Wrinkled TiNAgNW Nanocomposites for High-Performance Flexible Electrodes on TEMPO-Oxidized Nanocellulose.

In this study, we present a novel method for fabricating semi-transparent electrodes by combining silver nanowires (AgNW) with titanium nitride (TiN) layers, resulting in conductive nanocomposite coatings with exceptional electromechanical properties. These nanocomposites were deposited on cellulose nanopaper (CNP) using a plasma-enhanced pulsed laser deposition (PE-PLD) technique at low temperatures (below 200 °C). Repetitive bending tests demonstrate that incorporating AgNW into TiN coatings significantly enhances the microstructure, increasing the electrode's electromechanical robustness by up to four orders of magnitude compared to commercial PET/ITO substrates. Furthermore, the optical and electrical conductivities can be optimized by adjusting the AgNW network density and TiN synthesis temperature. Our results also indicate that the nanocomposite electrodes exhibit improved stability in air and superior adhesion compared to bare AgNW coatings.

Dry Two-Step Self-Assembly of Stable Supported Lipid Bilayers on Silicon Substrates.

Artificial membranes are models for biological systems and are important for applications. We introduce a dry two-step self-assembly method consisting of the high-vacuum evaporation of phospholipid molecules over silicon, followed by a subsequent annealing step in air. We evaporate dipalmitoylphosphatidylcholine (DPPC) molecules over bare silicon without the use of polymer cushions or solvents. High-resolution ellipsometry and AFM temperature-dependent measurements are performed in air to detect the characteristic phase transitions of DPPC bilayers. Complementary AFM force-spectroscopy breakthrough events are induced to detect single- and multi-bilayer formation. These combined experimental methods confirm the formation of stable non-hydrated supported lipid bilayers with phase transitions gel to ripple at 311.5 ± 0.9 K, ripple to liquid crystalline at 323.8 ± 2.5 K and liquid crystalline to fluid disordered at 330.4 ± 0.9 K, consistent with such structures reported in wet environments. We find that the AFM tip induces a restructuring or intercalation of the bilayer that is strongly related to the applied tip-force. These dry supported lipid bilayers show long-term stability. These findings are relevant for the development of functional biointerfaces, specifically for fabrication of biosensors and membrane protein platforms. The observed stability is relevant in the context of lifetimes of systems protected by bilayers in dry environments.

Spontaneous formation of nanopatterns in velocity-dependent dip-coated organic films: from dragonflies to stripes.

We present an experimental study of the micro- and mesoscopic structure of thin films of medium length n-alkane molecules on the native oxide layer of a silicon surface, prepared by dip-coating in a n-C32H66/n-heptane solution. Electron micrographs reveal two distinct adsorption morphologies depending on the substrate withdrawal speed v. For small v, dragonfly-shaped molecular islands are observed. For a large v, stripes parallel to the withdrawal direction are observed. These have lengths of a few hundred micrometers and a few micrometer lateral separation. For a constant v, the stripes' quality and separation increase with the solution concentration. Grazing incidence X-ray diffraction and atomic force microscopy show that both patterns are 4.2 nm thick monolayers of fully extended, surface-normal-aligned alkane molecules. With increasing v, the surface coverage first decreases then increases for v > v(cr) ∼ 0.15 mm/s. The critical v(cr) marks a transition between the evaporation regime, where the solvent's meniscus remains at the bulk's surface, and the entrainment (Landau-Levich-Deryaguin) regime, where the solution is partially dragged by the substrate, covering the withdrawn substrate by a homogeneous film. The dragonflies are single crystals with habits determined by dendritic growth in prominent 2D crystalline directions of randomly seeded nuclei assumed to be quasi-hexagonal. The stripes' strong crystalline texture and the well-defined separation are due to an anisotropic 2D crystallization in narrow liquid fingers, which result from a Marangoni flow driven hydrodynamic instability in the evaporating dip-coated films, akin to the tears of wine phenomenology.

Determination of halophenolic wood preservant traces in milk using headspace solid-phase microextraction and gas chromatography-mass spectrometry.

Extraction of 2,4,6-tribromophenol (TBP), pentachlorophenol (PCP) and pentachloroanisole (PCA) from whole fat cow milk using headspace solid-phase microextraction (HS-SPME) with polyacrylate (PA) and polydimethylsiloxane (PDMS) fibers was evaluated and compared. The PA was studied to extract PCA, TBP and PCP, while PDMS was used to extract PCA and acetyl derivatives of PCP and TBP. The parameters: fiber position, matrix effect, temperature and extraction time were studied. The analysis was made by gas chromatography coupled with mass spectrometry. The results show that the distance between fiber and milk had a significant effect on the extraction kinetics. Also, the fat content in milk was a critical parameter that clearly affected the extracted mass of each compound. By using a PA fiber, the sensitivity for PCA and TBP was higher than that obtained with PDMS fiber; however, PA fiber did not allow PCP determination. The recoveries from milk were 95+/-4%, 96+/-2% and 96+/-4% for PCP, TBP and PCA, respectively, with the PDMS fiber and 94+/-3% and 95+/-1% for TBP and PCA, respectively, with PA fiber. The method using PDMS fiber was applied to real whole milk samples.

NPC2 is expressed in human and murine liver and secreted into bile: potential implications for body cholesterol homeostasis.

The liver plays a critical role in the metabolism of lipoprotein cholesterol and in controlling its elimination through the bile. Niemann-Pick type C 2 (NPC2), a cholesterol-binding protein, is key for normal intracellular trafficking of lipoprotein cholesterol, allowing its exit from the endolysosomal pathway into the metabolically active pool of the cell. In addition, NPC2 is a secretory protein from astrocytes and epididymal cells. Although NPC2 mRNA is detected in the liver, plasma and biliary NPC2 protein levels and function have not been reported. This study demonstrates that NPC2 is present in murine and human plasma and bile. In addition, hepatic NPC2 protein expression was dramatically increased in NPC1-deficient mice but not regulated by cholesterol feeding or pharmacological modulation of various nuclear receptors involved in cholesterol and bile acid metabolism. Interestingly, biliary NPC2 levels were 3-fold increased in gallstone-susceptible C57BL6/J versus gallstone-resistant BALB/c mice. Furthermore, NPC2 was exclusively found in the cholesterol pro-nucleating ConA-binding fraction of human bile. In conclusion, NPC2 is secreted from the liver into bile and plasma, where it may have a functional role in cholesterol transport in normal and disease conditions.