New approach for fabrication of folded-structure SiO2 using oyster shell

Inspired by the phenomenological differences of layers in oyster shell and the morphological mimicry of SiO₂ thin film, a folded-structure SiO₂ was created by simple spray deposition system. The folded-structure SiO₂ was analyzed by scanning electron microscopy, energy dispersive spectrometer and microindentation. At the molecular level, the chalky and the folia were assembled and determined through biomineralization based on the differences of soluble protein in layers. At the macro-scale, the granular SiO₂ particles deposited at the surface of shell layers or Ca(OH)₂ and grew into thin film, thus leading to mimic the morphology of substrate.     

Effect of nanocomposite structure on the thermoelectric properties of 0.7-at% Bi-doped Mg2Si nanocomposite

Nanocomposites offer a promising approach to the incorporation of nanostructured constituents into bulk thermoelectric materials. The 0.7-at% Bi-doped Mg₂Si nanocomposites are prepared by spark plasma sintering of the mixture of nanoscale and microsized 0.7-at% Bi-doped Mg₂Si powders. Microstructure analysis shows that the bulk material is composed of nano- and micrograins. Although the nanograin hinders electrical conduction, the nanocomposite structure is more helpful to reduce thermal conductivity and increase the Seebeck coefficient, hence improving thermoelectric performance. A dimensionless figure of merit of 0.8 is obtained for the 0.7-at% Bi-doped Mg₂Si nanocomposite with 50-wt % nanopowder, which is about twice larger than that of the sample without nanopowder.     

Effect of the dispersibility of ZrO2 nanoparticles in Ni-ZrO2 electroplated nanocomposite coatings on the mechanical properties of nanocomposite coatings

ZrO₂ nanoparticles was uniformly co-deposited into a nickel matrix by electroplating of nickel from a Watts bath containing particles in suspension which were monodispersed with dispersant under DC electrodeposition condition. It was found that morphology, orientation and hardness of the nanocomposite coatings with monodispersed ZrO₂ nanoparticles had lots of difference from the nanocomposite coatings with agglomerated ZrO₂ nanoparticles and pure nickel coatings. Especially, the result of hardness showed that only a very low volume percent (less than 1 wt.%) of monodispered ZrO₂ nanoparticles in Ni-ZrO₂ nanocomposite coatings would result in higher hardness of the coatings. The hardness of Ni-ZrO₂ nanocomposite coatings with monodispersed and agglomerated ZrO₂ nanoparticles were 529 and 393 HV, respectively. The hardness value of the former composite coatings was over 1.3 times higher than that of the later. All these composite coatings were two-three times higher than that of pure nickel plating (207 HV) prepared under the same condition. The strengthening mechanisms of the Ni-ZrO₂ nanocomposite coatings based on a combination of grain refinement strengthening from nickel matrix grain refining and dispersion strengthening from dispersion state of ZrO₂ nanoparticles in the coatings.     

Scaling behavior of the thermopower of the archetypal heavy-fermion metal YbRh2Si2

We reveal and explain the scaling behavior of the thermopower S/T exhibited by the archetypal heavy-fermion (HF) metal YbRh₂Si₂ under the application of magnetic field B at temperature T. We show that the same scaling is demonstrated by different HF compounds such as β-YbAlB₄ and the strongly correlated layered cobalt oxide [BiBa_0.66K_0.36O₂]CoO₂. Using YbRh₂Si₂ as an example, we demonstrate that the scaling behavior of S/T is violated at the antiferromagnetic phase transition, while both the residual resistivity ρ₀ and the density of states, N, experience jumps at the phase transition, causing the thermopower to make two jumps and change its sign. Our elucidation is based on flattening of the single-particle spectrum that profoundly affects ρ₀ and N. To depict the main features of the S/T behavior, we construct a T –B schematic phase diagram of YbRh₂Si₂. Our calculated S/T for the HF compounds are in good agreement with experimental facts and support our observations.     

