Top electrode effects on resistive switching behavior in CuO thin films

Top electrode (TE) material on the resistive switching behavior of (TE)/CuO/SnO₂:F/Si substrate has been studied. We investigated the switching properties of CuO films deposited by sol-gel process. Two kinds of top electrode (TE) material on the resistive switching behaviors have been studied. The nonpolar and bipolar resistive switching phenomenon was observed in CuO thin films with different top electrodes. The filamentary mechanism was used to explain the two kinds of resistive switching behaviors. For the Pt/CuO/ATO device, it showed the nonpolar resistive switching where conducting path is formed and disappear due to the oxygen vacancy. For the Cu/CuO/ATO device, the resistance reduction is due to the existing Cu to form conduction Cu-rich pathways. An opposite bias takes the existing Cu back to the Cu electrode to its high-resistance state. CuO thin films are also observed by XRD, AFM and XPS.     

Dispersion stability and thermal conductivity of propylene glycol-based nanofluids

The dispersion stability and thermal conductivity of propylene glycol-based nanofluids containing Al₂O₃ and TiO₂ nanoparticles were studied in the temperature range of 20–80 °C. Nanofluids with different concentrations of nanoparticles were formulated by the two-step method and no dispersant was used. In contrast to the common belief, the average particle size of nanofluids was observed to decrease with increasing temperature, and nanofluids showed an excellent stability over the temperature range of interest. Thermal conductivity enhancement for both studied nanofluids was a nonlinear function of concentration and was temperature independent. Theoretical analyses were also performed using existing models compared with experimental results. The model based on the aggregation theory appears to be the best.     

Nanosecond laser ablation and deposition of silicon

Nanosecond-pulsed KrF (248 nm, 25 ns) and Nd:YAG (1064 nm, 532 nm, 355 nm, 5 ns) lasers were used to ablate a polycrystalline Si target in a background pressure of <10⁻⁴ Pa. Si films were deposited on Si and GaAs substrates at room temperature. The surface morphology of the films was characterized using scanning electron microscopy (SEM) and atomic force microscopy (AFM). Round droplets from 20 nm to 5 μm were detected on the deposited films. Raman Spectroscopy indicated that the micron-sized droplets were crystalline and the films were amorphous. The dependence of the properties of the films on laser wavelengths and fluence is discussed.     

In situ controlled synthesis of various TiO<Subscript>2</Subscript> nanostructured materials via a facile hydrothermal route

Various TiO₂ nanomaterials, such as nanosheets, nanoflowers, and nanowires were directly self assembled on titanium substrate on a large scale under hydrothermal conditions. The morphology of the formed TiO₂ nanomaterials could be easily tuned by varying the experimental parameters of temperature, reaction time, and the NaOH concentration. A possible formation mechanism was suggested on the basis of the shape evolution of TiO₂ nanostructures by SEM images in combination with XRD patterns of as-grown samples. The optical properties of TiO₂ nanosheets, nanoflowers, and nanowires were characterized by reflectance spectroscopy. The studies revealed that the absorption capability of visible light is obviously different for TiO₂ with different morphologies. Moreover, TiO₂ nanosheets exhibited better light trapping than TiO₂ nanoflowers and TiO₂ nanowires due to their unique nanostructure.     

Influence of NH<Subscript>3</Subscript> flow rate on pyridine-like N content and NO electrocatalytic oxidation of N-doped multiwalled carbon nanotubes

Nitrogen-doped multiwalled carbon nanotubes (N-MWCNTs) have been prepared by pyrolysis of pyridine and iron phthalocyanine over an iron catalyst at 850 °C at various ammonia gas (NH₃) flow rates. X-ray photoelectron spectroscopy results reveal that the pyridine-like nitrogen (N) content can be controlled by changing the flow rate of NH₃, and that pyridine-like N plays an important role: it can increase the electrocatalytic activity and the rate of nitric oxide (NO) electrooxidation and decrease the activation energy of NO electrooxidation. Cyclic voltammetry results demonstrate that the N-MWCNTs sample grown with 200 mL/min NH₃ flow has the maximum N content of 3.22 atomic %, and its content of pyridine-like N that is chemically active is also the highest among all the N-MWCNTs samples. Electrochemical impedance spectroscopy results indicate that two-step electron transfer process occurs at the N-MWCNT-modified electrode, and the control step is different in various potential regions. The stability of NO electrooxidation at the N-MWCNT-modified electrode is examined, and the reaction mechanism is discussed.     

