Characteristics of pulse plated ZnTe films

Stoichiometric films of ZnTe are electrodeposited on stainless steel and conducting glass substrates from an aqueous solution consisting of ZnSO₄ (50 mM), TeO₂ (17 μM) and H₂SO₄ to maintain a pH of 2.5. Structure, morphology, composition, and optical are studied using XRD, SEM, EDAX and optical transmittance spectroscopy The films are composed of small crystallites (50 nm) with cubic crystal structure. The films were polycrystalline in nature with peaks corresponding to the cubic phase. Direct band gap of 2.30 eV was observed. XPS studiers indicated the formation of ZnTe. EDAX measurements were made on the films and it was found that there was a slight excess of Te. AFM studies indicated a surface roughness of 15 nm and a crystallite size of 10–50 nm.     

Enhanced ferromagnetic and photocatalytic properties in Mn or Fe doped p-CuO/n-ZnO nanocomposites

Mn doped CuO/ZnO heterostructure exhibited significant room temperature ferromagnetism and visible light photocatalytic properties. Phase analysis for the pure, Mn and Fe doped CuO/ZnO nanocomposites evidently confirmed the formation of CuO and ZnO phases in each composite without any impurities. Based on Rietveld refinement analysis, the inclusion of Mn ions into CuO/ZnO nanocomposite decreased the unit cell volume of both oxides while Fe ions lead to lattice expansion. Mn ions induced the formation of ZnO hexagonal nanorods in CuO/ZnO nanocomposite. Nano-flakes and spherical nanoparticles shapes were seen for Fe doped CuO/ZnO nanocomposites. The characteristics IR absorption bands of CuO and ZnO overlapped together in their nanocomposites structure. From Kubelka-Munk plots, the incorporation of Mn ions enabled the ZnO band gap to absorb in the visible light region. Pure CuO/ZnO nanocomposite exhibited room temperature ferromagnetism with saturation magnetization (M_s) of 0.042 emu/g and coercivity (H_c) of 547 Oe. The ferromagnetic properties of the pure CuO/ZnO nanocomposite were greatly improved by Mn and Fe doping and the saturation magnetization extremely jumped to 0.86 and 0.85 emu/g, respectively. High photocatalytic activity, 98%, with good reusability for methyl orange (MO) degradation under visible light irradiation was achieved by 4 wt% Mn doped CuO/ZnO nanocomposite. A relation between the crystallinity, band gap and photocatalytic activity with dopant type (Mn or Fe) incorporated into CuO/ZnO nanocomposites was noticed. In contrary to Fe dopant, Mn as dopant played successful roles in improving the crystallinity, band gap and photocatalytic properties of CuO/ZnO nanocomposite. Multifunctional properties can be realized by combining different oxides in heterostructure form and using doping technique.     

Structure and optical properties of polycrystalline Cd1−xZnxTe thin films prepared by simultaneous evaporation

Cd_1–xZn_xTe films were deposited by simultaneous evaporation of CdTe and ZnTe. These Cd_1–xZn_xTe films were of cubic phase, and strongly (1 1 1) oriented as deposited. Predominant direct optical transitions were observed and the band gap varied with zinc content in a non-linear way. A structure development of CdS/CdTe/ZnTe : Cu solar cells with a Cd_1–xZn_xTe buffer layer was proposed.     

Synthesis of PbS/poly (vinyl-pyrrolidone) nanocomposite

A simple solution growth method for synthesis of nanocomposite of PbS nanoparticles in poly(vinyl-pyrrolidone) (PVP) polymer is described. The nanocomposite is prepared from methanolic solution of lead acetate (PbAc), thiourea (TU) and PVP at room temperature (∼27 °C). Optical absorption spectrum of PbS/PVP nanocomposite solution shows strong absorption from 300 to 650 nm with significant bands at 400 and 590 nm which is characteristic of nanoscale PbS. Spin-coated nanocomposite films on glass have an absorption edge at ∼650 nm with band gap of 2.55 eV. Fourier transform infrared (FTIR) spectroscopy of PbS/PVP nanocomposite and PVP shows strong chemical bond between PbS nanoparticles and host PVP polymer. The transmission electron microscope (TEM) images reveal that 5-10 nm PbS particles are evenly embedded in PVP polymer. The formation of PbS is confirmed by selective area electron diffraction (SAED) of a typical nanoparticle.     

