Fabrication of UV-Curing Linalool-Polysiloxane Hybrid Films with High Refractive Index and Transparency

In this article,a series of high refractive indices(1.50-1.53)thiol phenyl polysiloxane(TPS)were synthesized via hydrolytic sol-gel reaction.The Fourier transform infrared spectra(FT-IR)and nuclear magnetic resonance spectra(NMR)results showed that TPS conformed to the predicted structures.Natural terpene linalool was exploited as photocrosslinker to fabricate UV-curing linalool-polysiloxane hybrid films(LPH)with TPS via photoinitiated thiol-ene reaction.LPH rapidly cured under UV irradiation at the intensity of 80 mW/cm^(2) in 30 s,exhibiting good UV-curing properties.The optical transmittance of LPH in the wavelength of 300-800 nm was over 90%,exhibiting good optical transparency.The water contact angle and water vapor permeability results showed that the introduction of phenyl groups enhance the hydrophobicity and water vapor barrier properties of LPH.The results indicated the potential of LPHs in the applications of optical functional coatings.

Preparation and Characterization of Ternary Europium ComplexDoped Thin SolGel Hybrid Film by Fluorescence Spectroscopy

ＩｎｔｒｏｄｕｃｔｉｏｎＴｈｅｌｏｗ－ｔｅｍｐｅｒａｔｕｒｅｐｒｏｃｅｓｓｉｎｇｏｆｔｈｅｓｏｌ－ｇｅｌｍａｔｅｒｉａｌｍａｋｅｓｉｔｐｏｓｓｉｂｌｅｔｏｅｎｔｒａｐｏｒｇａｎｉｃｓｐｅｃｉｅｓｅａｓｉｌｙｗｉｔｈｉｎａｒｉｇｉｄｇｌａｓｓｍａｔｒｉ...

Degradation of Pollutant and Antibacterial Activity of Waterborne Polyurethane/Doped TiO_2 Nanoparticle Hybrid Films

The waterborne polyurethane/doped Ti O2 nanoparticle hybrid films were prepared. Nd, I doped Ti O2 was prepared with a 50 nm particle size firstly. The hybrid film was prepared by mixing doped Ti O2 with waterborne polyurethane, followed by heat treatment. The presence and nanometric distribution of doped Ti O2 nanoparticles in prepared membranes is evident according to SEM images. The photocatalytic activities of doped Ti O2 were signifi cantly enhanced compared with pure Ti O2 powders. After the hybrid fi lm fabrication, the photocatalytic activities were almost the same as the pure catalysts with kMB of 0.046. In the antibacterial testing, the hybrid fi lms can inhibit E. coli growth. A signifi cant decrease in membrane fl uidity and increase of permeability of E. coli were observed.

PREPARATION OF POLYIMIDE-BaTiO3 HYBRID FILMS BY A DISPERSION PROCESS AND THEIR MICROSTRUCTURE

Barium titanate (BaTiO3) powders with particle sizes of 30 similar to 50 nm were prepared from barium stearate, titanium alkoxides and stearic acid by stearic acid-gel method. Dispersing the agglomerate of BaTiO3 nanoparticles into poly(amic acid) solution followed by curing led to the formation of polyimide hybrid films. The hybrid films were transparent and well distributed with BaTiO3 nanoparticles when the BaTiO3 content was less than 1 wt%. Highly loaded hybrid film containing 30 wit % BaTiO3 was tough, had a smooth surface and possessed much higher dielectric and piezoelectric constants than the parent polyimide.

Preparation and Visible-light Photochromism of Phosphomolybdic Acid/Polyvinylpyrrolidone Hybrid Film

The visible-light photochromic hybrid film was constructed by entrapping phosphomolybdic acid（PMoA） into polyvinylpyrrolidone（PVPd） networks. The microstructure, photochromic properties and mechanism were inves- tigated with transmission electron microscopy（TEM）, atomic force microscopy（AFM）, Fourier transform infrared （FTIR） spectroscopy, ultraviolet-visible（UV-Vis） spectra and X-ray photoelectron spectroscopy（XPS）. The results in- dicate that the Keggin geometry of PMoA and the basic structure of PVPd are not destroyed during the composite process. Irradiated with visible light, the transparent PMoA/PVPd film changes color from colorless to blue and ex- hibits reversible photochromism in the presence of oxygen. According to the XPS analysis, the charge-transfer bridge of N-H-O has been built between PMoA and PVPd matrix via non-covalent bonding, and the appearance of Mo5＋ species indicates that the photo-reduction process is in accordance with the proton transfer mechanism.

