Electrophysical properties of Si/SiO<Subscript>2</Subscript> nanostructures fabricated by direct bonding

The results of experimental investigation of diode n ⁺⁺–p ⁺⁺-Si structures, which were fabricated by direct bonding and have tunneling-thin SiO₂ with Si nanoclusters embedded into the interface, are presented. The memristive effect with bipolar switching is demonstrated. The introduction of Si nanoclusters into the dielectric reduces the randomness of formation of a conducting channel. Intermediate metastable states are observed in the current–voltage characteristics. This may prove to be important for multibit data storage.     

SiO<Subscript>2</Subscript>/TiO<Subscript>2</Subscript> fibers from titanium-modified polycarbosilane

We developed a process for preparing SiO₂/TiO₂ fibers by means of precursor transformation method. After mixing PCS and titanium alkoxide, continuous SiO₂/TiO₂ fibers were fabricated by the thermal decomposition of titanium-modified PCS (PTC) precursor. The tensile strength and diameter of SiO₂/TiO₂ fibers are 2.0 GPa, 13 μm, respectively. Based on X-ray diffraction (XRD), scanning electron microscopy (SEM), and high resolution transmission electron microscopy (HRTEM) measurements, the microstructure of the SiO₂/TiO₂ fibers is described as anatase–TiO₂ nanocrystallites with the mean size of ~10 nm embedded in an amorphous silica continuous phase.     

Ultra-long SiO<Subscript>2</Subscript> and SiO<Subscript>2</Subscript>/TiO<Subscript>2</Subscript> tubes embedded with Pt nanoparticles using magnus green salt as templating structures

For the first time, magnus green salt (MGS, [Pt(NH₃)₄][PtCl₄]) fibers precipitated by solvent modification have been employed as a structure-directing modifier to synthesize single silica and silica/titania microtubes via a sol–gel process. In the case of titania tubes, tetraethylorthosilicate must be used as a capping agent to hinder the aggregation of primary MGS fibers and to serve as a protective layer against thermal stress during the metal salt fiber reduction. This implies that SiO₂/TiO₂ tubes result. The synthesized tubular materials were imaged by scanning and transmission electron microscopy, while their composition was determined by energy dispersive X-ray analysis and thermogravimetric analysis. Crystallinity and thermal stability of the tube walls were studied using X-ray diffraction analysis. The obtained oxide tubes possess high aspect ratios (80–200) because they are up to 60 μm in length, but only 300–700 nm in thickness. The key aspects of the synthesis approach are that the templating MGS fibers control the internal diameter of the oxide tubes, while the synthesis conditions control their wall thickness. The suggested method is a simple approach which produces, at low temperatures, very long oxide tubes with a very high amount of Pt (48–51 wt%) directly incorporated inside the tubes. To the best of our knowledge, filling of SiO₂ or SiO₂/TiO₂ nanotubes with such a dense population of Pt metal nanoparticles has not been demonstrated so far; our own experiments with [Pt(NH₃)₄](HCO₃)₂ as templating salt formed only tubes containing about 40 wt% Pt and were only about 20 μm long. The now formed more Pt-rich tubes are expected to have vivid applications in (photo)catalysis and in fabricating novel devices, such as nano- or sub-microcables.     

Fabrication and properties of SiO<Subscript>2</Subscript>/TiO<Subscript>2</Subscript> composites

Composites in the form of precipitated powders, hybrid xerogels, and SiO₂ core/TiO₂ shell particles have been produced via hydrolysis of precursors (alkoxides and inorganic derivatives of titanium and silicon) and have been characterized by differential thermal analysis, X-ray diffraction, adsorption measurements, and macroelectrophoresis. The results demonstrate that heat treatment of the composites leads to crystallization of the titanium-containing component and, accordingly, reduces their specific surface area. Hydrothermal treatment enables the fabrication of materials in which TiO₂ nanocrystals are evenly distributed over an amorphous SiO₂ matrix.     