Effect of various combinations of zirconia and organoclay nanoparticles on mechanical and thermal properties of an epoxy nanocomposite coating

An epoxy based nanocomposite coating containing various combinations of treated-zirconia and clay nanoparticles were prepared. Morphology and dispersion of nanoparticles within the nanocomposites were evaluated using optical microscopy, XRD and TEM analyses. Mechanical, thermal properties and corrosion resistance of nanocomposites were studied using; tensile strength measurements, DMTA and DSC analyses and salt spray test.The results showed that simultaneous use of spherical and plate-shape nanoparticles, have a positive effect on the clay exfoliation behavior in resulting nanocomposites.Mechanical properties of nanocomposites containing nano-zirconia slightly increased compared with neat-epoxy coating. Mechanical properties of nanocomposites containing various wt.% of clay or ZrO₂/clay nanoparticles slightly decreased; formation of physical barrier clay stacks, which leads to disturbing curing procedure and decreasing polymer cross-linking density, and development of nano-sized voids in the trapped regions by clay stacks. Corrosion performance of nanocomposites increased with addition of nanoparticles, due to improving barrier properties of the coating.     

Poly(3-hexylthiophene)/hexamine modified ZnO hybrid nanocomposite: structural,optical, thermal and electrical transport studies

This paper reports the synthesis of poly(3-hexylthiophene) (P3HT)/HA@ZnO nanocomposite by in situ polymerization and demonstrates their thermal, morphological and optoelectronic properties. Zinc oxide (ZnO) nanoparticles were prepared by the simple approach of co- precipitation method using zinc acetate dihydrate as precursor modified by hexamine (HA) acting as a capping agent. Structural and photo physical studies shows that conjugated polymer chains intimately contact with the inorganic semiconductor. ZnO has wurtzite structure with average crystallite size of 40 nm. The emission spectra indicate that modified ZnO nanoparticles results in more efficient photo induced charge transfer than that of the simple nanocomposite of P3HT/ZnO. The morphological studies revealed that the transformation of granular morphology of P3HT to the clusters in P3HT/HA@ZnO hybrid nanocomposites. Cyclic voltammeter elucidates the electrochemical behavior and the HOMO–LUMO energy levels of the nanocomposites. The results indicate that the P3HT/HA@ZnO nanocomposite has energy gap of 0.72 eV, indicating this composite has potential for the fabricating hybrid organic–inorganic solid state solar cells. A solar to electric energy conversion efficiency of 0.1238 % was attained with the system.     

温度梯度溶液法生长的Cr掺杂的ZnTe晶体的表征

以CrTe作为掺杂源、以Te作为溶剂, 用温度梯度溶液法生长了Cr掺杂的ZnTe晶锭。晶锭头部的晶粒尺寸较大(>10 mm×10 mm), 且Te夹杂相较少。Te夹杂相的大小、形状和分布可以反映晶锭中的温场分布。晶锭的径向非对称温场导致富Te相沿径向非对称分布。Te夹杂相在温度梯度作用下的热迁移会导致其相互融合长大、变长。Te夹杂相也会在晶体中引入裂纹和空洞等缺陷。部分未被掺入ZnTe中的CrTe富集于固液界面处, 表明温度梯度溶液法生长晶体时具有一定的排杂作用。Cr掺杂的ZnTe晶体的电阻率(约1000 Ω·cm)高于未掺杂的ZnTe(约300 Ω·cm)。Cr掺杂晶体在约1750 nm处的吸收峰表明Cr²⁺离子被成功地掺入了ZnTe中。但是Cr掺杂后晶体的红外透过率降低, 表明Cr掺杂引入了较多的缺陷。     

Magnetic and optical properties of polycarbonate/Fe nanocomposites

The magnetic and optical properties of polycarbonate (PC)/Fe nanocomposite films prepared by a solution blended process and the role of Fe additives are investigated. The saturation magnetization of the PC/Fe nanocomposites depends on the weight of Fe nanoparticles. Meanwhile, an increase of photoluminescence (PL) intensity with decreasing Fe additives is interpreted. The optical band gap corresponds to the increase of PL elements. The transmittance of the films increases with reduced Fe, and the PL peak energy of PC/Fe composites is also correlated to the weight ratio.     

