β-FeOOH纳米线的制备及表征

通过无机铁(III)盐的水解在常温条件下制备了β-FeOOH 纳米线, 并用透射电子显微镜(TEM)、高分辨透射电镜(HRTEM)、X射线衍射(XRD)及选区电子衍射(SAED)对其形貌及结构进行了表征. 电镜结果表明, 所得到的纳米线直径约 60 nm, 长度为4～5 μm, 且沿[001]方向生长. XRD结果表明纳米线为四方相β-FeOOH, 在常温下结晶性良好. 研究表明FeCl₃浓度对纳米线生长有很大影响, 只有当FeCl₃浓度合适时, 才能制备出高质量的纳米线.     

Synthesis and Magnetic Property of Fe-B Amorphous Alloy Nanowires by Inducing DC Magnetic Field

One dimension (1D) Fe-B amorphous alloy nanowires with diameter of 50-80 nm and length of several micrometers were synthesized under weak DC (direct current) magnetic field by KBH₄ reducing in aqueous solution. The structure, composition, and morphology were characterized by X-ray diffraction (XRD), inductively coupled plasma atomic emission spectrometry (ICP-AES), and scanning electron microscope (SEM), respectively. The results revealed that the magnetic field led to the fabrication of Fe-B amorphous alloy nanowire structure. Vibrating sample magnetometer (VSM) has been used to detect the magnetic properties of the samples. The results showed that the inducing of magnetic field had obvious effect on the magnetic properties of the samples.     

Spinel copper ferrite nanoparticles: Preparation,characterization and catalytic activity

The magnetic CuFe₂O₄ nanoparticles have been synthesized and characterized by various spectroscopic methods, including X‐ray diffraction (XRD), O K, Cu and Fe K ‐edge X‐ray absorption near edge structure (XANES), energy dispersive X‐ray analysis (EDX), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The azide‐alkyne cycloaddition by the reaction of various phenylacetylenes with a mixture of benzyl halides and NaN₃ and also three component (A³) coupling reaction of aldehyde, alkyne and amine catalyzed by CuFe₂O₄ nanoparticles under aerobic conditions led to the formation of the 1,4‐disubstituted‐1,2,3‐triazoles and propargylamines in excellent yields. The catalyst can be recovered by applying an external magnetic field for the subsequent cycloaddition reactions and reused without any tangible loss in catalytic efficiency.     

Phase‐Controlled Synthesis of Transition‐Metal Phosphide Nanowires by Ullmann‐Type Reactions

Transition‐metal phosphide nanowires were facilely synthesized by Ullmann‐type reactions between transition metals and triphenylphosphine in vacuum‐sealed tubes at 350–400 °C. The phase (stoichiometry) of the phosphide products is controllable by tuning the metal/PPh₃ molar ratio and concentration, reaction temperature and time, and heating rate. Six classes of iron, cobalt, and nickel phosphide (Fe₂P, FeP, Co₂P, CoP, Ni₂P, and NiP₂) nanostructures were prepared to demonstrate the general applicability of this new method. The resulting phosphide nanostructures exhibit interesting phase‐ and composition‐dependent magnetic properties, and magnetic measurements suggested that the Co₂P nanowires with anti‐PbCl₂ structure show a ferromagnetic–paramagnetic transition at 6 K, while the MnP‐structured CoP nanowires are paramagnetic with Curie–Weiss behavior. Moreover, GC‐MS analyses of organic byproducts of the reaction revealed that thermally generated phenyl radicals promoted the formation of transition‐metal phosphides under synthetic conditions. Our work offers a general method for preparing one‐dimensional nanoscale transition‐metal phosphides that are promising for magnetic and electronic applications.     

Magnetic nanowires via template electrodeposition

The magnetic NiFe_x nanowires were prepared via template-guided electrodeposition. Anodized nanoporous aluminum was used as a template. The pore density and dimensions of alumina templates can be controlled by anodization conditions. Magnetic nanorods (or nanowires) with various aspect ratios were prepared by controlling the electrodeposition time. SEM and TEM micrographs revealed the wire and rod shape morphologies with 50 nm in diameter and 1.5 ~ 10 μm in length. Elemental analysis and ESCA studies suggested that NiFe₃ magnetic alloy was formed. The X-ray diffraction pattern indicates that all the nanowires are stabilized in a BCC structure with a [1 1 0] texture oriented along the long axis of the nanowires. The magnetic measurement showed no hysteresis loops for the whole aspect ratios of the nanowires. Nevertheless, the magnetization is more temperature sensitive for nanowires with lower aspect ratio. This is caused by the fact that the easy magnetization axis is always parallel to the long axis of the nanowires.     

