Exchange bias and magnetothermal properties in Fe@Mn nanocomposites

We have studied the Exchange Bias (EB) effect in nanocomposite films consisting of Fe nanoparticles (mean size ∼1.9 nm) embedded in an antiferromagnetic Mn matrix. They were produced by co-deposition through a gas aggregation cluster source and molecular beam epitaxy and have different Fe volume filling fractions (2.2% and 24.8%). The exchange field, higher in the sample with higher Fe concentration (at T=5 K, H_ex∼460 Oe for 24.8% and ∼310 Oe for 2.2% ), in both the samples decreases with increasing T, finally disappearing at T∼40 K. The EB properties have been studied in conjunction with results on the thermal dependence of the magnetic coercivity, zero-field-cooled and field-cooled magnetization and thermoremanence. The different Fe content strongly affects the magnetothermal properties, featuring superparamagnetic relaxation in the diluted sample and a reentrant ferromagnet-type transition in the concentrated one. Hence, the EB properties of the two samples have been discussed in consideration of such peculiarities of the magnetic behavior and highlighting the role of the Mn matrix.     

Synthesis and surface modified hard magnetic properties in Co0.5Pt0.5 nanocrystallites from a rheological liquid precursor

Small crystallites of a metastable phase Co_0.5Pt_0.5 are precipitated by heating a rheological liquid precursor of cobalt–hydrazine complex and platinum chloride H₂PtCl₆·xH₂O in polymer molecules of poly(vinylpyrrolidone) (PVP) in ethylene glycol. The hydrazine co-reduces nascent atoms from the Co²⁺ and Pt⁴⁺ that recombine and grow as Co_0.5Pt_0.5. The PVP molecules cap a growing Co_0.5Pt_0.5 as it achieves a critical size so that it stops growing further in given conditions. X-ray diffraction pattern of a recovered powder reveals a crystalline Co_0.5Pt_0.5 phase (average crystallite size D∼8 nm) of a well-known Fm3m-fcc crystal structure with the lattice parameter a=0.3916 nm (density ρ=14.09 g/cm³). A more ordered L1₀ phase (ρ=15.91 g/cm³) transforms (D≥25 nm) upon annealing the powder at temperature lesser than 700 °C (in vacuum). At room temperature, the virgin crystallites bear only a small saturation magnetization M_s=5.54 emu/g (D=8 nm) of a soft magnet and it hardly grows on bigger sizes (D≤31 nm) in a canted ferromagnetic structure. A rectangular hysteresis loop is markedly expanded on an optimally annealed L1₀ phase at 800 °C for 60 min, showing a surface modified coercivity H_c=7.781 kOe with remnant ratio M_r/M_s=0.5564, and M_s=39.75 emu/g. Crystallites self-assembled in an acicular shape tailor large H_c from ideal single domains and high magnetocrystalline anisotropy of a hard magnet L1₀ phase.     

Nanoparticle kinetic effects experimentally observed in a magnetic fluid under a quasi-homogeneous magnetic field

The effect of a quasi-homogeneous external magnetic field on a created and decaying space nanoparticle structure and its distribution in a sample of a magnetic fluid was studied. This space structure was created as a grating by applying an interference field of two crossed Ar laser beams. The magnetic field was formed using two electromagnets and was applied in three main directions of the created nanoparticle grating. The magnetic field oriented parallel to the strips of the grating or perpendicular to the grating plain does not significantly change the shape of it. The magnetic field oriented in the perpendicular direction to the grating plain causes redistribution of the nanoparticles and as a consequence a perpendicular nanoparticle “quasi-grating” arises.     

Effect of nanoparticle size on magnetic damping parameter in Co92Zr8 soft magnetic films

Co₉₂Zr₈(50 nm)/Ag(x) soft magnetic films have been prepared on Si (111) substrates by oblique sputtering at 45°. Nanoparticle size of Co₉₂Zr₈ soft magnetic films can be tuned by thickening Ag buffer layer from 9 nm to 96 nm. The static and dynamic magnetic properties show great dependence on Ag buffer layer thickness. The coercivity and effective damping parameter of Co₉₂Zr₈ films increase with thickening Ag buffer layer. The intrinsic and extrinsic parts of damping were extracted from the effective damping parameter. For x=96 nm film, the extrinsic damping parameter is 0.028, which is significantly larger than 0.004 for x=9 nm film. The origin of the enhancement of extrinsic damping can be explained by increased inhomogeneity of anisotropy. Therefore, it is an effective method to tailor magnetic damping parameter of thin magnetic films, which is desirable for high frequency application.     