On the role of the colloidal stability of mesoporous silica nanoparticles as gene delivery vectors

Mesoporous silica nanoparticles have been synthesized and functionalized with four different types of molecules containing amino groups, i.e., with primary amines only, with quaternary amines, with quaternized cyclic amines, or with polyethylenimine (PEI), which is formed by primary, secondary, and tertiary amines. These nanoparticles were then incubated with reporter plasmids and the ability of the resulting complexes to transfect human cells was studied. Only nanoparticles functionalized with PEI were efficient for transfection. The agglomeration behavior and the electrokinetic potential of the nanoparticle–plasmid complexes have been studied, as well as their cell internalization behavior using a fluorescent-labeled plasmid that allows its monitorization by confocal microscopy. The results indicate that the efficiency of PEI-functionalized nanoparticles for transfection resides to some extent in the different characteristics imparted to the nanoparticles regarding agglomeration and surface charge behavior.     

Synthesis of the chain-shaped carbon fibers decorated with SiO<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript> beads by chemical vapor deposition

Chain-shaped carbon fibers decorated with SiO _x beads had been synthesized by using methyltriehlorosilane and normal carbon fibers as the raw materials, during which the chemical vapor deposition technique was applied. The products were characterized by scanning electron microscopy (SEM), energy dispersive spectrum (EDS), X-ray diffraction (XRD) and Raman spectroscopy. The as-received products show chain-shaped morphologies that have the normal carbon fibers as “strings” and possess regular SiO _x beads of 30–40 μm with relative smooth surface. The formation of the chain-shaped morphology is considered to involve the shrinkage of the absorbed silica layer and the possible growth mechanism is further proposed. It is thought that the chain-shaped carbon fibers are formed by two main stages.     

Synthesis and characterization of “mulberry”-like Fe<Subscript>3</Subscript>O<Subscript>4</Subscript>/multiwalled carbon nanotube nanocomposites

Nanocomposites composed of multi-wall carbon nanotubes (MWNTs) and Fe₃O₄ nanoparticles were fabricated using solvothermal method. Transmission and scanning electron microscopy, energy dispersive spectroscopy, and X-ray powder diffraction measurements confirmed that these mulberry-like Fe₃O₄ microparticles which were combined with the MWNTs in a random pattern are constructed with tiny nanocrystallites (12 nm in average diameter). The magnetic properties of the Fe₃O₄/MWNTs nanocomposites were measured using a vibrating sample magnetometer. Results showed that the Fe₃O₄/MWNTs nanocomposites exhibited superparamagnetism at room temperature and possessed a lower saturation magnetization (around 27.6 emu/g) than that of the pure Fe₃O₄ nanoparticles (around 33.7 emu/g). The Fe₃O₄/MWNTs nanocomposites have potential applications in engineering and medicine.     

Determination of Total Antioxidant Capacity by a New Spectrofluorometric Method Based on Ce(IV) Reduction: Ce(III) Fluorescence Probe for CERAC Assay

A Ce(IV)-based reducing capacity (CERAC) assay was developed to measure the total antioxidant capacity (TAC) of foods, in which Ce(IV) would selectively oxidize antioxidant compounds but not citric acid and reducing sugars which are not classified as antioxidants. The method is based on the electron-transfer (ET) reaction between Ce(IV) ion and antioxidants in optimized acidic sulphate medium (i.e., 0.3 M H₂SO₄ and 0.7 M Na₂SO₄) and subsequent determination of the produced Ce(III) ions by a fluorometric method. The fluorescent product, Ce(III), exhibited strong fluorescence at 360 nm with an excitation wavelength of 256 nm, the fluorescence intensity being correlated to antioxidant power of the original sample. The linear concentration range for most antioxidants was quite wide, e.g., 5.0 × 10⁻⁷–1.0 × 10⁻⁵ M for quercetin. The developed procedure was successfully applied to the TAC assay of antioxidant compounds such as trolox, quercetin, gallic acid, ascorbic acid, catechin, naringin, naringenin, caffeic acid, ferulic acid, glutathione, and cysteine. The proposed method was reproducible, additive in terms of TAC values of constituents of complex mixtures, and the trolox equivalent antioxidant capacities (TEAC coefficients) of the tested antioxidant compounds gave good correlations with those found by reference methods such as ABTS and CUPRAC.     

Interplay of information quantifiers and the modified Jaynes-Cummings model

The dynamics of the Buck and Sukumar model (B. Buck and C. V. Sukumar, Phys. Lett. A 81, 132 (1981)) is investigated using different semi-classical information-theory tools. Their interplay reveals somewhat unexpected features. A new signature for the classical-quantum barrier is encountered thereby.