Facile synthesis of flower-like nickel nanocrystals and properties

A solvo-hydrothermal synthesis approach for the preparation of a new type of flowerlike nickel nanostructure is reported. The as-synthesized flower-like nickel nanocrystallites were characterized by X-ray diffraction and scanning electron microscopy. The nickel flowers modified glassy carbon electrode can be prepared and used to detect methanol and ethanol in the solution. The results show that the nickel flowers give a very high activity for detecting the methanol and ethanol, which provide a new application of nickel flowers. Compared with that of bulk nickel, thus-prepared nickel flowers showed a much enhanced coercivity.     

Facile synthesis and magnetic properties of manganese doped ZnS nanorods

The synthesis of both Mn(II) doped and undoped ZnS nanorods were carried out using a simple soft-chemical route using mercaptoethanol as capping agent. Their morphological, structural and magnetic properties are presented. The crystal structures of the as obtained products were investigated through X-ray diffraction study reveals the formation of hexagonal wurtzite structure. The growth of the nanorods is achieved by careful control over the precursor addition, temperature and time duration. The nanorods are single crystalline and the diameter of the rods was found to vary in the range of 20-50 nm. Vibrating sample magnetometer measurements at room temperature show paramagnetic behavior for the doped nanorods.     

Chemical synthesis and magnetic properties of HCP and FCC nickel nanoparticles

In this study, we successfully synthesized single-phase hexagonal closed packed (HCP) and face-centered cubic (FCC) nickel nanoparticles via reduction of nickel nitrate hexahydrate and nickel acetate tetrahydrate, respectively, in polyethylene glycol-200. Structural information of the as-synthesized nickel nanoparticles are studied by X-ray diffraction (XRD) as a function of the molar concentration of the nickel precursor. XRD results reveal that low concentrations of nickel precursor (0.005?M and below) favor the HCP, while high concentrations favor the mixture of HCP and FCC crystal structures. Particle size of HCP structure is found in the range of ～15?nm via transmission electron microscope analysis. Vibratory sample magnetometer is employed to study its magnetic behavior and the results reveal that FCC crystalline phase shows ferromagnetic nature with high saturation magnetization (M _s?～?39.6?emu?gm^?1) as compared to metastable HCP crystalline structure (M _s?～?2?emu?gm^?1). The surfactants bonding on the surface of nickel nanoparticles are studied.     

Facile and rapid one-pot microwave-assisted synthesis of Pd-Ni magnetic nanoalloys confined in mesoporous carbons

An easy and rapid one-pot microwave-assisted soft-template synthesis method for the preparation of Pd-Ni nanoalloys confined in mesoporous carbon is reported. This approach allows the formation of mesoporous carbon and the growth of the particles at the same time, under short microwave irradiation (4 h) compared to the several days spent for the classical approach. In addition, the synthesis steps are diminished and no thermopolymerization step or reduction treatment being required. The influence of the Pd-Ni composition on the particle size and on the carbon characteristics was investigated. Pd-Ni solid solutions in the whole composition range could be obtained, and the metallic composition proved to have an important effect on the nanoparticle size but low influence on carbon textural properties. Small and uniformly distributed nanoparticles were confined in mesoporous carbon with uniform pore size distribution, and dependence between the nanoparticle size and the nanoalloy composition was observed, i.e., increase of the particle size with increasing the Ni content (from 5 to 14 nm). The magnetic properties of the materials showed a strong nanoparticle size and/or composition effect. The blocking temperature of Pd-Ni nanoalloys increases with the increase of Ni amount and therefore of particle size. The magnetization values are smaller than the bulk counterpart particularly for the Ni-rich compositions due to the formed graphitic shells surrounding the particles inducing a dead magnetic layer.

