Papers by Keyword: GDC

Abstract: Observation on the effects of rare earth impurities on the properties of Ce_0.9Gd_0.1O_0.195 (GDC) composite electrolyte has been performed. Indonesia has abundant rare earth elements especially CeO₂, which one of the resources is from monazite mineral. In this study, the GDC powders were synthesized via solid state technique. The two types of precursors were prepared and mixed into planetary ballmill, i.e., CeO₂ (Sigma Aldrich) with Gd₂O₃ (Sigma Aldrich) and CeO₂ (non-commercial, local product) with Gd₂O₃ (Sigma Aldrich), namely GDC commercial and GDC non-commercial, respectively. The composite electrolyte powders calcined at temperature of 800°C in the air atmosphere condition. The composite electrolytes were then characterized in terms of its morphology, elemental, phase structure and thermal properties of the powders. The GDC commercial and non-commercial powders both consist of face centered cubic fluorite ceria structure which was confirmed by X-Ray Diffraction (XRD). The peaks are matching well with the cerium oxide JCPDS card No: 34-394. There are no peaks detected for the gadolinium oxide. It indicates that the dopant ion is fully substituted into the CeO₂ lattice. The elemental analysis was performed using X-ray Fluorescence (XRF). The microstructures were observed under Scanning Electron Microscopy (SEM). The thermal properties characterizations were performed by using Thermal Gravimetric Analysis (TGA) and Differential Scanning Calorimetry (DSC) from room temperature to 1500°C. Both powders investigated are suitable for electrolyte IT-SOFC based on their physical and thermal characterization. Among the composite electrolytes investigated, the GDC commercial showed the better performance in terms of their physical and thermal properties.

Abstract: The surface modification of Gd doped ceria (GDC) and Sr-and Mg-codoped lanthanum gallate (LSGM) powders with cationic and anionic polyelectrolytes, Poly (diallyldimethylammonium chloride) (PDDA) and poly (2-acrylamido-2-methyl-1-propanesulfonic acid) (PAMPS), respevtively, was performed by the Layer by Layer (LbL) adsorption method to improve the surface-charging uniformity. The tri-layer of GDC/LSGM/GDC was deposited on a polypyrrole coated porous NiO-YSZ substrate by sequential EPD using the ethanol-based suspensions of the surface-modified powders. The topcoating of hydroxyl-propyl cellulose (HPC) on the deposited layers was conducted to control the drying rate with suppressing the cracking and peeling-off of the deposits. The advantage of the use of those polymers for the EPD process including the drying technique was demonstrated.

Abstract: Gravity die casting (GDC) and low pressure die casting (LPDC) methods were used to compare the mechanical properties and porosity distribution in a 5-step mould design. Commercially available A356 alloy was used for the experiments. Ar and Ar+H₂ mixture were used to achieve two different hydrogen levels, i.e. 0,1 and 0,2 ml/100g Al, respectively. Although the porosity level was lower in LPDC, the tensile properties were lower than GDC due to the fact that LPDC melt had 50 mm bifilm index, whereas GDC melt had 20 mm. This investigation has shown that the metal quality has a larger effect over the mechanical properties than the porosity content.

Abstract: Nanocrystalline GDC as small as 5 nm was successfully synthesized via the co-precipitation method. GDC/YSZ core-shell nanocrystals, which were GDC nanocrystals overcoated by a thin YSZ layer, was successfully synthesized by the addition of GDC nanocrystals in the YSZ source solution using sol-gel method. The core-shell structure was supported by its high-resolution transmission electron microscopy results and the composition was investigated by EDX method.

Abstract: Nickel coated gadolinium doped ceria (GDC) powder was synthesized by microwave radiation and combustion. For the synthesis, the precipitates of gadolinium cerium oxycarbonate hydrate (GdxCe2-xO(CO3)2·H2O) were formed by a microwave radiated reaction between cerium nitrate (Ce(NO3)3.6H2O) and gadolinium nitrate (Gd(NO3)3.6H2O) and urea (CO(NH2)2), then nickel coatings on the gadolinium cerium oxycarbonate hydrate were performed by further microwave reaction between nickel chloride and urea. The shape and size of the gadolinium cerium oxycarbonate hydrate particles were critically dependent on aging time during microwave radiation. The irregular particles were transformed to rod shape particles with well-crystallized with increasing aging time to 40 min at 70 - 80°C because of the gradual decomposition of urea during microwave radiation. Small nickel precursor particles were homogeneously coated on the gadolinium cerium oxycarbonate hydrate particles with rod shape with aid of microwave radiation at 80 °C for 40 min. As a result, the nickel coated GDC nanopowders were sucessfully produced by the microwave radiation synthesis and further microwave combusted at 450°C for 20 min.

Abstract: Extensive interfacial reactions are known to occur between Fe-Co based perovskite cathode materials and the standard solid oxide fuel cell (SOFC) yttria stabilized zirconia (YSZ) electrolyte. Thin films of gadolinia doped ceria (GDC) could be used as a diffusion barrier between the cathode and the electrolyte. The present work investigates spin coating thin diffusion reaction inhibiting films onto SOFC electrolytes. The chemical and structural evolution of ethylene glycol based precursor solution is studied by means of rheology, x-ray diffraction (XRD), high temperature XRD (HT-XRD), Fourier-transformed infrared spectroscopy (FTIR) and differential thermal analysis (DTA). The studies show that cerium formate is formed as an intermediate resin. Thin films, up to 500 nm thick, of gadolinia doped ceria (GDC) are successfully produced by multiple spin coating of polymerized ethylene glycol derived solutions on 200 1m thick YSZ tapes. The GDC and YSZ interfacial surface morphology and film thickness are studied by scanning electron microscopy (SEM) and atomic force microscopy (AFM). These films are shown to successfully prevent the creation of non-conducting reaction phases at the cathode-electrolyte interface by blocking interdiffusion.