Effect of morphology in the photocatalytic degradation of methyl violet dye using ZnO nanorods

In the present work, high purity ZnO nanorods were synthesized by solid state reaction method at different annealing temperatures (250–400 °C). The structural, morphological and optical characteristic of the ZnO nanorods were studied. X-ray diffraction results confirmed that the ZnO nanorods have Wurtzite structure with high crystal quality. The grain size has increased from 23 to 27 nm with increasing temperature. The scanning electron microscopy and high resolution-transmission electron microscopy photographs showed the formation of ZnO nanorods. The bonding natures of the synthesized nanorods were analyzed by Fourier transform infra-red spectroscopy. The blue shift in the absorption edge was observed from the UV–Vis spectrum. The photoluminescence spectra showed two emission peaks corresponding to blue and red emissions. The photocatalytic performance of these nanorods was evaluated using methyl violet dye. The result showed that photocatalytic performance is highly depends on the morphology of the nanorods.     

Preparation and photoluminescence study of mesoporous indium hydroxide nanorods

Mesoporous indium hydroxide nanorods were successfully synthesized by a mild one-step one-pot method. The obtained samples were characterized by X-ray diffraction, transmission electron microscopy with selected area electron diffraction, N₂ adsorption, ultraviolet-visible absorption and photoluminescence, respectively. Transmission electron microscopy showed that there were some pores in the samples, which were mainly composed of rod-like shapes with length of 300 nm and diameter of 90 nm. N₂ adsorption/desorption measurements confirmed that the prepared powder was mesoporous with average pore diameter of 3.1 nm. The ultraviolet-visible absorption spectroscopy analysis indicated that the band gap energy of the samples was 5.15 eV. Photoluminescence spectrum showed that there were two strong emissions under ultraviolet light irradiation. The growth mechanism of indium hydroxide nanorods and the role of cetyltrimethyl ammonium bromide were also discussed.     

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.     

Fabrication and properties of sulfur (S)-doped ZnO nanorods

Highly-aligned sulfur (S)-doped ZnO nanorods have been grown using the hydrothermal approach at 90 °C for 2 h onto quartz substrate pre-coated with ZnO seed layer deposited by radio frequency magnetron sputtering system. The morphology, crystal structure, and transmittance of the S-doped ZnO nanorods grown with varied sulfur concentration have been investigated. The scanning electron microscope images showed that the S-doped ZnO nanorods dimension is affected by sulfur doping. The nanorods doped with sulfur concentration of ~1, 1.5, and 2 at.% found to show nanorods with an average diameter of ~130, 170, and 270 nm respectively. X-ray diffraction measurements revealed that the sulfur-doped ZnO nanorods have hexagonal-wurtzite crystal structure and grown vertically in the (002) plane along c-axis perpendicular to the substrate. The nanorods doped with 1 at.% sulfur showed ~70 % transmittance in the visible region while the nanorods doped with 2 at.% sulfur showed transmittance of ~77 % and exhibited blue shift in the fundamental absorption edge.     

Comparative study of multilayered ZnO/TiO<Subscript>2</Subscript>/ZnO and TiO<Subscript>2</Subscript>/ZnO/TiO<Subscript>2</Subscript> thin films prepared by sol–gel dip coating method

The aim of this research work is to represent the comparative study of ZnO/TiO₂/ZnO (ZTZ) and TiO₂/ZnO/TiO₂ (TZT) thin films deposited by sol–gel dip coating on FTO substrates. After deposition, the films were annealed at 500 °C for 1 h. Structural, surface morphology, optical and electrical properties of these films were studied by X-ray diffractrometer (XRD), Raman spectra, atomic force microscope (AFM), photoluminescence spectra (PL) and four point probe technique respectively. XRD and Raman spectra confirmed the anatase, brookite phases of TiO₂ and cubic phase of ZnO. AFM confirmed the formation of nano particles with average sizes of 18.4 and 47.2 nm of TZT and ZTZ films respectively. According to PL spectra, both the multilayer films slowdown the electron hole recombination rate and enhances the optoelectronic properties of the materials. Also it showed the peaks in the visible region of spectrum. The four point probe results showed that the average sheet resistivity of the films is 450 and 120 (ohm-m) respectively.     

