Solid state reaction synthesis and total electrical conductivity of La_(0.7)Sr_(0.3)Cr_yMn_zCo_(1-y-z)O_(3-δ)

The La0.7Sr0.3CryMnzCo(1-y-z)O3-δ samples were prepared by solid state reaction.The phases,microstructure and properties of the samples were investigated by XRD,SEM,DC four-probe method and iodometry method.The single orthorhombic phase La0.7Sr0.3CryMnzCo(1-y-z)O3-δ perovskite oxides were obtained when sintered at l350 °C for 10 h.The oxygen nonstoichiometry of the materials varied inversely with the total electronic conductivity.The sample with composition of La0.7Sr0.3Cr0.5Mn0.35 Co0.15O3-δ had the maximal total electronic conductivity and the lowest oxygen nonstoichiometry which were 22.4 S/cm and 0.040 at 850 °C,respectively.The low total electronic conductivity is related to the low relatively density of the samples directly.The activation energy of conduction changed at 550 °C,and the activation energy of conduction at high temperature(T550 °C) was higher than that at low temperature range(T550 °C).     

Effect of Calcination Temperature on Structure and O2 Desorption Properties of CexPr1-xO2-δ Mixed Oxides

A series of CexPr1-xO2-δ (x=0,0.5,0.9,1.0) mixed oxide calcined at different temperatures were synthesized by sol-gel method and characterized by Raman, XRD and O2-TPD techniques. When x=0.9, only a cubic phase CeO2 is observed. When x=0.5, the compound was combined by Pr6O11 and CeO2 mixed oxides. For CexPr1-xO2-δ (x=0.5,0.9) samples 465cm-1 Raman peak is attributed to the Raman active F2g mode of Ceo2. The broad peak at about 570cm-1 can be linked to lattice defects resulting in oxygen vacancies. The crystallite size of the samples increased as increasing the calcined temperature. But the increased value of Ce0.9Pr0.1O2-δ and Ce0.5Pr0.5O2-δ is smaller than single CeO2 and Pr6O11 obviously. It reveals that the insertion of Pr atom into the ceria lattice could enhance the sintering resistance and thermal stability of the mixed oxides. Calcination temperatures had great effect on the peak intensity for CeO2 but less effect on Ce0.8Pr0.2O2-δ in Raman spectra, and it may be caused by the colors transformation of the mixed oxidfs. The result of O2-TPD experiment indicates that the formation of solid solution has elevation the stabilization and thermal stability of the mixed oxides.     

Electrical Properties and Microwave Synthesis of Mixed Rare Earth Oxide Ln0.7Sr0.3-xCaxCo0.9Fe0.1O3-δ

In order to lower the raw materials cost and develop a novel cathode materials for intermediate temperature solid oxide fuel cell(ITSOFC), using mixed rare earth replacing the expensive pure La2O3 as the raw materials, the powders of Ln0.7Sr0.3-xCaxCo0.9Fe0.1O3-δ (Ln=the mixed rare earth, x=0.05, 0.10, 0.15) for the applications as the cathode materials were prepared by microwave sintering process. The crystal structure and the particles morphology of the obtained powders were characterized by XRD and SEM, the electrical conductivity of all samples sintered at 1200 ℃ for 3 h was also measured as the function of the temperature from 100 to 800 ℃ by DC four-probe method in air. The experimental results show that due to the influence of mixed rare earth the powders of Ln0.7Sr0.3-xCaxCo0.9Fe0.1O3-δ synthesized at 1200 ℃ for 0.5 h with the mean particle size of 1～20 μm was of perovskite and cubic fluorite phase as well a little SrO phase, the electrical conductivity of the samples decreases with the adding Ca2+ content, and are all higher than 100 S·cm-1 from 500 to 700 ℃ when x≤0.10. Ln0.7Sr0.3-xCaxCo0.9Fe0.1O3-δ. Can meet the demand of the electrical properties for the cathode materials in ITSOFC.     

