Anode supported micro-tubular SOFC fabricated with mixed particle size electrolyte via phase-inversion technique

Cerium-gadolinium oxide is a promising material for electrolytes of intermediate temperature solid oxide fuel cells (IT-SOFCs) due to its high electrical conductivity at relatively lower temperatures of 400–700 °C. However, a high sintering temperature of up to 1550 °C is typically required to produce dense CGO electrolyte, eventually leading to an interfacial interdiffusion between the electrolyte and electrode components as well as generate a highly resistive interface which reduces ionic conductivity. Lowering the sintering temperature of the electrolyte will greatly benefit the fabrication of SOFCs. This study examines the effectiveness of introducing nano size CGO particles as an approach to get dense CGO electrolyte at lower sintering temperature. A series of dope suspensions with 0–50% nano size loading were prepared to observe rheology and measure viscosity. Then, 30% loading was selected and casting into flat sheet via phase-inversion technique. The flat sheet was characterized by morphology, surface roughness and mechanical strength tests. The suspension was extruded into dual-layer hollow fiber (DLHF) as well. The electrolyte/anode dual-layer hollow fibers (DLHFs) half-cell of micro-tubular solid oxide fuel cells (MT-SOFCs) were prepared via phase inversion based co-extrusion/co-sintering technique. The developed half-cell was characterized by morphological and gas tightness tests which further compared them with fully micron ones. The results show that the incorporation of 30% nanoparticle yielded to dense and tight CGO layers sintered at temperature 1450 °C, which about 50 °C lower than those reported previously for 100% micron particles. The I–V measurements demonstrated the maximum power density of 0.66 Wcm^?2 at temperatures 500 °C using 100% H₂ as fuel. Therefore, this approach is able to reduce the energy cost for the microstructural control of the prepared fiber and thus is recommended for the fabrication of low-cost dual-layer hollow fiber micro tubular SOFCs.     

Characterization of 3D microstructure,thermal conductivity,and heat flow of cement-based foam using imaging technique

This study presents the results of the 3D microstructure, thermal conductivity, and heat flow in cement-based foams and examines their changes with a range of densities. Images were captured using X-ray micro computed tomography (micro-CT) imaging technique on cement-based foam samples prepared with densities of 400, 600, and 800 kg/m³. These images were later simulated and quantified using 3D data visualization and analysis software. Based on the analysis, the pore volume of 11000 µm³ was determined across the three densities, leading to optimal results. However, distinct pore diameters of 15 µm for 800 kg/m³, and 20 µm for 600 and 400 kg/m³ were found to be optimum. Most of the pores were spherical, with only 10% appearing elongated or fractured. In addition, a difference of 15% was observed between the 2D and 3D porosity results. Moreover, a difference of 5% was noticed between the experimentally measured thermal conductivity and the numerically predicted value and this variation was constant across the three cast densities. The 3D model showed that heat flows through the cement paste solids and with an increase in porosity this flow reduces.     

Conductivity and Permittivity of Nickel-Nanoparticle-Containing Ceramic Materials in the Vicinity of Percolation Threshold

Conductivity and static permittivity of ceramic materials containing nanoparticles of Ni were measured in the vicinity of percolation threshold. It is found that, below this threshold, the experimentally obtained dependences of conductivity and static permittivity on the fractional Ni content in these materials are different from those calculated in the frame of the percolation theory. The origin of this discrepancy is discussed in terms of the network hierarchy model proposed recently by Balberg et al . for composite materials.     

Transient two-dimensional IR spectrometer for probing nanosecond temperature-jump kinetics

We have developed a Fourier transform two-dimensional infrared (2D IR) spectrometer to probe chemical reactions and biophysical processes triggered by a nanosecond temperature jump (T jump). The technical challenges for such a spectrometer involve (1) synchronization of a nanosecond T-jump laser and femtosecond laser system, (2) overcoming the decreased signal-to-noise ratio from low repetition rate data acquisition, and (3) performing an interferometric measurement through a sample with a density and index of refraction that varies with time delay after the T jump. The first challenge was overcome by synchronizing the two lasers to a clock derived from the Ti:sapphire oscillator, leading to timing accuracy of 2 ns for delays up to 50 ms. The data collection time is reduced by using undersampling with the improved signal-to-noise ratio obtained from a balanced detection scheme with a dual stripe array detector. Transient dispersed vibrational echo and 2D IR spectroscopy are applied to N-methylacetamide and ubiquitin, as examples, and the spectral responses by a temperature elevation and by structural changes of the protein are compared. The synchronization of 2D IR spectroscopy with a nanosecond temperature jump without losing its sensitivity at a low repetition rate opens a new applicability of the nonlinear spectroscopy to probe a variety of molecular structure changes induced by a nanosecond perturbation.