Synthesis and characterization of Co3O4 nanorods by thermal decomposition of cobalt oxalate

Cobalt oxalate was used as a precursor to prepare Co₃O₄ nanorods by thermal decomposition. The combinations of triphenylphosphine and oleylamine were added as surfactants to control the morphology of the particles. The products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared (FT-IR) spectroscopy and X-ray photoelectron spectroscopy (XPS). The diameters of Co₃O₄ nanorods are 20 nm and the average lengths are around 500 nm. The hysteresis loops of the obtained samples reveal the ferromagnetic behaviors, the enhanced coercivity (H_c) and decreased saturation magnetization (M_s) in contrast to their respective bulk materials. The study provides a simple and efficient route to synthesize Co₃O₄ nanorods at low temperature.     

Sonochemical synthesis of silver nanorods by reduction of sliver nitrate in aqueous solution

The sonochemical synthesis of sliver nanorods has been achieved by ultrasonic irradiation of the aqueous solution of sliver nitrate, methenamine (HMTA) and poly (vinyl pyrrolidone) (PVP) for 60 min. The silver nanorods obtained have lengths of 4–7 μm and mean diameters of about 100 nm. The structures of the samples were characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), selected area electron diffraction (SAED) and X-ray powder diffraction (XRD), and the chemical composition of the sample was examined by energy-dispersive X-ray spectrum (EDS). The effects of the irradiation time, the concentration of PVP and the reaction temperature on the morphology of silver nanorods were discussed, and the mechanism of the silver nanorods formation was tentatively inferred.     

BaMnO3 nanostructures: Simple ultrasonic fabrication and novel catalytic agent toward oxygen evolution of water splitting reaction

In the current paper, the main aim is to fabricate the BaMnO₃ nanostructures via the sonochemical route. The various factor, including precursors, reaction time and power of sonication can affect the shape, size, and purity of the samples. We utilized X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), and X-ray energy dispersive spectroscopy (EDS) to characterize the BaMnO₃ nanostructures. The optical property of BaMnO₃ nanostructures was explored by Ultraviolet–visible spectroscopy (UV–vis) and the energy gap was suitable for catalytic activity (about 2.75 eV). Changing the precursor can affect the size, nanoparticle shape, architectures, and uniformity of the samples. We employed the BaMnO₃ nanostructures for O₂ evolution reaction as catalysts. It can observe that increasing the homogeneity of the catalysts can increase the efficiency of the Oxygen evolution reaction. The maximum amount of the O₂ evolution and the highest TOF and TON are related to nanoplate disc using barium salicylate as a precursor of barium. As a result, we can nominate the BaMnO₃ nanostructures as an effective and novel catalyst for water-splitting reaction.     

Effect of the reaction conditions on the formation of the ZnO nanostructures

ZnO nanorods were synthesized through a simple chemical method by reacting Zn(C₂H₃O₂)₂·2H₂O and NaOH at low temperature and the effects of changing the order of addition of reactants on the morphological evolution of ZnO nanorods were investigated. The samples were characterized by using XRD, SEM, EDX, TEM, BET and Raman techniques. Optical properties of the ZnO nanostructures were too investigated by UV–Vis spectroscopy at room temperature.The hexagonal wurtzite phase of ZnO was confirmed by X-ray diffraction (XRD) for all the samples. SEM and TEM analysis indicated that different morphologies were obtained by changing the order of addition of reactants.     

Ultrasound assisted synthesis of {[Cu2(BDC)2(dabco)].2DMF.2H2O} nanostructures in the presence of modulator; new precursor to prepare nano copper oxides

As a new precursor to prepare nano copper oxide, nanostructures of porous metal organic framework (MOF) {[Cu₂(BDC)₂(dabco)].2DMF.2H₂O} (1) have been synthesized in the presence of acetic acid as a modulator via sonochemical method. Different concentrations of metal ion, organic linkers, modulator reagent and also different sonication times were held to improve the quality of nanostructures. Ultrasound irradiation helps nucleation step of the oriented attachment of modulation method and nanoparticles with a few nanorods has been prepared. As prepared MOF was calcinated at 500 °C to prepare nano CuO and Cu₂O. Compound 1, CuO and Cu₂O nanostructures were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray powder diffraction (XRD).     

