Acceptor related photoluminescence and field emission of ZnO:P nanostructures

ZnO:P nanobelts were self-assembly synthesized by thermal evaporation of Zn power and P₂O₅ mixture. The temperature dependence photoluminescence of ZnO:P nanostructures was studied from 81 to 291 K. As the temperature increased from 81 to 111 K, the PL intensity of DAP emission was obviously enhanced. The abnormal PL intensities were ascribed to the acceptor vibration with local phonon and lattice phonon assistant. The PL of zinc vacancy and its replica were well resolved due to the strenuous vibration of Zn vacancy. The replica of zinc vacancy emission increased while the visible emission gradually decreased with the temperature increase. It suggested that there were intensive deep acceptor vibration. The field emission properties of the ZnO:P nanostructures have been investigated according to the acceptor-related PL spectra. The influence of space charge effect on the field emission behaviors was also discussed.     

Controlling phosphorus doping concentration in ZnO nanorods by low temperature hydrothermal method

Phosphorous-doped ZnO nanorods (NRs) were synthesized with controllable morphology and doping concentration on top of the array of undoped natural n-type ZnO NRs by hydrothermal process. By changing the concentration of NH₄OH to adjust the pH of the reactant solution containing zinc acetate, hexamethylenetetramine, and ammonium phosphate, it was possible to control the morphology, doping concentration, and band structure of the ZnO nanostructures formed on the top side of the undoped NRs array. When the NH₄OH concentration was 1 vol% substitutional dopant P formed shallow acceptor levels in the ZnO NRs, while higher NH₄OH concentration resulted in the formation of donor levels as well as the compensation of the acceptors. A model p–n homojunction device based on the P-doped ZnO NRs consecutively attached to the initially synthesized n-type NRs showed a rectifying junction behavior confirming the formation of the p-type ZnO NRs with low doping concentration of P.     

Synthesis, optical and field emission properties of three different ZnO nanostructures

Three different ZnO nanostructures: nanocherries, nanomultipeds and nanospindles were successfully synthesized by thermal evaporation method under different experimental conditions. The X-ray diffraction peaks indicate that these ZnO nanostructures prefer to grow along the c-axis. Photoluminescence (PL) spectra show that they are partially related to morphologies. Comparing the field emission (FE) measurements of the three ZnO nanostructures, we found that the nanocherries structure has the lowest turn-on and threshold field, 2.31 V/μm and 5.83 V/μm, respectively, for nanospindles and nanomultipeds structures, they are 2.82 V/μm and 6.57 V/μm, 3.13 V/μm and 7.35 V/μm, revealing that the nanocherries structure may be one of the promising candidates for field emission displays.     

The fabrication and properties of field emission display based on ZnO tetrapod-liked nanostructure

ZnO tetrapod-liked nanostructure with fine crystalline structure and high purity was synthesized via CVD method. Each branch of the nanotetrapod was 50-200 nm in diameter and the nanotetrapod structure exhibited a high aspect ratio. Cathode emission materials with this nanostructure were employed to fabricate field emission display with 72 × 72 pixel array. The as-obtained device showed an ideal field emission property with a threshold electric field of 4.1 V/μm and an emission current density of 1 mA/cm² when the electric field reached 11.5 V/μm. The field enhancement factor of the nanotetrapods was calculated to be 1852. Using proper circuit drive, dynamic Chinese characters can be successfully displayed in the device.     

Efficient field emission properties of ZnO (core)/graphite (shell) nanowires

In this work the field emission studies of a new type of field emitter, zinc oxide (ZnO) core/graphitic (g-C) shell nanowires are presented. The nanowires are synthesized by chemical vapor deposition of zinc acetate at 1300 °C Scanning and transmission electron microscopy characterization confirm high aspect ratio and novel core–shell morphology of the nanowires. Raman spectrum of the nanowires mat represents the characteristic Raman modes from g-C shell as well as from the ZnO core. A low turn on field of 2.75 V/μm and a high current density of 1.0 mA/cm² at 4.5 V/μm for ZnO/g-C nanowires ensure the superior field emission behavior compared to the bare ZnO nanowires.     

