Thermal annealing induced structural and optical properties of Ca doped ZnO nanoparticles

In this letter, the effects of annealing on structural and optical properties of Ca doped ZnO nanoparticles have been investigated. X-ray diffraction analysis reveals that the prepared particles are in hexagonal wurtzite structure and formation of secondary phase related to the Calcite was found after thermal annealing. UV–Vis measurements show free exciton absorption band appeared at 372 nm and increase of band gap with annealing of samples. Room temperature photoluminescence (PL) spectrum of the prepared Ca doped ZnO nanoparticles shows bands which belong to the near band edge emission at 377 nm and green emission at 556 nm. Annealed samples exhibit enhancement in the blue emission band. Raman spectra show the increment in the electron–phonon coupling value with annealing.     

Structural and optoelectronic characterization of prepared and Sb doped ZnO nanoparticles

This paper briefly reports the structural and optoelectronics properties of prepared pure and Sb doped ZnO nanoparticles. Doping with suitable elements offers an efficient method to control and enhance the optical properties of ZnO nanoparticles, which is essential for various optoelectronics applications. Sb doped ZnO nanoparticles have significant concern due to their unique and unusual electrical and optical properties. In the present work, we report the synthesis of Sb doped ZnO successfully with average particle size range from 26 to 29 nm via direct precipitation method. The phase purity and crystallite size of synthesized ZnO and Sb doped nano-sized particles were characterized and examined via X-ray diffraction (XRD) and scanning electron microscopy (SEM). The elemental analyses of undoped and doped ZnO nanoparticles were examined by using energy-dispersive X-ray spectroscopy (EDAX).We investigated and measured the optoelectronics properties of synthesized ZnO and Sb doped ZnO nanoparticles by employing photoluminescence and UV–Visible spectroscopy. The influence of Sb doping on photoluminescence (PL) spectra of ZnO nanoparticles, which consists of UV emission and broad visible emission band, is found to be strongly dependent upon the Sb concentration for all the Sb doped ZnO nanoparticles samples under investigation. The UV–Visible absorption study shows an increase in band gap energy as Sb is incorporated on the ZnO nanoparticles.     

Microstructural and photoluminescence properties of tin dioxide modified by electron beam irradiation

A modified technique was developed by electron beam irradiation to prepare tin dioxide (SnO2) nanocrystals using the sol-gel method. SnO2 nanoparticles were radiated under a 1,400 KGy dose. The morphology and microstructure of the SnO2 nanocrystals were investigated by X-ray diffraction, high-resolution transmission electron microscopy (HRTEM), and Raman spectroscopy. The results indicate that the irradiated SnO2 nanoparticles have better crystallinity than unirradiated SnO2 nanoparticles, and the resulting nanocrystals have a tetragonal rutile crystalline structure. The HRTEM image proves that the average grain size is about 4 nm, and the clear lattice fringes indicate the improvement of SnO2 nanocrystals after irradiation. The Raman spectrum shows that there are new peaks at 535 cm(-1) and 691 cm(-1). The optical properties of SnO2 nanoparticles were characterized by ultraviolet-visible (UV-vis) and photoluminescence spectrophotometers. The band gap energy of the irradiated SnO2 was 3.29 eV smaller than that of the unirradiated SnO2 due to size effects and some defects of SnO2 nanocrystals. This work provides a novel approach for the improvement of SnO2 nanocrystals. The optical properties of the irradiated SnO2 nanomaterials are also expected to improve.     

Structural phase analysis,band gap tuning and fluorescence properties of Co doped TiO2 nanoparticles

This paper reports on structural and optical properties of Co (0, 3, 5 & 7 mol%) doped TiO₂ (titania) nanoparticles (NPs) synthesized by employing acid modified sol–gel method. The crystalline phase of the pure and doped NPs was observed with X-ray diffraction (XRD) followed by Raman scattering technique. Field emission scanning electron microscope and transmission electron microscopy give the morphological details. Fourier transform infrared spectra indicate the bonding interactions of Co ions with the titania lattice framework. Optical studies were attained with UV–visible absorption and fluorescence emission spectroscopy. XRD analysis reveals that all prepared samples have pure anatase phase with tetragonal symmetry devoid of any other secondary phase. The average crystallite size of all samples was calculated using Scherrer’s formula and was found to vary from 8 to 10 nm with doping concentration of Co. The Raman spectroscopy further confirmed the formation of TiO₂ in anatase structure in both pure and Co doped TiO₂ NPs. The most intense Raman active E_g peak of TiO₂ NPs shifted to higher energy on doping. Both UV–visible and fluorescence spectra show a blue shift in their absorption and band edge emission subsequently on increasing with Co percentage in titania host matrix, wherever there is an indication of quantum confinement effect with widening of band gap on decreasing in NPs size. There is also a possibility of strong Coulomb interaction effect on the optical processes involving the Co ions. However, the intensities of different emission spectra are not the same but decrease profoundly for doping samples due to concentration quenching effect.     