Synthesis and characterization of SnS/ZnO nanocomposite by chemical method

SnS nanorods and SnS/ZnO nanocomposite have been synthesized by chemical method. Structure and phase purity of the samples were confirmed by powder X-ray diffraction. Transmission electron microscope image of SnS nanorods showed the average diameter of nanorods was about 85 nm and length was several micrometers. Transmission electron microscope image of SnS/ZnO nanocomposite showed the average particle size of ZnO nanoparticle was about 12 nm. The formation of SnS/ZnO nanocomposite was confirmed by elemental analysis using energy dispersive X-ray spectroscopy. From the microRaman spectrum of SnS/ZnO nanocomposite, it was observed that the intensity of B_2g mode of SnS nanorods decreased dramatically compared to that of pure SnS nanorods, since the surface of the SnS nanorods were coated with ZnO nanoparticles. Both direct and indirect band gap transitions were observed for SnS nanorods from the optical absorption spectrum and the optical absorption spectrum of SnS/ZnO nanocomposite showed absorption in the visible region.     

Magnetic and optical properties of polycarbonate/Fe nanocomposites

The magnetic and optical properties of polycarbonate (PC)/Fe nanocomposite films prepared by a solution blended process and the role of Fe additives are investigated. The saturation magnetization of the PC/Fe nanocomposites depends on the weight of Fe nanoparticles. Meanwhile, an increase of photoluminescence (PL) intensity with decreasing Fe additives is interpreted. The optical band gap corresponds to the increase of PL elements. The transmittance of the films increases with reduced Fe, and the PL peak energy of PC/Fe composites is also correlated to the weight ratio.     

Synthesis,optoelectronic and thermal characterization of PMMA-MWCNTs nanocomposite thin films incorporated by ZrO2 NPs

PMMA polymer doped by multi-walled carbon nanotubes (MWCNTs) has attracted much attention as promising materials for photovoltaic and optoelectronic applications. The undoped poly(methyl methacrylate) (PMMA) and PMMA/MWCNTs nanocomposite films doped with varying concentrations of Zirconium dioxide nanoparticles (ZrO₂ NPs) are synthesized using the casting method. It is found that the transmittance (\(T\%\)) decreases significantly as wt%?=?5% of MWCNTs is injected into PMMA matrix. In addition, increasing the concentration of ZrO₂ NPs into PMMA- MWCNTs nanocomposite thin films results in a further reduction of the transmittance and a further increase of the reflectance (\(R\%\)). The optical band gap energy (E_g) of PMMA-MWCNTs/ZrO₂ NPs decreases from 4.063 \(eV\) to 3.845 \(eV\) upon injection of 5% of MWCNTs and gradually increasing the ZrO₂ concentration in PMMA matrix. Furthermore, other essential optical parameters are estimated using different classical models such as Drude, Spitzer-Fan, Sellmeier, and Wemple–DiDomenico (WDD). Interestingly, thermal stability of PMMA-MWCNTs nanocomposite films is enhanced dramatically upon increasing the content of ZrO₂ NPs. The synthesized nanocomposite thin films could be potential candidates for fabrication realistic scaled optoelectronic devices.

     

Synthesis, characterization and fluorescence property of CdS/P(N-iPAAm) nanocomposites

A novel nanocomposite in which CdS nanoparticles were embedded in poly(N-isopropylacrylamide) (P(N-iPAAm)) matrix have been fabricated. The particle size of CdS nanoparticles ranged from 10 nm to 40 nm could be adjusted with the varying of the inorganic contents. The nanocomposites have been characterized by X-ray diffraction (XRD), transmission electron microscope (TEM), thermo-gravimetric analysis (TGA), high resolution transmission electron microscope (HRTEM), UV-vis absorption and fluorescence spectra (FLS) measurements. The cell volume of CdS nanoparticles embedded in polymer matrix was smaller than the standard value and the nanocomposites with 12.0% inorganic content showed a good fluorescence property.     

Facile synthesis and characterization of novel nanocomposites of titanate nanotubes and rutile nanocrystals

The nanocomposites of one-dimensional (1D) titanate nanotubes and 0D rutile nanocrystals were fabricated by hydrothermal treatment of bulky rutile TiO₂ powders in a 10 M NaOH solution without using any templates and catalysts. The as-prepared samples were characterized with transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET) surface area, Fourier transform infrared spectroscopy (FTIR), UV–visible spectrophotometry (UV–vis), Raman spectroscopy and X-ray photoelectron spectroscopy (XPS). It was found that many small rutile nanocrystal particles of about 5 nm could uniformly attach to the outer surface and in the inner of the titanate nanotubes, forming an interesting and novel nanocomposite structure. Adjusting reaction time could control the amount of rutile nanoparticles in the nanocomposites. With increasing reaction time, the specific surface areas, porosity, pore volume, UV absorption and band gap energies of the nanocomposites gradually increased due to the fact that rutile particles were steadily turned into the tubular nanocomposites, finally completely formed titanate nanotubes.     

