Magnetically recoverable nano Pd/Fe<Subscript>3</Subscript>O<Subscript>4</Subscript>/ZnO catalyst: preparation,characterization, and application for the synthesis of 2-oxazolines and benzoxazoles

A novel palladium-based catalysts supported on Fe₃O₄/ZnO nanoparticles have been prepared by a simple method. The catalyst was characterized by transmission electron microscopy, X-ray powder diffraction, X-ray photoelectron spectroscopy, atomic absorption spectrophotometry, FT-IR, and BET analysis. The catalyst afforded efficient synthesis of 2-oxazolines and benzoxazoles from aromatic nitriles under solvent-free conditions. The significant features of this method are short reaction times, good to high yields of the products, simple operation, solvent-free condition, non-toxicity, reusability of the catalyst without significant loss of catalytic activity, and using ultra small amount of Pd (0.004 g of catalyst contains 9.16 × 10^?3 mmol Pd which was determined by ICP).     

Study on CaCO3-coated ZnO nanoparticles based dye sensitized solar cell

Dye sensitized solar cells (DSSCs) have been fabricated using ZnO and CaCO₃-coated ZnO nanoparticles. The effect of CaCO₃ coating on the performance of DSSC has been investigated. CaCO₃-coated ZnO nanoparticles have been synthesized by hydrothermal method. X-ray diffraction patterns of synthesized nanoparticles reveal that the ZnO and CaCO₃-coated ZnO nanoparticles have respectively wurtzite and rhomb-centred structure and both having hexagonal phase. Transmission electron microscopy study reveal that ZnO and CaCO₃-coated ZnO nanoparticles possess spherical symmetry and have average particle size respectively 6.2 and 6.7 nm. In case of CaCO₃/ZnO nanoparticles, the quenching in photoluminescence emission intensity has been attributed to the decrease in recombination rate of photo-generated electron–hole pairs. UV–Vis absorption spectra, confirms that the electrodes fabricated from the CaCO₃-coated ZnO nanoparticles have higher absorbance that shows their higher dye adsorbing power. The use of CaCO₃ coating has been found to enhance the efficiency of DSSC by over 100 %.     

ZnO nanostructures for efficient perovskite solar cells

Controlled ZnO nanostructures were synthesized via spin-coating and in situ thermal decomposition processing using ZnO paster with/without zinc acetate as precursor. The perovskite CH₃NH₃PbI₃ solar cells (PSCs) based on these ZnO nanostructures were fabricated and their photovoltaic performances have also been investigated. Effects of zinc acetate concentration on morphologies of ZnO nanostructures and the photovoltaic properties of corresponding PSCs have been discussed. Interestingly, the morphologies of ZnO nanostructures were varied from separate nanoparticles to interconnect net-like nanostructures and the space of ZnO nanoparticles became large when the concentration of zinc acetate was increased from 0 to 0.13 M. The space and the connection degree of ZnO nanostructure obtained from 0.05 M zinc acetate are the best choice for perovskite infiltration and charge transport, which leads to corresponding cells have highest power conversion efficiencies (PCE) of 9.30 %. Post-treatment of ZnO nanostructures improved further Voc and FF, leading to PCE to 13.1 %.     

Hollow ZnO from assembly of nanoparticles: photocatalytic and antibacterial activity

Hollow shells of ZnO were formed by the assembly of nanoparticles using PEG 400 wherein PEG-400 acted like both a solvent and a structure directing agent. The structure, morphology and optical properties were characterized by using PXRD, SEM, TEM and absorption studies. The hollow shells were found to possess high crystallinity with a surface area of 8 m² g^?1. The assembly was formed by nanoparticles ranging from 50 to 60 nm, whereas the size of the hollow shell ranged from 500 nm to 1 micron. Photocatalytic activity of these nanostructures was studied using Rhodamine B (RhB) and methyl orange (MO). Nearly 99% of the RhB dye was found to be degraded in 60 min while for MO, the degradation was 97% in 50 min. The pseudo-first-order rate constant was calculated as 0.072 min^?1 for the degradation of RhB and 0.075 min^?1 for the degradation of MO. The hollow shells were found to exhibit significant bacterial inhibiting efficacy at a low concentration of the particles. Comparative studies were carried out for photodegradation of Rhodamine B dye and antibacterial activity using spherical particles of ZnO and assembly of particles to form rods of ZnO. The results indicated that these hollow nanostructures could be used as a potential catalyst for the removal of dyes from water and as an antibacterial agent.     

