Electrochemical CO2 reduction with power generation in SOFCs with Cu-added LSCF–GDC cathode

Solid oxide fuel cell (SOFC) unit was constructed with Ni–GDC (gadolinia-doped ceria) as the anode, YSZ as the electrolyte, and Cu-added La_0.58Sr_0.4Co_0.2Fe_0.8O_3–δ–GDC as the cathode. Electrochemical CO₂ reduction occurs. The CO formation rate, the CO₂ conversion and the generated current density increase with increasing CO₂ concentration and temperature. The CO₂ conversion rate equals exactly the CO formation rate. No carbon deposition occurs. The activation energy is 2.72 kcal mol^?1. The electrochemical CO₂ reduction (dissociation) can have much lower activation barrier than the catalytic one. Simultaneous CO₂ reduction with power generation in SOFCs can be feasible.     

Experimental studies on drag reduction and rheology of mixed cationic surfactants with different alkyl chain lengths

Experimental studies of the effects of mixtures of cationic surfactants on their drag reduction and rheological behaviors are reported. Cationic alkyl trimethyl quaternary ammonium surfactants with alkyl chain lengths of C₁₂ and C₂₂ were mixed at different molar ratios (total surfactant concentrations were kept at 5 mM with 12.5 mM sodium salicylate (NaSal) as counterion). Drag reduction tests showed that by adding 10% (mol) of C₁₂, the effective drag reduction range expanded to 4–120 °C, compared with 80–130 °C with only the C₂₂ surfactant. Thus mixing cationic surfactants with different alkyl chain lengths is an effective way of tuning the drag reduction temperature range. Cryo-TEM micrographs revealed thread-like micellar networks for surfactant solutions in the drag reducing temperature range, while vesicles were the dominant microstructures at non-drag reducing temperatures. High extensional viscosity was the main rheological feature for all solutions except 50% C₁₂ (mol) solution, which also does not show strong viscoelasticity. It is not clear why this low extensional viscosity solution with relatively weak viscoelasticity is a good drag reducer. Received: 3 November 1999/Accepted: 5 January 2000     

Raman spectroscopic characterization of CH4 density over a wide range of temperature and pressure

The positions of the CH₄ Raman ν₁ symmetric stretching bands were measured in a wide range of temperature (from −180 °C to 350 °C) and density (up to 0.45 g/cm³) using high‐pressure optical cell and fused silica capillary capsule. The results show that the Raman band shift is a function of both methane density and temperature; the band shifts to lower wavenumbers as the density increases and the temperature decreases. An equation representing the observed relationship among the CH₄ ν₁ band position, temperature, and density can be used to calculate the density in natural or synthetic CH₄‐bearing inclusions. Copyright © 2014 John Wiley & Sons, Ltd.     

Kinetic roughening,global quantities,and fluctuation–dissipation relations

Growth processes and interface fluctuations can be studied through the properties of global quantities. We here discuss a global quantity that not only captures better the roughness of an interface than the widely studied surface width, but that is also directly conjugate to an experimentally accessible parameter, thereby allowing us to study in a consistent way the global response of the system to a global change of external conditions. Exploiting the full analyticity of the linear Edwards–Wilkinson and Mullins–Herring equations, we study in detail various two-time functions related to that quantity. This quantity fulfills the fluctuation–dissipation theorem when considering steady-state equilibrium fluctuations.     

Infrared Absorption,Nuclear Magnetic Resonance and Electronic Spectra of N-Hydroxyureas and Carbamates

During the course of investigating the anticancer activities of new compounds, we have synthesized a series of novel cyclic N-hydroxyurea derivatives and several carbamate intermediates^1–3. Infrared absorption, nuclear magnetic resonance, and electronic absorption spectra were examined in order to confirm the identities and to study the molecular structure of these compounds.     

Hole‐buffer polymer composed of alternating p‐terphenyl and tetraethylene glycol ether moieties: Synthesis and application in polymer light‐emitting diodes

Carrier balance is essential to obtain efficient emission in polymer light‐emitting diodes (PLEDs). A new polymer 3P5O composed of alternating p‐terphenyl and tetraethylene glycol ether segments is designed and synthesized by the Suzuki coupling reaction and successfully employed as hole‐buffer layer to improve carrier balance. Multilayer PLEDs [ITO/PEDOT:PSS/ 3P5O /SY/LiF/Al], with Super Yellow (SY) as the emitting layer and 3P5O as the hole‐buffer layer, reveal maximum luminance (17,050 cd/m²) and maximum current efficiency (6.6 cd/A) superior to that without the hole‐buffer layer (10,017 cd/m², 3.0 cd/A). Moreover, it also shows better performance than that using conventional BCP as hole‐blocking layer [ITO/PEDOT:PSS/SY/BCP/LiF/Al (80 nm): 13,639 cd/m², 4.1 cd/A]. The performance enhancement has been attributed to hole‐buffering characteristics of 3P5O that results in improved carrier recombination ratio and wider carrier recombination region. Current results indicate that the 3P5O is a promising hole‐buffer polymer to enhance the performance of optoelectronic devices. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 785–794