Transparent nanocomposites of high refractive index based on epoxy resin and TiO2 nanoparticle

A stepwise sol-gel method for the synthesis of stable colloidal TiO2 using hydrolysis and condensation reactions of titanium tetraisopropoxide (TTP) was investigated. The surface modification was carried out using 3-glycidoxypropyltrimethoxysilane (GPTMS). The particle size range of the modified TiO2 observed by TEM was 3-8 nm. The nanocomposites based on an epoxy resin and the modified TiO2 showed strong UV absorption, but maintained high transmittance within the visible region. TEM images of the nanocomposites confirmed the homogenous and fine dispersion of the TiO2 nanoparticles in the epoxy resin. The refractive index of the nanocomposites increased linearly with increasing TiO2 content. With 60% TiO2 by weight, the transmittance and refractive index of the nanocomposite were 98.4% and 1.657, respectively.     

Structural and optical characterization of ZnO doped PC/PS blend nanocomposites

PC50%/PS50% polymer blend nanocomposites, undoped and doped with different concentration of ZnO nanoparticles (1, 2, 3 wt%), have been prepared using solution casting method. Structural and optical studies have been performed using X-ray Diffraction (XRD), Scanning Electron Microscope (SEM) and Ultraviolet–Visible spectroscopy (UV–Vis). ZnO nanoparticles have been synthesized by chemical route method. The nanostructure of the ZnO nanoparticles has been ascertained through X-ray Diffraction (XRD) and Transmission Electron Microscopy (TEM). Optical Absorption Spectra has been used to study optical constants of prepared blend nanocomposites. Energy band gap of PC/PS – ZnO blend nanocomposites have been calculated by using Tauc relation. The band gap of the nanocomposites decreases as ZnO wt% increases. Extinction coefficient, refractive index and real & imaginary part of dielectric constants increase with increase in ZnO nanoparticles wt%.     

Cross‐Linked g‐C3N4/rGO Nanocomposites with Tunable Band Structure and Enhanced Visible Light Photocatalytic Activity

Cross‐linked rather than non‐covalently bonded graphitic carbon nitride (g‐C₃N₄)/reduced graphene oxide (rGO) nanocomposites with tunable band structures have been successfully fabricated by thermal treatment of a mixture of cyanamide and graphene oxide with different weight ratios. The experimental results indicate that compared to pure g‐C₃N₄, the fabricated CN/rGO nanocomposites show narrowed bandgaps with an increased in the rGO ratio. Furthermore, the band structure of the CN/rGO nanocomposites can be readily tuned by simply controlling the weight ratio of the rGO. It is found that an appropriate rGO ratio in nanocomposite leads to a noticeable positively shifted valence band edge potential, meaning an increased oxidation power. The tunable band structure of the CN/rGO nanocomposites can be ascribed to the formation of C?O?C covalent bonding between the rGO and g‐C₃N₄ layers, which is experimentally confirmed by Fourier transform infrared (FT‐IR) and X‐ray photoelectron (XPS) data. The resulting nanocomposites are evaluated as photocatalysts by photocatalytic degradation of rhodamine B (RhB) and 4‐nitrophenol under visible light irradiation (λ > 400 nm). The results demonstrate that the photocatalytic activities of the CN/rGO nanocomposites are strongly influenced by rGO ratio. With a rGO ratio of 2.5%, the CN/rGO‐2.5% nanocomposite exhibits the highest photocatalytic efficiency, which is almost 3.0 and 2.7 times that of pure g‐C₃N₄ toward photocatalytic degradation of RhB and 4‐nitrophenol, respectively. This improved photocatalytic activity could be attributed to the improved visible light utilization, oxidation power, and electron transport property, due to the significantly narrowed bandgap, positively shifted valence band‐edge potential, and enhanced electronic conductivity.     