Phase- and size-controllable synthesis with efficient photocatalytic activity of ZnS nanoparticles

We report a simple solution-based method to synthesize phase- and size-controllable ZnS nanoparticles at low temperature. Cubic ZnS (c-ZnS) and hexagonal ZnS nanoparticles (h-ZnS) were obtained by heating an aqueous solution of Zn(NO₃)₂·6H₂O and Na₂S₂O₃·5H₂O at different temperatures. When the system was heated at 65 °C for 24 h, hexagonal crystal structure of ZnS nanoparticles, with size of 50–350 nm, was obtained, as confirmed by X-ray diffraction and selected-area electron diffraction. When the reaction temperature was 100 °C under hydrothermal condition, c-ZnS nanoparticles were obtained and exhibited monodisperse nanoparticles with average size of 4 nm. Proper rate of S releasing tuned by the variation of pH value is believed to be critical to stabilize the hexagonal ZnS nanoparticles. Compared with large size of h-ZnS nanoparticles, c-ZnS nanoparticles show higher photocatalytic activity in degrading methyl orange (MO). The degradation efficiency of c-ZnS nanoparticles reaches 97% under UV irradiation for 120 min. The good ultraviolet absorbing ability, charge separation property, and large surface area of c-ZnS nanoparticles are believed to have a positive impact on improving the degradation rate and degradation efficiency of MO.     

Chemical vapor deposition-based growth of aligned ZnO nanowires on polycrystalline Zn<Subscript>2</Subscript>GeO<Subscript>4</Subscript>:Mn substrates

ZnO nanowires have been grown on polycrystalline Zn₂GeO₄:Mn substrates for the first time using a chemical vapor deposition method. Both Zn and ZnO sources were used to supply Zn vapor in the growth process of ZnO nanowires. The Zn₂GeO₄:Mn substrates were prepared using solid-state ceramic synthesis methods, and average grain sizes of ~1 μm were achieved. The nanowires of diameters in the range of 100–200 nm and length of ~30 μm were observed. In addition to nanowires, other morphologies of ZnO nanostructures, such as ZnO tetrapods, were observed when Zn powder was used as the source for the CVD growth. The results reveal that polycrystalline substrates are also promising as novel alternative substrates for growth of ZnO nanostructures. The as-synthesized ZnO nanowire/Zn₂GeO₄:Mn composites are being developed for future electroluminescent devices.     

Synthesis and Characterization of Superparamagnetic Co3O4@ZnO Nanocomposite

We report the sequential polyol synthesis of Co₃O₄@ZnO nanocomposite. Firstly, Co₃O₄ was synthesized and ZnO was produced on the surface of the as synthesized Co₃O₄ NPs in the same pot. The nanoparticles have been investigated by powder X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), transmission electron microscope (TEM), and physical properties measurement system (PPMS) of Quantum Design. The weight percentage of phases were found as 26.3 % for ZnO and 73.5 % Co₃O₄ (crystal thickness ratio \(D_{\mathrm{Co}_{3}\mathrm{O}_{4}}/ D_{\mathrm{ZnO}}= 1.38\) ) by using the generalized reference intensity ratios (RIRs) method. Superparamagnetism in Co₃O₄@ZnO nanocomposite at room temperature was first detected with high Ms value of 10 emu/g, and the non-hysteric curve with nearly saturated nature at high fields. This non-hysteric and nearly saturated nature at 15 kOe is the nature of superparamagnetic structures.     

Study of Structural and Magnetic Properties of Superparamagnetic Fe3O4–ZnO Core–Shell Nanoparticles

