Sub 5 nm magnetite nanoparticles: Synthesis,microstructure, and magnetic properties

Magnetite particles of 2–4 nm were synthesized by an economic, biocompatible chemical coprecipitation route, with their size tuned by the reaction temperature. The microstructure and morphology of the nanoparticles were characterized by X-ray diffraction (XRD) and high resolution transmission electron microscopy (HRTEM), whereas the magnetic properties were investigated by vibrating sample magnetometry (VSM) and superconducting quantum interference device (SQUID). It is found that the nanoparticles demonstrate well-defined superparamagnetic behavior as prepared and after annealing. Distinct lattices were observed which manifest the high crystallinity of such ultrasmall particles and the finite-size effect was revealed by analyzing the corresponding microstructure and magnetism.     

Synthesis of sub-5 nm Co-doped SnO2 nanoparticles and their structural,microstructural, optical and photocatalytic properties

A swift chemical route to synthesize Co-doped SnO₂ nanopowders is described. Pure and highly stable Sn_1−xCo_xO_2−δ (0 ≤ x ≤ 0.15) crystalline nanoparticles were synthesized, with mean grain sizes <5 nm and the dopant element homogeneously distributed in the SnO₂ matrix. The UV–visible diffuse reflectance spectra of the Sn_1−xCo_xO_2−δ samples reveal red shifts, the optical bandgap energies decreasing with increasing Co concentration. The samples' Urbach energies were calculated and correlated with their bandgap energies. The photocatalytic activity of the Sn_1−xCo_xO_2−δ samples was investigated for the 4-hydroxylbenzoic acid (4-HBA) degradation process. A complete photodegradation of a 10 ppm 4-HBA solution was achieved using 0.02% (w/w) of Sn_0.95Co_0.05O_2−δ nanoparticles in 60 min of irradiation.     

Multivalent assembly of ultrasmall nanoparticles: One-, two-, and three-dimensional architectures of 2 nm gold nanoparticles

The assembly of nanoparticles (NPs) into complex structures is a fundamental topic in nanochemistry. Although progress has been made in this respect, the classical treatment of NPs as hard building blocks that lack the ability to anisotropically “bond” to each other limits the construction of more complex assemblies. More importantly, extension of methods of assembly of robust NPs to the assembly of ultrasmall ones with size below 2 nm is still challenging. Here we report the controlled self-assembly of ∼2 nm gold NPs into one-dimensional (1D) nanochain, two-dimensional (2D) nanobelt and three-dimensional (3D) nanocomet architectures by kinetically controlling the diffusion of ultrasmall gold NPs with anisotropic surfaces in solution. This process is presumed to allow selective ligand exchange with linkers at different binding sites on the NP surface, and results in “multivalent” interactions between NPs. Different from the assembly of “hard building blocks”, our results demonstrate the significance of surface effects for ultrasmall NPs (or clusters) in determining the structure of complex self-assemblies, and suggest the possibility of assembling these “molecule-like” ultrasmall nanocrystals into novel complex materials on a nanoscale approaching that of real atoms or molecules.      

Functionalized magnetic nanoparticles for small-molecule isolation, identification, and quantification

Functionalized magnetic nanoparticles (MNPs) were synthesized to serve as laser desorption/ionization elements as well as solid-phase extraction probes for simultaneous enrichment and detection of small molecules in matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) analysis. Two laser-absorbing matrices were each conjugated onto MNP to give MNP@matrix which provided high ionization efficiency and background-free detection in MS leading to unambiguous identification of target small molecules in a complex mixture. MNP@matrix was demonstrated to serve as a general matrix-free additive in MALDI-TOF MS analysis of structurally distinct small molecules. Also, MNP@matrix provides a simple, rapid, and reliable quantitative assay for small molecules by mass without either the use of an internal standard or an isotopic labeling tag. Furthermore, the affinity extraction of small molecules from complex biofluid was achieved by probe protein-conjugated MNP@matrix without laborious purification. We demonstrated that a nanoprobe-based assay is a cost-effective, rapid, and accurate platform for robotic screening of small molecules.     

