Effects of low-energy hydrogen ion implantation on optical properties of ZnO nanowires

The low-energy hydrogen ions (2 keV; 1 × 10¹⁵ to 1 × 10¹⁸ cm⁻² per dose) implantation was used to study the passivation effect of defects and photoluminescence properties of ZnO nanowires. The implanted H⁺ effectively passivated deep level native defects, making the visible emission at 500 nm disappear completely and the UV emission (380 nm) of nanowires enhance for seven times. H⁺ implantation at higher dose induced a strongly new violet emission broad peak (around 410 nm) which may originate from the hydrogen related complex of defects. However, this violet emission disappeared after annealing in argon atmosphere at 300 °C, confirming that the new violet emission is related to hydrogen. All emission peaks vanished due to the formation of a large quantity of nonradiative recombination centers at high dose implantation. This controllable method of hydrogen doping may find potential application in UV/violet optoelectronic and especially in nano-optoelectronic devices.     

Synthesis and photoluminescence properties of aligned Zn2GeO4 coated ZnO nanorods and Ge doped ZnO nanocombs

Aligned Zn₂GeO₄ coated ZnO nanorods and Ge doped ZnO nanocombs were synthesized on a silicon substrate by a simple thermal evaporation method. The structure and morphology of the as-synthesized nanostructure were characterized using scanning electron microscopy and transmission electron microscopy. The growth of aligned Zn₂GeO₄ coated ZnO nanorods and Ge doped ZnO nanocombs follows a vapor-solid (VS) process. Photoluminescence properties were also investigated at room temperature. The photoluminescence spectrum reveals the nanostructures have a sharp ultraviolet luminescence peak centered at 382 nm and a broad green luminescence peak centered at about 494 nm.     

Synthesis, characterization and optical properties of sheet-like ZnO

Sheet-like ZnO with regular hexagon shape and uniform diameter has been successfully synthesized through a two-step method without any metal catalyst. First, the sheet-like ZnO precursor was synthesized in a weak alkaline carbamide environment with stirring in a constant temperature water-bath by the homogeneous precipitation method, then sheet-like ZnO was obtained by calcining at 600 °C for 2 h. The structures and optical properties of sheet-like ZnO have been characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), photoluminescence (PL) and UV-vis-NIR spectrophotometer. The results reveal that the product is highly crystalline with hexagonal wurtzite phase and has appearance of hexagon at (0 0 0 1) plane. The HRTEM images confirm that the individual sheet-like ZnO is single crystal. The PL spectrum exhibits a narrow ultraviolet emission at 397 nm and a broad visible emission centering at 502 nm. The band gap of sheet-like ZnO is about 3.15 eV.     

Effect of phosphorus incorporation on morphology and optical properties of ZnO nanorods

Phosphorus-doped ZnO nanorods have been prepared on Si substrates by thermal evaporation process without any catalyst. X-ray photoelectron spectroscopy and Raman spectra indicate that phosphorus entering into ZnO nanorods mainly occupies Zn site rather than O one. The introduction of phosphorus leads to the morphological changes of nanorods from hexagonal tip to tapered one, which should be attributed to the relaxation of the lattice strain caused by phosphorus occupying Zn site along the radial direction. Transmission electron microscopy shows that phosphorus-doped ZnO nanorods still are single crystal and grow along [0 0 0 1] direction. The effect of phosphorous dopant on optical properties of ZnO nanorods also is studied by the temperature-dependent photoluminescence spectra, which indicates that the strong ultraviolet emission is connected with the phosphorus acceptor-related emissions.     

Synthesis and optical properties of hierarchical pure ZnO nanostructures

We report the catalyst-free synthesis of hierarchical pure ZnO nanostructures with 6-fold structural symmetry by two-step thermal evaporation process. At the first step, the hexagonal-shaped nanowires consisting of a great deal of Zn and little oxide were prepared via the layer-by-layer growth mechanism; and at the second step, hierarchical pure ZnO nanostructures were synthesized by evaporating the Zn source on the basis of the step-one made substrate. Scanning electron microscopy, transmission electron microscope images, and the corresponding selected area electron diffraction pattern have been utilized to reveal the screw dislocation growth mechanism, through which the single crystal ZnO nanorods are epitaxially grown from the side-wall of central axial nanowires. Raman and photoluminescence spectra further indicate that, for the hierarchical ZnO nanostructures, the ultraviolet peak is related to the free exciton recombination, while the oxygen vacancies and high surface-to-volume ratio are responsible for the strong green peak emission.     