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Graphical abstract PdNi nanoalloys confined in mesoporous carbon exhibiting magnetic properties dependent on thealloys composition and size were synthesized by a fast microwave approach

     

Combustion synthesis of nickel ferrite powders: Effect of NaClO4 content on their characteristics and magnetic properties

Magnetic powders of nickel ferrite (NiFe₂O₄) were successfully synthesized by combustion synthesis in air using iron (Fe), iron oxide (Fe₂O₃), and nickel oxide (NiO) as reactants and sodium perchlorate (NaClO₄) as fuel (or oxidizing agent). The thermal behaviors were characterized using thermogravimetric analysis (TG) and differential thermal analysis (DSC). The as-combusted and final nickel ferrite powders were characterized in terms of chemical composition and morphology by X-Ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), and scanning electron microscopy (SEM) coupled with energy dispersive X-Ray spectroscopy (EDX). In addition, magnetic properties were examined by vibrating sample magnetometer (VSM). The results of TG/DSC analysis indicated that increasing the content of NaClO₄ increased the exothermicity of combustion reaction. XRD indicated that the final nickel ferrite powders formed a single spinel NiFe₂O₄ phase when the amount of NaClO₄ used was 0.08 or 0.10 mol. SEM revealed roughly octahedron particles with sizes in a sub-micrometer range (∼500 nm). All final products exhibited soft magnetism and, synthesis that included 0.1 mol of NaClO₄ produced pure NiFe₂O₄ powders that had a saturation magnetization (M_s) of 58.93 emu/g, which is higher than the reported value (55 emu/g) for the bulk product.     

Elastic and ultrasonic properties of single crystalline nickel nanowires

In the present paper, we have theoretically calculated the non linear elastic constants of single crystalline Ni NWs at very broad temperature range 20–300 K validating simple interaction potential model. The temperature dependent ultrasonic attenuation and other related properties are determined using their second and third order elastic constants (SOECs/TOECs). Where possible, the results are compared with experiments from literature. There is a correlation between the thermal conductivity and ultrasonic attenuation in the temperature range 100–300 K. Also, a correlation between the resistivity and ultrasonic attenuation in the temperature range 40–100 K has been established validating the theoretical approach.     

Microstructural and magnetic properties of CoPt nanowires

In this work, the magnetic and microstructural properties of CoPt nanowires are presented as a function of the electrolyte pH and current density during electrodeposition into anodized alumina templates. CoPt nanowires of high aspect ratio have been prepared using electrolyte pH values in the range from 2 to 6. The as-made samples exhibit a face centered cubic (fcc) structure with soft magnetic properties which transform into the face centered tetragonal (fct) L10 phase after thermal treatment. Different pH values of the electrolyte during electrodeposition lead to significantly different microstructures and, therefore, different magnetic properties. The CoPt nanowires prepared at high pH value are composed of fcc nanorods of about 25 nm in length. Thermal annealing of these samples leads to a preferred (0 0 1) orientation (along the direction perpendicular to the direction of nanowires) which increases with annealing time. On the other hand, the CoPt nanowires prepared at lower pH value are composed of uniform fcc nanograins with the size ∼2−3 nm. Magnetization curves for the later sample are virtually identical in both directions indicating an isotropic behavior.     

Facile synthesis of single-crystal silver nanowires through a tannin-reduction process

A facile aqueous-phase approach for the synthesis of silver nanowires is reported, in which tannin (C₇₆H₅₂O₄₆) is used as a mild reducing agent for silver nitrate. This synthesis is a root-temperature, seedless process, and does not need any surfactant or capping agent to direct the anisotropic growth of the nanoparticles. The obtained silver nanowires are about 25 nm in diameter and up to 20 μm in length. Unlike the usually reported cases of silver nanowires or nanorods, in which the silver nanocrystals were often generated with a multi-twinned structure, in our experiments the nanowires adopt a single-crystal structure with their growth direction along the [100] axis. Investigations on the influence of different experimental conditions indicate that slow rate of the reduction process is a key factor for inducing the anisotropic growth of the nanowires.     

Hydrothermal synthesis of MnO2 nanowires: structural characterizations,optical and magnetic properties

In this paper, 1D single-crystalline MnO₂ nanowires have been successfully synthesized by hydrothermal method using KMnO₄ and (NH₄)₂S₂O₈ as raw materials. X-ray diffraction patterns and high-resolution TEM images reveal pure tetragonal MnO₂ phase with diameters of 15–20 nm. Photoluminescence studies exhibited a strong ultraviolet (UV) emission band at 380 nm, blue emission at 452 nm and an extra weak defect-related green emission at 542 nm. UV–visible spectrophotometery was used to determine the absorption behavior of nanostructured MnO₂ and a direct optical band gap of 2.5 eV was acquired by Davis–Mott model. The magnetic properties of the products have been evaluated using vibrating sample magnetometer, which showed that MnO₂ nanowires exhibited a superparamagnetic behavior at room temperature. The magnetization versus temperature curve of the as-obtained MnO₂ nanowires shows that antiferromagnetic transition temperature is 99 K.     

