Preparation and characterization of vinyltriethoxysilane based inorganic–organic gel glasses dispersed 4′-n-pentyl-4-cyanobiphenyl nematic liquid crystal

Vinyltriethoxysilane based inorganic–organic glasses dispersed with 4′-n-pentyl-4-cyanobiphenyl nematic liquid crystal are designed to fabricate a new type of gel glass dispersed with liquid crystal. Scanning electron microscopy shows that the nematic liquid crystal phase, occupying the interconnected cavities, is continuously embedded in the inorganic–organic matrixes. The effect of the nematic liquid crystal weight concentration on the morphology is investigated. The differential scanning calorimetry shows that the nematic-isotropic transition temperature depends on the nematic liquid crystal weight concentration. The Raman spectra show that there are no obvious Raman frequency shifts, compared with pure nematic liquid crystal. The in situ diffuse reflectance FTIR spectra show that the integral intensity of bands of hydroxyls has not varied.     

Oxygen Barrier Properties of Waterborne Polyurethane/Silica Hybrids

The oxygen barrier properties of films obtained from waterborne polyurethane/silica hybrid dispersions were analyzed. Two different types of polyurethanes were used, based on poly(propylene glycol) and poly(1,4-butylene adipate). Three different strategies were followed in the preparation of the hybrid dispersions. In the first type of materials (series 1), the inorganic part came exclusively from the covalent incorporation of trifunctional silane groups into the polymeric chains. The other two series contained, in addition to the trifunctional silane groups, tetrafunctional silane groups either physically blended (series 2) or “in situ” generated (series 3). Materials of series 1 showed an increase of the oxygen permeability coefficient with the silane content. However, the other two types of materials presented just the opposite dependence. In this latter case, the systems containing “in situ” generated silica (series 3) presented higher permeability coefficient values, probably because of the steric hindrance imposed by the polyurethane that gave rise to silica networks containing silanol groups and free volume holes. Moreover, lower permeability coefficient values were obtained when larger size particles were added. This fact could mean that the polyurethane/silica interface effects were not totally hindered even when the organic/inorganic phases were covalently bonded.     

Spectrophotometric Studies of Entrapped Thymol Phtalein pH Indicator into Sol‐Gel Matrix

This research involves the behavior of thymol phtalein pH indicator entrapped into the sol‐gel derived inorganic matrix. The method is based on the physical entrapment of the reagent molecules in the sol‐gel matrix. The immobilized thymol phthalein pH indicator shows behavior similar to its solution counterpart. The UV/vis spectra indicate that the thymol phthalein retains its structure during the sol‐gel reactions in terms of response to pH. Thymol phthalein can be regarded as uniformly distributed in the sol‐gel matrix. This observation has been confirmed using polarized microscopy. This research shows that thymol phtalein can be immobilized in sol‐gel glasses and used as a solid pH sensor.     

A new sol–gel processing routine without chelating agents for preparing highly transparent solutions and nanothin films: engineering the role of chemistry to design the process

The great sensitivity of titanium alkoxides to hydrolysis makes their sol–gel transformation very fast and thus difficult to control. A method was proposed to alleviate this drawback. Preparation of highly transparent solutions and nanothin films is another objective of the present research. Employing nanoemulsion method and optimizing the processing conditions, a clear solution of well-dispersed nanosized particles was obtained. With the proposed process BaTiO₃ precursor sols and nanothin films with enhanced optical transparency towards the visible were prepared. The optimal formulation of the sol consists of acetic acid, barium acetate, 2-propanol, TTIP and deionized water with 6:1:1:1:150 M ratios, respectively. It was found that the reduction of the temperature in the initial stage of mixing of precursors controls the size of the forming species and accordingly improves the stability and transparency of the sol. The results also showed that the applied modifications and optimizations significantly downsize the particles within the sol to the nanometric scale and accordingly result in a significant improvement in the optical response of the products.     

Freeze–Thaw-Promoted Fabrication of Clean and Hierarchically Structured Noble-Metal Aerogels for Electrocatalysis and Photoelectrocatalysis

Noble-metal aerogels (NMAs) have drawn increasing attention because of their self-supported conductive networks, high surface areas, and numerous optically/catalytically active sites, enabling their impressive performance in diverse fields. However, the fabrication methods suffer from tedious procedures, long preparation times, unavoidable impurities, and uncontrolled multiscale structures, discouraging their developments. By utilizing the self-healing properties of noble-metal aggregates, the freezing-promoted salting-out behavior, and the ice-templating effect, a freeze–thaw method is crafted that is capable of preparing various hierarchically structured noble-metal gels within one day without extra additives. In light of their cleanliness, the multi-scale structures, and combined catalytic/optical properties, the electrocatalytic and photoelectrocatalytic performance of NMAs are demonstrated, which surpasses that of commercial noble-metal catalysts.     

