Synthesis and Characterization of La 0.8 Sr 0.2 MnO 3−δ Nanostructures for Solid Oxide Fuel Cells

La0.8Sr0.2MnO3-δ (LSM) perovskite was synthesized using different methods, such as solid state reaction, soft-chemical and sol-gel methods for solid oxide fuel cells (SOFCs) for use as a cathode material. The pristine material was characterized by X-ray diffraction, thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and scanning electron microscopy (SEM). X-ray diffraction results show that the pure phase of La0.8Sr0.2MnO3-δ (LSM) perovskite was formed at 1250oC. Scanning electron microscopy characterization shows that a highly porous material can be obtained using a soft-chemical method with different 3,3’,3”-nitrilotripropionic acid ( NTP) to metal-ion ratio R.


Introduction
Perovskite La 1−x Sr x MnO 3 (LSMO) has attracted attention because of its potential applications in magnetic sensors, reading heads for magnetic memories and as a cathode in solid oxide fuel cells (SOFCs) due to its excellent catalytic, thermal, electrical and magnetic properties [1][2][3][4].The cathode is one of the most essential components in a SOFC.The cathode materials for SOFCs have to meet several requirements in the operating temperature up to 800˚C -1000˚C: high electronic conductivity, resistance to sintering, thermal and chemical stability, high catalytic activity for oxygen reduction and a thermal expansion coefficient matching with other SOFC components [5].Strontium doped lanthanum manganite (LSM, La l−x Sr x MnO 3 ) is the most frequently used cathode material for zirconia based SOFCs.It is a perovskite material with intrinsic ptype conductivity and can meet these requirements.The p-type conductivity of LaMnO 3 is a result of the formation of cation vacancies and is enhanced by substituting with a lower valence ion as a dopant such as the alkaline earth in A and/or B sites.The LSM with the typical composition La 0.8 Sr 0.2 MnO 3−δ is broadly established as the cathode material for high temperature SOFCs.The particle size and microstructure of electrode are significant for the electrode performance.Several preparation techniques such as solid state reaction, gelcasting, drip pyrolysis, citrate-gel process, solgel process, hydrothermal, co-precipitation, pulse laser deposition, magnetron sputtering, molecular beam epitaxy, electrochemical deposition and aerosol pyrolysis methods are used to prepare LSM powders and films [6][7][8][9][10][11][12][13][14][15][16][17].For the SOFCs application, homogeneous nanosized and high purity powders are required.The LSM powders prepared by the solution chemistry methods regularly have smaller particle size than the solid state reaction method.The solid state reaction method influences the catalytic activity because the temperature during synthesis is too high.A poor surface area of LSM particles results from drip pyrolysis.Via the citrate-gel, sol-gel process and coprecipitation routes particle smaller sizes can be synthesized but also the powders frequently aggregate easily.The aim of this work is to find a suitable method to synthesis porous LSM powders.

Solid State Reaction
1.688 g of lanthanum oxide (La 2 O 3 ), 0.382 g of strontium carbonate (SrCO 3 ) and 1.0225 g of manganese oxide (Mn 2 O 3 ) were mixed together in a ball milling unit for 3 h and pressed into pellets.The pellets were fired at 1000˚C for 24 h, regrinded, pressed into pellets again and fired at 900˚C and 1250˚C for 24 h.

Sol-Gel Method
3.37 g of lanthanum nitrate (La(NO 3 ) 3 ), 0.55 g of strontium nitrate (Sr(NO 3 ) 2 ) and 2.32 g of manganese nitrate (Mn(NO 3 ) 2 ) were slowly dissolved in 75 mL distilled water.A transparent solution was formed after complete dissolution of the metal nitrates.A gel was formed under continuous stirring and mild heating at 90˚C.The gel was dried at 120˚C overnight and then heated at 400˚C for 12 h.The resulting powders were ground in an agate mortar and heated in air at 1250˚C for 12 h in a furnace.

Soft-Chemical Method
3,3',3"-Nitrilotripropionic acid (NTP) was synthesized using a green chemical method [18].3.37 g of lanthanum nitrate (La(NO 3 ) 3 ), 0.55 g of strontium nitrate (Sr(NO 3 ) 2 ) and 2.32 g of manganese nitrate (Mn(NO 3 ) 2 ) were slowly dissolved in 75 mL distilled water.A transparent solution was formed after complete dissolution of the metal nitrates.NTP was dissolved (for different values of the molar NTP to metal-ion ratio R (R = 0, 0.25, 0.5 and 0.75) in 100 mL of distilled water at 100˚C.This solution was added into the above mentioned transparent solution.The mixed solution was transferred into a 500 mL roundbottom flask and kept at 80˚C on a hot plate for 2h to evaporate the solution.A bulky gel of high viscosity was obtained after slowly evaporizing the solution at 80˚C by rotary evaporation.The obtained gel was heat treated at 120˚C for 24 h in oven.The final product was then ground and made pellets to fire at 400˚C and 1250˚C for 12 h in furnace.
Crystallographic information on the samples was obtained using an X-ray powder diffractometer (D8 Advanced Bruker) with graphite-monochromatized CuKα radiation (λ = 1.54187Å).Diffraction data were collected over the 2θ range 20˚ to 80˚.The morphologies of the resulting products were characterized using a scanning electron microscope (SEM, JEOL JSM 6390).For the TGA measurements a TA 600, operating in dynamic mode (heating rate = 5˚C/min), was employed.