Comparative study on thermal performance of helical screw tape inserts in laminar flow using Al2O3/water and CuO/water nanofluids

This paper presents a comparison of thermal performance of helical screw tape inserts in laminar flow of Al₂O₃/water and CuO/water nanofluids through a straight circular duct with constant heat flux boundary condition. The helical screw tape inserts with twist ratios Y = 1.78, 2.44 and 3 were used in the experimental study using 0.1% volume concentration Al₂O₃/water and CuO/water nanofluids. Nanofluids with required volume concentration of 0.1% were prepared by dispersing specified amounts of Al₂O₃ and CuO nanoparticles in deionised water. The performance analysis of helical screw tape inserts in laminar flow of Al₂O₃/water and CuO/water nanofluids is done by evaluating thermal performance factor for constant pumping power condition. Thermal performance factor of helical screw tape inserts using CuO/water nanofluid is found to be higher when compared with the corresponding value using Al₂O₃/water. Therefore, the helical screw tape inserts show better thermal performance when used with CuO/water nanofluid than with Al₂O₃/water nanofluid.     

Influence of ethanol on the electrocodeposition of Ni/Al2O3 nanocomposite films

The effect of ethanol on the electrocodeposition of nickel alumina nanocomposites was investigated using an acidic nickel sulfamate electrolyte. The surface charge and sedimentation behaviour of the 13 nm alumina particles in the nickel plating bath were characterized as a function of the ethanol concentration and the pH of the electrolyte. High ethanol contents cause a decrease in the surface charge and dispersion stability of the alumina particles in the plating electrolyte. The effects of the deposition conditions, i.e. ethanol content, current density, and particle content of the electrolyte on the codeposition of nickel alumina composites were investigated systematically. Low values of current density and high amounts of ethanol in the plating bath were found to be beneficial for the particle entrapment. The structure as well as the microhardness of the nickel films were investigated as a function of the electrolyte composition and the particle incorporation. A textural modification combined with a distinct grain refinement was found with increasing ethanol content of the electrolyte and due to the alumina incorporation. The microhardness of the layers increased with decreasing ethanol content of the electrolyte and increasing nanoparticle incorporation.     

Atomic force microscopy study of growth kinetics: Scaling in TiN-TiB2 nanocomposite films on Si(1 0 0)

We used the reactive unbalanced close-field dc-magnetron sputtering growth of TiN-TiB₂ on Si(1 0 0) at room temperature to determine if scaling theory provides insight into the kinetic mechanisms of two-phase nanocomposite thin films. Scaling analyses along with height-difference correlation functions of measured atomic force microscopy (AFM) images have shown that the TiN-TiB₂ nanocomposite films with thickness ranging from 70 to 950 nm exhibit a kinetic surface roughening with the roughness increasing with thickness exponentially. The roughness exponent α and growth exponent β are determined to be ∼0.93 and ∼0.25, respectively. The value of dynamic exponent z, calculated by measurement of the lateral correlation length ξ, is ∼3.70, agreeing well with the ratio of α to β. These results indicate that the surface growth behavior of sputter-deposited TiN-TiB₂ thin films follows the classical Family-Vicseck scaling and can be reasonably described by the noisy Mullins diffusion model, at which surface diffusion serves as the smoothing effect and shot noise as the roughening mechanism.     

Magnetic properties of the novel nanocomposite (Zn0.15Ni0.85Fe2O4)0.15/(SiO2)0.85 at room temperature