Construction of all-organic low dielectric polyimide hybrids via synergistic effect between covalent organic framework and cross-linking structure

Polyimide(PI)is a promising electronic packaging material,but it remains challenging to obtain an all-organic PI hybrid film with decreased dielectric constant and loss without modifying the monomer.Herein,a series of allorganic PI hybrid films were successfully prepared by introducing the covalent organic framework(COF),which could induce the formation of the cross-linking structure in the PI matrix.Due to the synergistic effects of the COF fillers and the cross-linking structure,the PI/COF hybrid film containing 2 wt%COF exhibited the lowest dielectric constant of 2.72 and the lowest dielectric loss(tanδ)of 0.0077 at 1 MHz.It is attributed to the intrinsic low dielectric constant of COF and a large number of mesopores within the PI.Besides,the cross-linking network of PI prevents the molecular chains from stacking and improves the fraction of free volume(FFV).The molecular dynamics simulation results are well consistent with the dielectric properties data.Furthermore,the PI/COF hybrid film with 5 wt%COF showed a significant enhancement in breakdown strength,which increased to 412.8 kV/mm as compared with pure PI.In addition,the PI/COF hybrid film achieve to reduce the dielectric constant and thermal expansion coefficient(CTE).It also exhibited excellent thermal,hydrophobicity,and mechanical performance.The all-organic PI/COF hybrid films have great commercial potential as next-generation electronic packaging materials.

Transparent and conductive PEDOT:PSS/Ag NW/PEDOT:PSS hybrid films prepared by spin-coating at room temperature

PEDOT：PSS/Ag NW/PEDOT：PSS hybrid films were deposited on PET substrates by the spin coating technique at room temperature. The optical transmittance, sheet resistance, crystallization and surface morphology were characterized by using the double beam spectrophotometer, Hall effect system, X-ray diffractometer and field emission scanning electron microscopy. XRD patterns of the hybrid films display characteristic diffraction peaks of Ag （111） and Ag （200）, and the Ag NW networks have a polycrystalline structure with a Ag （111） preferred orientation. A high transmittance of 83.95% at the 550 nm wavelength and a low sheet resistance of 21.98 Ω/□ are achieved for 3-PEDOT：PS S/5-Ag NW/3-PEDOT： PS S hybrid films.

A Simple Approach to the Fabrication of Graphene-Carbon Nanotube Hybrid Films on Copper Substrate by Chemical Vapor Deposition

In this study,graphene-carbon nanotube（CNT） hybrid films were directly synthesized on polycrystalline copper（Cu） substrates by thermal chemical vapor deposition（CVD） method.Graphene films were synthesized on Cu substrate at 1000 ℃ in mixture of gases:argon（Ar）,hydrogen（H2）,and methane（CH4）.Then,carbon nanotubes（CNTs） were grown uniformly on the surface of graphene/Cu films at 750 ℃ in mixture of Ar,H2.and acetylene（C2H2） gases.Ferric salt FeCl3solution deposited onto the surface of graphene/Cu substrate by spin coating method was used as precursor for the growth of the CNTs.The density and quality of the CNTs on the surface of graphene/Cu films can be controlled by varying the concentration of FeCl3salt catalyst.