Scanning transmission x-ray microscopy of polymer nanoparticles: probing morphology on sub-10 nm length scales

Water-processable nanoparticle dispersions of semiconducting polymers offer an attractive approach to the fabrication of organic electronic devices since they offer: (1) control of nanoscale morphology and (2) environmentally friendly fabrication. Although the nature of phase segregation in these polymer nanoparticles is critical to device performance, to date there have been no techniques available to directly determine their intra-particle structure, which consequently has been poorly understood. Here, we present scanning transmission x-ray microscopy (STXM) compositional maps for nanoparticles fabricated from poly(9,9-dioctyl-fluorene-2,7-diyl-co-bis-N, N'-(4-butylphenyl)-bis-N, N'-phenyl-1,4-phenylenedi-amine) (PFB) and poly(9,9-dioctylfluorene-2,7-diyl-co-benzothiadiazole) (F8BT) 1:1 blend mixtures. The images show distinct phase segregation within the nanoparticles. The compositional data reveals that, within these nanoparticles, PFB and F8BT segregate into a core-shell morphology, with an F8BT-rich core and a PFB-rich shell. Structural modelling demonstrates that the STXM technique is capable of quantifying morphological features on a sub-10 nm length scale; below the spot size of the incident focused x-ray beam. These results have important implications for the development of water-based 'solar paints' fabricated from microemulsions of semiconducting polymers.     

Barium hexaferrite nanoparticles: Synthesis and magnetic properties

Carbon combustion synthesis is applied to rapid and energy efficient fabrication of crystalline barium hexaferrite nanoparticles with the average particle size of 50-100 nm. In this method, the exothermic oxidation of carbon nanoparticles with an average size of 5 nm with a surface area of 80 m²/g generates a self-propagating thermal wave with maximum temperatures of up to 1000 °C. The thermal front rapidly propagates through the mixture of solid reactants converting it to the hexagonal barium ferrite. Carbon is not incorporated in the product and is emitted from the reaction zone as a gaseous CO₂. The activation energy for carbon combustion synthesis of BaFe₁₂O₁₉ was estimated to be 98 kJ/mol. A complete conversion to hexagonal barium ferrite is obtained for carbon concentration exceeding 11 wt.%. The magnetic properties H_c∼3000 Oe and M_s∼50.3 emu/g of the compact sintered ferrites compare well with those produced by other synthesis methods.     

Photoelectrochemical,optical and magnetic properties of magnetite nanoparticles

Magnetite magnetic nanoparticles are prepared using olive leaf extract as a green reducing and stabilizing agents. After reaction the product is heated up to get rid of the organic compounds and get pure magnetite nanoparticles. Differential scanning calorimetry is used to study the phase transformation as a function of heating temperature. Scanning electron microscope and high resolution transmission electron microscope show spherical and crystallized nanoparticles with a size of 5 nm. X-ray diffraction and Raman and x-ray photoelectron spectroscopy indicate the formation of Magnetite phase with high cristallinity and purity. The synthesized Magnetite nanoparticles are semiconductors with gap energy around 2 eV. Observed by transmission electron microscope graphite rods with stacked carbon disks are decorated with the prepared nanoparticles and show enhanced photocurrent. The vibrating sample magnetometer measurements indicate that the prepared Magnetite nanoparticles have superparamagnetic behavior. These results are very promising for clinical and water splitting applications.     

EuCuOSe: Crystal structure refinement, electrical and magnetic properties

The europium copper oxyselenide EuCuOSe has been prepared by reacting Eu, CuO and Se in the ratio 1:1:1 at 1123 K for a period of 10 days in sealed quartz ampoule. The structure has been determined by single-crystal X-ray methods. The compound crystallizes tetragonal in the space group P4/nmm (no. 129) with two formula units in the cell with dimensions a = 393.65(8) pm and c = 871.80(17) pm. The structure is composed of double layers separated by copper atoms, which are tetrahedrally coordinated to Se²⁻ anions. According to the resistivity measurements, EuCuOSe is a semiconductor. The magnetic susceptibility data shows the typical non-Curie-Weiss behavior of the ⁷F_J states of Eu in the 4f⁶ configuration.     

Superparamagnetic magnetite nanoparticles for cancer cells treatment via magnetic hyperthermia: effect of natural capping agent,particle size and concentration

Journal of Materials Science: Materials in Electronics - Superparamagnetic iron oxide nanoparticles (SPMNPs) continue to emerge as one of the most potential candidates in biomedical applications....     