The value of the effective magnetic anisotropy constant of the ferrimagnetic nanoparticles Zn_0.15Ni_0.85Fe₂O₄ embedded in a SiO₂ silica matrix, determined through ferromagnetic resonance (FMR), is much higher than the magnetocrystalline anisotropy constant. The higher value of the anisotropy constant is due to the existence of surface anisotropy. However, even if the magnetic anisotropy is high, the ferrimagnetic nanoparticles with a 15% concentration, which are isolated in a SiO₂ matrix, display a superparamagnetic (SPM) behavior at room temperature and at a frequency of the magnetization field equal to 50 Hz. The FMR spectrum of the novel nanocomposite (Zn_0.15Ni_0.85Fe₂O₄)_0.15/(SiO₂)_0.85, recorded at room temperature and a frequency of 9.060 GHz, is observed at a resonance field (B_0r) of 0.2285 T, which is substantially lower than the field corresponding to free electron resonance (ESR) (0.3236 T). Apart from the line corresponding to the resonance of the nanoparticle system, the spectrum also contains an additional weaker line, identified for a resonance field of ∼0.12 T, which is appreciably lower than B_0r. This line was attributed to magnetic ions complex that is in a disordered structure in the layer that has an average thickness of 1.4 nm, this layer being situated on the surface of the Zn_0.15Ni_0.85Fe₂O₄ nanoparticles that have a mean magnetic diameter of 8.9 nm.     

Surface characterization of the Zn-Ni-Al2O3 nanocomposite coating fabricated under ultrasound condition

Zn-Ni-Al₂O₃ nanocomposite coating, which was fabricated by eletrodeposition technique with the aid of ultrasound, was investigated by scanning electron microscopy (SEM), energy dispersive X-ray (EDX) analysis and X-ray photoelectron spectroscopy (XPS). The results reveal that 7.2 wt.% nano-alumina particles uniformly dispersed in the matrix of the composite coating. The XPS analyses demonstrate that the outermost layer of Zn-Ni-Al₂O₃ coating was composed of nano-alumina and Zn(OH)₂, while the transition layer between the outermost layer and the Zn-Ni matrix consisted of nano-alumina, metallic Zn, ZnO and metallic Ni. In order to investigate the influences of ultrasonic agitation and the incorporation of nano-alumina on the composition and surface structure of Zn-Ni matrix, the comparison studies of Zn-Ni-Al₂O₃ nanocomposite coating with Zn-Ni coatings fabricated with and without ultrasound were conducted. The results indicate that ultrasonic agitation resulted in a decrease of Ni content in the Zn-Ni matrix and an increase of the thickness of surface oxide layer; while the incorporation of nano-α-Al₂O₃ increased the Ni content in the Zn-Ni matrix.     

Super-hydrophilic properties of TiO2-DLC nanocomposite films fabricated by the simple electrochemical process

Anatase TiO₂ nanoparticles incorporated DLC films were successfully deposited on single crystalline silicon substrates by the electrolysis of TiO₂-methanol solution under ambient atmospheric pressure and low temperature. Anatase TiO₂ nanoparticles were embedded into amorphous carbon matrix, forming the typical nanocrystalline/amorphous nanocomposite films, confirmed by transmission electron microscopy (TEM). TiO₂ incorporation effectively increased the sp³-hybridized carbon concentration in the composite film, and further regulated the microstructure and surface morphology. Furthermore, the static contact testing completely displayed, TiO₂ incorporation got the composite films super-hydrophilic, which fundamentally improved the wetting ability of DLC film.     

Study on the surface erosion route to the fabrication of TiO2 hollow spheres

Three-dimensional (3D) architecture of TiO₂ hollow sphere has many excellent and interesting performances that attract significant attention nowadays. In this paper, a simple surface erosion approach to the fabrication of TiO₂ hollow spheres via the hydrothermal process has been developed. The morphologies and the phase were characterized by scanning electron microscopy (SEM) and X-ray diffractometer (XRD). The results indicate that the anatase-type TiO₂ hollow spheres with a diameter of ∼1 μm are successfully synthesized. The shell thickness of TiO₂ hollow spheres is ∼150 nm and the size of hollow cavity is ∼600 nm. By the control experiments, the influence of ammonium fluoride and hydrogen peroxide on the hollow spherical structures was studied. Hydrogen peroxide acts as both the oxidant and the bubble generator, ammonium fluoride is crucial for the erosion and dissolution of titanium, the detailed dissolution-crystallization mechanism for the formation of TiO₂ hollow spheres was also proposed.     