Role of additives; sodium dodecyl sulphate and manganese chloride on morphology of Zn1−xMnxO nanoparticles and their photoluminescence properties

In the present study Zn_1−xMn_xO (x = 0, 0.05 and 0.1) nanoparticles (NPs) have been synthesised in aqueous solution phase at mild reaction temperature 100 °C in moderate alkaline medium (pH = 9.5), and the role of external additives; like sodium dodecyl sulphate and manganese chloride on the morphology and size of the products has been explored on the basis of transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray diffraction (XRD) and Fourier transform infrared spectral analyses data. ZnO hexagonal nano-plates, core–shell like spherical/ellipsoidal Zn_0.95Mn_0.05O structures and thin sheets, thorn/needle mixed shaped Zn_0.9Mn_0.1O structures have been observed in TEM and SEM images. Zn(OH)₂ formed in moderate alkaline medium, converted to Zn(II) hydroxo complex ions on dissolution, which further recrystallizes to produce wurtzite ZnO at 100 °C. From XRD and EDX analysis, successful doping of Mn²⁺ ions at the Zn²⁺ sites in ZnO host has been proved. In the photoluminescence spectra, the observed blue shifts in NBE peaks and decrease of emissions intensity on Mn doping have thoroughly been discussed in the present investigation.     

Rapid synthesis, characterization and optical properties of TiO2 coated ZnO nanocomposite particles by a novel microwave irradiation method

A novel and rapid microwave method was used to prepare TiO₂ coated ZnO nanocomposite particles. The resulted particles were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), high resolution transmission electron microscopy (HR-TEM) and X-ray photoelectron spectroscopy (XPS). Results show that ZnO nanoparticles were coated with 6-10 nm amorphous TiO₂ layers. In addition, zeta potential analysis demonstrated the presence of TiO₂ layer on the surface of ZnO nanoparticles. Photoluminescence (PL) spectroscopy and UV-visible spectroscopy were used to investigate the optical properties of the nanoparticles. Compared to uncoated ZnO nanoparticles, the TiO₂ coated ZnO nanoparticles showed enhanced UV emission. The UV-visible diffuse reflectance study revealed the significant UV shielding characteristics of the nanocomposite particles. Moreover, amorphous TiO₂ coating effectively reduced the photocatalytic activity of ZnO nanoparticles as evidenced by the photodegradation of Orange G with uncoated and TiO₂ coated ZnO nanoparticles under UV radiation.     

Synthesis and characterization of porous ZnO nanoparticles by hydrothermal treatment of as pure aqueous precursor

The presence of the complexing agents in the growth solution poses risk of the unintentional doping in the synthesized product and hence is likely to adversely affect the intrinsic properties. Herein we report the synthesis of ZnO nanoparticles with porous microstructure using pure aqueous precursor. Crystalline ZnO nanoparticles were synthesized by thermal treatment of aqueous solution of zinc acetate in an open bath. The size of the nanocrystals was controlled by changing the initial precursor concentration. The structural and optical properties of the synthesized nanocrystals were analyzed by X-ray diffraction, high resolution transmission electron microscopy, UV-vis absorption and room temperature photoluminescence measurement techniques. The TEM and UV-vis spectral signature analyses confirmed the formation of dispersed single crystalline ZnO nanoparticles. The nanopowders were found to have disordered mesoporous structure. The synthesized nanocrystals exhibited characteristic band edge emission as well as to surface defect related deep level visible luminescence.     

Indium sulfide microflowers: Fabrication and optical properties

With the assistance of urea, uniform 2D nanoflakes assembled 3D In₂S₃ microflowers were synthesized via a facile hydrothermal method at relative low temperature. The properties of the as-obtained In₂S₃ flowers were characterized by various techniques. In this work, the utilization of urea and l-cysteine, as well as the amount of them played important roles in the formation of In₂S₃ with different nanostructures. Inferred from their morphology evolution, a urea induced precursor-decomposition associated with the Ostwald-ripening mechanism was proposed to interpret these hierarchical structure formation. Furthermore, the optical properties of these In₂S₃ microflowers were investigated via UV–vis absorption and photoluminescence (PL) spectroscopies in detail.     

Facile synthesis, optical and photoconductive properties of novel ZnO nanocones

Large-scale, uniform ZnO nanocones with tips about 200 nm and length about 50 μm have been synthesized by a facile hydrothermal method. The morphology and structures were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM) and high-resolution transmission electron microscope (HR-TEM). The effects of reaction time and PEG-400 on the morphology of ZnO nanostructures were investigated, also an oriented attachment mechanism has been briefly proposed. The optical properties were investigated by lasing confocal microscope and photoluminescence spectrum, a strong near band edge emission peak centered at 387 nm from the ZnO nanocones was observed in photoluminescence spectrum. Finally, we have fabricated UV photodetector based on single ZnO nanocone, which present good switching properties by turning the UV light on and off.     