磁性金属合金纳米粒子的合成与自组装

介绍了用高温液相法合成FePt、CoPt、FeCoPt和FeCoAg等磁性纳米粒子及其自组装的原理和方法，讨论了这些纳米粒子所具有的优异性能，并且指出了它们的最新应用。     

Zinc oxide micro- and nanoparticles: Synthesis, structure and optical properties

Zinc oxide (ZnO) spherical nanoparticles (SNPs) and bitter-melon-like (BML) microparticles were synthesized by a hydrothermal route using a zinc (Zn) plate as a source and substrate at various synthesis conditions. The structural analysis confirmed the formation of ZnO with hexagonal wurtzite phase on the hexagonal Zn substrate with growth of the ZnO microparticles along the [1 0 1] direction. The UV-vis absorption spectra of the ZnO microparticles indicated absorption peaks in the UV region which can be attributed to the band gap of ZnO. The room temperature photoluminescence (PL) of the ZnO microparticles exhibited a broad emission band, which is fitted with four Gaussian peaks and were assigned to transitions involving free excitons and various defect centers. The growth model for the formation of ZnO micro- and nanoparticles is presented.     

Structural,optical and magnetic properties of cobalt-doped CdSe nanoparticles

Pure and Co-doped CdSe nanoparticles have been synthesized by hydrothermal technique. The synthesized nanoparticles have been characterized using X-ray diffraction (XRD), ultraviolet-visible spectroscopy (UV–Visible), photoluminescence spectroscopy (PL), energy dispersive spectroscopy (EDS), transmission electron microscopy (TEM) and superconducting quantum interference device (SQUID), at room temperature. From XRD analysis, pure and cobalt-doped CdSe nanoparticles have been found to be polycrystalline in nature and possess zinc blende phase having cubic structure. In addition to this, some peaks related to secondary phase or impurities such as cobalt diselenide (CoSe₂) have also been observed. The calculated average crystallite size of the nanoparticles lies in the range, 3–21 nm, which is consistent with the results obtained from TEM analysis. The decrease in average crystallite size and blue shift in the band gap has been observed with Co-doping into the host CdSe nanoparticles. The magnetic analysis shows the ferromagnetic behaviour up to 10% of Co-doping concentration. The increase of Co content beyond 10% doping concentration leads to antiferromagnetic interactions between the Co ions, which suppress the ferromagnetism.     

Size-controlled synthesis, microstructure and magnetic properties of Ni nanoparticles

Ni nanoparticles with different mean diameters of 15-83 nm were synthesized by solution reduction process. The size of Ni nanoparticles can be controlled by varying the concentration of NiCl₂·6H₂O and synthesis temperature. The samples were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), infrared spectroscopy (IR) and X-ray photoelectron spectroscopy (XPS). Results show that the synthesized particles are single-phased Ni with a face-centered cubic crystal structure. Magnetic measurements indicate that Ni nanoparticles are ferromagnetic. The lattice constants and coercivities of the samples are size-dependent.     

Superparamagnetic iron oxide nanoparticles assembled magnetic nanobubbles and their application for neural stem cells labeling

Micro/nanobubbles for use as ultrasound contrast agents have been fabricated with different shell materials.When various biomedical nanoparticles have been embedded in the shells of bubbles,the composite structures have shown promising applications in multi-modal imaging,drug/gene delivery,and biomedical sensing.In this study,we developed a new gas-liquid interface self-assembly method to prepare magnetic nanobubbles embedded with superparamagnetic iron oxide nanoparticles(SPIONs).The diameter of the generated assembled nanobubbles was 227.40±87.21 nm with a good polydispersity index(PDI)of 0.29.Under the condition of 150 compression cycles,the nanobubble concentration could reach about 6.12×10⁹/mL.Transmission electron microscopy(TEM)and scanning electronic microscopy(SEM)demonstrated that the assembled nanobubbles had a hollow gas core with SPIONs adsorbed on the surface.Ultrasound(US)imaging and magnetic resonance imaging(MRI)experiments indicated that the assembled magnetic nanobubbles exhibited good US and MR contrast capabilities.Moreover,the assembled magnetic nanobubbles were used to label neural stem cells under ultrasound exposure.After 40 s US exposure,the magnetic nanobubbles could be delivered into cells with 2.80 pg Fe per cell,which could be observed in the intracellular endosome by TEM.Compared with common incubation methods,the ultrasound exposure method did not introduce the potential cytotoxicity of transfection reagents and the efficiency was about twice as high as the efficiency of incubation.Therefore,the assembled magnetic nanobubbles prepared through the pressure-driven gas-liquid interface assembly approach could be a potential US/MRI dual model imaging nanocarrier for regenerative applications.     

