Synthesis and Optical Properties of Films Formed by the Sol‐Gel Method in Mesoporous Matrices

The main laws governing the formation of films by the solgel method in the mesopores of anodic aluminum oxide, porous silicon, and synthetic opals have been considered. Investigations of the luminescence at 1.5 m in the structure porous silicon–gel, doped with erbium, have been analyzed. Special features of the synthesis of the film structure microporous xerogel–mesoporous anodic aluminum oxide, doped with erbium, terbium, and europium, and the possible factors that enhance the photoluminescence of lanthanides in the structure are shown.     

Characterization of Mn—Doped Ba1—xSrxTiO3 Thin Films Prepared by the Sol—Gel Method

Undoped and Mn-doped Ba1-xSrxTiO3(BST) thin films have been fabricated on Pt/Ti/SiO2/Si by an aqueous acetate sol-gel method.The BST stock solution can be easily mixed with an aqueous metal ion solution and is stable at room temperature.The annealing temperature of the doped and undoped films is between 650-750℃.The x-ray photoelectron spectra results show that the Mn2p3/2 valence state in the BST is the sampe as that of the original Mn(Ⅱ） dopant,The dielectric constant of the BST thin films can be increased to 800,and the loss tangent can be decreased to 0.01 due to the Mn(Ⅱ） doping.The leakage current of the BST films can also be greatly reduced.     

Synthesis and Characterization of New Organic–Inorganic Hybrid Nanosilica Fillers Prepared by Sol–Gel Reaction

In light of the success of making multicomponent sol–gel glasses, in this study the synthesis of new hybrid nanosilicas with controlled hydrophilic/hydrophobic properties was carried out by incorporating organic based species with appropriate functional groups to inorganic based alkoxides by co-condensation reaction. Furthermore, in this study the acidity and the water content during reaction synthesis was proven to be critical in controlling the structure of the hybrid nanosilicas. These nanosilicas with different hydrophobicity were obtained by using TEOS (tetraethylorthosilicate) and 10 wt% two organic modifiers (tris-hydroxymethylaminomethane — TRIS — and 1,1,1,3,3,3-hexamethyldisilazane-HDMS). The average diameter of the nano-particles ranged between 7 and 10 nm. The addition of the organic modifiers changed the pH of the hybrid nanosilicas, to a different extent depending on the nature of the organic modifier. The hydrophobicity in the hybrid nanosilicas estimated from pH measurements in water and ethanol, and from IR spectroscopy, can be tailored by incorporating different organic modifiers on the network during synthesis. Finally, the measurement of pH of the hybrid nanosilicas by using solvents with different polarity/acidity was a simple and efficient method of assessing the hydrophobicity of the nanosilicas.     

Holographic Recording Media Based on Poly‐N‐Epoxypropylcarbazole Films Doped with Organic Dyes

A comparative analysis of the recording media based on polyNepoxypropylcarbazole films doped with cationic, anionic, and intraionic organic dyes has been carried out for the purposes of holographic interferometry. It is shown that in the case of application of intraionic dyes recording media have satisfactory information characteristics. The use of anionic and cationic dyes does not give a positive result because of the absence of the photoconductivity effect in the anionic dyes and of the high electrical conductivity of the films on increase of the temperature of the cationic dyes. The effect of longterm storage of a latent image in the films with intraionic dyes makes it possible to use them for recording holograms with several exposures.     

Luminophors Based on the Phosphate Compounds of Uranyl With Rare‐Earth Elements at a High Concentration of Active Ions (Review)

A review of the works concerned with investigation of the spectroscopic and kinetic properties of the emission of luminescent materials based on phosphate compounds of uranyl with rareearth elements is presented. The characteristic features of electron excitation energy transfer from UO₂ ²⁺ to Ln³⁺ at an abnormally high (from the viewpoint of concentration quenching) concentration of active ions in phosphate matrices are considered.     

Optical Properties of SiO2 Films Obtained by the Sol‐Gel Method in the Presence of Modifiers of Different Nature

The degrees of hydrolysis of tetraethoxysilane (TEOS) in filmforming compositions containing hydrolysis catalysts and modifiers of different nature have been determined. The TEOS hydrolysis depth has been estimated by the IR spectroscopic method. It is shown that the optical absorption of films depends on the amount of the immobilized indicator and the initial conditions for film formation.     