Studies on the structural and optical properties of zinc oxide nanobushes and Co-doped ZnO self-aggregated nanorods synthesized by simple thermal decomposition route

Pure and Co-doped zinc oxide nanomaterials were prepared by a simple low temperature synthesis and were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), high resolution-transmission electron microscopy (HR-TEM), diffused reflectance spectroscopy (DRS) and electron paramagnetic resonance (EPR) techniques. The results showed the formation of nanobushes that consists of several nanowires for pure ZnO and the nanorods formed by self-aggregation for Co-doped ZnO. The presence of Co²⁺ ions replacing some of the Zn²⁺ in the ZnO lattice was confirmed by EPR and DRS studies. The mechanism for the formation of self-aggregated and self-aligned ZnO rods after the incorporation of cobalt in the lattice by the building block units is discussed in this study. Morphological studies were carried out using SEM and HR-TEM, which supports the validity of the proposed mechanism for the formation of ZnO nanobushes and Co-doped ZnO nanorods. The synthesized nanomaterials were found to have good optoelectronic properties.     

Synthesis and optical properties of elliptic Pb(OH)Br microdiskettes

The novel elliptic Pb(OH)Br microdiskettes were controllably synthesized by a simple sonochemical process. The structure characterizations of the microdiskettes were investigated in detail by means of XRD, SEM, and HRTEM. The results indicate that the orthorhombic phase of Pb(OH)Br with good crystallinity can be obtained. Meanwhile, controlled experiments show that the concentration of cetyltrimethylammonium bromide (CTAB) play an important role in the formation of the microdiskettes. Moreover, the ultraviolet-visible (UV-vis) absorbance spectra and photoluminescence (PL) microdiskettes show their ultraviolet absorption and green emitting behavior, indicating that the elliptic Pb(OH)Br microdiskettes have great potential to be applied in luminescent and optoelectronic devices.     

Growth and photocatalytic properties of one-dimensional ZnO nanostructures prepared by thermal evaporation

Aligned ZnO nanorods and nanotubes were grown on the silicon substrates by thermal evaporation of high pure zinc powders without any other metal catalyst. The morphology evolution of ZnO nanostructures with prolonged growth time suggested that the growth of the ZnO nanorods and nanotubes follows the vapor–liquid–solid mechanism. ZnO nanoneedle and nanoparticle films were also synthesized by the same way, and their photocatalytic performances were tested for the degradation of organic dye methylene blue. The ZnO nanoneedle films exhibited very high photocatalytic activities. The decomposition kinetics of the organic pollutant was discussed. Moreover, it is found that the ZnO nanoneedle films showed very stable photocatalytic activity.     

Effect of thickness on the structural, electrical and optical properties of ZnO films

A series of ZnO films of different thickness have been deposited on glass substrates using sol-gel technique by varying the number of spin coatings and the effect of film thickness on the structural, electrical and optical properties have been investigated. The XRD results indicate that the full width at half maximum (FWHM) of the (0 0 2) diffraction peak and the strain along c-axis are decreased as the film is grown up to a thickness of 300 nm. Above 300 nm, the strain again becomes appreciable. The surface morphology shows that the grains become more uniform and bigger in size as the film thickness increases. Electrical result shows that although ZnO film with thickness of around 260 nm has the highest resistivity but is better for current conduction. The excitonic nature in the absorption spectrum becomes prominent for a film with thickness of around 260 nm. The band gap increases and then decreases as the film grows thicker.     

Zinc oxide micro- and nanoparticles: Synthesis, structure and optical properties

Zinc oxide (ZnO) spherical nanoparticles (SNPs) and bitter-melon-like (BML) microparticles were synthesized by a hydrothermal route using a zinc (Zn) plate as a source and substrate at various synthesis conditions. The structural analysis confirmed the formation of ZnO with hexagonal wurtzite phase on the hexagonal Zn substrate with growth of the ZnO microparticles along the [1 0 1] direction. The UV-vis absorption spectra of the ZnO microparticles indicated absorption peaks in the UV region which can be attributed to the band gap of ZnO. The room temperature photoluminescence (PL) of the ZnO microparticles exhibited a broad emission band, which is fitted with four Gaussian peaks and were assigned to transitions involving free excitons and various defect centers. The growth model for the formation of ZnO micro- and nanoparticles is presented.     