Preparation and characterization of SrSnO3 nanorods

Perovskite strontium stannate (SrSnO₃) nanorods were prepared by annealing the precursor SnSr(OH)₆ nanorods at 600 °C for 3 h. The precursor nanorods were hydrothermally synthesized at 160 °C for 16 h using Sr(NO₃)₂ and SnCl₄·5H₂O as starting materials in the presence of surfactant cetyltrimethyl ammonium bromide (CTAB). As-prepared samples were characterized by X-ray diffraction (XRD), thermogravimetric-differential thermal analysis (TG-DTA), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and infrared ray spectroscopy (IR). The results show that the as-synthesized powders are made of SrSnO₃ one-dimensional nanorods of about 0.2-1 μm length and 100-150 nm diameter. Possible formation mechanism of SrSnO₃ with nanorod structure under certain conditions was preliminarily analyzed, in which it was thought that CTAB played an important role in the formation process of the nanorod structure. Electrochemical performance of the samples versus Li metal was also evaluated for possible use in lithium-ion batteries.     

From crystalline V2O5 to nanostructured vanadium oxides using aromatic amines as templates

Nanoneedles, nanorods of B-VO₂, and vanadium oxide nanotubes with high crystallinity were synthesized via a one-step hydrothermal treatment using crystalline V₂O₅ as a precursor and aromatic amines (C₆H₅-(CH₂)_n-NH₂ with n=0, 1, 3) as structure-directing templates. Samples were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray powder diffraction (XRD), thermal analysis, nitrogen adsorption/desorption isotherms and infrared spectroscopy. Nanoneedles, 0.5-5 μm in length and about 50 nm in average diameter and VO₂(B) nanorods about 20-100 nm wide and up to 2.5 μm long, have been obtained. The inner and the outer diameters of the vanadium oxide nanotubes vary, respectively, between 15-25 and 70-100 nm with a length up to 4 μm.     

Large-scale synthesis of Ag<Subscript>1.8</Subscript>Mn<Subscript>8</Subscript>O<Subscript>16</Subscript> nanorods and their electrochemical lithium-storage properties

Ag_1.8Mn₈O₁₆ nanorods have been synthesized on a large scale by a facile hydrothermal route. The effects of experimental conditions including reaction time and reactant concentration on the phase and morphology of the final products were investigated systematically. The products were characterized by using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and energy-dispersive X-ray (EDX) spectroscopy. Electrochemical lithium-storage capabilities of the as-formed nanostructured Ag_1.8Mn₈O₁₆ were also evaluated. Interestingly, the as-formed Ag_1.8Mn₈O₁₆ nanorods possess the unique one-dimensional structure and in situ silver loading, which are beneficial features for electrochemical lithium-storage applications. The results suggest their potential use as cathode materials for lithium-ion batteries.     

Fabrication of porous BaSnO3 hollow architectures using BaCO3@SnO2 core-shell nanorods as precursors

We present a strategy to synthesize porous BaSnO₃ hollow architectures with that were 150-300 nm in diameter and 1.5-5 μm in length using precursor of BaCO₃@SnO₂ nanorods prepared by hydrothermal treatment. BaCO₃@SnO₂ nanorods, consisting of a BaCO₃ core and a SnO₂ shell, could be used effectively for the solid-state synthesis of polycrystalline BaSnO₃ powder at 800 °C (lower than convention for BaCO₃ and SnO₂ mixtures). The core/shell structure of the precursor could play a role as a structural directing template for preparing BaSnO₃ hollow architectures during the calcination process. The X-ray diffractometer (XRD), scanning electron microscope (SEM), and transmission electron microscope (TEM) are employed to characterize the structures and morphologies. When applied to DSSC, the porous BaSnO₃ hollow architectures exhibit distinct photovoltaic effect.     

Sonochemical synthesis and characterization of NiMoO4 nanorods

NiMoO₄ nanorods have been successfully synthesized by sonochemical method process by using Ni(CH₃COO)₂·4H₂O and (NH₄)₆Mo₇O₂₄·4H₂O as starting materials. Some parameters including ultrasonic power, ultrasonic irradiation time, stirring effect, solvent effect, and surfactant effect were investigated to reach optimum condition. The as synthesized nanostructures were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmittance electron microscopy (TEM), photoluminescence (PL) spectroscopy, Fourier transform infrared (FT-IR) spectra and energy dispersive X-ray microanalysis (EDX). Facile preparation and separation are important features of this route. This work has provided a general, simple, and effective method to control the composition and morphology of NiMoO₄ in aqueous solution, which will be important for inorganic synthesis methodology.     

