Silica Films with Bimodal Pore Structure Prepared by Using Membranes as Templates and Amphiphiles as Porogens

Extended porous silica films with thicknesses in the range of 60 to 130 μm and pores on both the meso‐ and macroscale have been prepared by simultaneously using porous membrane templates and amphiphilic supramolecular aggregates as porogens. The macropore size is determined by the cellulose acetate or polyamide membrane structure and the mesopores by the chosen ethylene‐oxide‐based molecular self‐assembly (block copolymer or non‐ionic surfactants). Both the template and the porogen are removed during an annealing step leaving the amorphous silica material with a porous structure that results from sol–gel chemistry occurring in the aqueous domains of the amphiphilic liquid‐crystalline phases and casting of the initial template membrane. The surface area and total pore volume of the inorganic films vary from 473 to 856 m² g^–1, and 0.50 to 0.73 cm³ g^–1, respectively, depending on the choice of template and porogen. The combined benefits of both macro‐ and mesopores can potentially be obtained in one film. Such materials are envisaged to have applications in areas of large molecule (biomolecule) separation and catalysis. Enhanced gas and liquid flow rates through such membranes, due to the presence of the larger pores, also makes them attractive as supports for other catalytic materials.     

基于光学异常透射现象的光纤传感器的设计与研究

基于光学异常透射现象的光纤传感器,因其具有高度的近场增强效应和介电环境的高度敏感性等优点,在化学、生物医学等领域有广泛的应用前景。但是由于在光纤端面加工周期纳米结构需要复杂的工艺或者昂贵的微加工仪器,限制了基于光学异常透射现象的光纤传感器的发展。针对这一问题,提出了模板转移法在光纤端面加工金属周期纳米结构,并搭建实验系统对应用该方法制作的光纤传感器的传感特性及其物理机理进行了研究。实验结果表明,模板转移法能够很好地完成在光纤端面加工高质量的周期金属纳米结构。应用该方法制作的光纤传感器具有很好的传感特性,传感器的最高灵敏度达到594.45 nm·RIU-1,品质因数值达到33.12。     

[C10N2H10][ZnCl(HPO4)]2: A New Templated Zincophosphate Containing Tetrahedral Nets with 63 Topology

The crystal structure of [C₁₀N₂H₁₀][ZnCl(HPO₄)]₂ contains corrugated tetrahedral layers with 6³ topology. Charge balance is achieved by insertion of diprotonated 4,4′‐bipyridine between the layers. Crystal data: monoclinic, P2₁/n (no. 14), a = 4.8832(2) Å, b = 22.673(2) Å, c = 8.1643(4) Å, β = 104.02(1)°; V = 877.0(1) ų; Z = 4; R1 = 0.041 and wR2 = 0.088 for 1836 reflections [I > 2σ(I)]. Tetrahedral layers are also observed in other organo‐ammonium templated compounds. However, their topologies are characterized by 4.8² nets. With the title compound a layered tetrahedral net with 6³‐topology is reported for the first time.     

Organic Tube/Rod Hybrid Nanofibers with Adjustable Segment Lengths by Bidirectional Template Wetting

Segmented nanotubes and nanorods exhibiting a variation in their composition along their long axes represent a new and exciting class of nanomaterials. It is shown that bidirectional template wetting enables the integration of functional and complex polymeric materials into segmented nanofibers. First, a template is wetted under conditions in which a solid polymeric thread with adjustable length fills a pore segment starting from one template surface. Subsequently, a second wetting step starting from the opposite template surface yields segmented nanofibers. The exploitation of different wetting mechanisms results in the formation of tube/rod hybrid nanofibers.     

Nanoporous Organosilicate Films Prepared in Acidic Conditions Using Tetraalkylammonium Bromide Porogens

Organosilicate films with narrow pore size distribution tunable in the range of 1–3.4 nm were prepared by spin‐coating of silicon wafers with sols prepared in acidic conditions using tetraethyl orthosilicate, methyltrimethoxysilane, and tetraalkylammonium bromide (TAABr) porogen. The pore size was defined by the alkyl chain length of the quaternary ammonium molecule and the porogen concentration. The pore network in the films and the hydrophobicity of the pore surfaces were characterized using ellipsometric porosimetry with toluene and water adsorbates. In the absence of TAABr, the pore volume was 9 vol% and the pore size 1 nm. By using TAABr porogens, monomodal pore size distributions were obtained in the range of 1.2–3.5 nm. The pore volume was in the range from 18 vol% at 1.2 nm pore diameter up to 54 vol% at 3.5 nm diameter. The hydrophobicity of the pores was dependent on the pore diameter, with smaller pores being the least hydrophobic. The increase of hydrophobicity with pore size was explained by an increased distance between silanol groups on the curved pore surfaces. The mechanical properties and dielectric constant of these films were comparable to reference materials prepared using more sophisticated porogens reported in the literature.     