Growth of aligned hexagonal ZnO nanorods on FTO substrate for dye-sensitized solar cells (DSSCs) application

This article reports a facile growth of well-crystalline aligned hexagonal ZnO nanorods on fluorine-doped tin-oxide (FTO) substrate via non-catalytic thermal evaporation process. The morphological investigations done by field-emission scanning electron microscope (FESEM) and transmission electron microscopy (TEM) reveal that the grown products are aligned hexagonal ZnO nanorods which are grown in a very high density over the whole substrate surface. The detailed structural properties observed by high-resolution TEM equipped with selected area electron diffraction (SAED) and X-ray diffraction (XRD) pattern confirmed that the synthesized nanorods are well-crystalline possessing wurtzite hexagonal phase and preferentially grown along the c-axis direction. A sharp and strong UV emission at 381 nm in room-temperature photoluminescence (PL) spectrum showed that the as-grown ZnO nanorods possess excellent optical properties. The as-grown nanorods were used as photo-anode for the fabrication of dye-sensitized solar cells (DSSCs) which exhibits an overall light-to-electricity conversion efficiency (ECE) of 0.7% with V(oc) of 0.571 V, J(sc) of 2.02 mA/cm2 and FF of 0.58.     

Effect of leavening agent on structural and photocatalytic properties of ZnO nanorods

In the present work, we have demonstrated a simple, facile, one-step, rapid and cost effective synthesis of ZnO nanorods through the thermal decomposition of zinc acetate and leavening agent (NaHCO₃). The silver nanoparticles (AgNPs) were deposited on the surface of ZnO nanorods by photocatalytic reduction of Ag (I) to Ag(0). As synthesized ZnO nanorods and Ag–ZnO nanocomposites were characterized by using X-ray Diffraction, field emission scanning electron microscope, high-resolution transmission electron microscope and diffuse reflectance spectroscopy. The photocatalytic activities of the ZnO nanorods and Ag–ZnO nanocomposites were evaluated for the photodegradation of Methyl Orange (MO) under UV and sunlight irradiation. The use of common leavening agent helps to prevent the aggregation of ZnO nanorods, further it hinders crystallite growth and narrowing the diameter of nanorods by the evolution of carbon dioxide during calcination. The ZnO nanorods and Ag–ZnO nanocomposite exhibited an enhanced photocatalytic activity and separation of photogenerated electron and hole pairs. Due to effect of leavening agent and AgNPs deposited on surface of ZnO nanorods finds best catalyst for the 99% degradation of MO within 30 min compared to ZnO.     

ZnO@CdS core–shell thin film: fabrication and enhancement of exciton life time by CdS nanoparticle

In the present study photoluminescence behavior of ZnO and ZnO@CdS core–shell nanorods film has been reported. ZnO nanorods were grown on the glass coated indium tin oxide (ITO) surface by seeding ZnO particle followed with nanorods growth. These nanorods were coated with CdS by chemical bath deposition techniques to have ZnO@CdS thin film and further annealed at 200 °C for their adherence to the ITO surface. The coating was characterized for surface morphology using SEM and optical behavior using UV–visible spectrophotometer. Energy dispersive X-ray (EDX) was used for compositional analysis and time resolve photoluminescence decay for excitons life time measurement. The absorption spectrum reveals that the absorption edge of ZnO@CdS core–shell heterostructure shifted to 480 nm in the visible region whereas ZnO nanorods have absorption maxima at 360 nm. The excitons lifetime of ZnO@CdS was found to be increased with the thickness of the CdS layer on ZnO nanorod. These ZnO@CdS core–shell nanostructures will be of great use in the field of photovoltaic cell and photocatalysis in a UV–visible region.     

CeO2 quantum dot functionalized ZnO nanorods photoanode for DSSC applications

Cerium oxide quantum dots (CeO₂ QDs) decorated zinc oxide nanorods (ZnO NRs) heterostructures were grown by a combination of solvothermal and chemical bath deposition methods and used for dye sensitized solar cell (DSSC) applications. Transmission electron microscope images showed the formation of CeO₂/ZnO NRs, where ~5 nm CeO₂ QDs were decorated on ZnO NRs having 1–2.5 μm length and 100–150 nm width. Photoluminescence spectra showed the significant increase in UV emission after decoration of ZnO NRs with CeO₂ QDs. DSSC results revealed that the ZnO NRs with CeO₂ QDs leads to an increase in the open circuit voltage and fill factor and exhibited a maximum efficiency of 2.65 %, which was 2.01 times higher than that of unmodified ZnO NRs. The decoration of CeO₂ QDs on the ZnO NRs surface may lead to the formation of barrier layer and hindered the back electron transfer and thereby high light harvesting efficiency.     