Structure and magnetic properties of Co nanowires electrodeposited into the pores of anodic alumina membranes

Cobalt nanowires were obtained in the process of electrodeposition into pores of an alumina membrane. Structural research (XRD, TEM) of Co revealed the face-centered cubic structure. However, the existence of the hexagonal structure cannot be excluded due to strong texture. The influences of an external magnetic field and Al₂O₃ membrane geometry on magnetic properties of obtained wires were examined. It was found that cobalt nanowires exhibit pronounced shape anisotropy in a direction parallel to the wire axis. The highest influence on the magnetic properties is ascribed to the nanowires geometry i.e., height, diameter, and distances between single wires. Application of an external magnetic field in a perpendicular direction to the sample surface during cobalt electrodeposition increases magnetic anisotropy with a privileged direction along the wire axis. Application of the magnetic field in a parallel direction to the sample surface changes the direction of magnetization.     

PREPARATION AND CHARACTERIZATION OF PVA COATED MAGNETIC NANOPARTICLES*

Polyvinyl alcohol coated magnetic particles (PVA ferrofluids) have been synthesized by chemical co-precipitationof Fe(Ⅱ)/Fe(Ⅲ) salts in 1.5 mol/L NH_4OH solution at 70℃ in the presence of PVA. The resultant colloidal particles havecore-shell structures, in which the iron oxide crystallites form the cores and PVA chains form the shells. The hydrodynamicdiameter of the colloidal particles is in the range of 108 to 155 nm, which increases with increasing PVA concentration from5 wt% to 20 wt%. The size of the magnetic cores is ca. 5～10 nm, which is relatively independent of PVA concentration.Under transmission electron microscopic (TEM) examination, the magnetic cores exhibit somewhat irregular shapes varyingfrom spherical, oval, to cubic. Magnetometry measurement revealed that the PVA coated magnetic particles aresuperparamagnetic. The saturation magnetization of 5 wt% and 20 wt% PVA ferrofluids at 300 K is 54 and 49 emu/g.respectively. All the PVA ferrofluids exhibited excellent colloidal stability in pure water and phosphate buffer saline (PBS,pH=7.4). The ferrofluids can remain stable in above solutions for more than three months at 4℃.     

Hierarchical Titanate Nanostructures through Hydrothermal Treatment of Commercial Titania Powders

Hierarchical titanate nanostructures were hydrothermally synthesized in concentrated base solutions using commercial titania powders as starting materials. By varying the base concentration, nanowire arrays, flowers of nanosheets and nanotubes, and urchin‐like nanostructures of nanowires and nanotubes were sequentially fabricated. If the NaOH concentration was higher than 6 M , hydrated Na₂Ti₆O₁₃ nanowire arrays, with nanowire diameters of 20–90 nm and an aspect ratio of 1100–5000, were produced at suitable reaction temperatures over a large area. In 10 M KOH solutions, aligned nanowires with a diameter of 30 nm and a lenght of 80 μm formed. In 4 M NaOH solutions, micrometer‐sized flowers of nanotubes and nanosheets formed. Reactions in 2 M NaOH solutions produced urchin‐like materials with a size of ca. 10 μm that were composed of nanotubes and nanowires. The adsorption behavior of the urchin‐like materials resembled macroporous materials with micropores. Since both base concentration and reaction temperature affected the reaction rate, the formation of various titanate nanostructures was proposed as a growth speed controlled process.     

A Mössbauer and X-ray study of Fe2P1−xBx compounds (x < 0.15)

Boron/phosphorus substitution in Fe₂P has been studied by ⁵⁷Fe Mössbauer spectroscopy. The magnetic ordering temperature increases rapidly with increasing boron content. Replacement of a phosphorus atom by boron in the immediate environment of an iron atom results in a substantial increase of the magnetic hyperfine field, while the centroid shift and the quadrupole splitting are almost unchanged. The hyperfine parameters for iron atoms at larger distances from the boron atom remain unaffected. Boron substitutes preferentially for phosphorus at the singlefold P(2) position in the Fe₂P structure.     