Influence of Different Subsistence States of CeO2-ZrO2 Mixed Oxides in Catalyst Coating on Catalytic Properties

The metallic substrate-catalysts with different subsistence states of CeO2-ZrO2 mixed oxides were prepared and the catalytic properties were investigated. The studies on CeO2-ZrO2-V2O5-CuO mixed oxides which were prepared by coprecipitation, show that the doping of V5 and Cu2 in CeO2-ZrO2 mixed oxides can enhance the catalytic activity and thermal stability of coating materials. Moreover, different additives were doped in slurries of γ-Al2O3 to investigate the influence of additives on oxidation activity of catalysts. The mixture of ceria-zirconia, alkali metals and other rare earths acting as additives exhibits promotion effect on oxidation activity by optimizing the distribution of oxygen on the surface and in the bulk of ceria species. This mentioned mixture was mixed with γ-Al2O3 and a newly proposed active component to prepare a new catalyst. Afterward, the influence of thermal treatment on the new catalyst were investigated by calcinations at 500, 650, 750, 800, 850 and 900 ℃ for 2 h. The light-off curves of CO and HC show that after being treated at 650～750 ℃, catalysts present the best activity. XRD patterns show that ceria and zirconia species in the newly proposed active component form a phase of extra CeO2-ZrO2 mixed oxides on the surface of catalysts after the thermal treatment at 750 ℃, which has practical value for improving the preparation process and promoting the catalytic properties. Moreover, XPS results imply the existence of Ce1-xPdxO2-σ and Ce1-xPtxO2-σ on the surface of these treated samples, which may show influence on the catalytic activities.     

Phase Constitution in Mixed Gd_2O_3 and B_4C by Sintering at High Temperature

The phase constitution in mixed Gd2O3 and B4C by sintering in graphite tube furnace at the temperature of 100～1489 ℃ in argon atmosphere was studied by means of XRD and TG-DTA. The results show that the impurity C reacts with O in the B4C at the temperature of 367～458 ℃. When the temperature is 800 ℃, Gd2O3 reacts with B4C, and the reaction products include GdB6, GdB4, GdBO3, GdBC and B. GdBC changes into GdB4 at 1200 ℃. When the temperature is 1470 ℃, GdB6 is obtained by the reaction of GdB4 with elemental B. The content of GdB6 is increasing with the prolonging time.     

Effect of Hot Pressing on Microstructure and Mechanical Properties of Bulk Nanocrystalline Fe3Al Materials Containing Manganese Element

 Bulk nanocrystalline Fe3Al materials containing manganese of 10% were prepared by aluminothermic reaction. Hot pressing of those materials was performed at different temperatures and times. The microstructures of the alloy were investigated by optical microscope (OM) and electron probe microanalyzer (EPMA). The grain sizes of the materials were analyzed by X-ray diffraction (XRD) and transmission electron microscope (TEM). The results showed that the grain sizes of the materials increase after hot pressing. The grain sizes of the materials decrease with increasing the hot pressing times at the same temperature and the grain sizes of the materials increase with increasing hot pressing temperatures at identical times. The hardness and compressibility of the materials were also tested. The results showed that the hardness decreases with increasing hot pressing times at 800 ℃ and hardness increases with increasing the hot pressing temperatures. The variation of hardness with grain size of the nanocrystalline Fe3Al materials after hot pressing is contrary to the Hall-Petch relation. The materials are not broken during hot pressing and exhibit good plasticity and compressibility.     

Preparation and Physicochemical Characterization of La1-xCexCoO3+δ Perovskite Catalyst and Its Methane Catalytic Combustion

Perovskite oxide LaCoO3 methane catalytic material was synthesized with citric acid complexation and bubbling method.The effect of doped cerium was studied on the series of La1-xCexCoO3 δ materials by means of BET,XRD and SEM techniques.Their catalytic behaviors were studied with methane catalytic complete combustion as probe reaction.The results show that doped cerium has great effect on crystal phase formation.When doped cerium is less than 0.3 (molar ratio),the crystal phase of oxide has little changed.When doped cerium is up to 0.5,Co3O4 phase is obviously discovered and the perfectibility of LaCoO3 perovskite crystal phase is deteriorated.When x is over 0.7,perovskite crystal phase is weakened or completely disappeared.Considering the crystal phase of oxides,the optimum doped cerium is about 0.3.The perovskite oxides can be formed at a low calcinations temperature of 700 ℃.When x is 0.3,the highest catalytic activity of T10% (390 ℃) and T90% (603 ℃) is obtained on the series of La1-xCexCoO3 δ materials calcined at 800 ℃.     