Wear and mechanical properties of epoxy/SiO<Subscript>2</Subscript>-TiO<Subscript>2</Subscript> composites

Preparation of epoxy/SiO₂-TiO₂ composites is investigated in this paper. The products are characterized by FT-IR spectroscopy. Results of FT-IR spectroscopy and atom force microscope (AFM) demonstrated that epoxy chains have been covalently bonded to the surface of the SiO₂-TiO₂ particles. The particles sized of SiO₂-TiO₂ are about 20–50 nm, which characterized by AFM. The properties of composites such as impact strength, flexural strength, tensile strength and ring-on-block wear are also investigated. Dry sliding wear tests showed that the SiO₂-TiO₂ particles could improve the wear resistance of the epoxy matrix even though the content of the SiO₂-TiO₂ particles was at a relatively low level (1.95–2.65 wt%). This makes it possible to develop novel type of epoxy-based materials with improved wear resistance for various applications. The worn surface was observed by scanning electron microscopy (SEM), and mechanisms for the improvement are discussed in this paper     

Influence of C<Subscript>4</Subscript>F<Subscript>8</Subscript>/Ar/O<Subscript>2</Subscript> plasma etching on SiO<Subscript>2</Subscript> surface chemistry

The plasma assisted etching of SiO₂ in a commercial RF reactor with a variety of C₄F₈/Ar/O₂ chemistries has been studied by XPS, SIMS and FTIR. A simple model of surface reactions is proposed. In particular, the role of oxygen in the etch process has been investigated. According to our experiments, oxygen inhibits the formation of CFH based polymeric films on the surface. As the etching process is due to an exchange reaction between the oxygen in the SiO₂ and the gaseous fluorine species in the plasma, the presence of oxygen in the etch hinders this process by occupying adsorption sites on the surface. The results would confirm that argon does not participate in chemical reactions with the SiO₂ substrate but provides energy for reactions in which F, C and O are involved. The results also indicate that a thick fluorocarbon layer only forms on the surface in the absence of oxygen, regardless of the oxygen source. Consequently, only when the SiO₂ layer has been substantially removed does this film form.     

Preparation of La<Subscript>2</Subscript>NiMnO<Subscript>6</Subscript> thin films on Pt/TiO<Subscript>2</Subscript>/SiO<Subscript>2</Subscript>/Si substrates by pulsed laser deposition

Double perovskite La₂NiMnO₆ thin films were prepared on Pt/TiO₂/SiO₂/Si substrates by the pulsed laser deposition process, and the crystal structure and microstructures were investigated. The temperature and the oxygen pressure played the primary roles dominating the crystallization behavior and the morphology of La₂NiMnO₆ thin films. The well crystallized La₂NiMnO₆ thin films could be obtained at 873 and 923 K under all oxygen pressures investigated here, and the fine morphology was obtained under the oxygen pressures equal to or higher than 50 and 100 Pa, respectively, while phase constitution was significantly affected by the oxygen pressure for La₂NiMnO₆ thin films prepared at 1,023 K where the higher oxygen pressure led to the appearance of some secondary phase.     

Antireflecting coating from Ta<Subscript>2</Subscript>O<Subscript>5</Subscript> and SiO<Subscript>2</Subscript> multilayer films

Sol-gel method is important for depositing antireflective coating that allows control over thickness as well as the index of refraction. Antireflective coatings which are produced from Ta₂O₅ and SiO₂ multi-layer thin films using sol-gel spin coating method are presented. The refractive index and the thickness are controlled by the composition and the concentration of the solution respectively. The thickness, refractive index and extinction coefficient of the films were calculated through transmission and reflection measurement by an NKD analyser. Mechanical properties of the films were checked by the cross tape test and dry sun test at 760 W/m². The result shows that the sample heat treated at 450^∘C for 15 min approaches a reflectance with less than 0.5% at around 840 nm.     

Synthesis and characterization of nanoporous SiO<Subscript>2</Subscript>/pHEMA biocomposites

Porous SiO(2)/pHEMA biocomposites were synthesized in situ by incorporating silica nanoparticles with a hydroxyethyl methacrylate (HEMA) monomer, following a UV-induced photopolymerization. The nanostructure of the composites was characterized and the resulting physical properties were examined. The release kinetics of the model molecule-vitamin B12-and the hemocompatibility of the porous SiO(2)/pHEMA composites were investigated. Heterogeneous reaction kinetics is proposed to be the formation mechanism of the nanoporosity in the pHEMA matrix as a result of incorporating silica nanoparticles following photopolymerization. Experimental results also demonstrated that the incorporation of the silica nanoparticles into the pHEMA matrix not only enhanced the mechanical property but also maintained a good hemocompatibility of the resulting biocomposites. In addition, it was observed that the drug release profile of the composites (in the form of a membrane) can be precisely regulated from a two-stage pattern to one-stage pattern by varying the concentration of both the SiO(2) nanoparticles and HEMA monomer during synthesis. The permeability of the model drug was enhanced by two orders of magnitude from 4.22 x 10(-7 )cm(2)/h to 3.92 x 10(-5 )cm(2)/h by controlling the micro-to-nanostructure of the composites. The platelet adhesion experiment demonstrated low aggregation of the platelets on the surface of the biocomposite membranes, indicating a promising antithrombotic property.     