In this work, Fe₃O₄–ZnO core–shell nanoparticles have been successfully synthesized using a simple two-step co-precipitation method. In this regard, Fe₃O₄ (magnetite) and ZnO (zincite) nanoparticles (NPs) were synthesized separately. Then, the surface of the Fe₃O₄ NPs was modified with trisodium citrate in order to improve the attachment of ZnO NPs to the surface of Fe₃O₄ NPs. Afterwards, the modified magnetite NPs were coated with ZnO NPs. Moreover, the influence of the core to shell molar ratio on the structural and magnetic properties of the core–shell NPs has been investigated. The prepared nanoparticles have been characterized utilizing transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy and vibrating sample magnetometer (VSM). The results of XRD indicate that Fe₃O₄ NPs with inverse spinel phase were formed. The results of VSM imply that the Fe₃O₄–ZnO core–shell NPs are superparamagnetic. The saturation magnetization of prepared Fe₃O₄ NPs is 54.24 emu/g and it decreases intensively down to 29.88, 10.51 and 5.75 emu/g, after ZnO coating with various ratios of core to shell as 1:1, 1:10 and 1:20, respectively. This reduction is attributed to core–shell interface effects and shielding. TEM images and XRD results imply that ZnO-coated magnetite NPs are formed. According to the TEM images, the estimated average size for most of core–shell NPs is about 12 nm.     

Performance of Eu2O3 coated ZnO nanoparticles-based DSSC

To provide an inherent energy barrier between the electrode and electrolyte interface, the surface of the ZnO nanoparticles has been modified by Eu₂O₃ layer. The synthesis of ZnO, Eu₂O₃ coated ZnO nanoparticles have been carried out by chemical precipitation method and solvothermal treatment. The synthesized samples were characterized by XRD and the diffraction plane (222) of Eu₂O₃ detected, demonstrating the existence of Eu₂O₃ on the surface of ZnO, which is further verified using energy dispersive X-ray spectroscopy and Fourier transform infrared spectroscopy. The strong quenching in photoluminescence emission, in case of Eu₂O₃/ZnO nanoparticles, has been attributed to the decrease in recombination rate of photo-generated electron–hole pairs. Compared to ZnO electrodes, Eu₂O₃ coated ZnO electrodes adsorbed more dye. The photoelectrochemical properties of the Eu₂O₃/ZnO electrodes have been found to improve and the energy conversion efficiency increase from 0.44 to 1.45 % under the illumination of simulated light of 100 mW/cm².     

Low-temperature synthesis of ZnO nanoparticles for inverted polymer solar cell application

Zinc oxide (ZnO) nanoparticles were synthesized by a simple wet chemical method at low temperature. Morphologies, crystalline structure, and optical transmission of ZnO nanoparticles were investigated. The results showed that the average diameter of as-synthesized ZnO nanoparticles was about 4.9 nm, the nanoparticles were wurtzite-structured (hexagonal) ZnO and had optical band gap of 3.28 eV. Very high optical transmission (>80 %) in visible light region of ZnO nanoparticulate thin films was achieved. Furthermore, an inverted polymer solar cell consisted of ZnO nanoparticles and polymer were fabricated. The device exhibited an open circuit voltage (V_oc) of 0.50 V, a short circuit current density (J_sc) of 1.76 mA/cm², a fill-factor of 38 %, and a power conversion efficiency of 0.42 %.     

Promoting Photocatalytic Performance of ZnO Particles by Photochemically Reducing Ag+ on the Particle Surfaces

Dispersive Ag nanoparticles were formed on the surface of crystalline ZnO particles, using a photochemical reduction technique, to produce the Ag/ZnO with high photocatalytic performance. The prepared Ag/ZnO particles, as well as the ZnO particles without Ag attachments, were characterized using x-ray diffractometer, transmission electron microscope, and surface area analyzer. The abilities of the ZnO and the Ag/ZnO particles to photocatalytically decompose methylene blue under 365-nm ultraviolet light irradiation were evaluated by determining the corresponding specific reaction rate constant, k′_MB,m (based on the mass of the photocatalyst used). While the ZnO crystalline particles (k′_MB,m > 0.43 m³/(kg min)) already possessed better photocatalytic performance than the commercial photocatalyst P25 (k′_MB,m = 0.39 m³/(kg min)), the Ag/ZnO particles exhibited much better photocatalytic performance than the ZnO particles. The highest k′_MB,m for the Ag/ZnO particles was 1.93 m³/(kg min), which was about five times that of the P25.     