Temperature controlled synthesis of SrCO3 nanorods via a facile solid-state decomposition rout starting from a novel inorganic precursor

Strontium carbonate nanorods have been successfully synthesized via solid-state decomposition of a new precursor, [Sr(Pht)(H₂O)₂]. The obtained nanorods were found to be orthorhombic with the length of 70-100 nm and the diameter of about 10-15 nm. The Effect of calcinations temperature on morphology and purity of the products has been investigated. Strontium carbonate nanorods were formed at 500 °C. The products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and Fourier transform infrared (FT-IR) spectroscopy. In addition, further evidence for the purity and stoichiometry of the product was obtained by XPS (X-ray photoelectron spectroscopy) spectrum.     

Synthesis and characterization of nanophased silver tungstate

Silver tungstate (Ag₂WO₄) nanoparticles in two different morphologies are prepared by controlling the reaction kinetics of aqueous precipitation. X-ray diffraction studies reveal that the silver tungstate nanoparticles are in the α-phase. SEM images show the rod-like and fiber-like morphologies of the nanoparticles with high aspect ratios. The TGA and DTA studies show the high thermal stability of the nanorods. The average crystallite sizes (20–30 nm) of the rod-like silver tungstate estimated from TEM is consistent with the XRD results     

Sonochemical synthesis of cobalt aluminate nanoparticles under various preparation parameters

Cobalt aluminate (CoAl₂O₄) nanoparticles were synthesized using a precursor method with the aid of ultrasound irradiation under various preparation parameters. The effects of the preparation parameters, such as the sonochemical reaction time and temperature, precipitation agents, calcination temperature and time on the formation of CoAl₂O₄ were investigated. The precursor on heating yields nanosized CoAl₂O₄ particles and both these nanoparticles and the precursor were characterized by means of X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and atomic force microscopy (AFM). The use of ultrasound irradiation during the homogeneous precipitation of the precursor reduces the duration of the precipitation reaction. The mechanism of the formation of cobalt aluminate was investigated by means of Fourier transformation infrared spectroscopy (FT-IR) and EDX (energy dispersive X-ray). The thermal decomposition process and kinetics of the precursor of nanosized CoAl₂O₄ were investigated by means of differential scanning calorimetry (DSC) and thermogravimetry (TG). The apparent activation energy (E) and the pre-exponential constant (A) were 304.26 kJ/mol and 6.441 × 10¹⁴ s^?1, respectively. Specific surface area was investigated by means of Brunauer Emmett Teller (BET) surface area measurements.     

Fabrication of chain-like Mn2O3 nanostructures via thermal decomposition of manganese phthalate coordination polymers

A novel manganese coordination polymer [Mn(Pht)(H₂O)]_n as a precursor was obtained by chemical precipitation involving an aqueous solution of anhydrous manganese acetate and phthalate anion as a potential O-banded ligand. Fourier transform infrared (FT-IR) results proved that phthalate anions coordinate to metal cations as a chelating bidentate ligand, making polymeric structure. The Mn₂O₃ nanostructures have been prepared via thermal decomposition of as-prepared manganese phthalate polymers as precursor in the presence of oleic acid (OA) and triphenylphosphine (TPP) as a stabilizer and capping. Different approaches such as FT-IR, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were applied to characterize the products. TEM images and XRD analysis indicated that the as-synthesized chain-like Mn₂O₃ has a crystal phase of cubic syngony with a mean size of ∼40 nm.     

Synthesis of magnetite nanorods and porous hematite nanorods

Fe₃O₄ nanorods with average diameters of 40-50 nm and lengths of up to 1 μm were synthesized through hydrolysis of FeCl₃ and FeSO₄ solutions containing urea in the temperature range from 90 to 95 °C in reflux condition for 12 h, following an aging time of 12 h. The porous hematite nanorods were prepared by calcination of the precursor which was obtained from hydrolysis of FeCl₃ and FeSO₄ solutions containing urea at a temperature of 90 °C for 10 h in hydrothermal condition. The formation of the porosity of hematite was due to the decomposition of FeCO₃ and FeOOH. Urea played a key role in the formation of the iron oxide nanorods. Transmission electron microscopy (TEM) images showed that the morphology of magnetite particles is homogeneous in the shape of rods and hematite rods are full of porosity. The values of saturation magnetization (M) and coercivity (H) of magnetite nanorods are 67.55 emu/g and 114 Oe, respectively. The samples were also characterized by X-ray powder diffraction (XRD) and electron diffraction (ED). At last, the forming mechanism of both the magnetite and porous hematite nanorods was discussed.     

