Effect of pH on the morphology and optical properties of modified ZnO particles by SDS via a precipitation method

ZnO particles were synthesized directly from an aqueous solution of zinc acetate dihydrate in the presence of sodium dodecyl sulfate (SDS) and sodium hydroxide at 70 °C. The morphological changes were investigated in the range of pH 8-12. The hexagonal prism-like shape was formed at pH 8 and 10 by inhibition of growth along the c direction whereas the small rod-like shape was observed at pH 12. The estimated band gap and the room temperature photoluminescence intensity in a visible region are dependent upon the geometrical shape and size of the ZnO particles.     

Electrical and optical properties of Al-doped ZnO and ZnAl2O4 films prepared by atomic layer deposition

ZnO/Al₂O₃ multilayers were prepared by alternating atomic layer deposition (ALD) at 150°C using diethylzinc, trimethylaluminum, and water. The growth process, crystallinity, and electrical and optical properties of the multilayers were studied with a variety of the cycle ratios of ZnO and Al₂O₃ sublayers. Transparent conductive Al-doped ZnO films were prepared with the minimum resistivity of 2.4 × 10⁻³ Ω·cm at a low Al doping concentration of 2.26%. Photoluminescence spectroscopy in conjunction with X-ray diffraction analysis revealed that the thickness of ZnO sublayers plays an important role on the priority for selective crystallization of ZnAl₂O₄ and ZnO phases during high-temperature annealing ZnO/Al₂O₃ multilayers. It was found that pure ZnAl₂O₄ film was synthesized by annealing the specific composite film containing alternative monocycle of ZnO and Al₂O₃ sublayers, which could only be deposited precisely by utilizing ALD technology.     

ZnO assisted photocatalytic degradation of acridine orange in aqueous solution using visible irradiation

A detailed investigation of photocatalytic degradation of the dye, acridine orange, has been carried out in aqueous heterogeneous medium containing ZnO as photocatalyst in a batch reactor. Visible light in the absence of ZnO has negligible effect on degradation. The disappearance of the dye, monitored spectrophotometrically, follows approximately pseudo-first order kinetics according to the Langmuir–Hinshelwood model. The total degradation of dye was tested using the chemical oxygen demand (COD) method. The addition of an optimal amount of hydrogen peroxide and potassium persulphate increases the degradation rate while NaCl and Na₂CO₃ decreases. The effect of addition of cationic and anionic surfactants has also been investigated. Bubbling of nitrogen in the reaction solution decreases the reaction rate. ZnO has been found experimentally to be a highly efficient photocatalyst for the degradation of acridine orange dye and hence there is a great potential in the treatment of organic pollutants such as dyes.     

Annealing atmospheres induced structural and morphological transformation of zinc tin hydroxide nanostructures

The variation in crystallinity, morphology and phase of zinc tin hydroxide nanostructures are investigated after annealing at different (oxidizing, non-oxidizing and reducing) atmospheres. The zinc tin hydroxide nanostructures are prepared using hydrolysis assisted co-precipitation method. Annealing in oxidizing (oxygen and air) and non-oxidizing (nitrogen and argon) atmospheres do not have a significant effect on morphological and structural properties. However, the annealing in the reducing (ammonia) atmosphere converts the cubic nanostructures into nanorods and spherical particles. The zinc tin hydroxide forms three new phases (ZnON, SnO₂ and Sn) after annealing in reducing atmosphere. The formation of ZnON and SnO₂ phases are evident in Raman and XPS analysis. The reducing atmosphere (ammonia) changes the reaction kinetics leading to diffusion control crystal growth that could be responsible for such structural and morphological transformation. The bandgap is significantly changed after morphological and structural transformation with notable variation in photocurrent density, charge transfer resistance, and charge carrier concentration.     

