovskite La0.6Sr0.4Co0.8Fe0.2O3-δ obtained has been confirmed from the XRD pattern, and no peak of SrCO3 was found by XRD of the oxides synthesized at a relatively low temperature of 800℃. The reducibility of La0.6Sr0.4Co0.8Fe0.2O3-δ was also characterized by the temperature programmed reduction （TPR） technique. Disk shaped dense La0.6Sr0.4Co0.8Fe0.2O3-δ membrane was prepared by the isostatical pressing method. The oxygen flux rate of dense La0.6Sr0.4Co0.8Fe0.2O3-δ membrane was （2.8-18）× 10^-8 mol/（cm^2.s） in the temperature range of 800-1000 ℃.展开更多
文章采用柠檬酸络合法制备了La_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O_(3-δ)钙钛矿,采用低温N_2物理吸附、X-射线衍射(X-ray diffraction,XRD)、氢气程序升温还原(hydrogen temperature programmed reduction,H_2-TPR)、氧气程序升温脱附(ox...文章采用柠檬酸络合法制备了La_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O_(3-δ)钙钛矿,采用低温N_2物理吸附、X-射线衍射(X-ray diffraction,XRD)、氢气程序升温还原(hydrogen temperature programmed reduction,H_2-TPR)、氧气程序升温脱附(oxygen temperature programmed desorption,O_2-TPD)和X-射线光电子能谱(X-ray photoelectron spectroscopy,XPS)表征了其物理化学性质,并考察了甲烷催化燃烧活性。结果表明,当柠檬酸/金属离子摩尔比(citric acid to metal ions molar ratio,CMMR)为1.25时,所制得的催化剂催化活性最佳。XRD表征结果表明,CMMR为1.25或1.50时,形成的钙钛矿晶型更完整。H_2-TPR表征结果表明,CMMR为1.25时,催化剂中的Fe^(4+)和Co^(3+)的还原温度较低,还原性能好。XPS表征结果表明,CMMR为1.25时,催化剂表面上吸附氧晶格氧之比最大。O_2-TPD表征结果表明,随着CMMR增加,催化剂中可移动晶格氧量减小,脱附温度增加,非化学计量比显著减小。CMMR为1.25时,催化剂表面吸附氧较易活化,形成活性物种。展开更多
NiO-La0.3Ce0.7O2-δ(LDC30) novel anode was investigated for IT-SOFCs(Intermediate Temperature-Solid Oxide Fuel Cells) with LaGaO3-based electrolyte. The results showed that LDC30 has a suitable chemical compatibility ...NiO-La0.3Ce0.7O2-δ(LDC30) novel anode was investigated for IT-SOFCs(Intermediate Temperature-Solid Oxide Fuel Cells) with LaGaO3-based electrolyte. The results showed that LDC30 has a suitable chemical compatibility with NiO and NiO-LDC30 has a good thermal expansion matching with LDC30 interlayer and LSGM(La0.8Sr0.2Ga0.8Mg0.2O3-δ) electrolyte, so NiO-LDC30/LDC30 was considered as a feasible and novel anode system. It was also shown that NiO content plays a key role on polarization performance and morphology of the anode. When the content of NiO was 60%(mass fraction), the polarization loss of anode was the lowest. Next we will optimize the porosity and sintering procedure to modify the microstructure and performance of the anode.展开更多
Mixed ionic-electronic conductors in the family of LaxSr1-xCoyFe1-y O3-δ have been widely studied as cathode materials for solid oxide fuel cells （SOFCs）. However, the long-term stability was a concern. Here we rep...Mixed ionic-electronic conductors in the family of LaxSr1-xCoyFe1-y O3-δ have been widely studied as cathode materials for solid oxide fuel cells （SOFCs）. However, the long-term stability was a concern. Here we report our findings on the effect of a thin film coating of La0.85Sr0.15MnO3-δ （LSM） on the performance of a porous La0.6Sr0.4Co0.2Feo.8O3-δ（LSCF） cathode. When the thicknesses of the LSM coatings are appropriate, an LSM-coated LSCF electrode showed better stability and lower polarization （or higher activity） than the blank LSCF cathode without LSM infiltration. An anode-supported cell with an LSM-infiltrated LSCF cathode demonstrated at 825 ℃ a peak power density of -1.07 W/cm2, about 24% higher than that of the same cell without LSM infiltration （-0.86 W/cm2）. Further, the LSM coating enhanced the stability of the electrode; there was little degradation in performance for the cell with an LSM-infiltrated LSCF cathode during 100 h operation.展开更多
Effects of SO2 in ambient air on the performance and durability of solid oxide fuel cell（SOFC） cathode were evaluated by galvanostatic measurement. Comparison between two cathode materials was made to consider the c...Effects of SO2 in ambient air on the performance and durability of solid oxide fuel cell（SOFC） cathode were evaluated by galvanostatic measurement. Comparison between two cathode materials was made to consider the cathode degradation mechanisms. The degradation performance is associated with a slow decomposition of the La0.6Sr0.4Co0.2Fe0.8O3（LSCF） due to the segregation of strontium oxide. Negligible deterioration for （La0.7Sr0.3）MnO3 （LSM） cathode was caused by SO2 poisoning under a current density of 200 mA/cm2. Metal sulphate formation may explain a slight deterioration under increasing high the concentration of SO2. It was verified that the poisoning mechanism for the two cathode materials resulted from the gradual decomposition of the cathode materials.展开更多
基金Sponsored by SRF for ROCS, key lab of enhanced heat transfer and energy conservation (MOE)Guangdong provincial natural science foundation (04020126).