Sol-gel-derived Hybrid Conductive Films for Electromagnetic Interference (EMI) Shielding

The conductive nano-sized zinc particles were embedded in an insulating amorphous silica matrix,and the hybrid films were obtained by a sol-gel method.The stable hybrid sol solution was prepared by hydrolysis and condensation of Methyltrimethoxysilane （MTMS） with a one-step acidic catalyst process.Hybrid films were dip-coated on silicon wafer and cured at 120℃ for 60minutes.The structural characterization of hybrid films were investigated by means of attenuated total reflection infrared （ATR-IR） spectroscopy and X-ray diffraction （XRD）.The electrical properties of the films were examined with four-point probe.Hybrid films showed to be relatively dense,uniform and defect free.The conductivity of hybrid films was varied with the different contents of zinc nanoparticles and the thickness of the film.It was observed that there was the percolation threshold for the film＇s electrical properties.

Photoelectrocatalytic oxidation of GMP on an ITO electrode modified with clay/[Ru(phen)_2(dC18bpy)]^(2+) hybrid film

An indium tin oxide (ITO) electrode modified with monolayer clay/[Ru(phen)2(dC18bpy)]2+ (phen= 1,10-phenanthroline, dC18bpy = 4,4′-dioctadecyl-2,2′ bipyridyl) hybrid film has been fabricated by the Langmuir-Blodgett (LB) method. Atomic force microscopy revealed that the single-layered hybrid film of clay/[Ru(phen)2(dC18bpy)]2+ (denoted as Clay-Ru) was closely packed at a surface pressure of 25 mN-m-1 and had a thickness of 3.4±0.5 nm. Cyclic voltammograms showed that the redox current of Ru(Ⅱ) complex decreased when incorporated into the clay film, suggesting that the clay layer acts as a barrier against electron transfer. When applied to oxidizing the mononucleotide of guanosine 5′-monophosphate (GMP), a large catalytic oxidative current was achieved on the Clay-Ru(Ⅱ) modified ITO electrode at the external potential above 900 mV (vs. Ag|AgCl|KCl ) and, more significantly, this response was further enhanced by light irradiation (λ>360 nm), in which the photocurrent is increased about 11 times in comparison with that of a bare ITO. Mechanism of the photoelectrocatalytic effect was proposed in terms of the reduction of the photoelectrochemically generated Ru(Ⅲ) complex in the Clay-Ru film by GMP.

Hybrid Self-Assembled Multilayer Films Formed by Alternating Layers of Keggin Polyoxometalates and 1,10DAD

Hybrid self-assembled multilayer films were prepared by alternate adsorption of 1,10-diaminodecane (1,10-DAD) and Keggin polyoxometalates of SiW12O404-, SiW11VO405-, and PMo12O403-, respectively. The films were reproducibly grown at each adsorption cycle as monitored by UV spectroscopy.

Hybrid Luminescent Films Obtained by Covalent Anchoring Terbium Complex to Silica-based Network

New monomer N-(4-carboxyphenyl)-NL-(propyltriethoxysilyl)urea (1) which acts as both a ligand for Tb3+ ion and a sol-gel precursor has been synthesized and characterized by 1H NMR, and MS. Hybrid luminescent thin films consisting of organoterbium covalently bonded to a silica-based network have been obtained in situ via a sol-gel approach. Strong line emission of Tb3+ ion was observed from the hybrid luminescent films under UV excitation.

Monte Carlo simulations of biaxial structure in thin hybrid nematic film based upon spatially anisotropic pair potential

Hybrid nematic films have been studied by Monte Carlo simulations using a lattice spin model, in which the pair potential is spatially anisotropic and dependent on elastic constants of liquid crystals. We confirm in the thin hybrid nematic film the existence of a biaxially nonbent structure and the structure transition from the biaxial to the bent-director structure, which is similar to the result obtained using the Lebwoh-Lasher model. However, the step-like director＇s profile, characteristic for the biaxial structure, is spatially asymmetric in the film because the pair potential leads to K1 ≠ K3. We estimate the upper cell thickness to be 69 spin layers, in which the biaxial structure can be found.