High carrier mobility low-voltage ZnO thin film transistors fabricated at a low temperature via solution processing

Wide-bandgap ZnO TFTs have many potential applications in large-area, flexible electronics and transparent devices because of their low cost, high performance and excellent optical transmittance. High-performance ZnO TFTs fabricated via simple solution processing have been widely studied. However, the key issues of solution-processable ZnO TFTs are the relatively high processing temperature (> 300?°C) and the high operating voltage for achieving the desired electrical properties. Here, we successfully fabricated low-voltage ZnO TFTs at an annealing temperature of ≤?250?°C. The resulting ZnO transistors with high-k terpolymer P(VDF-TrFE-CFE) showed a mobility of up to 5.3?cm² V^?1 s^?1 and an on/off ratio of >?10⁵ at 3?V. Furthermore, the influence of the dielectric constant on the carrier mobility was investigated. A lower k-value dielectric resulted in a high carrier mobility under the same carrier density. Therefore, with a low-k CYTOP dielectric applied to modify the interface between the ZnO semiconductor and the P(VDF-TrFE-CFE) layer, ZnO transistors annealed at 250?°C showed an electron mobility of 13.6?cm² V^?1 s^?1 and an on/off ratio of >?10⁵ at 3?V. To the best of our knowledge, this mobility is the highest value reported to date among the low-voltage solution-processable undoped ZnO TFTs annealed at temperatures of ≤?300?°C.     

Hexagonal core-shell and alloy Au/Ag nanodisks on ZnO nanorods and their optical enhancement effect

Au and Ag hybrid hexagonal nanodisks were synthesized on ZnO nanorods'' (0002) surface via a new two-step deposition-annealing method. The structural, compositional, as well as optical investigations were carried out systematically to find out the nanodisks'' formation mechanism and optical enhancement effect. It was shown that the core-shell Au/Ag nanodisk can be formed under rapid annealing temperature of 500°C, while Au/Ag alloy nanodisks are formed if higher temperatures (>550°C) are applied. The optical effect from these nanodisks was studied through photoluminescence and absorption spectroscopy. It was found that the carrier-plasmon coupling together and carrier transfer between metal and ZnO contribute to the emission enhancement. Furthermore, the results suggest that the composition of nanodisk on the vicinity of metal/ZnO interface plays an important role in terms of the enhancement factors.     

Cu-doped ZnO nanorod arrays: the effects of copper precursor and concentration

Cu-doped ZnO nanorods have been grown at 90°C for 90 min onto a quartz substrate pre-coated with a ZnO seed layer using a hydrothermal method. The influence of copper (Cu) precursor and concentration on the structural, morphological, and optical properties of ZnO nanorods was investigated. X-ray diffraction analysis revealed that the nanorods grown are highly crystalline with a hexagonal wurtzite crystal structure grown along the c-axis. The lattice strain is found to be compressive for all samples, where a minimum compressive strain of −0.114% was obtained when 1 at.% Cu was added from Cu(NO₃)₂. Scanning electron microscopy was used to investigate morphologies and the diameters of the grown nanorods. The morphological properties of the Cu-doped ZnO nanorods were influenced significantly by the presence of Cu impurities. Near-band edge (NBE) and a broad blue-green emission bands at around 378 and 545 nm, respectively, were observed in the photoluminescence spectra for all samples. The transmittance characteristics showed a slight increase in the visible range, where the total transmittance increased from approximately 80% for the nanorods doped with Cu(CH₃COO)₂ to approximately 90% for the nanorods that were doped with Cu(NO₃)₂.     

Controllable synthesis of ZnO nanostructures on the Si substrate by a hydrothermal route

In this paper, controllable synthesis of various ZnO nanostructures was achieved via a simple and cost-effective hydrothermal process on the Si substrate. The morphology evolution of the ZnO nanostructures was well monitored by tuning hydrothermal growth parameters, such as the seed layer, solution concentration, reaction temperature, and surfactant. X-ray diffraction and photoluminescence measurements reveal that crystal quality and optical properties crucially depend on the morphology of the ZnO nanostructures. The ease of synthesis and convenience to tune morphology and optical properties bring this approach great potential for nanoscale applications.     

Influence of gas carrier on morphological and optical properties of nanostructured In2O3 grown by solid-vapour process

Nanostructured indium oxide (In₂O₃) thin film was prepared by solid-vapour deposition method under NH₃ and Ar atmosphere. The influence of gas nature on the growth of In₂O₃ thin film was investigated in terms of structure, morphology and optical properties. X-ray diffraction, Raman spectroscopy and photoluminescence analyses indicated the formation of pure In₂O₃ phase with strong preferred orientation along c-axis, from cubic- to needles-like morphologies. The as-fabricated nanostructured In₂O₃ thin films with tailored morphology, enhanced crystallinity and optical quality can be used for gas sensing, solar cells and other potential applications. In addition, the potential use of NH₃ as carrier gas for an efficient control of morphology/size and optical properties can be proposed for the fabrication of other nanostructured oxides.     