Graphene oxide modified ZnO nanorods hybrid with high reusable photocatalytic activity under UV-LED irradiation

In this work, graphene oxide/zinc oxide (GO/ZnO) hybrid was prepared through a facile hydrothermal process. Transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectra and N₂ adsorption and desorption isotherms were used to investigate the morphology, crystal structure, optical properties and specific surface area of GO/ZnO hybrid. It was shown that the well-dispersed ZnO nanorods were deposited on GO homogeneously. Photocatalytic properties of GO/ZnO nanorods hybrid were evaluated under 375 nm light-emitting diode light irradiation for photodegradation of methylene blue (MB). The synergic effect between GO and ZnO was found to lead to an improved photo-generated carrier separation. An optimal GO content has been determined to be 3 wt%, and corresponding the apparent pseudo-first-order rate constant kapp$k_{\text{app}}$ is 0.0248 min⁻¹, 4.3 times and 2.5 times more than that of pure ZnO nanorods and commercial P25 photocatalyst, respectively. Moreover, the cyclic photocatalytic test indicated that GO/ZnO hybrid can be reused for degradation of MB, suggesting the possible application of GO/ZnO hybrid as excellent candidate for water treatment.     

Enhanced field emission from ZnO nanoneedles on chemical vapour deposited diamond films

ZnO nanoneedles were coated on hot filament chemical vapour deposited diamond thin films to enhance the field emission properties of ZnO nanoneedles. The virgin diamond films and ZnO nanoneedles on diamond films were characterized using scanning electron microscopy, X-ray photoelectron spectroscopy and Raman spectroscopy. The field emission studies reveal that the ZnO nanoneedles coated on diamond film exhibit better emission characteristics, with minimum threshold field (required to draw a current density ~ 1 μA/cm²) as compared to ZnO needles on silicon and virgin diamond films. The better emission characteristic of ZnO nanoneedles on diamond film is attributed to the high field-enhancement factor resulting due to the combined effect of the ZnO nanoneedles and diamond film.     

Novel low temperature synthesis of ZnO nanostructures and its efficient field emission property

We have developed a novel, simple and cost effective wet chemical synthetic route for the production of ZnO nanoneedles and nanoflowers at low temperature. The synthesis process does not require any surfactant, template or pre-seeding. The synthesized ZnO nanoneedles have very sharp tips with their lengths in the range 2-3 μm, while for the case of nanoflowers, the nanoneedles were bunched together. X-ray diffraction study and X-ray photoelectron spectroscopic studies confirmed the formation of pure ZnO phase. Studies on the electron field emission property of the grown nanostructures showed that they are very efficient field emitter. The turn-on fields and the threshold fields are 3.6 V/μm, 4.4 V/μm and 5.4 V/μm, 6.8 V/μm for the ZnO nanoneedles and ZnO nanoflowers, respectively. The enhanced field emission property was attributed to the presence of sharp tips of the nanostructures.     

Synthesis of large-area single-walled carbon nanotube films on glass substrate and their field electron emission properties

Large-area and homogeneous single-walled carbon nanotube (SWCNT) films have been deposited via arc discharge directly on glass substrate coated with a layer of indium tin oxide film. The characterization, by means of electron microscopy and Raman spectroscopy, shows that the as-grown films are uniformly woven and consist of SWCNT with diameters ranging from 0.82 to 1.15 nm. As a cathode material, the field emission test indicates the films have low turn-on field of ∼1.2 V/μm at 10 μA/cm² emission current, and high emission intensity causing luminance of about 7000 cd/cm² with fine uniformity. The best performing sample exhibits a constant degradation of less than 3% per hour at an emission current of around 1 mA. Measuring with the high voltage (2000 V) on the films for 2.0 h increased the field enhancement factor from 4500 to 5400 at the high field region. The results are of significance to the development of field emission display using nanoemitters.     