Microwave strengthens decomposition of mixed rare earth concentrate: Microwave absorption characteristics

The potential application of microwave heating technology for processing the mixed rare earth concentrate was systematically investigated by analyzing the microwave absorption characteristics in this study. The complex permittivity was measured through resonant cavity perturbation method. The variations of permittivity, the loss factor, loss tangent and the penetration depth with the increasing temperature were investigated numerically. The results indicate that the permittivity increases as the temperature increases, and temperature has a pivotal effect on it. The mixed concentrate is high loss material at the temperature range from 600 to 800℃ according to theoretical analyses of loss tangent and penetration depth. The results of phase transition analysis prove that the variation of microwave absorption characteristics of mixed concentrate is caused by the changes of crystal and lattice structures.The reflectivity, loss factor and penetration depth of the mixed concentrate were also calculated, and the results indicate that processing the mixed concentrate by microwave heating is of high feasibility and industrial potential.     

Preparation and Characterization of Gd3Sc2Ga3O12 Polycrystalline Material by Co-Precipitation Method

Gd3Sc2Ga3O12 polycrystalline material for single crystal growth was prepared with Ga, Gd2O3 and Sc2O3 as starting materials and aqueous ammonia as the precipitator by co-precipitation method. The precursors sintered at various temperatures were characterized by infrared spectra （IR）, X-ray diffractometry （XRD） and transmitted electron microscopy （TEM）. The results showed that pure GSGG phase could be obtained at 900 ℃. The sintered powders were well-dispersed and less-aggregated in the sintered temperature range of 900 - 1000 ℃. XRD and TEM show that the polycrystalline particle sizes of the polycrystalline powders were about 20 - 50 nm. Compared with the method that Ga2O3, Gd2O3 and Sc2O3 were mixed directly and sintered to get polycrystalline materials, the synthesized temperature was lower and sintered time was shorter. Thus co-precipitation was a good method to synthesize GSGG polycrystalline material.     

Synthesis and characterization of calcium and manganese-doped rare earth oxide La_(1-x)Ca_xFe_(0.9)Mn_(0.1)O_(3-δ) for cathode material in IT-SOFC

In order to develop novel cathode materials with high performance for intermediate temperature SOFC(IT-SOFC),Ca and Mn doped rare earth oxides La1-xCaxFe0.9Mn0.1O3-δ(x=0.1,0.3 and 0.5,denoted as LCFM9191,LCFM7391 and LCFM5591) were synthesized by solid state reaction(SSR) method.The formation process,phase structure and microstructure of the synthesized samples were characterized using thermogravimetry/differential scanning calorimetry(TG/DSC),X-ray diffraction(XRD) and scanning electron microscopy(SEM).The thermal expansion coefficients(TEC) of the samples were analyzed at 100-900 oC by thermal dilatometry.The electrical conductivities of the samples were measured with direct current(DC) four-terminal method from 300 to 850 oC.The results indicated that the samples(x=0.1 and 0.3) exhibited a single phase with orthorhombic and cubic perovskite structure,respectively after being sintered at 1200 oC for 3 h.The electrical conductivity of the samples increased with temperature up to a maximum value,and then decreased.The small polaron hopping was regarded as the conducting mechanism for synthesized samples at T≤600 oC.The negative temperature dependence occurring at higher temperature was due to the creation of oxygen vacancies for charge balance.LCFM7391 had higher mixed conductivity(>100 S/cm) at intermediate temperature and could meet the demand of cathode material for IT-SOFC.In addition,the average TECs of LCFM9191 and LCFM7391 were 11.9×10-6 and 13.1×10-6 K-1,respectively,which had good thermal match to the common electrolytes.     

Preparation and Characterization of Component Materials for Intermediate Temperature Solid Oxide Fuel Cell by Glycine-Nitrate Process

La1-xSrxGa1-yMgyO3-δ (LSGM) electrolyte, La1-xSrxCr1-yMnyO3-δ (LSCM) anode and La1-xSrxFe1-yMnyO3-δ (LSFM) cathode materials were all synthesized by glycine-nitrate process (GNP). The microstructure and characteristics of LSGM, LSCM and LSFM were tested via X-ray diffraction(XRD), scanning electron microcopy (SEM), A C impedance and four-probe direct current techniques. XRD shows that pure perovskite phase LSGM electrolyte and electrode (LSCM anode and LSFM cathode) materials were prepared after being sintered at 1400 ℃ for 20 h and at 1000 ℃ for 5 h, respectively. The max conductivities of LSGM (ionic conductivity), LSCM (total conductivity) and LSFM (total conductivity) materials are 0.02, 10, 16 S·cm-1 in the air below 850 ℃, respectively. The conductivity of LSCM becomes smaller when the atmosphere changes from air to pure hydrogen at the same temperature and it decreases with the temperature like metal. The porous and LSGM-based LSCM anode and LSFM cathode films were prepared by screen printing method, and the sintering temperatures for them were 1300 and 1250 ℃, respectively. LSGM and electrode (LSCM and LSFM) materials have good thermal and chemical compatibility.     