Color tuning of up-conversion emission in ytterbium,erbium, aluminum tri-doped zinc oxide crystal by adjusting aluminum concentration

Ytterbium, erbium, aluminum tri-doped zinc oxide crystal was synthesized, which can turn color from red to green up-conversion luminescence through adjusting aluminum content. When the aluminum concentration reached 4?mol%, the color of up-conversion emission first turn from red to green. Meanwhile, the ratio of red to green emission reduced from 25.32 to 0.26, and the coordinates of chromaticity coordinate calculation changes from (0.5749, 0.3378) to (0.2190, 0.7169) with aluminum concentration range from 0 to 4?mol%. The up-conversion emission peaks at 521, 542, and 660?nm of sample originate from the transitions of ²H_11/2 → ⁴I_15/2, ⁴S_3/2 → ⁴I_15/2, and ⁴F_9/2 → ⁴I_15/2 of erbium ions, respectively. X-ray diffraction patterns perform the better crystallization degree with increasing aluminum concentration. The scanning electron microscopy images show the porous and lamellar structures with different aluminum concentrations. A convenient but effective design to obtain ytterbium, erbium, aluminum tri-doped zinc oxide up-conversion luminescence is reported, which can turn color from red to green.     

Leakage currents in ferroelectric thin films

The main mechanisms of leakage currents in thin lead zirconate titanate (PZT) ferroelectric films prepared by the sol–gel method are discussed. Four specific regions are determined in I–V dependencies. At very weak fields (10–20 kV/cm), the current falls with the voltage increase as a result of depolarization. In the low fields region (about 70–100 kV/cm), the leakage current decreases with the decrease of voltage ramp speed and its components are the ohmic and displacement currents. In the high fields region (≥130 kV/cm), the leakage current increases with the decrease of step voltage ramp in contrast to the previous case. Possible conductivity mechanisms are the Poole– Frenkel emission and hopping conduction. In the transition region between above-mentioned ones (from 80–90 to ～130 kV/cm), an abrupt unstable increase of current is observed caused by breakdown of reverse bias Schottky barrier. Depolarization currents are studied for sol–gel PZT films prepared at different preparation conditions.     

脉冲激光法连续制备纳米钴乙醇溶胶的研究

纳米钴因其优异的磁性能在磁记录材料 [1]、超顺磁材料 [2 ]、巨磁材料 [3 ]和雷达吸波 [4 ]方面具有重要应用 .金属钴有面心立方、密排六方和非晶态 3种结构 [5] .目前 ,用等离子加热及碳电弧法制备的纳米钴粉基本上都是面心立方结构 [6] .Gibson等 [7]用超声化学方法获得了密     

Portable Fibre Optic Oxygen Sensor Based on Room-Temperature Phosphor escence Lifetime

 A portable fibre optic instrument for oxygen sensing based on luminescence lifetime is presented. The instrument is based on measurement of the quenching by oxygen of the room temperature phosphorescence (RTP) emitted by aluminium tris(8-hydroxy-7-iodo-5-quinolinesulfonic acid) chelate incorporated in an inorganic matrix by sol–gel technology. The comparatively long RTP lifetime of this sensing material (450 μs) and the large singlet–triplet splitting (λ_exc 390 nm, λ_em 590 nm) allow the use of simple opto-electronic circuits and low-cost processing electronics. Standard electronic components have been applied in development of the low-cost lifetime-measurement instrumentation presented here. Two optical sensor configurations, “flow-through cell” and “probe”, have been designed and evaluated for the determination of very low levels of oxygen, in gaseous argon streams and in waters. The basic technology, design parameters and performance characteristics of the optical sensors are discussed. Applications to determination of dissolved oxygen in river, tap and sewage waters are described. The advantages of luminescence lifetime measurements over conventional RTP intensity measurements for oxygen sensing are discussed. Received April 1, 1999. Revision November 4, 1999.     

Synthesis of Nano‐Sized TiO2 Colloidal Sol and Its Optical Properties

Nano‐sized TiO₂ sol was prepared through a wet synthesis process. The synthesis procedure involved hydrolysis of TiCl₄, acid treatment, and a SiO₂ surface‐modifying process. Before surface modification, the TiO₂ suspension was treated with acid to remove Na ions, soluble TiO_2, and other impurities. The acid treatment of a TiO₂ suspension at a higher temperature was proved to be useful for effective SiO₂ modification. The colloidal sol provided high transparency in visible light as well as excellent UV‐shielding properties. Surface modification of TiO₂ particles with SiO₂ greatly improved both the dispersing stability in neutral pH and the photostability of TiO₂ colloidal sol.