Effects of Na-doping on the efficiency of ZnO nanorods-based dye sensitized solar cells

Na-doped ZnO nanorods (Zn_1?xNa_xO: x = 0.0, 0.02, 0.04) were grown by a chemical bath deposition method on ZnO seeded FTO substrates. The influence of Na-doping on the efficiency of ZnO nanorods-based dye-sensitized solar cells (DSSCs) was investigated. Undoped and Na-doped ZnO nanorods were used as photo-anodes for the fabricated DSSCs. X-ray diffraction measurements exhibited that all the samples had a wurtzite structure of ZnO with a preferred orientation of (002) plane. Scanning electron microscopy images of the samples revealed that all the samples displayed hexagonal shaped nanorods. It was observed from optical measurements that the band gap energy gradually decreased from 3.29 to 3.21 eV for undoped and 4 at.% Na-doped ZnO nanorods, respectively. Photoluminescence spectrum for undoped ZnO showed three peaks located at 379, 422, and 585 nm corresponding to UV emission, zinc vacancy, and deep level emission (DLE) peaks, respectively. When ZnO nanorods were doped with 2 at.% Na, the intensity of UV peak increased whereas the intensity of DLE peak decreased. The maximum conversion efficiency of DSSCs was found to be 0.22 % with a J_sc of 0.80 mA/cm², V_oc of 0.49 V, and fill factor of 0.523 as ZnO nanorods were doped with 2 at.% Na atoms.     

Optically poled SHG and THG effects in cesium doped zinc oxide nanorods

The hexagonal wurtzite structure of the synthesized undoped and cesium (Cs) doped zinc oxide (ZnO) nanorods were confirmed with X-ray diffraction patterns. Further analysis with field emission scanning electron microscope images and energy dispersive X-ray spectra revealed the c-axis oriented hexagonal morphology of the samples with chemical composition. Optical poling through 337 nm nitrogen laser has been adopted to enhance the nonlinear optical properties. When the power density of the fundamental laser beam from Nd:YAG laser of 1064 nm matched with the band edge of the samples, resonant absorption takes place leading to the enhanced NLO properties. The interstitial occupancy of the dopants in 3 and 5 mol% CsZnO increases the band tailing in the forbidden energy gap. The minimum of Urbach energy calculated from UV–Vis absorption spectra corresponding to 1 mol% CsZnO revealed more ordering in the sample. More enhanced second and third order NLO effects were observed in this sample having larger crystallite size, lesser diameter, lesser band gap, minimum urbach energy and higher electron–phonon interaction.     

Synthesis of silica/Au core-shell nanostructures by galvanic replacement of silica/Ag in aqueous and alkaline medium

We present here a facile one-step method for the synthesis of silica/Au core-shell nanostructures by exploiting the potential difference of AuCl₄^? and Ag in aqueous as well as alkaline media. Initially, silica/Ag core-shell nanostructures were synthesised by coating Ag nanoparticles on silica core (size ～150 nm) in a two-step process (seeding and growth) and were characterised for their morphological, structural and optical behaviours. A complete coverage of silica core with Ag nanoparticles was seen from scanning electron microscope and transmission electron microscope images. The presence of resonance peaks in the optical spectrum manifests the nature of the shell (thin shell ～413 and 650 nm, thick shell ～434 nm). Galvanic replacement of silica/Ag core-shell nanostructures in chloroauric acid solution (HAuCl₄) was studied in both the aqueous and alkaline medium, where an aqueous environment results into fast and effective replacement as compared to an alkaline medium, which has been confirmed from optical absorption studies. The optical studies showed that in an alkaline environment, on galvanic replacement of Ag with Au, the individual absorption peak of Ag (～414 nm) and Au (～520 nm) disappeared, whereas new absorption wavelengths in higher region (600–800 nm) of electromagnetic spectrum were observed. A detailed mechanism is proposed for the same to explain this behaviour. A range of novel new plasmonic core-shell nanomaterials can be synthesised as an intermediate of this facile one-step reaction.     

Facile preparation of Ag/ZnO nanoparticles via photoreduction

Ag/ZnO nanoparticles can be obtained via photocatalytic reduction of silver nitrate at ZnO nanorods when a solution of AgNO₃ and nanorods ZnO suspended in ethyleneglycol is exposed to daylight. The mean size of the deposited sphere like Ag particles is about 5 nm. However, some of the particles can be as large as 20 nm. The ZnO nanorods were pre-prepared by basic precipitation from zinc acetate di-hydrate in the ionic liquid 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide. They are about 50–300 nm in length and 10–50 nm in width. Transmission electron microscopy (TEM), energy-dispersive X-ray analysis (EDS), X-ray powder diffraction (XRD), UV–Vis spectroscopy, X-ray photoelectron spectroscopy (XPS), and photoluminescence (PL) were used to characterize the resulting Ag/ZnO nanocomposites.     

Growth and optical properties of ZnO nanorods by introducing ZnO sols prior to hydrothermal process

ZnO nanorods of 25 nm with quite homogeneous size and shape have been fabricated by introducing ZnO sols as nucleation centers prior to the hydrothermal reaction. The samples were characterized by scanning electron microscope, transmission electron microscope, X-ray diffraction, photoluminescence and resonant Raman spectra. After ZnO sols are introduced, the width of the resulting nanorods decreases above an order of magnitude and the aspect ratio increases 5 times. The increase of the intensity ratio of ultraviolet to visible emissions in room-temperature photoluminescence spectrum and the decrease of the Raman linewidths show the improvement in the quality of ZnO nanorods. Influences of the number of seed nuclei and the aging time of ZnO sols on the morphology of ZnO nanorods are discussed.     