Synthesis of AgBr/ZnO nanocomposite with visible light-driven photocatalytic activity

AgBr/ZnO nanocomposite was synthesized via chemical precipitation from pure ZnO nanowires, AgNO₃, and NaBr. Inductively coupled plasma optical emission spectroscopy, X-ray diffraction, and high resolution transmission electron microscopy results confirmed the forming of AgBr/ZnO nanocomposite. High resolution transmission electron microscopy results of the as-synthesized AgBr/ZnO nanocomposite revealed that AgBr nanoparticles were attached to the surface of ZnO nanowires. UV-vis diffuse reflectance spectra of both pure ZnO and AgBr/ZnO nanocomposite displayed a band gap edge at about 350-380 nm. However, compared with pure ZnO, an additional broad tail from approximately 400 nm to 700 nm appeared in the UV-vis diffuse reflectance spectrum of AgBr/ZnO nanocomposite. The photocatalytic studies indicated that the as-synthesized AgBr/ZnO nanocomposite was a kind of promising photocatalyst in remediation of water polluted by some chemically stable azo dyes under visible light.     

Synthesis and structural, optical and electrical properties of TiO2/SiO2 nanocomposites

Sole components of titania (TiO₂), silica (SiO₂) nanoparticles, and binary TiO₂–SiO₂ nanocomposites with various molar ratios of silica contents were prepared by modified sol–gel method. The samples were calcined at 500 °C for 5 h and characterized by X-ray diffraction, Fourier transform infrared spectroscopy (FTIR), UV–Vis spectroscopy, Brunauett–Emmett–Teller (BET), and photoconductivity. The crystallite size for TiO₂/SiO₂ nanocomposites was calculated using Scherrer’s formula and found to be 5 nm for TiO₂ nanoparticles. The binary oxide shows the anatase type of TiO₂ at the mole ratio up to 80 mol% of TiO₂ added. The band gap for as-synthesized nanocomposites was calculated and it was found that the band gap decreases with increase of SiO₂ content and then decreases with excess SiO₂ content. FTIR confirms that both TiO₂ and SiO₂ phases have been formed. The BET surface area for TiO₂/SiO₂ nanocomposite is found to be 303 m²/g, and pore size distribution has an average pore diameter about 10 nm for 40 mol% of TiO₂ added. It also confirms the absence of macropores and the presence of micro and mesopores. The field-dependent dark and photoconductivity studies reveal that the dark and photocurrent increase linearly with applied field confirming the ohmic nature of the electric contacts. The dark and photocurrent increase slightly with increase of SiO₂ content and decrease with excess amount of SiO₂.     

Melting, crystallization and optical behaviors of poly (ethylene terephthalate)-silica/polystyrene nanocomposite films

Poly (ethylene terephthalate) (PET)-silica (SiO₂)/polystyrene (PS) nanocomposite films were prepared by melting PET with the core-shell SiO₂/PS nanoparticles. Differential scanning calorimetry (DSC) results showed that the crystallization temperature of PET-SiO₂/PS nanocomposite films with 2 wt.% PS-encapsulated SiO₂ nanoparticles reached 205.1 °C, 11.6 °C higher than that of PET. For crystallized PET-SiO₂/PS nanocomposite films, double melting peaks appeared in DSC curves similar to PET. Scanning electron microscopy revealed a netlike fibre morphology for the amorphous PET-SiO₂/PS nanocomposite films with 2 wt.% PS-encapsulated SiO₂ nanoparticles. The light transmittance of these amorphous PET-SiO₂/PS nanocomposite films reached 87.9%, compared to 84.2% for PET. With the increase of annealing temperature from 110 to 150 °C, the transmittance of PET-SiO₂/PS nanocomposite films decreased slowly from 69.9 to 46.9%, while their haziness increased slightly from 45.8 to 48.2%. All these phenomena are suggested to result from the strongly heterogeneous nucleation of PS-encapsulated SiO₂ nanoparticles in PET.     

Synthesis and characterization of nanostructured SnO<Subscript>2</Subscript> film

Nanostructured tin dioxide (SnO₂) film was deposited on glass substrate by thermal evaporation of tin metal followed by thermal oxidation at 600 °C for 2 h. XRD investigation confirms that grown film is crystalline tetragonal rutile. The average optical transmittance of the film was as high as 90%. The optical band gap of the nanostructured SnO₂ was estimated from transmittance data and found to be 3.4 eV. The variation of electrical conductivity with temperature was investigated. The root mean square (RMS) roughness and topography of the film were investigated by atomic force microscopy and found to be 2 nm with grain size of 17 nm.