Preparation and characterization of La0.9Sr0.1Ga0.8Mg0.2O3–δ thin film deposited by radio frequency magnetic sputtering

La0.9Sr0.1Ga0.8Mg0.2O3-δ (LSGM) electrolyte materials were synthesized by the solid state reaction method.The conductivity of LSGM materials was detected by four probe method,and it was 0.08 S/cm at 850 ℃.Dense and uniform films of LSGM materials were deposited by the magnetic sputtering on substrates of Si and La0.7Sr0.3Cr0.5Mn0.5O3-δ (LSCM).The experimental results showed that the deposition rates dropped and the average grain sizes of the films enlarged with increase in the substrate temperatures.In the sputtering process,the LSGM film was deposited with preferred growth direction.After annealing,the preferred growth direction disappeared and the film surface became smoother and denser.Through observing the deposition process,deposition mechanism was proposed,which was consistent with a model of island growth.     

Characterization and Stability of La0.5Sr0.5CoO2.91 Perovskite-Type Oxide

Compositely doped oxide La0.5Sr0.5CoO2.91 （LSC） was synthesized using solid state reaction and citric acid-nitrate low temperature self-propagating combustion methods. The crystal structure and the particle size micrograph of LSC powders synthesized by different methods were investigated with XRD and SEM. The experimental results show that the single perovskite phase of LSC can be synthesized by solid state reaction method, but LaSrCoO4 phase appears in LSC powder synthesized by citric acid-nitrate low temperature self-propagating combustion method. The LSC particle by citric acid-nitrate low temperature self- propagating combustion method has smaller size. To analyze the character of cathode material based on Ceo.gGdo.101.95（GDC） electrolyte, two types of cathode wafers were fabricated with the two kinds of LSC and GDC powders at the mass rate of 6：4, respectively. The electrical conductivity of the sintered samples was measured by four probe DC method from 300 to 800 ℃. The cathode with LSC particle by citric acid- nitrate low temperature self-propagating combustion method has higher electrical conductivity. In order to investigate the stability, the two samples were put into the muffle furnace to heat up in air at 800℃for 800 h. To analysis the reason for reduced electrical conductivity, the crystal structure and the particle micrograph of the cathode wafers before and after an exposure were investigated with XRD and SEM. The result shows that new crystal structure appears in both the two kinds of cathode wafers and crystal micrographs change a lot.     

Preparation and Fluorescence Properties of TiO2 ：Eu Nano-Materials

A series of europium-doped titanium dioxide (TiO2) fluorescent nano-materials prepared by sol-gel method is presented. The phase structure and crystalline sizes of TiO2:Eu, which is doped with different europium content and then heat-treated at different temperature, were investigated by XRD ,TG, DTA and TEM. The results show that europium could be introduced into TiO2 under high temperature and it can suppress the structural phase transition from anatase to rutile and the crystal growth of TiO2 in TiO2:Eu nano-materials. The fluorescence spectra were examined by fluorescence spectrophotometer, and the results show that the fluorescence intensity is the strongest when europium content is 2.68% (molefraction) and the heat-treated temperature is 700℃. From the measurement results of the fluorescence lifetimes, it can be seen that the fluorescence lifetime could be prolonged when europium is incorporated in TiO2.     

Preparation and Physicochemical Characterization of La1-x Cex Co03＋δ Perovskite Catalyst and Its Methane Catalytic Combustion

Perovskite oxide LaCoO3 methane catalytic material was synthesized with citric acid complexation and bubbling method. The effect of doped cerium was studied on the series of La1-x,Ce,CoO3 8 materials by means of BET, XRD and SEM techniques. Their catalytic behaviors were studied with methane catalytic complete combustion as probe reaction.The results show that doped cerium has great effect on crystal phase formation. When doped cerium is less than 0.3(molar ratio), the crystal phase of oxide has little changed. When doped cerium is up to 0.5, Co3O4 phase is obviously discovered and the perfectibility of LaCoO3 perovskite crystal phase is deteriorated. When x is over 0.7, perovskite crystal phase is weakened or completely disappeared. Considering the crystal phase of oxides, the optimum doped cerium is about 0.3. The perovskite oxides can be formed at a low calcinations temperature of 700℃. When x is 0.3, the highest catalytic activity of T10%(390℃) and T90%(603℃) is obtained on the series of La1-xCexCoO3 δ materials calcined at 800℃.     