Understanding the solar photo-catalytic activity of TiO2-ITO nanocomposite deposited on low cost substrates

In this work, we report on the photo-catalytic properties of TiO₂-ITO nanocomposite deposited on low cost conventional clay ceramic substrates. The nanocomposite was formed by spraying a solution prepared from the P25 TiO₂ powder (Degussa) mixed with an organometallic paste of a dissolved combination of indium and tin. A TiO₂-ITO powder-like nanocomposite was prepared for X-ray diffraction (XRD) and transmission electron microscopy (TEM) characterization. The mean particle size of the TiO₂-ITO nanocomposite was found to be larger than that of pure TiO₂. The optical features of TiO₂-ITO-based layers (deposited on glass substrates) were investigated using UV-vis spectroscopy. The TiO₂-ITO nanocomposite deposited layers were found to have higher light absorption than the P25 TiO₂ powder. The photo-catalytic properties of the TiO₂-ITO nanocomposite (deposited on low cost clay ceramic substrates) were tested under solar irradiation using a well-known polluting dye. It was shown that the TiO₂-ITO nanocomposite exhibits higher degradation rates towards the pollutant dye than the P25 TiO₂ powder. The optical band gap of the TiO₂-ITO nanocomposite (2.79 eV) was found to be lower than that of pure TiO₂ (3.1 eV), while ITO (indium tin oxide) has a band gap of about 4.2 eV. ITO was found to be entirely transparent to sun light, while it exhibits a slight photo-catalytic activity, signifying the possible existence of an indirect photo-catalysis phenomenon (sensitized semiconductor photocalysis) and potential degradation (oxidation) of the pollutant through electron transfer from the dye to conduction band of the semiconductor. All photo-catalytic activity results were discussed in light of the optical band gap of the various compounds.     

利用电子束蒸发制备铝隧道结工艺研究

采用电子束蒸发的方法在Si片上制备超导铝(Al)薄膜。利用X射线衍射和直流四电极电阻法分别测试了厚度从100埃到5000埃的Al薄膜物向组成,超导转变温度(Tc)和临界电流密度(Jc)。当Al薄膜厚度大于500埃时,超导转变温度Tc=1.2K。电子束蒸发制备的Al薄膜性能良好,具有较高的结晶质量,为制备Al超导隧道结奠定了良好基础。对小面积的Al超导隧道结工艺进行了研究,该超导隧道结两层的超导体材料为Al薄膜,中间势垒层材料为Al2O3。其中Al薄膜利用电子束蒸发制备,势垒层通过直接氧化Al薄膜表面实现,该工艺和采用直接蒸发氧化物薄膜工艺相比不仅简单而且能有效防止势垒层不连续造成的弱连接。     

Preparation and characterisation of ZnFe2O4/ZnO polymer nanocomposite sensors for the detection of alcohol vapours

During the last 10 years, a large interest has developed in the preparation of nanocomposite structures by embedding inorganic nanoparticles into polymeric materials. These materials combine the properties of the inorganic fillers with the processability and flexibility of polymers. The versatility of polymer nanocomposite systems is of special interest to the gas sensor industry where arrays of polymer/carbon black composites have been used to identify gases and odours. These polymer gas sensors provide selectivity based on their chemical structures and operate at room temperature, which provide advantages over thick-film metal oxide gas sensors. ZnFe₂O₄ and ZnO have excellent stability, high sensitivity, low fabrication complexity and moderate operating temperatures, which are ideal properties for a gas sensing material. In this work, the development of a thick-film ZnFe₂O₄/ZnO sensor, which operates at room temperature and a drop-coated conducting polymer composite sensor containing 30 w/w% ZnFe₂O₄/ZnO nanoparticles is discussed. The sensors were tested in a fully automated test rig and showed promising results for the detection of alcohol vapours.     