Results and Discussion
Phase purity and crystallographic information of the synthesized La 0.8 Sr 0.2 MnO 3−δ perovskite nanostructures were characterized using powder X-ray diffraction.The XRD patterns of LSM perovskite nanostructures synthesized by three methods are shown in Figure 1.All diffraction patterns of La 0.8 Sr 0.2 MnO 3−δ perovskite nanostructures show characteristic peaks of the perovskite phase.The XRD patterns are in good agreement with the standard data for hexagonal symmetry with a = 5.5163 Å and c = 13.329Å (JCPDS # 00-056-0616).No second phases were observed presumably because a pure phase of La 0.8 Sr 0.2 MnO 3−δ (LSM) perovskite was formed at 1250˚C [19].
In the synthesis of La 0.8 Sr 0.2 MnO 3−δ (LSM) perovskite nanostructures the carrier (3,3',3"-nitrilotripropionic acid (NTP)) helped in obtaining a homogeneous mixture of the cations in solution through forming metal complexes, it also helped in the reduction of nitrates in a combustion process, releasing a large amount of heat.This is shown by an exothermic peak at 400˚C on a DSC curve (Figure 2).During the solid-state reduction process, metal cations and oxygen anions stay in the reaction mixture during the formation of the perovskite phase in this combustion process.The large heat released during combustion might help to overcome the lattice energy, which is required for the formation of the perovskite phase, and also in the completion of the nucleation by the rearrangement of atoms by short distance diffusion.The fast combustion process might not be of help for the diffusion of atoms far from each other and hence the particle size of LSM powder remained in the nanometer range.Thermogravimetric analysis and differential scanning calorimetry (TGA-DSC) curves with NTP-assisted LSM dried as a gel at 120˚C are shown in Figure 2. The weight losses happened in three steps.The total weight loss was 4.75 mg from room temperature to 1300˚C.The first weight loss is 0.26 mg in the temperature range 22˚C -157˚C; this can be attributed to evaporation of water from the layers of LSM.
The second weight loss is 3.97 mg in the temperature range 157˚C -357˚C and the third weight loss is 0.55 mg in the temperature range 357˚C -840˚C.The second and third weight losses are attributed to decomposition of the carrier (NTP) and evaporation of structurally bounded water.The peaks located at about 380˚C and 400˚C are exothermic on the DSC curve due to decomposition of nitrates and organic matter and correspond to the second weight loss of 3.97 mg from about 157˚C to 400˚C as observed in the TGA curve.The decomposition of all nitrates is finished below 400˚C, which promotes formation of the complex oxides.Here NTP played two roles: One is to form the metal ion complexes and secondly, it serves as a fuel for the combustion reaction, while the nitrates act as an oxidant, so the decomposition reactions can be finished at lower temperatures.
DSC-TGA curves of LSM gel synthesized at 120˚C by sol-gel and soft-chemical methods without using chelating agents are shown in Figures 3 and 4. The total weight losses are 3.43 mg and 7.02 mg for the sol-gel and soft-chemical method materials from room temperature to 1300˚C in three steps.The first weight losses are 0.96 mg and 1.37 mg, they can be attributed to evaporation of water.The second weight losses are 2.44 mg and 4 mg, these correspond to decomposition of the nitrates.The third weight losses are 0.36 mg and 1.65 mg due to eva-poration of structurally bounded water.The highest de-composition temperature is about 600˚C in both SG and SC methods, which is due to the presence of strontium nitrate.
Figure 5 shows a SEM image of LSM microstructures prepared by solid state (SS) reaction at 1250˚C.It shows, that the powder-like material consists of irregular micro-slabs of several micrometers in length.A SEM image of LSM nanoparticles synthesized by sol-gel (SG) method is shown in Figure 6.The particle size distribution is more uniform and the size of the particle is about 300 nm -400 nm.

Conclusion
LSM nanostructures were successfully synthesized by sol-gel and soft-chemical methods.Pure phase pervoskite LSM is formed at 1250˚C.The decomposition temperature where LSM is obtained is higher in SG and SC methods without NTP when compared to the NTP-assisted SC method.With the latter method highly porous materials were obtained at various 3,3',3"-nitrilotripropionic acid (NTP) to metalion ratios.

Figure 5 .
Figure 5. SEM image of LSM micro slabs synthesized by solid state reaction.higherporosity (Figures7(b)-(d)) contrast to those methods SS, SG and SC without NTP.

Figure 6 .
Figure 6.SEM image of LSM nanoparticles prepared by SG method.