Role of annealing temperature on structural and optical properties of zinc oxy-nitride films synthesized by powder vapor transport technique

Zinc oxy-nitride (ZnON) is an emerging semiconductor having tunable energy bandgap (Eg) and refractive index (n). Herein, the effect of annealing temperature on ZnON films synthesized on glass substrates at different (50, 100 and 150 sccm) nitrogen gas flow rates (NGFR) by simple powder vapor transport (PVT) technique is studied. All the synthesized ZnON films are annealed at 300 °C for 60 min. The unannealed and annealed ZnON (Un-&-An-ZnON) films are characterized by XRD, SEM, Raman and UV spectroscopies. XRD analysis confirms the formation of polycrystalline ZnN films and no diffraction plane related to oxide phase. The crystallinity of Un-ZnN films is increased after annealing, however, it is maximum for 100 sccm NGFR. Raman analysis indicates the presence of vibrational modes related to ZnN and ZnO phases, thereby confirming the formation of ZnON films. After annealing, the surface morphologies of Un-ZnON films is transformed from nano-sheets/nano-blocks to rounded nanoparticles. The change in structural and morphological features of ZnON films, associated with annealing temperature causes to create stresses and defects and hence Eg and n. The values of n (1.85–1.87) and Eg (2.6–2.7 eV) of Un-ZnON films are increased to (1.98–2.62) and (3.16–3.25 eV), after annealing, respectively. These inexpensive but high quality ZnON films can be used for semiconducting and optoelectronic devices.     

Annealing impact on the structural and optical properties of electrospun SnO2 nanofibers for TCOs

Tin oxide (SnO₂) nanofibers were fabricated by electrospinning technique and subsequent annealed at different temperatures. The structure, morphology and optical properties of the annealed samples were characterized by X-ray diffraction (XRD), Raman, scanning electron microscopy/energy dispersive spectroscopy (SEM/EDS), transmission electron microscopy (TEM), Fourier transformed infrared (FTIR),and optical absorption techniques. The phase of SnO₂ of all samples is rutile (tetragonal), and at higher annealing temperatures, good crystallinity and lower absorption were obtained. Annealing of the samples at 600 °C caused the lower absorption and higher optical band gap, and the decrease of the absorption was probably because the fiber structure changed from solid to hollow structure. From PL spectra, it was observed that the SnO₂ hollow nanofibers annealed at 600 °C revealed green emission at 530 nm.     

Annealing temperature and environment effects on ZnO nanocrystals embedded in SiO2: a photoluminescence and TEM study

We report on efficient ZnO nanocrystal (ZnO-NC) emission in the near-UV region. We show that luminescence from ZnO nanocrystals embedded in a SiO₂ matrix can vary significantly as a function of the annealing temperature from 450°C to 700°C. We manage to correlate the emission of the ZnO nanocrystals embedded in SiO₂ thin films with transmission electron microscopy images in order to optimize the fabrication process. Emission can be explained using two main contributions, near-band-edge emission (UV range) and defect-related emissions (visible). Both contributions over 500°C are found to be size dependent in intensity due to a decrease of the absorption cross section. For the smallest-size nanocrystals, UV emission can only be accounted for using a blueshifted UV contribution as compared to the ZnO band gap. In order to further optimize the emission properties, we have studied different annealing atmospheres under oxygen and under argon gas. We conclude that a softer annealing temperature at 450°C but with longer annealing time under oxygen is the most preferable scenario in order to improve near-UV emission of the ZnO nanocrystals embedded in an SiO₂ matrix.     

Effect of zinc precursor ratio on morphology and luminescent properties of ZnO nanoparticles synthesized in CTAB medium

In this study, the effect of zinc precursor ratio on structural, morphology and luminescent properties of zinc oxide (ZnO) nanoparticles (NPs) prepared by cationic surfactant-assisted method was studied. ZnO NPs were prepared at room temperature by increasing Zn²⁺: CTAB mole ratio. The pristine ZnO samples showed phase-purity (without need for calcination) as shown by X-ray diffractograms (XRD). Nitrogen adsorption ? desorption analysis showed that the samples exhibit Type III isotherm and H3 hysteresis with mesoporosity. The triangular- to quadrilateral-shaped morphological evolution of the ZnO NPs with increasing concentrations of zinc ions was confirmed by SEM and TEM images of the samples. The UV–Vis–DRS studies showed blue-shifted λ_max (band gap) in all the ZnO samples which indicated their nanostructured nature. The photoluminescence spectra of these ZnO samples show emissions in UV and visible regions. The mechanism of formation of nanostructured ZnO was suggested based on the model reported for mesoporous silica synthesized in CTAB medium.     