Scaling behaviour of the energy gap of spin-1/2 AF-Heisenberg chains in both uniform and staggered fields

The energy gap of the 1D AF-Heisenberg model in the presence of both uniform (H) and staggered (h) magnetic fields is investigated using the exact diagonalization technique. The opening of the gap in the presence of a staggered field is found to scale with h^ν, where ν=ν(H) is the critical exponent, and depends on the uniform field. With respect to the range of the staggered magnetic field, two regimes are identified through which the dependence of the real critical exponent ν(H) on H can be calculated numerically. Our numerical results are in good agreement with the results obtained by other theoretical approaches.     

Highly active Ce1−xCuxO2 nanocomposite catalysts for the low temperature oxidation of CO

A series of Ce_1−xCu_xO₂ nanocomposite catalysts with various copper contents were synthesized by a simple hydrothermal method at low temperature without any surfactants, using mixed solutions of Cu(II) and Ce(III) nitrates as metal sources. These bimetal oxide nanocomposites were characterized by means of XRD, TEM, HRTEM, EDS, N₂ adsorption, H₂-TPR and XPS. The influence of Cu loading (5-25 mol%) and calcination temperature on the surface area, particle size and catalytic behavior of the nanocomposites have been discussed. The catalytic activity of Ce_1−xCu_xO₂ nanocomposites was investigated using the test of CO oxidation reaction. The optimized performance was achieved for the Ce_0.80Cu_0.20O₂ nanocomposite catalyst, which exhibited superior reaction rate of 11.2 × 10⁻⁴ mmol g⁻¹ s⁻¹ and high turnover frequency of 7.53 × 10⁻² s⁻¹ (1% CO balanced with air at a rate of 40 mL min⁻¹, at 90 °C). No obvious deactivation was observed after six times of catalytic reactions for Ce_0.80Cu_0.20O₂ nanocomposite catalyst.     

Low temperature fabrication of 5-10 nm SiO2/Si structure using advanced nitric acid oxidation of silicon (NAOS) method

We have developed the advanced nitric acid oxidation of Si (NAOS) method to form relatively thick (5-10 nm) SiO₂/Si structure with good electrical characteristics. This method simply involves immersion of Si in 68 wt% nitric acid aqueous solutions at 120 °C with polysilazane films. Fourier transform infrared absorption (FT-IR) measurements show that the atomic density of the NAOS SiO₂ layer is considerably high even without post-oxidation anneal (POA), i.e., 2.28 × 10²² atoms/cm², and it increases by POA at 400 °C in wet-oxygen (2.32 × 10²² atoms/cm²) or dry-oxygen (2.30 × 10²² atoms/cm²). The leakage current density is considerably low (e.g., 10⁻⁵ A/cm² at 8 MV/cm) and it is greatly decreased (10⁻⁸ A/cm² at 8 MV/cm) by POA at 400 °C in wet-oxygen. POA in wet-oxygen increases the atomic density of the SiO₂ layer, and decreases the density of oxide fixed positive charges.     

Study of the fabrication parameters of large core Yb2O3 doped optical fibre through solution doping technique

Double clad large core Yb₂O₃ doped fibres with core diameter up to 20 μm have been fabricated by the solution doping technique through deposition of multiple porous core layers. The process parameters have been optimized with respect to the uniform doping of Al₂O₃ and Yb₂O₃ within the large core preform through soaking of the deposited multiple porous layers of fixed SiO₂-P₂O₅ composition with an alcoholic solution of a mixture of suitable strength of AlCl₃·6H₂O and YbCl₃·6H₂O to get the desired low NA around 0.09-0.11. The most critical parameters associated in this process are the deposition temperature with respect to uniform deposition of un-sintered layers of equal thickness with suitable porosity, viscosity of the soaking solution, pre-sintering temperature, proper mixing of the inlet gas mixture as well as proper drying of the thick porous layer after solution soaking process. This investigation will be very useful for development of large core Yb₂O₃ doped laser fibre technology.