Fabrication of Microporous Film and Microspheres Hybrids

Hybrids consisting of a microporous film and polymeric microspheres were fabricated via a simple method without a special apparatus. Highly ordered microporous polymer films with honeycomb structure were fabricated by a dissipative process utilizing amphiphilic poly(acrylic acid)- block-polystyrene, which was synthesized by atom transfer radical polymerization followed by an acid-catalyzed ester cleavage reaction. In order to embed the microsphere efficiently, the dried microporous films should be soaked in methanol to alter the surface functionality and to improve the wettability of the film surface. The introduction of amino functionality to polystyrene microspheres by seeded polymerization of N,N-dimethylaminoethyl methacrylate drastically improved the embedding efficiency. The effect of open pore size was also investigated.

Electrocatalytic oxidation of GMP on an ITO electrode modified by the photodeposition of Pd nanoparticles onto a monolayer TiO_2 nanosheets/[Ru(phen)_2(dC18bpy)]^(2+) hybrid film

An indium tin oxide(ITO)electrode coated with monolayer TiO2/[Ru(phen)2(dC18bpy)] 2+ (phen=1,10-phenanthroline, dC18bpy=4,4′-dioctadecyl-2,2′-bipyridyl)hybrid film(denoted as ITO/TiO2-Ru)has been prepared using the modified Langmuir-Blodgett(LB)method,and the electrocatalytic oxidation of mononucleotide of guanosine 5′-monophosphate(GMP)on an ITO/TiO2-Ru electrode after Pd-photodeposition(denoted as ITO/TiO2-Ru/Pd)has been studied.Atomic force microscopy reveals that the single-layered hybrid film of TiO2 nanosheets/[Ru(phen)2(dC18bpy)] 2+is closely packed at a surface pressure of 25 mN m 1and has a thickness of(3.20±0.5)nm.X-ray photoelectron spectra show the formation of Pd nanoparticles on the surface of hybrid film with radii of 20–200 nm by the reduction of[Pd(NH3)4] 2+ under light irradiation.When it is applied to oxidize GMP,a larger catalytic oxidative current is achieved on the ITO/TiO2-Ru/Pd electrode at the external potential above 700 mV(vs.Ag|AgCl|KCl)in comparison with the naked ITO electrode and ITO/TiO2-Ru electrode.Such a result indicates that the Pd nanoparticles are able to hamper the combination of electron hole pairs and reduce the counterwork of insulating long alkyl chains of amphiphilic Ru(II)complexes,and thus develops the electron transfer efficiency and produces the enhanced redox current.

Organic-inorganic Hybrids Towards the Preparation of Nanoporous Composite Thin Films for Microelectronic Application

Silicon containing materials have traditionally been used in microelectronic fabrication. Semiconductor devices often have one or more arrays of patterned interconnect levels that serve to electrically couple the individual circuit elements forming an integrated circuit. These interconnect levels are typically separated by an insulating or dielectric film. Previously, a silicon oxide film was the most commonly used material for such dielectric films having dielectric constants( k ) near 4 0. However, as the feature size is continuously scaling down, the relatively high k of such silicon oxide films became inadequate to provide efficient electrical insulation. As such, there has been an increasing market demand for materials with even lower dielectric constant for Interlayer Dielectric(ILD) applications, yet retaining thermal and mechanical integrity. We wish to report here our investigations on the preparation of ultra low k ILD materials using a sacrificial approach whereby organic groups are burnt out to generate low k porous ORMOSIL films. We have been able to prepare a variety of organically modified silicone resins leading to highly microporous thin films, exhibiting ultra low k from 1 80 to 2 87, and good to high modulus, 1 5 to 5 5 GPa. Structure property influences on porosity, dielectric constant and modulus will be discussed.

Deterioration Process of the Hybrid Films during Wear Test--Polyacrylate Emulsion Modified by Silica Particles

The hybrid materials are widely used in various fields for excellent performance. However, there are few researches studying their failure process. In order to prepare the hybrid materials with better performance, the failure process needs to be well studied. Two kinds of silica/polyacrylate films are successfully prepared to study the effect of organic-inorganic interaction on performance. The average diameter of silica particles is measured to be around 342 nm by scanning electron microscope（SEM）. Wear test demonstrates the hybrid film, which is obtained by grafting polyacrylate onto silica particles, possesses more excellent properties than the one filled directly with silica particles. The stronger interaction between organic and inorganic components leads to a better distribution of inorganic particles within the polymer matrix. In this work, a model is presented to illustrate the deterioration process of the hybrid films, which allows us to further understand the hybrid materials.