Synthesis and characterization of solar photoactive TiO2 nanoparticles with enhanced structural and optical properties

The structural, morphological, and optical properties of the sol–gel derived TiO₂ nanoparticles at different pH and calcination temperature were investigated in the present study. X-ray diffraction (XRD), Thermogravimetric analysis (TGA), Field emission scanning electron microscopy (FE-SEM), Transmission electron microscopy (TEM), UV–Visible(Vis) spectroscopy, energy dispersive studies (EDS), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, X-ray photoluminescence (PL) spectroscopy, BET surface area analysis, and Barrett-Joyner-Halenda (BJH) pore size distribution and pore volume analysis were used to characterize the prepared TiO₂ photocatalyst. The range of crystallite size and band gap of the synthesized TiO₂ samples were in the range of 20–80?nm and 2.5–3.2?eV respectively. The photocatalytic performance of prepared TiO₂ photocatalysts was evaluated by photodegradation of Methylene Blue (MB) solution under simulated solar irradiation. Results illustrate that the synthesized TiO₂ exhibits visible light activity at higher calcination temperature. Crystallinity and surface area plays a vital role in the overall performance of the prepared TiO₂ photocatalyst.     

Effect of Zn source concentration on structural,optical and electrical properties of zinc sulphide–polyaniline (ZnS–PANI) nanocomposite thin films

Zinc sulphide–polyaniline (ZnS–PANI) nanocomposites are prepared by preparing ZnS nanoparticles in the same reaction bath for synthesis of PANI. Three different composites have been prepared by varying the concentration of zinc source. The films obtained from the colloidal dispersion are characterized by Scanning electron microscopy, energy dispersive analysis of X-rays, transmission electron microscopy, X-ray diffraction studies, Fourier transform infrared spectroscopy, UV–visible optical absorption, photoluminescence and current–voltage studies. Broadening of X-ray diffraction peaks suggest change in crystallite size and this is in agreement with the results from transmission electron microscopy. Fourier transform infrared spectra indicate crosslinking in the composite film. UV–visible absorption spectra of the film exhibit enhancement of doping level which is assigned to the existence of greater number of charges on the polymer backbone. Optical properties of the films are studied by measuring photoluminescence spectra. This shows decrease in intensity and blue shift with the increase in zinc source concentration. The blue shift indicates strong quantum confinement. Current–voltage characteristics exhibit excellent light response indicating tunneling type of conduction.     

Influence of Co-doping on the structural, optical and magnetic properties of ZnO nanoparticles synthesized using auto-combustion method

In the present work, we have interested to understand the influence of cobalt doping on the various properties of ZnO nanoparticles, a series of samples were successfully synthesized using sol–gel auto-combustion method. The effects of Co doping on the structural and optical properties of ZnO:Co nanoparticles were investigated using X-ray diffraction (XRD), scanning electron microscopy, fourier transform infrared (FTIR) spectroscopy, ultraviolet–visible spectroscopy, photoluminescence spectroscopy and vibrating sample magnetometer (VSM). With the sensitivity of the XRD instrument, the structural analyses on the undoped and Co-doped ZnO samples reveal the formation of polycrystalline hexagonal-wurtzite structure without any secondary phase. FTIR spectra confirm the formation of wurtzite structure of ZnO in the samples. The optical absorption spectra showed a red shift in the near band edge which indicates that Co²⁺ successfully incorporated into the Zn²⁺ lattice sites. The room temperature PL measurements show a strong UV emission centered at 392 nm (3.16 eV), ascribed to the near-band-edge emissions of ZnO and defect related emissions at 411 nm (violet luminescence), 449 nm (blue luminescence) and 627 nm (orange-red luminescence), respectively. Magnetic study using VSM reveals that all the samples are found to exhibit room temperature ferromagnetism.     