DNA-controlled assembly of a NaTl lattice structure from gold nanoparticles and protein nanoparticles

The formation of diamond structures from tailorable building blocks is an important goal in colloidal crystallization because the non-compact diamond lattice is an essential component of photonic crystals for the visible-light range. However, designing nanoparticle systems that self-assemble into non-compact structures has proved difficult. Although several methods have been proposed, single-component nanoparticle assembly of a diamond structure has not been reported. Binary systems, in which at least one component is arranged in a diamond lattice, provide alternatives, but control of interparticle interactions is critical to this approach. DNA has been used for this purpose in a number of systems. Here we show the creation of a non-compact lattice by DNA-programmed crystallization using surface-modified Qβ phage capsid particles and gold nanoparticles, engineered to have similar effective radii. When combined with the proper connecting oligonucleotides, these components form NaTl-type colloidal crystalline structures containing interpenetrating organic and inorganic diamond lattices, as determined by small-angle X-ray scattering. DNA control of assembly is therefore shown to be compatible with particles possessing very different properties, as long as they are amenable to surface modification.     

聚合物包覆纳米铁粒子的结构及其磁性能研究进展

纳米铁粒子具有极大的反应活性而被氧化.本文简要综述了聚合物包覆的纳米铁及其磁性能的研究进展.     

The preparation and magnetic properties of GdxBiY2−xFe5O12 nanoparticles

Gd_xBiY_2−xFe₅O₁₂ (x = 0, 0.1, 0.2, 0.4, 0.6, 0.8) nanocrystals were synthesized by sol–gel method. Samples were characterized by using of X-ray diffraction (XRD), thermal gravity analysis (TGA), differential thermal analysis (DTA), transmission electron microscopy (TEM), and vibrating sample magnetometer (VSM).The average size of the particles was calculated by Scherrer's formula from XRD data, which are from 43 to 50 nm. The effect of Gd³⁺ substitution for Y³⁺ on magnetic properties of BiY₂Fe₅O₁₂ has been investigated.     

Formation, characterization and magnetic properties of carbon-encapsulated iron carbide nanoparticles

Fe₃C nanoparticles encapsulated in carbon shell with a size range of 20–50 nm were obtained in large scale by reacting anhydrous FeCl₃, hexamethylenetetramine and metal Na in an autoclave at 650 °C. Magnetization measurements show that the as-obtained materials display superparamagnetic properties at room temperature. A possible formation mechanism of the core–shell nano-structures was discussed.     

Bulk synthesis, growth mechanism and properties of highly pure ultrafine boron nitride nanotubes with diameters of sub-10 nm

As a structural analogue of the carbon nanotube (CNT), the boron nitride nanotube (BNNT) has become one of the most intriguing non-carbon nanostructures. However, up to now the pre-existing restrictions/limitations of BNNT syntheses have made the progress in their research rather modest. This work presents a new route toward the synthesis of highly pure ultrafine BNNTs based on a modified boron oxide (BO) CVD method. A new effective precursor--a mixture of Li?O and B--has been proposed for the growth of thin, few-layer BNNTs in bulk amounts. The Li?O utilized as the precursor plays the crucial role for the present nanotube growth. The prepared BNNTs have average external diameters of sub-10 nm and lengths of up to tens of μm. Electron energy loss spectrometry and Raman spectroscopy demonstrate the ultimate phase purity of the ultrafine BNNTs. Property studies indicate that the ultrafine nanotubes are perfect electrical insulators exhibiting superb resistance to oxidation and strong UV emission. Moreover, their reduced diameters lead to a dramatically decreased population of defects within the tube walls and result in the observation of near-band-edge (NBE) emission at room temperature.     

Functionalization of carbon nanotubes with magnetic nanoparticles: general nonaqueous synthesis and magnetic properties

A novel approach has been developed to synthesize magnetic nanoparticle and carbon nanotube (CNT) core-shell nanostructures, such as CoO/CNTs and Mn(3)O(4)/CNTs, by the nonaqueous solvothermal treatment of metal carbonyl on CNT templates using hexane as the solvent. The morphological and structural characterizations indicate that numerous cubic CoO or tetragonal Mn(3)O(4) nanoparticles are deposited on the surfaces of the CNTs to form CNT-based core-shell nanostructures. It is revealed that the hydrophobic interaction between nanoparticles and CNTs in hexane plays the critical role for the formation of CNT-based core-shell nanostructures. A physical property measurement system (PPMS-9, Quantum Design) analysis indicates that the CoO/CNT core-shell nanostructures show weak ferromagnetic performance at 300?K due to the ferromagnetic Co clusters and the uncompensated surface spin states, while the Mn(3)O(4)/CNT core-shell nanostructures display ferromagnetic behavior at low temperature (34.5?K), which transforms into paramagnetic behavior with increasing temperature.