Effect of annealing temperature on the energy transfer in Eu-doped ZnO nanoparticles by chemical precipitation method

Eu-doped ZnO nanoparticles were synthesized by the chemical precipitation method and the annealing temperature effect on the structures and photoluminescence (PL) properties of the nanoparticles were briefly investigated. The X-ray diffraction and energy dispersive spectroscopy results indicated that the Eu³⁺ was successfully incorporated into the crystal lattice of ZnO host when the annealing temperature was fixed at 400 °C, but the Eu³⁺ ions were partly precipitated from the host with the annealing temperature increasing. The as-obtained ZnO: Eu nanocrystals composed of nanoparticles had an average size of 10 nm, and the valence states of europium ions in the nanocrystals were determined as tervalent. PL spectroscopy indicated that the characteristic red emissions of Eu³⁺ ions were attributed to the ⁵D₀ → ⁷F₀, ⁵D₀ → ⁷F₁ and ⁵D₀ → ⁷F₂ transitions, respectively. Moreover, the annealing temperature was found to have effect on the red emission of Eu³⁺ ions. That is to say, the energy transfer in the doped nanocrystals could be adjusted by different annealing temperatures.     

Chemical,morphological, structural,optical, and magnetic properties of Zn<Subscript>1−x</Subscript>Nd<Subscript>x</Subscript>O nanoparticles

In the present investigation, we made an endeavor to fabricate the ZnO nanoparticles and achieved the tunable properties with Nd doping. The Nd-doped ZnO nanoparticles were characterized via X-ray diffraction (XRD), Raman, and X-ray photoelectron spectroscopy (XPS) studies that confirmed the successful doping of Nd ions in the ZnO crystal lattice without amending its hexagonal phase. The particle morphology revealed nearly spherical particles with uniform size distribution. The band gap of these samples was determined using diffuse-reflectance spectra (DRS) and was found to vary from 3.17 to 3.21 eV with increasing Nd concentration. A broad and intense emission band at 1083 nm for Nd doped ZnO nanoparticles is observed and is assigned to corresponding emission transition ⁴F_3/2?→?⁴I_11/2 of Nd³⁺ ions. Furthermore, the magnetic studies indicate that the Nd doping altered the magnetic behavior of nanocrystalline ZnO particles from diamagnetic to ferromagnetic at 300 K and that the magnetization of these samples decreased with increasing Nd concentration. The tunable optical band gap as well as room-temperature ferromagnetism of these samples may find applications in both optoelectronics and spintronics.     

Optical properties of amorphous/crystalline ZnO nano-powder prepared by solid state reaction

This paper presents a simple and efficient method to prepare amorphous and crystalline ZnO nano-powders via thermal decomposition of the mixture of Zn(CH₃COO)₂·2H₂O and NaHCO₃. X-ray diffraction (XRD) pattern and transmission electron microscope (TEM) images indicated that thermal decomposition of the mixture at 160° C for 3 h, amorphous ZnO powder was obtained. Otherwise, temperature above 160°C, the amorphous ZnO would begin transform into crystalline. Photoluminescence (PL) spectra of amorphous ZnO revealed it had very strong UV emission, but its visible emission was barely observed. The UV intensity of amorphous ZnO was about 3 times of that of crystalline ZnO. This can be explained by quantum size effect.     

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.     

Photoluminescence and photoconductivity studies of ZnO nanoparticles prepared by solid state reaction method

In the present work, the effect of annealing temperature on the luminescence and photoconductivity properties of ZnO nanoparticles (NPs) has been investigated. The ZnO NPs have been prepared at low temperature by a simple one step solid state reaction method using ZnSO₄·7H₂O as a starting precursor. X-ray diffraction results show, the prepared samples have a hexagonal wurtzite structure of ZnO NPs. FE-SEM reveals that the prepared ZnO nanoparticles have perfect spherical shape with little agglomeration. UV–visible absorption spectrum of as-prepared ZnO sample shows an absorbance peak at ~372 nm (~3.32 eV), which is blue shifted as compared to bulk ZnO (~386 nm). The annealed sample exhibits red shift of absorption peak. The photoluminescence spectra of as-prepared sample as well as annealed samples show one emission peak in UV region, and violet, blue, blue-green and green emissions in visible region. The sample annealed at 650 °C results in a significant reduction in luminescence as compared to that of the sample annealed at 450 °C. The photoconductivity properties such as voltage dependence of photocurrent, growth and decay of photocurrent as well as wavelength dependence of photocurrent have been studied in detail.     