Performance of mesoporous CeO2-Cr2O3 mixed metal oxides applied to benzene catalytic combustion

In this paper,a hydrothermal method was used to prepare(Ce,Cr)-MOF with different Ce/Cr molar ratios and then a series of CeO₂-Cr₂O₃ mixed metal oxides(CeCr-MMO) with mesoporous structure were prepared by thermal decomposition of these MOFs at different temperatures.After a series of characterization techniques were applied to test the physicochemical properties of the materials,it is found that thermal decomposition temperature(TDT) and Ce/Cr molar ratios have i...     

Study on Properties of LSGM Electrolyte Made by Tape Casting Method and Applications in SOFC

Solid oxide fuel cell is attracting more attention in recent years for its lower pollution emission and high energy convert efficiency. La0.9Sr0.1Ga0.8Mg0.2O3-δ is a new kind of electrolyte for intermediate temperature SOFC. In this paper, La0.9Sr0.1Ga0.8Mg0.2O3-δ (LSGM) was prepared by solid state reaction method and formed by tape casting process to make a planar electrolyte. The appropriate amount of the dispersive was obtained by viscosity test. The densities of sintered samples increase with the increasing sintering temperature. It was found that the relative density of electrolyte can approach the value of 95% by the isostatic pressing treatment of the green tape. The average thermal expansion coefficient of the LSGM is 11.4×10-6/℃ at temperature range (200～1200 ℃). Measurements of the current-voltage and power-current characteristics of the H2-Air cell show that the open-circuit voltage is 1.067 V at 800 ℃, peak current density is 0.56 A·cm-2 and the maximum power output is 0.147 W·cm-2.     

Fabrication and Characterization of SOFC Anode, Ni-SDC Cermet

NiO and Ce0.8Sm0.2O1.9 were synthesized by the combination of sol gel and citric acid-nitrate low temperature self-propagating combustion method. Anode precursors which include home-made NiO and Ce0.8Sm0.2O1.9 were prepared by different NiO content and fabrication condition. The anode precursors with pure hydrogen at 820 ℃ for 2.5 h were reduced, The electrical conductivity was tested, and the effect of microstructure on electrical conductivity of Ce0.8Sm0.2O1.9 composite anodes was investigated. The results show that the anode electrical conductivity depends strongly on the anode microstructure that is dramatically affected by Ni content and fabrication condition.     

XPS Studies on Rare Earth Oxide LSCO／YSZ Electrodes

The X-ray diffraction spectra and X-my photoelectron spectroscopy were measured for Sr-doped Lal-xSrx CoO3 materials with perovskite structure prepared by the solid-state reaction method. The influence of heat-treatment tempera-ture on the average crystal size of Lal-xSrx CoO3 was studied. The surface chemical states of Lal-xSrxCoO3 cathodes with different Sr-doped content were discussed. The experimental results show that average crystal size of Lal-xSrxCoO3 under the condition of heat-treatment in the range of 900- 1200℃ is larger than that at other temperatures, which is of benefit to forming porous electrodes. When La is replaced by Sr gradually, the oxygen vacancy concentration increases. It is of benefit to enhancing the transport property of oxygen ion.     

Synthesis and Luminescence Properties of Gd2O3：Eu^3＋ Phosphors

Gd2O3: Eu^3 phosphors were prepared by urea homogeneous precipitation with different surfactant and sol-gel method. XRD patterns show that all the obtained samples are in cubic Gd2O3, and the results of FTIR and fluorescent spectra conformed that OP is a good surfactant for preparing the Gd2O3:Eu^3 phosphors. The SEM photographs show that the particles prepared by urea homogeneous precipitation method are all spherical and well-dispersed, and grain morphology can be controlled by different surfactant. XRD and SEM indicate that the particle sizes prepared by sol-gel method are in the range of 5-30 nm, and the grain sizes increase with increasing of heated temperatures. Luminescence spectra indicat that the main emission peaks of all samples are at 610 nm, the intensities are different from samples prepared with different surfactant and the luminescence intensities increase with increasing of annealed temperatures.