Synthesis,structural and optical properties of nanoparticles (Al,V) co-doped zinc oxide

The synthesis by the sol–gel method, structural and optical properties of ZnO, Zn_0.99Al_0.01O (AlZ), Zn_0.9V_0.1O (VZ) and Zn_0.89Al_0.01V_0.1O (AlVZ) nanoparticles was reported. The approach was slow release of water for hydrolysis by esterification reaction followed by a supercritical drying in ethyl alcohol. After thermal treatment at 500^°C in air, the obtained nanopowders were characterized by various techniques such as transmission electron microscopy, X-ray diffraction and photoluminescence (PL) spectroscopy. The structural properties showed that the ZnO nanoparticles with an average particle size of 25 nm exhibit hexagonal wurtzite structure. From the optical studies, it was found that the optical band gap was located between 2.97 and 3.17 eV. The obtained electrical properties showed the potential application of the samples in optoelectronic devices. The powder of AlVZ presented a strong luminescence band in the visible range. The PL band energy position presented a small blue shift with the increase of measurement temperature. Different possible attributions of this emission band will be discussed.     

Structural and optical characterization of tin dioxide nanoparticles prepared by a surfactant mediated method

In this study tin dioxide nanoparticles were synthesized using a cationic surfactant (cetyl-trimethyl ammonium bromide) as the organic template and the hydrous tin chloride and liquid ammonia as the inorganic precursor. Samples were characterized by X-ray diffraction, transmission electron microscopy and UV–visible absorption, photoluminescence and Raman spectroscopy. The X-ray diffraction pattern of the as prepared sample is indexed to rutile phase of tin dioxide without any trace of an extra phase and particle size 7–8 nm which is further confirmed by electron microscopy. The UV–visible spectrum shows that the absorption edge is blue shifted and the band gap of the prepared sample is 4.0 eV which is larger than the bulk tin dioxide (3.6 eV).     

Thickness dependent structural, electronic, and optical properties of Ge nanostructures

In the present paper, we have investigated structural, optical as well as electronic properties of electron beam evaporated Ge thin films having layer thicknesses ranging from ultra-thin (5 nm) to thick (200 nm). The Raman spectra show that all peaks are shifted towards lower wave number as compared to their bulk counterparts and are considered as a signature of nanostructure formation and quantum confinement effect. The Raman line exhibits transformation from nanocrystalline to microcrystalline phase with a reduction in blue shift of peak position with increase in Ge film thickness (>5 nm). Similarly, the optical absorption spectra corresponding to these films also show reduction in blue shift effect, although Ge 5 nm film shows the absorption behaviour quite different from higher thickness films. The corresponding band gap values obtained from absorption measurements are much larger than bulk Ge and are mainly attributed to the effect of quantum confinement as expected for small size particles calculated from GIXRD patterns. AFM data in each case are correlated and discussed with structural as well as optical results to support the effect of growth morphology on the above-mentioned observations. The results are further supported by photoelectron spectroscopy (PES), photoluminescence (PL) and resistivity measurements and are interpreted in terms of crystallinity and quantum confinement effect.     

Structural and optical properties of Co-doped ZnS nanoparticles synthesized by a capping agent

Cobalt-doped Zinc sulfide (ZnS) nanoparticles were prepared by a simple chemical method using alkyl hydroxyl ethyl dimethyl ammonium chloride (YH) as capping agent. The structural and optical properties of prepared cobalt-doped ZnS nanoparticles have been characterized. X-ray diffraction patterns and transmission electron microscope images reveal pure cubic ZnS phase with size of about 5–2 nm for all cobalt-doped ZnS nanoparticles. The lattice constant of the samples decreases slightly by the introduction of Co²⁺ The absorption edge of the ZnS:Co²⁺ nanoparticles is blue-shifted as compared with that of bulk ZnS, indicating the quantum confinement effect. The photoluminescence emission band exhibits a blue shift for Co-doped ZnS nanoparticles as compared to the ZnS nanoparticles.     

Optical studies of electrodeposited ZnCuTe ternary nanowire arrays

The optical properties of electrodeposited zinc copper telluride (ZnCuTe) ternary nanowires on ITO substrate using polycarbonate membrane (Whatman) of diameter 200,100 and 50?nm have been studied and reported in this paper. Scanning electron microscopy confirmed the formation of the standing nanowires having uniform diameter equal to the diameter of the template used. UV–vis absorption and photoluminescence (PL) spectroscopy were used for optical studies. The optical band gaps of 200, 100 and 50?nm have been calculated as 3.19, 3.39 and 3.57?eV, respectively using UV–vis spectroscopy. The UV–visible absorption spectrometry reveals the absorption spectra of 200, 100 and 50?nm shows a blue shift. UV–visible absorption depicts that the band gap increases with decrease in the diameter size of the nanowires. Several broad emission lines have been observed over a wide wavelength range (390–690?nm) of visible light spectrum in the PL spectra of ZnCuTe nanowires of diameter 200, 100 and 50?nm. A good emission peak at around 615?nm has been observed in all nanowires.     

