Search Results (7)

A mixture of lanthanum strontium cobalt ferrite (LSCF) and nickel oxide (NiO) makes for a desirable cathode material for an IT-SOFC due to its excellent oxygen reduction capability. This study investigates the effect of NiO addition into LSCF cathode on its physical and electrochemical properties. To optimise the amount of NiO addition, both electrochemical impedance spectra and bode phase were used to examine various weight ratios of nickel oxide and LSCF cathode. Brunauer-Emmett-Teller (BET) and thermal analyses validated the electrochemical observation that the LSCF:NiO ratio yields sensible oxygen reduction reaction and stoichiometric findings. Initial characterisation, comprising of phase and bonding analyses, indicated that LSCF-NiO was successfully synthesised at 800 °C using an improved modified sol gel technique. The addition of 5% nickel oxide to LSCF results in the lowest area specific resistance (ASR) value overall. The Bode phase implies that the addition of 5% nickel oxide to LSCF reduces the impedance at low frequencies by 64.28 percent, indicating that a greater oxygen reduction process happened at the cathode. After the addition of 5 wt% NiO, a single LSCF-NiO cell may function at temperatures as low as 650 °C and the LSCF cathode power density is increased by 25.35%. The surface morphology of the LSCF-NiO cathode reveals that the average particle size is less than 100 nm, and mapping analysis demonstrated a homogenous NiO distribution over the cathode layer. Consequently, the synthesis of LSCF-NiO at intermediate temperatures (800–600 °C) revealed outstanding chemical compatibility, bonding characteristics, and electrochemical performance. Full article

The objective of this paper is to manufacture free-standing solid oxide cells (SOCs) through the atmospheric plasma spray process (APS), without the aid of a metallic support nor the need for a post-process heating treatment. A five-layered cell was fabricated. Fused and crushed yttria-stabilized zirconia (YSZ) powder in the 5–22 μm particle size range was used in order to achieve a dense electrolyte layer, yet still permitting satisfactory ionic diffusivity. Nickel oxide (NiO) powder that was obtained by in-house flame spray (FS) oxidation of pure nickel (Ni) powder was mixed and sprayed with the original Ni-YSZ feedstock, so as to increase the porosity content in the supporting electrode. Two transition layers were sprayed, the first between the support electrode and the electrolyte (25% (Ni/NiO)–75% YSZ) and the second at the electrolyte and the end electrode interface (50% YSZ–50% lanthanum strontium manganite (LSM)). The purpose of intercalation of these transition layers was to facilitate the ionic motion and also to eliminate thermal expansion mismatches. All the as-sprayed layers were separately tested by an in-house developed acetone permeability comparative test (APCT). Electrodes with adequate porosity (25–30%) were obtained. Concerning electrolytes, relatively thick (150–200 µm) layers derived from fused and crushed YSZ were found to be impermeable to acetone, while thinner YSZ counterparts of less than 100 µm showed a low degree of permeability, which was attributed mostly to existent microcracks and insufficient interparticle cohesion, rather than to interconnected porosity. Full article

A nickel-ceria-yttria stabilized zirconia (Ni-CYSZ) cermet material was synthesized and tested as the anode for the direct oxidation of methane in a solid oxide fuel cell (SOFC) with YSZ as the electrolyte and strontium-doped lanthanum manganite (LSM) as the cathode. Initially, the electrochemical behavior was investigated under several load demands in wet (3% H₂O) CH₄ at 850 °C during 144 h using I-V curves, impedance spectra, and potentiostatic measurements. Long-term tests were subsequently conducted under 180 mA·cm^–2 in wet CH₄ for 236 h and dry CH₄ for 526 h at 850 °C in order to assess the cell stability. Material analysis was carried out by SEM-EDS after operation was complete. Similar cell performance was observed with wet (3% H₂O) and dry CH₄, and this indicates that the presence of water is not relevant under the applied load demand. Impedance spectra of the cell showed that at least three processes govern the direct electrochemical oxidation of methane on the Ni-CYSZ anode and these are related to charge transfer at high frequency, the adsorption/desorption of charged species at medium frequency and the non-charge transfer processes at low frequency. The cell was operated for more than 900 h in CH₄ and 806 h under load demand, with a low degradation rate of ~0.2 mV·h^–1 observed during this period. The low degradation in performance was mainly caused by the increase in charge transfer resistance, which can be attributed to carbon deposition on the anode causing a reduction in the number of active centers. Carbon deposits were detected mostly on the surface of Ni particles but not near the anode/electrolyte interface or the cerium surface. Therefore, the incorporation of cerium in the anode structure could improve the cell lifetime by reducing carbon formation. Full article