Oxygen plasma assisted end-opening and field emission enhancement in vertically aligned multiwall carbon nanotubes

This paper highlights the changes in micro-structural and field emission properties of vertically aligned carbon nanotubes (VACNTs) via oxygen plasma treatment. We find that exposure of very low power oxygen plasma (6 W) at 13.56 MHz for 15–20 min, opens the tip of vertically aligned CNTs. Scanning electron microscopy and transmission electron microscopy images were used to identify the quality and micro-structural changes of the nanotube morphology and surfaces. Raman spectra showed that the numbers of defects were increased throughout the oxygen plasma treatment process. In addition, the hydrophobic nature of the VACNTs is altered significantly and the contact angle decreases drastically from 110° to 40°. It was observed that the electron field emission (EFE) characteristics are significantly enhanced. The turn-on electric field (ETOE) of CNTs decreased from ∼0.80 V μm⁻¹ (untreated) to ∼0.60 V μm⁻¹ (oxygen treated). We believe that the open ended VACNTs would be immensely valuable for applications such as micro/nanofluidic based filtering elements and display devices.     

Preparation,characterization, and photoluminescence study of PVA/ZnO nanocomposite films

ZnO nanoparticles with average diameter of 25 nm were synthesized by a modified sol–gel method and used in the preparation of (in wt.%) (100 − x) poly(vinyl alcohol) (PVA)/x ZnO nanocomposite films, with x = 0, 1, 2, 3, 4, and 5. The PVA/ZnO films were exposed to UV radiation for 96 h and their thermal, morphological, and spectroscopic properties were investigated. In inert atmosphere, the nanocomposite films showed lower thermal stability than the pure PVA film, and the calorimetric data suggest an interaction between PVA and ZnO in the nanocomposite films. Some crystalline phases could be seen in the films with ZnO, and a direct dependence on the ZnO concentration was also observed. The original structure of ZnO nanoparticles remained unaltered in the PVA matrix and they were uniformly distributed on the film surface. The roughness of the PVA film was not modified by the addition of ZnO; however, it increased after 96 h of UV irradiation, more significantly in the nanocomposite films. The films showed an absorption band centered at 370 nm and a broad emission band in the UV–vis region when excited at 325 nm.     

Field emission of carbon nanotubes grown on nickel substrate

Carbon nanotubes (CNTs) have been synthesized directly on the electrically conducting nickel substrate without additional catalyst. Field emission properties of the as-prepared sample were characterized using parallel plate diode configurations. It was observed that the field emission qualitatively follows the conventional Fowler–Nordheim (F–N) theory from the straight line of ln(I/V²) versus 1/V plot at the high applied field region. The uniformity and stability of the electron emission have also been examined. The low electron turn-on field (E_to) and high emission current density indicates the potential applications of this new CNT-based emitter.     

Field emission characteristics from tapered ZnO nanostructures grown onto vertically aligned carbon nanotubes

Zinc oxide (ZnO) nanostructures were grown on vertically aligned carbon nanotubes (CNTs) using thermal chemical vapor deposition (CVD) to enhance the field emission characteristics. The shape of ZnO nanostructure was tapered. Scanning electron microscopy (SEM) image showed the ZnO nanostructures were grown onto CNT surface uniformly. The field electron emission of pristine CNTs and ZnO-coated CNTs were measured. The results showed that ZnO nanostructures grown onto CNTs could improve the field emission characteristics. The ZnO-coated CNTs had a threshold electric field at about 3.1 V/μm at 1.0 mA/cm². The results demonstrated that the ZnO-coated CNT is an ideal field emitter candidate material. The stability of the field emission current was also tested.     

Field emission properties of electrodeposited cobalt nanowire arrays grown in anodic aluminum oxide

The excellent vertically aligned cobalt nanowire arrays were electrodeposited into anodic aluminum oxide (AAO) templates. Each nanowire has the same length with 20 μm and the diameter with 60 nm. The field emission characteristics of the nanowires were firstly studied based on current-voltage measurements and the Fowler-Nordheim equation. The electron field emission measurements on the samples showed a turn-on field (1 mA/cm²) of 1.66 V/μm, a field enhancement factor of β = 3054 and a current density of 600 mA/cm² at a relatively low voltage of 4.3 V/μm. The nanowire arrays could be an ideal alternative to carbon nanotubes and ZnO nanowires for the fabrication of flat panel displays.     