Preparation and Optical Patterning of Organic-Inorganic Hybrid Color-Filter Films Using Latent Pigments by Utilizing Photo-Acid-Generator and Microwave Irradiation

Preparation and photo-patterning characteristics of organic-inorganic hybrid thin film containing latent pigment by using photo-acid-generator (PAG) and microwave irradiation have been investigated. The acrylic thin film modified with methoxysilane containing PAG was formed on a glass substrate and irradiated with ultraviolet rays to promote sol-gel reaction by catalytic action of acid which was generated from PAG. And then the film was hardened with microwave irradiation, yielding organic-inorganic hybrid polymer film having hardness, highly transparency and strong adhesion with a glass substrate. Since this reaction only occurred in the optically (UV) irradiated regions, by exploiting the difference between the adhesivenesses of these regions photo-irradiated through photomask with a glass substrate, it was possible to form a patterned film with pitch of 100 to 50 μm by a simple lift-off method. A pigment-containing film using latent pigments (with subtractive three primary colors of coloring materials) and a patterned film were prepared, and it was possible to make these films multi-colored by varying the mixing ratio of the pigments. This multi-colored film-preparation method is effective for simply and efficiently forming a color-filter film by applying optical and microwave irradiation.

Tribological Behavior of Binary B-C Films Deposited by Sputtering-PBII Hybrid System

In this article, the authors report on the use of Radio Frequency (RF) Magnetron Sputtering combined with Plasma-Based Ion Implantation (PBII) technique to synthesize the Boron-Carbon (B-C) films. High purity of boron carbide (99.5%) disk was used as a target with an RF power of 300 W. The mixtures of Argon (Ar)-Methane (CH4) ware used as reactive gas under varying CH4 partial flow pressure at the specified range of 0 - 0.15 Pa and fixed total gas pressure and total gas flow at 0.30 Pa and 30 sccm, respectively. The effect of CH4 flow ratio on the friction coefficient of B-C films was studied. The friction coefficient of the film depended on the concentration of B. When it was 10% or lower, the coefficient decreased to 0.2 or lower. In this concentration range of B, the specific wear rate also decreased to the order of 10-7 mm3/Nm, and excellent wear resistance was displayed.

Intercalating Ultrathin MoO_3 Nanobelts into MXene Film with Ultrahigh Volumetric Capacitance and Excellent Deformation for High-Energy-Density Devices

The restacking hindrance of MXene films restricts their development for high volumetric energy density of flexible supercapacitors toward applications in miniature,portable,wearable or implantable electronic devices.A valid solution is construction of rational heterojunction to achieve a synergistic property enhancement.The introduction of spacers such as graphene,CNTs,cellulose and the like demonstrates limited enhancement in rate capability.The combination of currently reported pseudocapacitive materials and MXene tends to express the potential capacitance of pseudocapacitive materials rather than MXene,leading to low volumetric capacitance.Therefore,it is necessary to exploit more ideal candidate materials to couple with MXene for fully expressing both potentials.Herein,for the first time,high electrochemically active materials of ultrathin MoO3 nanobelts are intercalated into MXene films.In the composites,MoO3 nanobelts not only act as pillaring components to prevent restacking of MXene nanosheets for fully expressing the MXene pseudocapacitance in acidic environment but also provide considerable pseudocapacitive contribution.As a result,the optimal M/MoO3 electrode not only achieves a breakthrough in volumetric capacitance(1817 F cm-3 and 545 F g-1),but also maintains good rate capability and excellent flexibility.Moreover,the corresponding symmetric supercapacitor likewise shows a remarkable energy density of 44.6 Wh L-1(13.4 Wh kg-1),rendering the flexible electrode a promising candidate for application in high-energy-density energy storage devices.