Effects of annealing temperature on the phase formation,optical, photoluminescence and magnetic properties of sol-gel YFeO3 films

YFeO₃ (YFO) thin films were deposited onto quartz substrates via sol-gel spin-coating technique and annealed at different temperature ranged between 650 and 900 °C. The impact of annealing temperature on the phase formation, microstructural, optical, photoluminescence (PL) and magnetic properties of the films were systematically investigated. X-ray diffraction analysis revealed an amorphous structure in film annealed at 650 °C and formation of hexagonal-YFO (h-YFO) phase in films annealed at 750–800 °C. The films annealed at 850–900 °C exhibited an orthorhombic-YFO (o-YFO) structure. Atomic force microscopy images of h-YFO films showed homogeneous surface with uniform particles size and shape. The particle size increased and had irregular shape in o-YFO films. The average particle size was 44 and 117 nm, while the root square roughness was 1.38 and 2.55 nm for h- and o-YFO films annealed at 750 and 850 °C, respectively. The optical band gap (E_g) was 2.53 and 2.86 eV for h- and o-YFO films annealed at 750 and 850 °C, respectively. The PL spectra of h-YFO films were red-shifted compared with that of o-YFO films. The PL emission related to near band edge was observed at 459.0 and 441.9 nm for h- and o-YFO films annealed at 750 and 850 °C, respectively. The magnetization was enhanced with the increasing of annealing temperature and has the value of 4.8 and 12.5 emu/cm³ at 5000 Oe for h- and o-YFO films annealed at 750 and 850 °C, respectively.     

Multifunctional ZnO/Fe-O and graphene oxide nanocomposites: Enhancement of optical and magnetic properties

ZnO is a semiconductor with a great interest, but it has several deficiencies which limit its use in technologic applications. One important limitation is having the band gap in the UV which reduces its use in optical devices. To solve this problem, in this work, composites based in ZnO with goethite and graphene oxide (GO) by sol-gel are prepared. The obtained samples (powders and thin films) were characterized microstructurally (DTA, XRD, micro-Raman, FE-SEM), optically (transmittance and photoluminescence) and magnetically (SQUID). The ZnO band gap of multifunctional composites shows a red-shift towards visible range (E_g ∼3.01 eV) with high transmittance ∼85% (thickness of 362 nm) over the visible wavelength range. A long-range magnetic order at room temperature appears in these nanocomposites (Ms = 1.60·10⁻² emu/g). The combination of both dopants allows modifying the functional properties of ZnO, opening a great field of applications in ZnO composites, such as spintronic and optoelectronic devices.     

Effect of ignition temperature and fuel amount on photocatalytic activity of solution combustion synthesized ZnO

Nanocrystalline zinc oxide (ZnO) photocatalyst has been synthesized by a simple solution combustion method using zinc nitrate as the oxidizer and urea as the fuel. Effect of fuel to oxidizer ratio and ignition temperature on the mechanism of combustion synthesis, crystallinity, morphology, surface area, and optical properties were investigated by thermal analysis, X-ray diffraction (XRD), Scanning electron microscopy (SEM), Diffuse reflectance UV–Visible spectra and Photoluminescence analyses. Photocatalytic activity of the synthesized materials was evaluated by degrading an azo dye at ambient temperature and solution pH. The prepared photocatalysts at the fuel-rich condition possess small crystallite size and more surface area; consequently, a higher photocatalytic dye degradation capability.The powder samples synthesized at the fuel-oxidant ratio of 1.8 and the ignition temperature at 400 °C have shown the maximum percentage (99%) of dye degradation in 180 min. The pseudo-first order photocatalytic dye degradation rate constant of a catalyst sample synthesized at the fuel-oxidant ratio of 1.8 was 0.0253 min⁻¹and it is 3.14 and 2.88 times higher than that of samples synthesized at fuel-oxidant ratios of 0.6 and 1.The outcomes of the present article help to design more pronounced experiments for the synthesis of photocatalysts by varying ignition temperatures and fuel amounts.     