Directed growth of 1D cadmium sulfide by chemically anchored Al2O3 and ZnO nanoparticles

Cadmium sulfide nanowires were synthesized on in-situ generated alumina nanoparticles using a one pot hydrothermal method. As grown hexagonal-phase cadmium sulfide nanowires have diameters ranging from 40 to 50 nm. Mechanistic aspects reveal that the alumina template based growth of cadmium sulfide nanowires is due to the fact that S²⁻ ions will preferably attach to the aluminum due to the Lewis acidic character of Al³⁺ (~ 0.5 on Brown's scale of average Lewis acid strength). To support the proposed mechanism, we have further shown the growth of cadmium sulfide nanowires on zinc ions having similar Lewis acidic strength.     

Characterization and enhanced field emission properties of carbon nanotube bundle arrays coated with N-doped nanocrystalline anatase TiO2

Anatase TiO₂ nanocrystals (NCs) were deposited onto patterned carbon nanotube (CNT) bundle arrays to form a TiO₂/CNT composite using metal organic chemical vapor deposition (MOCVD) using titanium-tetraisopropoxide (Ti(OC₃H₇)₄) as a source reagent. The N-doped TiO₂/CNT composite was then fabricated using nitrogen plasma treatment. The structural and spectroscopic properties of TiO₂/CNT composites were characterized by field-emission scanning electron microscopy, micro-Raman spectroscopy and X-ray photoelectron spectroscopy. The combined geometrical structure and low electron affinity effects of N-doped TiO₂ led to a low turn-on field of 1.0 V μm⁻¹ at a current density of 10 μA cm⁻², a low threshold field of 1.9 V μm⁻¹ at a current density of 1 mA cm⁻², a high field enhancement factor of 3.0 × 10³, and long-term stability for the N-doped TiO₂/CNT composite. The results revealed that the N-doped TiO₂/CNT composite can be a potential candidate for field emission devices.     

One-step approach to prepare magnetic iron oxide/reduced graphene oxide nanohybrid for efficient organic and inorganic pollutants removal

An environmentally friendly effective technique was demonstrated to prepare iron oxide/reduced graphene oxide nanohybrid (IO/RGO) at room temperature by using banana peel ash aqueous extract as the base source and Colocasia esculenta leaves aqueous extract as the reducing agent. The nanohybrid was characterized by Fourier transform infrared spectroscopy, X-ray diffractometry, transmission electron microscopy, vibrating sample magnetometry, Raman spectroscopy and thermal studies. The results indicated the decoration of superparamagnetic IO nanoparticles on the surface of the RGO. Both organic and inorganic pollutants were effectively removed from the contaminated water (for Pb²⁺ and Cd²⁺ within 10 min, whereas for tetrabromobisphenol A within 30 min) by IO/RGO. The study revealed that adsorption followed pseudo-second order kinetics and isotherms were well described by the Langmuir model in all the cases. The thermodynamics parameters (ΔG°, ΔS° and ΔH°) were calculated from the temperature dependent isotherms and indicated that the adsorptions were endothermic and spontaneous.     

Field emission characteristics of CuO nanowires by hydrogen plasma treatment

CuO nanowires were formed on copper-coated silicon substrates by a wet chemical process, immersing them in a hot alkaline solution. The effect of hydrogen plasma treatment on the field emission characteristics of the CuO nanowires was investigated. The results showed that hydrogen plasma treatment enhanced the field emission characteristics of the CuO nanowires showing a decrease in turn-on voltage as well as an increase of field enhancement factor. It is believed that hydrogen plasma treatment plays an important role in the improvement of field emission characteristics of CuO emitters.