Perovskite derived Ni catalysts offer the remarkable benefit of regeneration after catalyst poisoning or Ni particle growth through the reversible segregation of Ni from the perovskite-type oxide host. Although this property allows for repeated catalyst regeneration, improving Ni catalyst stability towards sulfur poisoning by H₂S is highly critical in solid oxide fuel cells. In this work Mn, Mo, Cr and Fe were combined with Ni at the B-site of La_0.3Sr_0.55TiO_3±δ to explore possible benefits of segregation of two transition metals towards sulfur tolerance. Catalytic activity tests towards the water gas shift reaction were carried out to evaluate the effect of the additional metal on the catalytic activity and sulfur stability of the Ni catalyst. The addition of Fe to the Ni perovskite catalyst was found to increase sulfur tolerance. The simultaneous segregation of Fe and Ni from La_0.3Sr_0.55Ti_0.95-xNi_0.05Fe_xO_3±δ (x ≤ 0.05) was investigated by temperature programmed reduction, X-ray diffraction and X-ray absorption spectroscopy and catalytic tests after multiple redox cycles. It is shown that catalytic properties of the active phase were affected likely by the segregation of Ni/Fe alloy particles and that the reversible segregation of Ni persisted, while it was limited in the case of Fe under the same conditions. Full article

Irreversible hydrocolloids (IR) is a dental impression material commonly used in Brazilian and European dental practice because it is inexpensive, easy to handle, has good reproductive detail and is comfortable for the patient. This research aimed to analyze the chemical composition of eight different IRs for dental use. A sample of 0.2 g was weighed and transferred to a Teflon beaker moistened with drops of distilled or deionized water; 5 mL of nitric acid was added until total solubility of the sample; the solution was transferred to a 100 mL volumetric flask, the volume was filled with distilled or deionized water and homogenized. Thirty-five chemical elements were found: Lithium, Beryllium, Boron, Sodium, Magnesium, Aluminum, Silicon, Phosphorus, Potassium, Titanium, Manganese, Cobalt, Nickel, Vanadium, Zinc, Rubidium, Arsenic, Iron, Copper, Strontium, Yttrium, Zirconium, Niobium, Molybdenum, Ruthenium, Cadmium, Tin, Antimony, Barium, Lanthanum, Cerium, Mercury, Lead, Thorium and Uranium. Only one of the samples contained no Nickel, Antimony and Lead; and Arsenic and Uranium were found in 2 samples. This study provided evidence of high toxicity of the IR brands, pointing out the need for better quality control of this product, in order to prevent health damage in dentists, prosthesis technicians and patients. Full article

Mechanical damage is a major factor limiting the long-term stability of solid oxide fuel cells (SOFCs). Here, the mechanical stability of planar SOFCs consisting of Ni-YSZ anode/YSZ electrolyte/LSM-YSZ cathode (Ni=Nickel, YSZ=yttria-stabilized zirconia, LSM=lanthanum strontium manganite) is analyzed by a structural mechanics model with composition dependent mechanical properties. Influencing factors considered include: the Ni and LSM volume fractions, the thicknesses of anode, cathode and electrolyte layers, and the cell types of anode-, cathode-, and electrolyte-supported designs. It is found that (i) the anode failure probability increases with the Ni content. However, SOFCs remain mechanically safe if the Ni volume fraction is below 65%. (ii) An LSM volume fraction of over 40% is required to maintain the mechanical integrity of cathode. (iii) For an anode-supported cell with a 20 μm thick electrolyte, the anode thickness should be more than 0.5 mm to be mechanically stable. (iv) The anode-supported cell is found to be mechanically safer than that of the electrolyte-supported cell. Full article

This review summarizes the current state of polymer composites used as dielectric materials for energy storage. The particular focus is on materials: polymers serving as the matrix, inorganic fillers used to increase the effective dielectric constant, and various recent investigations of functionalization of metal oxide fillers to improve compatibility with polymers. We review the recent literature focused on the dielectric characterization of composites, specifically the measurement of dielectric permittivity and breakdown field strength. Special attention is given to the analysis of the energy density of polymer composite materials and how the functionalization of the inorganic filler affects the energy density of polymer composite dielectric materials. Full article