Formation of Nanocomposite Solid Oxide Fuel Cell Cathodes by Preferential Clustering of Cations from a Single Polymeric Precursor.

Conventional composite cathodes used in solid oxide fuel cells (SOFCs) are fabricated by co-sintering of electrocatalyst and ionic conductor powders at 1100-1250 °C. The relatively high-temperature heat treatments required to ensure bonding among the powders and between the powders and electrolyte results in the formation of resistive phases and coarse microstructures corresponding to short triple-phase boundary (TPB) length and, consequently, low oxygen reduction activity. In the present work, to achieve long TPBs and avoid resistive phase formation, we propose to fabricate nanocomposite La0.8Sr0.2MnO3-Ce0.8Sm0.2O2 (LSM-SDC) and La0.8Ca0.2MnO3-Ce0.8Sm0.2O2 (LCM-SDC) thin film cathodes by a low-temperature method, which involves the use of a single polymeric precursor solution containing all the respective cations. Owing to the molecular level mixing and the liquid lack of any powder-based starting material, we envision that preferential clustering of cations forming nanoscale electrocatalyst and ionic conductor particles will take place upon heat treatment at relatively low temperatures of 600-800 °C. Here, we report for the first time in the literature, a correlation between the heat-treatment temperature-phase evolution-cluster formation-surface chemistry evolution and electrochemical activity of nanocomposite thin film cathodes fabricated from a single polymeric precursor. Our experiments reveal that highest electrochemical activity is achieved when the electrocatalyst phase is poorly crystallized, complete clustering of cations takes place, and A-site dopant segregation at the surface is minimal.

Electrochemistry of La(0.3)Sr(0.7)Fe(0.7)Cr(0.3)O(3-δ) as an oxygen and fuel electrode for RSOFCs.

The use of a single porous mixed ion-electron conducting (MIEC) material as both the oxygen and fuel electrodes in reversible solid oxide cells is of increasing interest, primarily due to the resulting simplified cell design and lower manufacturing costs. In this work, La(0.3)Sr(0.7)Fe(0.7)Cr(0.3)O(3-δ) (LSFCr-3) was studied in a 3-electrode half-cell configuration in air, pure CO2 and in a 1 : 1 CO2 : CO mixture, over a temperature range of 650-800 °C. A detailed analysis of the impedance (EIS) data, under both open circuit and polarized conditions, as well as the cyclic voltammetry response of LSFCr-3 has shown that it is very active in all of these environments, but with oxygen evolution being somewhat more facile that oxygen reduction, and CO2 reduction more active than CO oxidation. Evidence for a chemical capacitance, associated with the Fe(3+/4+) redox process in LSFCr-3, was also obtained from the EIS and CV data in all gas environments.

First-time electrical characterization of nanotubular ZrO2 films for micro-solid oxide fuel cell applications.

In this work, anodically grown ZrO2 nanotubes (NTs) are examined for the first time for use in micro solid oxide fuel cell (µ-SOFC) applications. This is due to their high surface area to volume ratio and useful nanoscale morphological features (e.g., 5-100 nm thick NT bases that could serve as the electrolyte layer). To understand their full potential for these applications, the determination of their electrical properties is necessary. Therefore, ZrO2 NTs, in the form of a uniform and crack-free film, were obtained by the two-step anodization of Zr foil in aqueous solutions. The films exhibited excellent adhesion to the Zr substrate, which facilitated impedance spectroscopy analyses, used for the first time to obtain the resistivity of the nanotubular array separately from the contact resistances. This gave a conductivity of the ZrO2 NTs of 1.6 × 10(-6) S cm(-1) at 600 °C in N2, approximately twice that reported for dense ZrO2 films measured at the same temperature in air, and also a very reasonable activation energy of 0.90 eV in the 400-600 °C temperature range.

A Novel Label-Free Optical Biosensor Using Synthetic Oligonucleotides from E. coli O157:H7: Elementary Sensitivity Tests.

SiO(2)-TiO(2) thin films for use as fiber optic guiding layers of optical DNA biosensors were fabricated by the sol-gel dip coating technique. The chemical structure and the surface morphology of the films were characterized before immobilization. Single probe DNA strands were immobilized on the surface and the porosity of the films before the hybridization process was measured. Refractive index values of the films were measured using a Metricon 2010 prism coupler. On the surface of each film, 12 different spots were taken for measurement and calculation of the mean refractive index values with their standard deviations. The increased refractive index values after the immobilization of single DNA strands indicated that immobilization was successfully achieved. A further refractive index increase after the hybridization with target single DNA strands showed the possibility of detection of the E. coli O157:H7 EDL933 species using strands of 20-mers (5'-TAATATCGGTTGCGGAGGTG -3') sequence.