Structural, vibrational, optical and magnetic properties of sol–gel derived Nd doped ZnO nanoparticles

Nd doped ZnO (Zn_1-xNd_xO, x = 0.0, 0.03, 0.06 and 0.10) nanoparticles were prepared by sol–gel method. Phase identification and effect of Nd ions substitution in ZnO lattice were confirmed by Rietveld analysis of XRD patterns. UV–Visible absorption spectra of pure and Nd doped ZnO nanoparticles showed the variation of the band gap in the range of 3.31–3.26 eV. The FTIR analysis of pure and Nd doped ZnO nanoparticles exhibited similar patterns in Zn/Nd–O bond length as obtained from the Rietveld refinement. Raman analysis confirmed the formation of a wurtzite structure wherein the local structure of ZnO nanoparticles is distorted due to Nd substitution. Magnetization-magnetic field hysteresis curves for pure and Nd doped ZnO nanoparticles revealed diamagnetic and paramagnetic behaviour, respectively. The paramagnetic behaviour of doped ZnO nanoparticles increased with increasing Nd concentration. However, the weak ferromagnetic behaviour of doped ZnO nanoparticles is observed after subtracting paramagnetic components, whereas the ferromagnetic behavior increased up to x = 0.06 samples, which further declined for x = 0.10 sample due to competition between paramagnetic and ferromagnetic ordering. The reduction in the ferromagnetic behavior for x = 0.10 sample indicates that the solubility limit of Nd atoms in ZnO lattice has been reached and paramagnetically coupled Nd atoms increased due to the increasing secondary phases.     

Effect of synthesized temperature on microstructure, infrared emissivity and dielectric property of Fe-doped ZnO powder

Fe-doped ZnO powder has been synthesized by coprecipitation method under different synthesized temperature, using zinc nitrate as the staring material, urea as the precipitator, and ferric nitrate as the doping source, respectively. The prepared powders have been characterized by XRD and SEM. Results show that when the synthesized temperature is below 700 °C the prepared powders are ZnO(Fe) solid solution powders and the ZnFe₂O₄ impurity phase appeared for the Fe-doped ZnO powder synthesized at 700 °C. The electric permittivities in the frequency range of 8.2–12.4 GHz and average infrared emissivity at the waveband range of 8–14 μm of prepared powders have been determined. The real part and imaginary part of electric permittivities of prepared powders have increased firstly and then decreased with increasing synthesized temperature. The average infrared emissivity has presented the opposite changing trend.     

Sol-gel synthesis,structural and enhanced photocatalytic performance of Al doped ZnO nanoparticles

In this research ZnO and Zn_1?x Al_xO (x = 1, 3, 5, 7% mol) nanoparticles were synthesized by sol-gel method. The effect of Al concentration on the structure, morphology, absorption spectra and photocatalytic properties investigated by using X-ray, TEM, EDS and UV–Vis spectrophotometer approaches. Hexagonal, spherical and rod-like structure was achieved as the dominant structure for undoped nanoparticles, low and high concentrations of doped Al, respectively. Photocatalytic activity of nanoparticles was measured by degradation of methyl orange as a pollutant under radiation of ultraviolet (UV). The experimental test results indicate that the best photocatalytic performance is at of 5% of Al. Furthermore, the doped ZnO nanoparticles have more activity in visible area compared with undoped nanoparticles. The absorption amount in this area increases by raising the Al concentrations. Furthermore, the band gap of the particles decreases from 3.22 eV to 2.93 eV by increasing Al percentage.     

Green synthesis of ZnO and Mg doped ZnO nanoparticles,and its optical properties

The Zinc oxide nanoparticles (ZnO NPs) and Magnesium doped ZnO nanoparticles (Mg doped ZnO NPs) are synthesized by Psidium guajava leaf extract. X-ray diffraction studies confirmed that, synthesized nanoparticles were retained the wurtzite hexagonal structure. In FESEM and HRTEM image analysis, ZnO and Mg doped ZnO NPs morphology were trigonal and spherical shape. Elemental compositions were identified by EDAX analysis. From FTIR result, the Zn–O stretching was observed at 453 and 448 cm^?1 for both ZnO samples. In Raman spectra, the high intensive E₂ ^high mode observed for 438 cm^?1 for ZnO NPs. But Mg doped ZnO NPs intensity of E₂ ^high mode decreased as compared to the pure ZnO NPs, it is due to the Mg²⁺ ion in to ZnO lattice site. The photoluminescence measurements revealed that the broad emission was composed of seven different bands due to zinc vacancies, oxygen vacancies and surface defects.