Cr掺杂ZnO纳米线电子性质和磁性质

本文采用第一性原理密度泛函理论系统的研究了Cr原子单掺杂和双掺杂两种尺寸ZnO纳米线的电子性质和磁性质.所有掺杂纳米线的形成能都比纯纳米线的形成能低,表明掺杂增强了纳米线的稳定性.研究发现Cr原子趋于替代纳米线表面的Zn原子.所有掺杂纳米线都显示了金属性.纳米线的总磁矩主要来源于Cr原子3d轨道的贡献.由于杂化,相邻的O原子和Zn原子也产生了少量自旋.在超原胞内,Cr和O原子磁矩反平行排列,表明它们之间是反铁磁耦合.表面双掺杂纳米线铁磁态能量比反铁磁态能量低149 meV,表明Cr掺杂ZnO纳米线可能获得室温铁磁性.     

Large-scale synthesis of ZnO nanowires using a low-temperature chemical route and their photoluminescence properties

Single-crystalline zinc oxide (ZnO) nanowires were synthesized from zinc powder and H₂O through a simple chemical route at 730 °C in Ar atmosphere. The potential exists for bulk synthesis of ZnO nanowires at temperatures significantly less than the 200–300 °C of thermal evaporation methods reported formerly. Scanning electron microscopy and transmission electron microscopy observations reveal that the ZnO nanowires are structurally uniform, have lengths up to several hundreds of micrometers and diameters of about 40–60 nm and crystallize in a hexagonal structure. The growth of ZnO nanowires is controlled by the vapor–solid crystal-growth mechanism. Photoluminescence measurements show that the ZnO nanowires have a strong near-band ultraviolet emission at 380 nm and a green light emission at 520 nm caused by oxygen vacancies. PACS 81.05.Ys; 78.55.Et     

Facile alcohothermal synthesis of large-scale ceria nanowires with organic surfactant assistance

Well monodispersed and large-scaled ceria nanowires with cubic fluorite structure and high aspect ratios were successfully prepared at 80 °C without further sintering via a facile surfactant-assisted alcohothermal route. The X-ray diffraction, transmission electron microscopy with selected-area electron diffraction indicated that the as-prepared ceria nanowires had a cubic fluorite-structure and the morphologies of the products were uniform, with diameters of about 50–100 nm. The TG-DTA and XPS measurements revealed the existence of both trivalent and quadrivalent cerium and an oxidization process took place gradually with increase of the reaction time. Compared with as-reported method, the present process is more convenient and feasible.     

Synthesis and magnetic properties of Mn doped CuO nanowires

Study of diluted magnetic semiconductor nanowires is one of the important topics in materials science. By using Mn-Cu alloy as the starting material, Mn doped CuO nanowire arrays have been synthesized in air at the temperature of 550 °C. X-ray diffraction measurements and scanning electron microscopic study shows that the nanowires were grown on Cu₂O substrate. Transmission electron microscopic study shows the single crystal property of the nanowires. Magnetic measurements show ferromagnetic property in the Mn doped CuO nanowires with the critical temperature higher than 80 K.     

Synthesis and magnetic properties of Mn doped ZnO nanowires

Mn doped ZnO nanowires have been synthesized using a simple autocombustion method. The as-synthesized Mn doped ZnO nanowires were characterized by X-ray diffraction and transmission electron microscopy. An increase in the hexagonal lattice parameters of ZnO is observed on increasing the Mn concentration. Optical absorption studies show an increment in the band gap with increasing Mn content, and also give evidence for the presence of Mn²⁺ ions in tetrahedral sites. All Zn_1−xMn_xO (0≤x≤0.25) samples are paramagnetic at room temperature. However, a large increase in the magnetization is observed below 50 K. This behavior, along with the negative value of the Weiss constant obtained from the linear fit to the susceptibility data below room temperature, indicate ferrimagnetic behavior. The origin of ferrimagnetism is likely to be either the intrinsic characteristics of the Mn doped samples, or due to some spinel-type impurity phases present in the samples that could not be detected.     