Antireflective coatings based on SiO<Subscript>2</Subscript> nanoparticles

Single-layer antireflective coatings, produced by sol-gel method on soda-lime glass substrates, were studied. Optimal parameters of the silica sols synthesis and coating procedure of the antireflective coatings based on SiO₂ nanoparticles on soda-lime glasses for producing composite glasses with high optical transmittance within the visible range of wavelengths were obtained.     

Sorption of U(VI) onto TiO<Subscript>2</Subscript>/ZrO<Subscript>2</Subscript>/SiO<Subscript>2</Subscript> Mesoporous Materials from Sulfate Solutions

New nanostructured mesoporous materials of the composition TiO₂/ZrO₂/SiO₂ were prepared by the template sol–gel method using a siloxane–acrylate emulsion as a template. The morphology and structure of these materials and their ability to take up U(VI) were studied. The influence of various factors (ZrO₂ content, pH of solution) on the sorption properties was studied. The suggested materials allow efficient sorption of U(VI) from sulfate solutions with low U(VI) concentrations and can be used in final purification processes.     

Excimer laser crystallization of InGaZnO<Subscript>4</Subscript> on SiO<Subscript>2</Subscript> substrate

In this paper, we were able to crystallize InGaZnO₄ (IGZO) by excimer laser on SiO₂ substrate. It was observed that uniform [0001] textured polycrystalline IGZO film has been obtained without any grain boundaries and oxygen vacancies on SiO₂ substrate. This process is very promising in fabricating high quality IGZO thin film transistors (TFT) at low temperature without seed substrate.     

Memory characteristics of Al<Subscript>2</Subscript>O<Subscript>3</Subscript>/LaAlO<Subscript>3</Subscript>/SiO<Subscript>2</Subscript> multilayer structures with tunnel oxide thickness variation

Charge trap flash (CTF) memory devices are candidates to replace NAND flash devices. In this study, Pt/Al₂O₃/LaAlO₃/SiO₂/Si multilayer structures with lanthanum aluminate charge traps were fabricated for nonvolatile memory device applications. An aluminum oxide film was used as a blocking oxide for low power consumption in the program/erase operation and to minimize charge transport through the blocking oxide layer. The thickness of SiO₂ as tunnel oxide layer was varied from 30 to 50 Å. Thicknesses of oxide layers were confirmed by high resolution transmission electron microscopy (HRTEM) and all the samples showed amorphous structure. From the C–V measurement, a maximum memory window of 3.4 V was observed when tunnel oxide thickness was 40 Å. In the cycling test for reliability, the 30 Å tunnel oxide sample showed a relatively large memory window reduction by repeated program/erase operations due to the high electric field of ~10 MV/cm through tunnel oxide. The other samples showed less than 10% loss of memory window during 10⁴ cycles.     

Ultrasound velocity and absorption in BeO,Al<Subscript>2</Subscript>O<Subscript>3</Subscript>, ZrO<Subscript>2</Subscript>, and SiO<Subscript>2</Subscript> ceramics

We have measured the ultrasound velocity and absorption in BeO, Al₂O₃, ZrO₂, and SiO₂ ceramics. The results indicate that the ultrasound velocity in oxide ceramics depends on the nature of the basic oxide component, the density of the material, and the preferential alignment of the grains. The ultrasound velocity in ceramics is shown to correlate with their thermal conductivity: with increasing thermal conductivity, the ultrasound velocity increases. The ultrasound absorption in oxide ceramics decreases with decreasing temperature, and vice versa, with increasing temperature, the ultrasound attenuation coefficient increases.     

Electric conductivity of a bulk composite based on Bi<Subscript>2</Subscript>Te<Subscript>3</Subscript>/SiO<Subscript>2</Subscript> core-shell nanoparticles

Composite Bi₂Te₃/SiO₂ nanoparticles of the core-shell type have been synthesized for the first time with a view to creating bulk composites possessing high thermoelectric figure of merit (conversion efficiency). It is suggested that bulk composited based on Bi₂Te₃/SiO₂ nanoparticles will provide a combination of low lattice heat conduction due to SiO₂ insulator and rather high electric conduction due to charge-carrier tunneling via dielectric spacers between adjacent Bi₂Te₃ semiconductor grains. The electric resistance of the composite increases with increasing temperature in the range of 130–300 K. This temperature dependence can be described in terms of a tunneling conduction model.     