Growth of High Magnetic α-Fe2O3 and Fe3O4 Nanowires via an Oxide Assisted Vapor-Solid Process

We describes a controllable synthesis procedure for growing α-Fe₂O₃ and Fe₃O₄ nanowires. High magnetic hematite α-Fe₂O₃ nanowires are successfully grown on Fe_0.5Ni_0.5 alloy sub-strates via an oxide assisted vapor-solid process. Experimental results also indicate that previous immersion of the substrates in a solution of oxalic acid causes the grown nanowires to convert gradually into magnetite (Fe₃O₄) nanowires. Additionally, the saturated state of Fe₃O₄ nanowires is achieved as the oxalic acid concentration reaches 0.75 mol/L. The aver-age diameter and length of nanowires expands with an increasing operation temperature and the growth density of nanowires accumulates with an increasing gas flux in the vapor-solid process. The growth mechanism of α-Fe₂O₃ and Fe₃O₄ nanowires is also discussed. The results demonstrate that the entire synthesis of nanowires can be completed within 2 h.     

Magnetic Co3O4 nanowires,preparation and properties

The Co₃O₄ nanowires have been successfully synthesized via modified template method.The as-prepared products have been characterized by EDS,TEM and HRTEM analysis.The magnetic behavior of it is investigated by a magnetic property measurement system.The nanowires exhibit some novel magnetic properties,which are different from its bulk material.The temperature dependence curves of magnetization in zero-field-cooling and field-cooling exhibit two peaks of antiferromagnetic at blocking temperature of～23 K and～31 K,respectively.The field dependent M（H） curves of the Co₃O₄ nanowires at T = 5 and 300 K both exhibit PM properties.Moreover,the diameter of nanowires is hence determined according to the finite size effect as approximately 7-11 nm,in consistent with the characterizations by HRTEM.     

Synthesis and visible light photocatalytic activity of β-AgVO3 nanowires

β-AgVO₃ nanowires are synthesized by the hydrothermal method. The synthesis yields nanowires with a monoclinic phase structure. Typical nanowires have diameter of about 200–700 nm and length up to 300 μm. Photocatalytic degradation of Rhodamine B dye is investigated. It is found that the β-AgVO₃ nanowires possess excellent catalytic degradation activity owing to its effective visible light absorption and well crystallization. The highly photocatalytic activity suggest its possible application in the organic pollutant treatment under visible light irradiation.     

磁场诱导制备Fe-B非晶态合金纳米线及其磁学性质

通过引入外加直流电磁场, 采用KBH4还原法在室温下制备了一维Fe-B非晶态合金纳米线, 并采用X射线衍射(XRD)、电感耦合等离子原子发射光谱仪(ICP-AES)和扫描电子显微镜(SEM)等表征方法研究了产物的结构、组成和形貌. 结果表明, 在直流电磁场的作用下得到了Fe-B非晶态合金纳米线, 所得样品的直径在50-80 nm之间, 长度达到数微米. 通过振动样品磁强计(VSM)研究其磁学性质, 发现外加磁场的引入会显著影响Fe-B非晶态合金的磁学性质. 随着引入磁场强度的增强, 所得样品的饱和磁感应强度和矫顽力明显区别于未引入磁场制备的Fe-B非晶态合金.     

Synthesis and characterization of magnetic nanoparticles

Magnetic nanoparticles with average diameter in the range of 6.4-8.3 nni have been synthesized by a chemical co-precipitation of Fe(Ⅱ)and Fe(Ⅲ)salts in 1.5 M NH4OH solution.The size of the magnetic particles is dependent on both temperature and the ionic strength of the iron ion solutions.The magnetic particles formed at higher temperature or lower ionic strength were slightly larger than those formed at lower temperature or higher ionic strength respectively.In spite of the different reaction conditions,all the resultant nanoparticles are nearly spherical and have a similar crystalline structure.At 300 K,such prepared nanoparticles are superparam-agnetic.The saturation magnetizations for 7.8 and 6.4 nm particles are 71 and 63 emu/g respectively,which are only ~ 20-30% less than the saturation magnetization(90 emu/g)of bulk Fe3O4 Our results indicated that a control of the reaction conditions could be used to tailor the size of magnetic nanoparticles in free precipitation.     