General solution-based route to V–VI semiconductors nanorods from hydrolysate

V–VI (Bi₂Se₃, Bi₂Te₃, Sb₂Se₃, and Sb₂Te₃) semiconductors nanorods with the diameters of 40–90 nm have been synthesized starting from BiCl₃ (or SbCl₃) and Na₂SeO₃ (or Na₂TeO₃) by using NaH₂PO₂·H₂O as the reduced agent at 140°C for 24 h. The samples were characterized by XRD, SEM and TEM. XPS spectra of the products show the obtained samples are close to stoichiometry. The hydrolysate of the starting materials could be served as the precursor and sharply decreases the growth of the samples; a possible hydrolyzation–reduction–crystallization process was also proposed to explore the formation mechanism of these nanorods.     

Synthesis and photoluminescence of single-crystal GaN nanorods prepared by sol-gel method

A new method was applied to prepare GaN nanorods. In this method, gallium oxide (Ga₂O₃) gel was firstly formed by a sol-gel processing using gallium ethanol, Ga(OC₂H₅)₃, as a new precursor. GaN nanorods were successfully synthesized after annealing of the Ga₂O₃ gel at 1000 °C for 20 min in flowing ammonia. The as-prepared nanorods were confirmed as single crystalline GaN with wurtzite structure by X-ray diffraction (XRD), selected-area electron diffraction (SAED) and high-resolution transmission electron microscopy (HRTEM). Transmission electron microscopy (TEM) displayed that the GaN nanorods were straight and smooth, with diameters ranging from 200 nm to 1.8 μm and lengths typically up to several tens of microns. When excited by 280 nm light at room temperature, the GaN nanorods had a strong ultraviolet luminescence peak located at 369 nm and a blue luminescence peak located at 462 nm, attributed to GaN band-edge emission and the existence of the defects or surface states, respectively.     

Synthesis, characterization and photoluminescent properties of rare-earth hydroxides and oxides nanorods by hydrothermal route

The stable and crystalline pure phase Ln(OH)₃ (Ln=La, Nd, Sm, Eu, Gd, Tb, and Dy) nanorods are synthesized by a facile hydrothermal method using the simple chemical materials (rare-earth chloride hexahydrate LnCl₃?6H₂O and NH₃?H₂O) and polymer polyvinypyrrolidone (PVP). The as-prepared Ln(OH)₃ nanorods can be successfully converted to Ln₂O₃ nanorods via calcination under appropriate conditions. X-ray diffraction (XRD) spectra, Fourier transformed infrared (FTIR) spectrum, scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-Resolution TEM (HRTEM), and Raman spectroscopy were used to examine the morphologies and microstructures to find out the cause. The analyzed results indicate that the obtained nanorods are rare-earth hydroxides and oxides with 1D nanostructures. The formation mechanism of the Ln(OH)₃ and Ln₂O₃ nanorods was investigated. Optical properties of the Ln(OH)₃ and Ln₂O₃ nanorods were determined by photoluminescence (PL). Ln(OH)₃ and Ln₂O₃ nanorods exhibit a strong blue emission with the strongest narrow bands at about 469 nm corresponding to the intra-4f transitions ⁵D₂→⁷F₆, which have potential applications in fluorescent devices.     

Solvothermal synthesis of CdS nanorods using hydroxyethyl cellulose as a template

CdS nanorods were solvothermally produced from Cd(CH₃COO)₂ and S powder using ethylenediamine (en) as a solvent and hydroxyethyl cellulose (HEC) as a template. The phase with hexagonal structure was detected using XRD and SAED, which is in perfect accordance with the results obtained by simulation. SEM, TEM and HRTEM revealed the development of nanorods with a number of atoms arranged in crystal lattices. When the appropriate amount of HEC was used, the longest nanorods, with preferential growth in the [0 0 1] direction, were produced. Raman spectra showed the fundamental and overtone modes at the same wavenumbers of 301 and 599 cm⁻¹, respectively. Their relative intensities at each temperature were strongly influenced by the anisotropic geometry of the products. Photoluminescence caused by electron-hole recombination was detected at 470 nm, and by surface trapping induced emission at 575 nm. The formation mechanism of CdS nanorods was also proposed based on the experimental results.     

A novel precursor for synthesis of metallic copper nanocrystals by thermal decomposition approach

[Bis(2-hydroxy-1-naphthaldehydato)copper(II)] complex, as a novel precursor, was employed in thermal decomposition process to synthesize metallic copper nanoparticles using oleylamine (C₁₈H₃₇N) as capping agent. The products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared (FT-IR) spectroscopy, thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS) and ultraviolet-visible (UV-vis) spectroscopy. The synthesized copper nanoparticles have a fcc structure with average size 20-35 nm.