CTAB-assisted hydrothermal synthesis of single-crystalline copper-doped ZnO nanorods and investigation of their photoluminescence properties

A simple CTAB-assisted hydrothermal synthesis of undoped and copper-doped ZnO nanorods is reported. The phase and structural analysis carried out by X-ray diffraction, shows the formation of hexagonal wurtzite structure of ZnO. Morphology of the ZnO nanorods was investigated by electron microscopy techniques which showed the formation of well dispersed regular shape ZnO nanorods of 100 ± 10 nm in diameter and 900 ± 100 nm in length. However, size of the copper doped ZnO nanorod slightly increased with increasing copper concentration. Furthermore, the selected area electron diffraction pattern and high resolution transmission electron microscopy reveal that both the undoped and copper doped ZnO nanorods were single crystalline in nature and preferentially grew up along [0001] direction. Optical property was investigated by photoluminescence spectroscopy. The effects of copper doping on the photoluminescence property of ZnO nanorods were investigated.     

Ferromagnetism in Gd-doped CdS dilute magnetic semiconducting nanorods

Cd _x Gd_1?x S (x = 0–0.15) nanorods have been synthesized by solvothermal technique. X-ray diffraction study reveals that pure and Gd-doped CdS nanorods exhibits hexagonal wurtzite structure. Transmission electron microscopy reveals nanorods like morphology of synthesized CdS having 14 and 26 nm size of pure and 15 % doped CdS nanorods. UV–Visible absorption study confirms the blue shift in the energy band energy due to the quantum confinement effects. Photoluminescence spectra confirm the defect free nature of the synthesized nanorods with peaks emerging around 528 and 540 nm due to the green emission. The magnetic study shows that the pure and Gd-doped CdS nanorods exhibits ferromagnetic character and the magnetisation increased by five times from 0.074 to 0.422 emu/g upon Gd-doping.     

A simple microwave-assisted decomposing route for synthesis of ZnO nanorods in the presence of PEG400

In the paper, a simple microwave-assisted decomposing reaction in the presence of PEG400 has been successfully developed to synthesize ZnO nanorods with 10-25 nm of diameter and 60-200 nm of length. The product was analyzed and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and HRTEM. Ultraviolet-visible (UV-vis) absorption peak of ZnO nanorods shows a distinct blue shift from that of the bulk and the Photoluminescence (PL) spectrum exhibits a strong near-band-edge emission at 385 nm. Further experiments have also been designed, and the results show that microwave radiation and surfactant PEG400 all played an important role on the formation of ZnO nanorods.     

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.     

Synthesis, characterization and photoluminescence studies of ZnOrod@SnO2 nanocomposites

The synthesis of II-VI semiconductor (ZnO_rod@SnO₂) nanocomposite materials with core-shell morphology has been reported. ZnO nanorods were grown by hydrothermal technique using zinc acetate as the reactant. SnO₂ was coated on the nanorods by a simple technique of colloid chemistry. The formation of tin dioxide shell on the ZnO nanorods was confirmed by the TEM images of the resultant materials. The formation of the nanocomposite was also supported by XRD pattern. The effect of tin dioxide shell on the optical properties of ZnO was investigated by photoluminescence spectroscopy and Raman spectroscopy.     

A Novel one-step synthesis of Ag-doped ZnO nanoparticles for high performance photo-catalytic applications

In this report, pure and silver (Ag) doped zinc oxide (ZnO) nanoparticles with various concentrations of silver (5 and 10 wt%) was successfully synthesized by a novel and one step microwave irradiation method. Powder X-ray diffraction results indicates that all of the as-synthesized samples including the highest Ag (10 wt%) doping have a hexagonal wurtzite type structure and average crystalline size was found to be 28, 21 and 16 nm for pure and Ag doped ZnO respectively. Spherical shaped morphology with an average diameter of around 32–13 nm was observed by Transmission electron microscope analysis. UV–Vis spectra revealed that, Ag doped samples exhibits a red shift in the absorption band edge with increasing Ag dopant concentration. The photocatalytic degradation of methyl violet (MV), phenol and rhodamine B (RHB) was investigated by using Ag-ZnO catalyst under UV light irradiation. The result showed that the photocatalytic property was significantly improved by Ag doping. The improved photocatalytic mechanism by Ag doping was also discussed. The samples were further characterized by photoluminescence spectra and Fourier Transform Infrared Spectra (FTIR) analysis.