Anisotropy of dielectric losses in Al<Subscript>2</Subscript>O<Subscript>3</Subscript> and SiO<Subscript>2</Subscript> single crystals

The procedure and results of measurements of the dielectric loss tangent using the dielectric resonator technique on azimuthal modes of the HE (quasi-E) and EH (quasi-H) types are considered. The measurements were performed for uniaxial anisotropic single crystals of Al₂O₃ (at a frequency of 11 GHz) and SiO₂ (at 39 GHz) in a temperature range of 80–373 K and for an isotropic single crystal of Y₃Al₅O₂ (YAG) at room temperature in a frequency range of 9–15 GHz. The proposed method revealed the anisotropy of dielectric losses in Al₂O₃ and SiO₂ single crystals in the temperature range studied. According to this, losses along the optical axis of these crystals are lower than in the transverse plane. In the YAG crystal, the Q values for modes of the two types with the same frequency are close, which corresponds to isotropic losses. The dielectric losses in YAG increase in proportion to the frequency.     

Enhanced thermal stability in K<Subscript>2</Subscript>O-metakaolin-based geopolymer concretes by Al<Subscript>2</Subscript>O<Subscript>3</Subscript> and SiO<Subscript>2</Subscript> fillers addition

Based on the principle of stability of geopolymer gel as refractory binder, a geopolymeric paste in the K₂O–Al₂O₃–SiO₂ system was developed and used to produce refractory concretes by adding various amount of α-quartz sand (grain size in the range 0.1 μm to 1 mm) and fine powder alumina (grain size in the range 0.1–100 μm). The consolidated samples were characterized before and after sintering using optical dilatometer, DSC, XRD and SEM. The total shrinkage in the range of 25–900 °C was less than 3%, reduced with respect to the most diffused potassium or sodium based geopolymer systems, which generally records a >5% shrinkage. The maximum shrinkage of the basic geopolymer composition was recorded at 1000 °C with a 17% shrinkage which is reduced to 12% by alumina addition. The temperature of maximum densification was shifted from 1000 °C to 1150 or 1200 °C by adding 75 wt% α-quartz sand or fine powder alumina respectively. The sequences of sintering of geopolymer concretes could be resumed as dehydration, dehydroxylation, densification and finally plastic deformation due to the importance of liquid phase. The geopolymer formulations developed in this study appeared as promising candidates for high-temperature applications: refractory, fire resistant or insulating materials.     

Analysis of weakly bonded oxygen in HfO<Subscript>2</Subscript>/SiO<Subscript>2</Subscript>/Si stacks by using HRBS and ARXPS

We have used transmission electron microscopy, high-resolution Rutherford backscattering spectrometry (HRBS), and angle-resolved X-ray photoelectron spectroscopy (ARXPS) to investigate the interfacial oxidized states of hafnium oxide/silicon oxide/Si gate oxide stacks. The atomic concentrations and profiles of HRBS analysis are similar before and after annealing; however, ARXPS shows a clear difference in bond status. These results imply that weakly bonded oxygen atoms existed in the stacks alongside the suboxides. In the as-deposited layers, dioxides are found at the interfaces and suboxides in the layers whereas after annealing suboxides are found at the interfaces and dioxides are found in the layers because of redistribution of bonds during annealing. The combination of HRBS and ARXPS analyses indicated that the main oxidized states transformed from the suboxides to the dioxides with no obvious quantitative difference in the content of oxygen atoms, suggesting that reactions of the weakly bonded oxygen atoms occurred with the suboxides within the layers.     

Crystallization and microstructure of a glass seal for rapid laser sealing in the system CaO/Al<Subscript>2</Subscript>O<Subscript>3</Subscript>/SiO<Subscript>2</Subscript>

A glass with the composition 61 CaO·30 Al₂O₃·9 SiO₂ was studied with respect to its crystallization behavior and its suitability as a rapidly crystallizing material for laser sealing. The glass was studied by differential scanning calorimetry; from the profiles recorded, Avrami activation energies and Avrami coefficients were calculated. The latter are in the range between 0.99 and 1.55 which is supposedly attributed to sole surface crystallization. During thermal treatment as well as during laser sealing, Ca₁₂Al₁₄O₃₃, CaAl₂O₄ and Ca₃Al₂O₆ are formed. These phases were also observed in SEM micrographs as evidenced by electron backscatter diffraction from the attributed Kikuchi patterns. Transmission electron microscopy showed a crystallized CaO- and SiO₂-enriched interface which strongly adhered to the Al₂O₃ ceramic. The porosity of the crystallized seal was in the order of few percent. The studied glass proved suitable as crystallizing seal for rapid laser sealing.