Quasi-Hexagonal Ordered Arrays of FePt Nanoparticles Prepared by a Micellar Method

Hexagonally ordered arrays of magnetic FePt nanoparticles on Si substrates are prepared by a self assembly of diblock copolymer PS-b-P2VP in toluene, a dip coating process and finally plasma treatment. The as-treated FePt nanoparticles are covered by an oxide layer that can be removed by a 40 s Ar＋ sputtering. The effects of the sequence of adding salts on the composition distribution are revealed by x-ray photoelectron spectroscopy measurements. No particle agglomeration is observed after 600℃annealing for the present ordered array of FePt nanoparticles, which exhibits advantages in patterning FePt nanoparticles by a micellar method. Moreover, magnetic properties of the annealed FePt nanoparticles at room temperature are investigated by a vibrating sample magnetometer.     

Influence of Thermal Annealing and Deposition Conditions on the Structure and Optical Properties of GRS‐Active Substrates Based on Silver Films

Using the methods of atomicforce microscopy, xray diffractometry, and spectrophotometry, we have studied the morphological, structural, and optical characteristics of GRSactive substrates based on original and annealed silver films. We show that the backing temperature during deposition is the factor which exerts the most substantial effect on the morphological and optical properties of silver films and also on their stability with time. The coefficients of the correlation of the deposition rate with the characteristics of the optical density spectra of silver films are calculated. It is found that hightemperature (350°C) annealing of a silver film leads to the selforganization of its surface into a quasiperiodic structure with semiellipsoidal islets. The contribution of the processes of excitation of plasma resonances to the formation of the optical density spectra is discussed. It is shown that as a result of thermal modification the concentration of the crystalline phase of silver in a silver film increases 2–3 times and also the dispersion of the orientation of crystallites decreases.     

Optical Properties of Multilayer BaTiO3/SiO2 Film Structures Formed by the Sol–Gel Method

Physics of the Solid State - Multi-layer film structures BaTiO3/SiO2 with a thickness of ~1 μm containing up to 14 pairs of layers were synthesized by the sol–gel method with sequential...     

The Influence of Thermal Treatment on the Formation Mechanism of the Cu,Fe-Containing Nanocomposite Material Synthesized by the Sol–Gel Method

Physics of the Solid State - The nanocomposite samples, containing copper and iron species in the silica matrix, were prepared by annealing at temperatures up to 1100°C. The samples were...     

Magnetic Properties and Magnetoresistance of CdMnS：Au Based Structures Prepared by Co-evaporation

Polycrystalline CdMnS and CdMnS：Au films with hexagonal structure on Si（111） substrates are prepared by co-evaporation, and exhibit ferroelectric and ferromagnetic properties, respectively. Under optimized growth conditions, CdMnS：Au samples with an average crystallite size of 90nm and Mn concentration of 5.0at.% are obtained, and an all-semiconductor spin valve device of Co/Au/CdMnS：Au/CdMnS/Pt is fabricated. Electrical measurement of the device reveals the clear dependence of resistance on applied magnetic field, with a relative magnetoresistance of 0.06% and a switching field of 100 Oe at 77K.     

Comment on “Quantum Key Distribution and Quantum Authentication Based on Entangled State”

Shi et al. (Phys. Lett. A 281:83–87, 2001) proposed a scheme which allows simultaneous realization of quantum key distribution and quantum authentication. However, this study points out a weakness in Shi et al.’s scheme, in which a malicious user can impersonate a legitimate participant without being detected. Furthermore, an improved scheme is proposed to avoid this weakness.     

Influences of Branched Side Chains and Cross‐linking Network on the Solid State Structures of Oligo‐ and Poly (p‐phenyleneethynylene)s

To investigate the influences of side chains and cross‐linking network on the packing fashion and the formation of aggregates and excimers of poly(p‐phenyleneethynylene)s (PPEs) chains in the solid state, a series of cross‐linkable unsubstituted oligo (p‐phenyleneethynylene)s (OPEVs) and alkoxy‐substituted PPEs (EO‐PPEVs) with vinyl end‐groups were synthesized and characterized. By a thermal cross‐linking reaction, cross‐linked polymers were obtained. The oligomer chains in the cross‐linked polymers containing no residual vinyls are packed randomly, forming no aggregates or excimers; however, aggregates and excimers exist in the cross‐linked polymers if they contain residual vinyls. The chains of EO‐PPEVs with sterically hindered side chains form aggregates in films. The network, leading to a pronounced increase of the film photoluminescence quantum yields, can depress these aggregates. These EO‐PPEVs are fully processable and can become insoluble in normal organic solvents after thermal curing; therefore, they are favorable candidates as active layers for fabrication of high performance multilayer devices.     