Enhanced visible luminescence and modification in morphological properties of cadmium oxide nanoparticles induced by annealing

Cadmium oxide nanoparticles synthesised by a simple sol–gel synthesis method showed luminescence properties in the visible region of the electromagnetic spectrum. Both green and blue emissions were observed in photoluminescence spectra. We have investigated luminescence properties by changing the synthesis conditions. An enhanced luminescence of CdO nanoparticles was realised when these particles were annealed at different temperatures. Cadmium interstitial vacancies and oxygen vacancies played an important role in luminescence properties. X-ray diffraction confirmed annealing-induced changes in morphological properties. A good correlation between all the experimental results was obtained. Optical properties were investigated by diffuse reflectance spectra and photoluminescence spectra. Structural properties were investigated by high-resolution transmission electron microscopy.     

Quantum confinement effect of CdS nanoparticles dispersed within PVP/PVA nanocomposites

Nanocomposite films of CdS nanoparticles within PVP/PVA blend were prepared. The prepared films were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy, Ultraviolet–visible spectroscopy (UV–vis), transmission electron microscopy (TEM) and photoluminescence (PL) spectra. The amount of Cd⁺ used strongly influenced the size of the CdS nanoparticles, which was confirmed by XRD, UV–vis absorption spectra, PL emission spectra and TEM images. Smaller sized CdS nanoparticles were formed in higher content of cadmium. The results of XRD indicate that CdS nanoparticles were formed with hexagonal phase in the polymeric matrix. PL and UV–vis spectra reveal that nanocomposite films shows quantum confinement effect. Optical band gap and particle size were calculated and is in agreement with the results obtained from TEM data. The direct energy band gap was increased up to 2.86 eV.     

Temperature-induced modification on the structural, optical and morphological properties of Zn0.96Cu0.04O nanoparticles

Zn_0.96Cu_0.04O nanoparticles synthesized by co-precipitation method were annealed at different temperatures, 400, 500, 600 and 700 °C for 2 h in air atmosphere. Crystalline phases and optical studies of the nanoparticles were studied by X-ray diffraction (XRD) and ultraviolet (UV)–visible photo-spectrometer. Elemental composition was studied by the energy dispersive X-ray (EDX) analysis and the microstructure was examined by scanning electron microscope. The XRD showed that the prepared nanoparticles had different microstructure without changing a hexagonal wurtzite structure. The average crystallite size increased from 28 to 60 nm when the annealing temperatures increased from 400 to 700 °C. The EDX analyses confirmed the presence of Cu in ZnO system and the weight percentage was nearly equal to their nominal stoichiometry within the experimental error. The optical band gap was varied between 3.75 and 3.86 eV and found maximum, 3.86 eV at 500 °C. Existence of functional groups and bonding were analyzed by fourier transform infrared spectra. The observed blue shift in UV emission from 400 to 500 °C in photoluminescence spectra was due to the intrinsic and extrinsic impurities whereas the red shift after 500 °C was due to the increase of crystalline size and relaxation of tensile strain. The reduction in intensity of green band emission with temperature was due to the reduction of intrinsic and extrinsic defects in Zn–O–Cu lattice.     

Growth and characterization of NiS and NiCoS nanoparticles in mordenite zeolite host

We report the optical and structural properties of NiS and the ternary NiCoS nanoparticles in mordenite zeolite. The samples were obtained by sulfidation of the Ni²⁺ and Co²⁺ ion-exchange zeolite in a Na₂S solution at room temperature. The optical properties of the samples were studied by UV–visible spectroscopy. Their crystalline structure and morphology were studied by XRD and scanning electron microscopy. The results show that the nanoparticles are inside the zeolite channels and cavity. Exciton absorption peaks at higher energy than the fundamental absorption edge of bulk NiS and CoS indicate quantum confinement effects in nanoparticles as a consequence of their small size. The absorption spectra show that the optical band gap varies in the range 3.53–3.9 eV, depending on the semiconductor material and their relative concentration.     