Densely packed single-crystal Bi2Fe4O9 nanowires fabricated from a template-induced sol-gel route

Densely packed single-crystal Bi₂Fe₄O₉ nanowires were successfully synthesized by a template-induced citrate-based sol-gel process. The structural properties of the nanowires were characterized using many techniques. The results of scanning electron microscopy (SEM) and transmission electron microscopy (TEM) revealed that Bi₂Fe₄O₉ nanowires possessed a uniform length and diameter, which were controlled by the thickness and the pore diameter of the applied porous anodic aluminum oxide (AAO) template, respectively. The results of X-ray diffraction (XRD) and the selected area electron diffraction (SAED) indicated that Bi₂Fe₄O₉ nanowires had an orthorhombic single-crystal structure. Furthermore, the energy-dispersive X-ray (EDX) spectroscopy demonstrated that the stoichiometric Bi₂Fe₄O₉ was formed. The possible formation mechanism of nanowires was also discussed.     

Magnetically Assembled Multisegmented Nanowires and Their Applications

Here we report a cost effective and versatile way of synthesizing and assembling multi‐functional (e.g., gold‐polypyrrole‐nickel‐gold) nanowires. Multisegmented nanowires were synthesized using electrodeposition method for precise control over segment dimensions for proper expression of material functionality. The nanowires were integrated on microfabricated electrodes using magnetic dipole interactions between the ferromagnetic segment in the nanowire and the ferromagnetic electrodes. The electrical properties of multisegmented nanowires showed semiconducting behavior with the activation energy of ca. 0.27 eV for the conducting polymer segment of the nanowire. These nanowire devices showed response towards light and exposure to ammonia, demonstrating their potential use as photonic device and gas sensor, respectively.     

Extraction of Rutin and Rhoifolin by Inorganic Borate Functionalized Magnetic Particles

We demonstrate a facile approach for smart time‐saving extraction of active components of rutin and rhoifolin by a new kind of magnetic particles (MPs). The inorganic borate functionalized magnetic particles are quasi‐spherical with an average diameter of 200–220 nm. The MPs were characterized by scanning electron microscopy and X‐ray diffraction techniques. The inorganic boron content in MPs was confirmed by electron‐dispersive X‐ray spectroscopy. The extraction and release efficiency of MPs were investigated. The smart borate‐decorated magnetic particles show a specific extraction towards the active components containing cis‐1,2 diol moieties. Rutin and rhoifolin were extracted at 16.55 and 22.49 mg/g, respectively. The recycling test shows that MPs can be reused and maintain a significant efficiency for seven cycles. Hence, a novel structured and reusable magnetic nanomaterial for extracting rutin and rhoifolin was developed. This strategy of specific extraction will be an important method to obtain the active components with some structure features through designing various structured particles.     

Circular Dichroism Study of the Mechanism of Formation of DNA Templated Nanowires

In order to control the fabrication method, the mechanism used in the formation of DNA templated nanowires is investigated through circular dichroism (CD) spectroscopy. Metallic (Au) and magnetic (Fe₂O₃ and CoFe₂O₄) nanoparticles (NP) are aligned along the DNA strand at various mass ratios. The DNA templated nanowires are compared to the structure of B‐form dsDNA through CD experiments. Absorbance and thermal melting tests are performed to verify the structural changes of DNA templated nanowires. Low concentrations of nanoparticles preserve the DNA B‐form through electrostatic interactions. Conversely, at higher concentrations of nanoparticles aligned along the DNA strand, the template is denatured. Information on the mode of nanoparticle binding and DNA helix alterations are explored for metallic and magnetic nanowires based upon the results.     

High rate performances of hydrogen titanate nanowires electrodes

In this study, H₂Ti₃O₇ nanowires were successfully synthesized via a hydrothermal process and post-treatments. The diameter of the nanowires is found to be about 30 nm and the length up to several micrometers. A lithium battery using H₂Ti₃O₇ nanowires as the active material of the positive electrode exhibits a discharge capacity of 100 mA hg⁻¹ and still keeps stable after 200 cycles at a current density as high as 40 Ag⁻¹, demonstrating excellent high rate performance.     

Large‐Scale Synthesis of Necklace‐Like Single‐Crystalline PbTiO3 Nanowires

Summary: We show in this communication that large‐scale necklace‐like single‐crystalline tetragonal perovskite PbTiO₃ nanowires can be obtained via a simple electrospinning method. The morphology and the crystal structure are investigated by SEM, XRD, and HRTEM. The length of the necklace‐like PbTiO₃ nanowires is from tens to several tens of micrometers, the wider the diameter of it is between 100 and 200 nm and the thinner the part is between 20 and 50 nm. The necklace‐like PbTiO₃ nanowires exhibit high surface photovoltage under the action of external electric field, which is probably applicable in displaying photoelectric devices of heterojunction structure.

SEM image of the electrospinning necklace‐like PbTiO₃ nanowires.