Synthesis,structural and morphological characteristics,magnetic and optical properties of Co doped ZnO nanoparticles

Zn_1−xCo_xO (x==0.05, 0.10, 0.15) nanoparticles have been synthesized by an alternative wet-chemical synthesis route using the SimAdd technique. The as-obtained powders were investigated by FT-IR spectroscopy, X-ray diffraction and thermal analysis correlated with evolved gas analysis (TG–DTA–FT-IR) in order to determine their chemical nature, crystalline structure and to establish the decomposition sequences. The precipitates are generally amorphous, but low-intensity reflection peaks assigned both to the zinc oxalate dihydrate, and zinc hydroxide can be observed in the recorded patterns, indicating that hydroxy-oxalate precipitates were obtained. The structure, morphology and magnetic properties of the thermally treated samples have been investigated by X-ray diffraction, FT-IR, HRTEM, SAED, UV–vis and EPR. XRD studies reveal a hexagonal wurtzite-type structure for all Zn_1−xCo_xO samples. TEM investigations show particle size between 28 and 37 nm, with spherical and polyhedral shapes and with tendency to form aggregates. The presence of a Co₃O₄ secondary phase was evidenced by XRD, UV–vis and EPR for the Zn_0.85Co_0.15O sample. The ferromagnetic behavior of the samples was revealed. The paper highlights that by varying the cobalt concentration it is possible to modulate the structural, morphological, optical and magnetic properties.     

Modification of optical and electrical properties of zinc oxide-coated porous silicon nanostructures induced by swift heavy ion

Morphological and optical characteristics of radio frequency-sputtered zinc aluminum oxide over porous silicon (PS) substrates were studied before and after irradiating composite films with 130 MeV of nickel ions at different fluences varying from 1 × 10¹² to 3 × 10¹³ ions/cm². The effect of irradiation on the composite structure was investigated by scanning electron microscopy, X-ray diffraction (XRD), photoluminescence (PL), and cathodoluminescence spectroscopy. Current–voltage characteristics of ZnO-PS heterojunctions were also measured. As compared to the granular crystallites of zinc oxide layer, Al-doped zinc oxide (ZnO) layer showed a flaky structure. The PL spectrum of the pristine composite structure consists of the emission from the ZnO layer as well as the near-infrared emission from the PS substrate. Due to an increase in the number of deep-level defects, possibly oxygen vacancies after swift ion irradiation, PS-Al-doped ZnO nanocomposites formed with high-porosity PS are shown to demonstrate a broadening in the PL emission band, leading to the white light emission. The broadening effect is found to increase with an increase in the ion fluence and porosity. XRD study revealed the relative resistance of the film against the irradiation, i.e., the irradiation of the structure failed to completely amorphize the structure, suggesting its possible application in optoelectronics and sensing applications under harsh radiation conditions.     

Effect of precursor concentration on structural,morphological and opto-electric properties of ZnO thin films prepared by spray pyrolysis

Sprayed ZnO films were grown on glass substrate at 400 °C using zinc chloride as precursor with different molar concentrations varying from 0.05 to 0.2 M. X-ray diffraction patterns reveal that ZnO films are polycrystalline with hexagonal wurtzite structure with preferred orientation in (002) plane. Optical measurements show that transmittance reaches a maximum value of 95% in the visible region for ZnO films prepared from precursor with 0.05 M concentration. The films obtained from the precursor with 0.1 M concentration have the highest electrical conductivity and photocurrent values.     

Structural and optical properties of ZnO nanorods by electrochemical growth using multi-walled carbon nanotube-composed seed layers

We reported the enhancement of the structural and optical properties of electrochemically synthesized zinc oxide [ZnO] nanorod arrays [NRAs] using the multi-walled carbon nanotube [MWCNT]-composed seed layers, which were formed by spin-coating the aqueous seed solution containing MWCNTs on the indium tin oxide-coated glass substrate. The MWCNT-composed seed layer served as the efficient nucleation surface as well as the film with better electrical conductivity, thus leading to a more uniform high-density ZnO NRAs with an improved crystal quality during the electrochemical deposition process. For ZnO NRAs grown on the seed layer containing MWCNTs (2 wt.%), the photoluminescence peak intensity of the near-band-edge emission at a wavelength of approximately 375 nm was enhanced by 2.8 times compared with that of the ZnO nanorods grown without the seed layer due to the high crystallinity of ZnO NRAs and the surface plasmon-meditated emission enhancement by MWCNTs. The effect of the MWCNT-composed seed layer on the surface wettability was also investigated.