Photocatalytic degradation of dye pollutants under solar,visible and UV lights using green synthesised CuS nanoparticles

A green method for the solvothermal synthesis of copper sulphide nanoparticles (CuS NPs) using xanthan gum as a capping agent was developed. The CuS NPs were characterised by scanning electron microscopy, transmission electron microscopy (TEM), X-ray diffraction, Brunauer–Emment–Teller, zeta analysis, thermal gravimetric– differential thermal analysis, Fourier transform infrared and UV–visible absorption spectra. These characterisations together determine the composition, structural, thermal and optical properties. The UV–visible spectrum had a broad absorption in the visible range. The particle size of the products was observed by TEM in the range of 8–20 nm. The photocatalytic performance of the CuS NPs was evaluated for the degradation of organic dyes (methylene blue, rhodamine B, eosin Y and congo red) under irradiation of solar, visible and UV lights. The CuS NPs showed good photocatalytic activity. Kinetic analyses indicate that the photodegradation rates of dyes usually follow pseudo-first-order kinetics for degradation mechanisms.     

Effect of deposition time on structural, optical and photoluminescence properties of Cd0.9Zn0.1S thin films by chemical bath deposition method

The present work investigates the effect of deposition times on the structural, optical and photoluminescence properties of Cd_0.9Zn_0.1S thin films deposited on glass substrate by chemical bath deposition method. The deposition time was varied from 30 to 90 min. The deposited films were uniform and adherent to the glass substrates and amorphous in nature. Structural, optical and photoluminescence properties of Cd_0.9Zn_0.1S thin films were studied through X-ray diffraction, energy dispersive X-ray, scanning electron microscopy, UV–Vis absorption, fourier transform infra red spectroscopy and photoluminescence spectroscopy. The average crystal size was increased from ~1.3 to 2.5 nm with increase in deposition times. The absorption of the films was increased and the absorption peak shifted to lower wavelength side when deposition time increases. The increased energy gap from 2.4 to 2.49 eV with deposition time was due to quantum size effect and better crystallization. The presence of functional groups and chemical bonding were confirmed by FTIR. PL spectra showed two well distinct and strong bands; blue band around 407–415 nm and green band around 537–541 nm due to size effect.     

Synthesis and optical properties of nanocrystalline V-doped ZnO powders

This paper reports the synthesis and optical properties of nanocrystalline powders of V-doped ZnO (i.e. Zn_0.95V_0.05O, Zn_0.90V_0.10O, and Zn_0.85V_0.15O) by a simple sol–gel method using metal acetylacetonates of Zn and V and poly(vinyl alcohol) as precursors. Structure of the prepared samples was studied by X-ray diffraction, FTIR spectroscopy, and selected-area electron diffraction (SAED) analysis. The morphology of the powders revealed by SEM and TEM was affected by the amount of V, causing the formations of both nanoparticles and nanorods in the Zn_0.95V_0.05O sample, nanorods in the Zn_0.90V_0.10O sample, and nanoparticles in the Zn_0.85V_0.15O sample. The optical properties of the samples were investigated by measuring the UV–VIS absorbance and photoluminescence spectra at room temperature. All the samples exhibited UV absorption at below 400 nm (3.10 eV) with a well-defined absorbance peak at around 364 nm (3.41 eV) and 288 nm (4.31 eV). The band gap of the V-doped samples shows a decrease with increasing V concentration. The photoluminescence spectra of all the samples showed a strong UV emission band at 2.98 eV, a weak blue band at 2.82 eV, a week blue–green band at 2.56 eV, and a weak green band at 2.34 eV, which indicated their high structural and optical quality.     

Annealing effects on the structural and optical properties of growth ZnO thin films fabricated by pulsed laser deposition (PLD)

Annealed ZnO thin film at 300, 350, 400, 450 and 500 °C in air were deposited on glass substrate by using pulsed laser deposition. The effects of annealing temperature on the structural and optical properties of annealed ZnO thin films by grazing incident X-ray diffraction (GIXRD), transmittance spectra, and photoluminescence (PL) were investigated. The GIXRD reveal the presence of hexagonal wurtzite structure of ZnO with preferred orientation (002). The particle size is calculated using Debye–Scherrer equation and the average grain size were found to be in the range 5.22–10.61 ± 0.01 nm. The transmittance spectra demonstrate highly transparent nature of the films in visible region (>70 %). The calculation of optical band gap energy is found to be in the range 2.95–3.32 ± 0.01 eV. The PL spectra shows that the amorphous film gives a UV emission only and the annealed films produce UV, violet, blue and green emissions this indicates that the point defects increased as the amorphous film was annealed.