Investigations on the surface modification of ZnO nanoparticle photocatalyst by depositing Pd

In this paper, ZnO nanoparticle photocatalysts were modified by depositing Pd on their surfaces with a photoreduction method. We mainly investigated the modification mechanisms as well as the effects on the photocatalytic activity of ZnO nanoparticles of deposited Pd by means of XPS and SPS (Surface Photovoltage Spectroscopy), and the effects of Pd content on SPS responses were also discussed from the point of the electronic energy level. The results showed that the content of crystal lattice oxygen on the surface of ZnO nanoparticle decreased after an appropriate amount of Pd was deposited, while that of adsorbed oxygen increased, indicating that Pd was mainly deposited on the crystal lattice oxygen. At the same time, the intensity of SPS responses of ZnO nanoparticles remarkably decreased. In addition, the activity of ZnO nanoparticles could be greatly improved by depositing an appropriate amount of Pd in the gas phase photocatalytic oxidation of n-C₇H₁₆. Thus, it could be concluded that the increase in surface content of adsorbed oxygen could facilitate the photocatalytic reaction, and there were close relationships between the SPS response and photocatalytic activity, i.e. the weaker the SPS response, the higher the photocatalytic activity, of Pd-deposited ZnO nanoparticles.     

SnO2纳米粒子-花生酸LB膜有序组合体的研究

采用胶体化学法制备了稳定的SnO2纳米粒子（nanoparticleNP）水溶胶，用膜天平和原位布儒斯特角显微镜（BAM）考察了经典成膜材料花生酸（AA）在此水溶胶气-液界面的成膜性，并用LB膜技术在不同基底上制得了单层和多层AA-Sno2NP复合LB膜，通过TEM、小角X-ray、IR和UV-VIS光谱，进一步考察了该有序组装体的结构和周期性，以及组装作中Sno2纳米粒子的形貌、粒度分布和表面聚集状态.结果表明，用这种方法能够制得粒度分布均匀、农致密的Sno2纳米粒子复合LB膜，并且多层复合膜具有良好的周期性.     

Metal oxide nanoparticles: synthesis, characterization and application

The synthesis of metal oxide nanoparticles is described in terms of precursor formation, nucleation, growth, and aging processes. The main parameters governing these processes are the solution properties, including the solvent viscosity, dielectric constant and the presence of adsorbing anions, the solubility of the metal oxide, and the metal oxide surface energy.     

Degradation behaviors of star-shaped poly(ethylene glycol)-poly(?-caprolactone) nanoparticles in aqueous solution

Star-shaped poly(ethylene glycol) (PEG)-poly(?-caprolactone) (?-PCL) block copolymers were synthesized via a ring-opening polymerization. Nanoparticles prepared by the precipitation/solvent evaporation technique exhibit a core-shell structure. The hydrolytic degradation of 3-arm PEG-PCL copolymeric nanoparticles was studied by dynamic light scattering (DLS), nuclear magnetic resonance (NMR) and gel permeation chromatography (GPC). It was found that copolymers with shorter PCL block length degraded faster. The sizes of nanoparticles fluctuated during the initial degradation period, and then increased slightly before finally dropping off. The degradation mainly occurred at CL-CL linkages firstly then at the EO-CL linkages. The CL/EO molar ratios and the molecular weights of copolymers decreased as degradation time and a zero-order degradation behavior was observed.     

Rayleigh and Hyper-Rayleigh Scatterings from the Nanometer SnO_2 Particle in Solution

Nano-materials have been extensively studied in the past[1]. The quantum effect makes the properties of nano-materials dif- ferent from that of bulk materials. A few of publications regard- ing the catalysis, electronic structure, and optics of the nanome…     

Mechanochemical-hydrothermal synthesis of calcium phosphate powders with coupled magnesium and carbonate substitution

Magnesium- and carbonate-substituted calcium phosphate powders (Mg-, CO₃-CaP) with various crystallinity levels were prepared at room temperature via a heterogeneous reaction between MgCO₃/Ca(OH)₂ powders and an (NH₄)₂HPO₄ solution using the mechanochemical-hydrothermal route. X-ray diffraction, infrared spectroscopy, and thermogravimetric analysis were performed. It was determined that the powders containing both Mg²⁺ and CO₃²⁻ ions were incorporated uniformly into an amorphous calcium phosphate phase while in contrast, the as-prepared powder free of these dopants was crystalline phase-pure, stoichiometric hydroxyapatite. Dynamic light scattering revealed that the average particle size of the room temperature Mg-, CO₃-CaP powders was in the range of 482 nm-700 nm with a specific surface area between 53 and 91 m²/g. Scanning electron microscopy confirmed that the Mg-, CO₃-CaP powders consisted of agglomerates of equiaxed, ≈20-35 nm crystals.