Magnetic properties of one-dimensional embedded nickel nanostructures in gold nanowires

Magnetic nanostructures of nickel embedded in gold were successfully fabricated by electrochemical deposition in porous alumina templates. Structural characterization of the samples confirmed the formation of pure phase, crystalline multi-segmented Au-Ni-Au nanowires. Magnetic characterization of the wires reveals that ferromagnetism arises as a result of Ni embedded in Au segments. An interesting behavior of coercivity was observed that showed a rapid decrease of coercivity for smaller Ni segments while a monotonic decrease was found for the larger segments. Finally, the saturation magnetization of the wires exhibited a slower increase for smaller Ni segments while a sharp increase was observed for larger Ni segments.     

Chemical synthesis and studies on structural and magnetic properties of fine grained nickel cadmium ferrites

The cadmium substituted nickel ferrites Ni_1−xCd_x Fe₂O₄ (x=0.2, 0.4, 0.6) has been prepared by the self-propagating auto combustion method. Phase identification of the samples was studied by XRD patterns which are characteristics of cubic spinel structure ferrites. As the content of cadmium in the ferrites increases the lattice parameter. The tetrahedral and octahedral vibrations in the samples were studied by Fourier Transform Infrared (FT-IR) spectra. The SEM study reveals the fine-grained nature of ferrites with little agglomeration. The decrease in the drift mobility is found with increase in cadmium content. DC resistivity indicates the semiconducting nature of the samples. The Super Quantum Interference Device measurements were taken to study the magnetic properties of the samples.     

Sonochemical synthesis and optical properties of amorphous ZnO nanowires

Large-scale amorphous wire-like ZnO nanostructures were prepared by ultrasonic spray pyrolysis Zn(CO)₅ without involvement of any template or patterned catalyst. The as-obtained amorphous ZnO nanowires were characterized using scanning/transmission electron microscopy, X-ray diffraction/photoelectron spectroscopy, energy-dispersed X-ray spectrometry, selected area electronic diffraction, and high-resolution transmission electron microscopy. The results reveal the as-made noncrystalline samples are about 30–60 nm in diameter and several tens of microns in length and the growth mechanism is tentatively proposed as the self-assembly soft template mechanism. The photoluminescence spectra in all of the as-studied specimens exhibit one wide visible emission peak in about 508 nm. The corresponding PL intensity greatly increased with an annealing temperature, which has an application for a high efficiency vacuum fluorescent displays and a low-voltage phosphor.     

电沉积法制备的泡沫镍的晶体结构与磁性能

 采用X射线衍射仪、振动样品磁强计分别测试了电沉积法制备的泡沫镍的晶体结构和磁性能，研究了电流密度、温度、占空比、脉冲频率对镍沉积层的晶体结构和磁性能的影响；并用扫描电子显微镜、透射电子显微镜观察了泡沫镍的组织结构与微观形貌。制备出的3维网络状泡沫镍密度为0.25 g/cm³，孔隙率为97.5%、孔径分布为400～500 μm。沉积层大颗粒粒径为1 μm，沉积层晶粒尺寸在10nm以下;泡沫镍为超顺磁材料，具有低的矫顽力和高的磁导率，其磁导率和饱和磁化强度随沉积层晶粒尺寸的增加而增大。     

Magnetic properties of a two-dimensional spatially ordered array of nickel nanowires

The structural and magnetic characteristics of two-dimensional spatially ordered arrays of magnetic nickel nanowires embedded in the anodized alumina template have been investigated. It has been shown using small-angle polarized-neutron diffraction that, there exists the samples under investigation, in a highly ordered hexagonal structure of pores and magnetic nanowires separated by a characteristic distance d = 106 ± 2 nm. An analysis has been made of different contributions to neutron scattering, such as the nonmagnetic (nuclear) contribution, the magnetic contribution dependent on the magnetic field, and the interference contribution indicating a correlation between the magnetic and nuclear structures. The performed analysis of the results obtained has demonstrated that, when the magnetic field is applied perpendicular to the longitudinal axis of the nanowire in a completely magnetized sample, there arise demagnetizing fields around each nanowire that form a regular hexagonal lattice.