文摘Single-phase perovskite La0.6Sr0.4Co0.8Fe0.2O3-δ has been successfully prepared by using citrate-EDTA complexation method at relatively low calcination temperature. The structure and thermal decomposition process of the complex precursor have been investigated by means of differential scanning calorimetry-thermal gravimetric analysis （DSC/TGA）, X-ray diffraction （XRD）, and Fourier transform infrared spectroscopic （FT-IR） measurements. The precursor decomposed completely and started to form perovskite-type oxide above 420 ℃ according to the differential scanning calorimetry （DSC） and thermal gravimetric analysis （TGA） results. Single-phase perovskite La0.6Sr0.4Co0.8Fe0.2O3-δ obtained has been confirmed from the XRD pattern, and no peak of SrCO3 was found by XRD of the oxides synthesized at a relatively low temperature of 800℃. The reducibility of La0.6Sr0.4Co0.8Fe0.2O3-δ was also characterized by the temperature programmed reduction （TPR） technique. Disk shaped dense La0.6Sr0.4Co0.8Fe0.2O3-δ membrane was prepared by the isostatical pressing method. The oxygen flux rate of dense La0.6Sr0.4Co0.8Fe0.2O3-δ membrane was （2.8-18）× 10^-8 mol/（cm^2.s） in the temperature range of 800-1000 ℃.
文摘文章采用柠檬酸络合法制备了La_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O_(3-δ)钙钛矿,采用低温N_2物理吸附、X-射线衍射(X-ray diffraction,XRD)、氢气程序升温还原(hydrogen temperature programmed reduction,H_2-TPR)、氧气程序升温脱附(oxygen temperature programmed desorption,O_2-TPD)和X-射线光电子能谱(X-ray photoelectron spectroscopy,XPS)表征了其物理化学性质,并考察了甲烷催化燃烧活性。结果表明,当柠檬酸/金属离子摩尔比(citric acid to metal ions molar ratio,CMMR)为1.25时,所制得的催化剂催化活性最佳。XRD表征结果表明,CMMR为1.25或1.50时,形成的钙钛矿晶型更完整。H_2-TPR表征结果表明,CMMR为1.25时,催化剂中的Fe^(4+)和Co^(3+)的还原温度较低,还原性能好。XPS表征结果表明,CMMR为1.25时,催化剂表面上吸附氧晶格氧之比最大。O_2-TPD表征结果表明,随着CMMR增加,催化剂中可移动晶格氧量减小,脱附温度增加,非化学计量比显著减小。CMMR为1.25时,催化剂表面吸附氧较易活化,形成活性物种。
文摘NiO-La0.3Ce0.7O2-δ(LDC30) novel anode was investigated for IT-SOFCs(Intermediate Temperature-Solid Oxide Fuel Cells) with LaGaO3-based electrolyte. The results showed that LDC30 has a suitable chemical compatibility with NiO and NiO-LDC30 has a good thermal expansion matching with LDC30 interlayer and LSGM(La0.8Sr0.2Ga0.8Mg0.2O3-δ) electrolyte, so NiO-LDC30/LDC30 was considered as a feasible and novel anode system. It was also shown that NiO content plays a key role on polarization performance and morphology of the anode. When the content of NiO was 60%(mass fraction), the polarization loss of anode was the lowest. Next we will optimize the porosity and sintering procedure to modify the microstructure and performance of the anode.
基金supported by the Department of Energy (National Energy Technology Laboratory) SECA Core Technology Program under Award Number DE-NT0006557 and DE-FE0009652by NSFC under grant No.51002182
文摘Mixed ionic-electronic conductors in the family of LaxSr1-xCoyFe1-y O3-δ have been widely studied as cathode materials for solid oxide fuel cells （SOFCs）. However, the long-term stability was a concern. Here we report our findings on the effect of a thin film coating of La0.85Sr0.15MnO3-δ （LSM） on the performance of a porous La0.6Sr0.4Co0.2Feo.8O3-δ（LSCF） cathode. When the thicknesses of the LSM coatings are appropriate, an LSM-coated LSCF electrode showed better stability and lower polarization （or higher activity） than the blank LSCF cathode without LSM infiltration. An anode-supported cell with an LSM-infiltrated LSCF cathode demonstrated at 825 ℃ a peak power density of -1.07 W/cm2, about 24% higher than that of the same cell without LSM infiltration （-0.86 W/cm2）. Further, the LSM coating enhanced the stability of the electrode; there was little degradation in performance for the cell with an LSM-infiltrated LSCF cathode during 100 h operation.
基金Supported by the National Natural Science Foundation of China(No.50872041)the Research Funds of Industrial Technology Research and Development Projects of Jilin Province, China(No.JF2012C024)+1 种基金the Natural Science Foundation of Jilin Province,China(No.201215109)the Science and Technology Research Projects of Education Department of Jilin Province, China(No.2011205)
文摘Effects of SO2 in ambient air on the performance and durability of solid oxide fuel cell（SOFC） cathode were evaluated by galvanostatic measurement. Comparison between two cathode materials was made to consider the cathode degradation mechanisms. The degradation performance is associated with a slow decomposition of the La0.6Sr0.4Co0.2Fe0.8O3（LSCF） due to the segregation of strontium oxide. Negligible deterioration for （La0.7Sr0.3）MnO3 （LSM） cathode was caused by SO2 poisoning under a current density of 200 mA/cm2. Metal sulphate formation may explain a slight deterioration under increasing high the concentration of SO2. It was verified that the poisoning mechanism for the two cathode materials resulted from the gradual decomposition of the cathode materials.