Synthese und Kristallstruktur von [N(Hex)4][Cu2(CN)3]

Synthesis and Crystal Structure of [N(Hex)₄] [Cu₂(CN)₃] [N(Hex)₄][Cu₂(CN)₃] has been prepared by solvothermal reaction of CuCN with Tetra‐n‐hexylammoniumiodide in acetone. The crystal structure is built up by condensed (CuCN)₆ and (CuCN)₇ rings, forming a zeolith type cyanocuprate(I) framework [Cu₂(CN)₃^—]. Space group R3; α = 44.482(6), c = 21.283(4) Å, V = 36471(9) ų; Z = 9.     

Growth of La2CuO4 nanofibers under a mild condition by using single walled carbon nanotubes as templates

La₂CuO₄ nanofibers (ca. 30 nm in diameter and 3 μm in length) have been grown in situ by using single walled carbon nanotubes (SWNTs; ca. 2 nm in inner diameter; made via cracking CH₄ over the catalyst of Mg_0.8Mo_0.05Ni_0.10Co_0.05O_x at 800 °C) as templates under mild hydrothermal conditions and a temperature around 60 °C. During synthesis, the surfactant poly(ethylene glycol)-block-poly(propylene glycol)-block-poly(ethylene glycol) and H₂O₂ were added to disperse SWNTs and oxidize the reactants, respectively. The structure of La₂CuO₄ nanofibers was confirmed by powder X-ray diffraction (XRD) and their morphologies were observed with field emission scanning electron microscope (FESEM) at the hydrothermal synthesis lasting for 5, 20 and 40 h, respectively. The La₂CuO₄ crystals grew from needle-like (5 h) through stick-like (20 h) and finally to plate-like (40 h) fibers. Twenty hours is an optimum reaction time to obtain regular crystal fibers. The La₂CuO₄ nanofibers are probably cubic rather than round and may capsulate SWNTs.     

Tuning the size of silver deposits by templated electrodeposition using agarose gels

Tuning the size of electrochemically deposited silver crystals is possible by using template layers of agarose gels of certain concentrations on platinum electrodes. The size of the silver crystals can be controlled in the range of 100 to 400 nm by choosing the appropriate agarose concentration. The obtained crystal sizes match very well with the size of the pores that have been reported in literature for the used agarose concentrations. This is also a good proof of the correctness of the earlier pore-size estimations applying other techniques.     

Fabrication of Conducting Polymer and Complementary Gold Microstructures Using Polymer Brushes as Templates

This article describes a strategy to fabricate a conducting polymer and complementary gold microstructures through selective electrodeposition and wet chemical etching on a chemically tethered polymer brush template that is prepared by surface‐initiated atomic transfer radical polymerization (ATRP) and subsequent photopatterning. The polymer brush acts as a sufficient insulating barrier and thus the polypyrrole (PPy) can be grown from the exposed area of the polymer brush template. Different polymer brushes provide different protection actions in selective etching, which is utilized to generate complementary (negative or positive) gold pattern on a single template in different manners.     

Making nanometer thick silica glass scaffolds: an experimental approach to learn about size effects in glasses

A convenient method for the synthesis of very well defined porous silica glasses using ionic liquids as templates is presented. Depending on template concentration, these systems form a homologous series of mesoporous systems with diverse shapes, with the pores having constant thickness of about 2.4 nm. These nanostructures allow the analysis of the two-dimensional behavior of glasses, either from a liquid to be embedded in the pore or of the silica glass forming the wall. For the walls, the third reduced dimension can be varied in a systematic fashion. This approach is exemplified by analyzing the static glass structure of 2D-silica by WAXS.