Controlled growth and properties of Pb doped ZnO nanodisks

Pb²⁺ doped zinc oxide nanodisks have been grown through a facile solvothermal method. The nanodisks have perfect hexagonal shape with about 1 μm in diagonal and 100 nm in thickness. The existence of Pb²⁺ is vital to the formation of the disk morphology. Room temperature photoluminescence measurements show two photoluminescence peaks centered at 518 and 648 nm. The mechanism of the nanodisk growth is also discussed.     

Hydrothermally-induced morphological transformation of GdVO4:Eu

The aim of the present study is to investigate the effect of a wide pH range on morphology and luminescence properties of europium-doped gadolinium vanadate (GdVO₄:Eu³⁺). GdVO₄:Eu³⁺ powders were hydrothermally synthesized at 180 °C for 24 h in a wide pH range. The as-synthesized powders were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and photoluminescence (PL) spectroscopy. The XRD results showed that GdVO₄:Eu³⁺ with the tetragonal structure formed at pH < 13 as a single phase and Gd(OH)₃ formed at pH ≥ 13 as a secondary phase. The SEM and TEM observations demonstrated the hydrothermally-induced morphological transformation of GdVO₄:Eu³⁺ powders by altering the pH of the synthesis solution. The possible mechanism for the morphological transformation was proposed. The intensities of the prominent peaks at 618 nm in the PL emission spectra of GdVO₄:Eu³⁺ powders considerably shift according to the specific morphology. The luminescence intensity of the octahedron- and rod-like GdVO₄:Eu³⁺ powders hydrothermally obtained at pH = 3 was the strongest one due to high packing density and high crystallinity as well as the extended reduction of the concentration of inherent defect states or adsorbed species.     

Spectroscopic and structural investigations of Er doped zinc bismuth borate glasses

Erbium doped glasses having composition 20ZnO·xBi₂O₃·(79.5 − x)B₂O₃ (15 ≤ x ≤ 35, x in mol%) were prepared by melt-quench technique. The spectroscopic properties were investigated using optical absorption and fluorescence spectra. The Judd–Ofelt intensity parameters, Ω_λ (λ = 2, 4, 6) were determined from the spectral intensities of absorption bands in order to calculate the radiative transition probability (A_R), radiative life time (τ_R), branching ratio (β_R) for various excited luminescent states. Using the emission spectra, full width at half maximum (FWHM), stimulated emission cross-section (σ_e) and figure of merit (FOM) were evaluated. The high values of Judd–Ofelt parameters indicate a substantial mixing of other electronic configuration into the 4f^N configuration by the random crystal field in the glasses. All the intensity parameters (Ω_λ) decrease with increase in Bi₂O₃ content and the effect is found to be most pronounced for Ω₂ values. The structural investigations of the glasses were carried out by recording the IR transmission spectra. A correlation between the network forming units with the multi-phonon relaxation rate and hence with the possibility of radiative quantum efficiency has been made. In addition, various physical and optical parameters have been determined from the measured density and refractive index values.     

Effect of a ZnSe buffer layer on the surface, structural, and optical properties of the ZnTe/ZnSe/GaAs heterostructures

Lattice-mismatched ZnTe epilayers on GaAs (1 0 0) substrates with and without ZnSe buffer layers were grown by using molecular beam epitaxy. AFM, XRD, and TEM measurements were performed to investigate the surface and structural properties of the ZnTe thin films. Photoluminescence, Raman scattering, and TEM measurements showed that the crystallinity of a ZnTe epilayer grown on a GaAs substrate was remarkably improved by using a ZnSe buffer layer. Photoreflectance measurements showed that the strain of the ZnTe layer with the ZnSe buffer layer was smaller than that without the ZnSe buffer layer. These results indicate that ZnTe epitaxial films grown on GaAs substrates with ZnSe buffer layers hold promise for potential applications in optoelectronic devices operating in the blue-green spectral region.     

Third-order nonlinear optical properties of Bi2S3 nanocrystals doped in sodium borosilicate glass studied with Z-scan technique

The third-order nonlinear optical properties of Bi₂S₃ nanocrystals doped in sodium borosilicate glass are measured by Z-scan technique. The microstructures of the glass are characterized by means of X-ray diffraction, transmission electron microscopy, scanning transmission electron microscopy, energy dispersion X-ray spectra, and high-resolution transmission electron microscopy. The results show that the Bi₂S₃ nanocrystals ranging from 10 to 30 nm are determined to be of the orthorhombic crystalline phase, and the third-order optical nonlinear refractive index γ, absorption coefficient β, and susceptibility χ⁽³⁾ of the glass are determined to be 2.56 × 10⁻¹⁶ m² W⁻¹, 4.13 × 10⁻¹⁰ mW⁻¹, and 1.43 × 10⁻¹⁰ esu, respectively.