The Preparation and Study on Ultrahigh Molecular Weight Polypropylene Gel‐spun Fibers

A novel polypropylene (PP) fiber was prepared by using gel spinning/crystallization from dilute solutions of ultrahigh molecular weight isotactic polypropylene (i‐UHMWPP), and subsequently drawing at various temperatures. The influence of drawing temperature on the properties of the resulted fibers was investigated. We found that the draw‐ability and mechanical as well as crystallization properties of the fibers obtained were dramatically improved with increasing drawing temperature. When the drawing temperature is below the α‐crystal relaxation temperature of PP, which was measured by wide‐angle X‐ray diffraction (WAXD) analysis as 100–120°C, the fibers are characterized by lower crystallinity and smaller crystals with less perfection, resulting in brittle fracture and subsequently poor mechanical durability. With drawing at temperatures above the α‐crystal relaxation temperature of PP, a novel UHMWPP fiber with Young's modulus of 27 GPa and tensile strength of 1.3 GPa was obtained. Higher crystallinity and larger crystals with better perfection and orientation were observed in this fiber.     

The Effect of Crystallization on the Solid State Polycondensation of Poly(L‐lactic Acid)

Melt solid polycondensation is an approach to increase the molecular weight of poly (L‐lactic acid) (PLLA). For this report, the effect of crystallization time of PLLA prepolymer on the molecular weight of the biomaterial was studied. In this process, PLLA prepolymer with a molecular weight of 18,000 was first prepared by the ordinary melt‐polycondensation process. The prepolymer was crystallized at 105°C for various times, and then heated at 135°C for 15–50 h for further solid state polycondensation (SSP). The differential scanning calorimetry (DSC) and viscosity measurements were used to characterize the crystalline properties and molecular weight of the resulting PLLA polymers, respectively. The results showed that the molecular weight of PLLA reached a maximum value under the condition of a crystallization time of 30 min and SSP of 35 h.     

Investigation of the Melt‐Crystallization of Polypropylene by a Temperature Slope Method

Abstract

To investigate the in‐situ ordering process of isotactic polypropylene (iPP) from a melt state, a stationary growth front was prepared by the temperature slope crystallization (TSC) method. During the melt‐crystallization, iPP was crystallized into the α‐phase or β‐phase depending on the crystallizing conditions. The mechanism of the melt‐crystallization at the growth front was precisely observed by wide‐angle and small‐angle x‐ray scattering (WAXS and SAXS) using a strong synchrotron beam. In the TSC apparatus, the sample was crystallized in between a heater, controlled to 220°C, and a cooler, cooled by water to 25°C. We define the z‐axis parallel to the temperature gradient. A‐lamellae and B‐lamellae are also defined as those whose lamellar normal are perpendicular and parallel to the z‐axis, respectively. In a sample‐stop (SS) stage before the TSC, the original α‐phase lamellae became thicker, approaching to the melt‐solid boundary by annealing. The annealing process showed that the α‐phase B‐lamellae remained and the SAXS reflection was stronger on the meridian near the melt‐solid boundary in the SS stage. In the beginning of the TSC, the α‐phase B‐lamellae developed as a primary crystallization. During secondary crystallization under high supercooling, the SAXS cross pattern appeared showing that the α‐phase developed both A‐ and B‐lamellae. As the growth direction of A‐lamellae is parallel to the z‐axis, A‐lamellae grow faster than B‐lamellae. By the self‐epitaxial mechanism on the side surface of the A‐lamellae, the B‐lamellae grow on the base of the A‐lamellae. Following appearance of a spontaneous β‐nucleus, the β‐phase lamellae grew preferentially, excluding the α‐phase, and occupied the whole area of the sample. In this case also, A‐lamellae are advantageous to grow because of the growth direction parallel to the z‐axis. As a result, the SAXS β‐phase reflection appeared on the equator.