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At least 829 records · Page 46
All sourcesNASA NTRSDOE OSTI
DOE OSTI2015

Role of intensive milling in the processing of barium ferrite/magnetite/iron hybrid magnetic nano-composites via partial reduction of barium ferrite

In this research a mixture of barium ferrite and graphite was milled for different periods of time and then heat treated at different temperatures. The effects of milling time and heat treatment temperature on the phase composition, thermal behavior, morphology and magnetic properties of the samples have been investigated using X-ray diffraction, differential thermal analysis, high resolution transmission electron microscopy and vibrating sample magnetometer techniques, respectively. X-ray diffraction results revealed that BaFe{sub 12}O{sub 19}/Fe{sub 3}O{sub 4} nanocomposites form after a 20 h milling due to the partial reduction of BaFe{sub 12}O{sub 19}. High resolution transmission electron microscope images of a 40 h milled sample showed agglomerated structure consisting of nanoparticles with a mean particle size of 30 nm. Thermal analysis of the samples via differential thermal analysis indicated that for un-milled samples, heat treatment up to 900 °C did not result in α-Fe formation, while for a 20 h milled sample heat treatment at 700 °C resulted in reduction process progress to the formation of α-Fe. Wustite was disappeared in an X-ray diffraction pattern of a heat treated sample at 850 °C, by increasing the milling time from 20 to 40 h. By increasing the milling time, the structure of heat treated samples becomes magnetically softer due to an increase in saturation magnetization and a decrease in coercivity. Saturation magnetization and coercivity of a sample milled for 20 h and heat treated at 850 °C were 126.3 emu/g and 149.5 Oe which by increasing the milling time to 40 h, alter to 169.1 emu/g and 24.3 Oe, respectively. High coercivity values of milled and heat treated samples were attributed to the nano-scale formed iron particles. - Graphical abstract: Display Omitted - Highlights: • Barium ferrite and graphite were treated mechano-thermally. • Increasing milling time increases reduction progress after heat treatment. • Composites including iron nano-crystals forms by milling and heat treatment. • Shorter milling time results in higher H{sub C} of the milled and heat treated samples.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2015

PVA and PEG functionalised LSMO nanoparticles for magnetic fluid hyperthermia application

La{sub 0.7}Sr{sub 0.3}MnO{sub 3} magnetic nanoparticles are synthesized by a solution combustion method and functionalised with polyvinyl alcohol and polyethylene glycol. The induction heating characteristics of coated magnetic nanoparticles (42 °C) were observed at a reasonably low concentration (5 mg/mL). Remarkably, coated magnetic nanoparticles exhibited a promisingly high specific absorption rate with varying magnetic field and constant frequency. The surface analysis is carried out by X-ray photoelectron spectroscopy. A reduction in the agglomeration of the particles was observed when the magnetic nanoparticles were functionalised with polyvinyl alcohol or polyethylene glycol and can be confirmed by transmission electron microscopy and dynamic light scattering studies. Vibrating sample magnetometer measurements indicate superparamagnetic behaviour at room temperature before and after coating. Colloidal stability revealed a considerably higher zeta potential value for coated system. In vitro cytotoxicity test of the magnetic nanoparticles indicates that coated nanoparticles have no significant effect on cell viability within the tested concentrations (1–5 mg mL{sup -1}) as compared to uncoated La{sub 0.7}Sr{sub 0.3}MnO{sub 3}. All these findings explore the potentiality of La{sub 0.7}Sr{sub 0.3}MnO{sub 3} nanoparticles for magnetic fluid hyperthermia. - Highlights: • Surface functionalization of LSMO nanoparticles — first time with PVA • Surface functionalization of LSMO nanoparticles — first time with PEG • BSA protein — first time used as dispersion medium for stability of LSMO nanoparticles • The heating ability observed at low concentration • Improved efficiency of magnetic fluid hyperthermia treatment with surfactants.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2015

Utilizing maleic acid as a novel fuel for synthesis of PbFe{sub 12}O{sub 19} nanoceramics via sol–gel auto-combustion route

PbFe{sub 12}O{sub 19} nanostructures were prepared in an aqueous solution by the sol–gel auto-combustion method using Pb(NO{sub 3}){sub 2} and Fe(NO{sub 3}){sub 3} as starting materials and various carboxylic acids, including oxalic acid, malonic acid, succinic acid and maleic acid as fuel and reducing and capping agents. The as-synthesized products were characterized by X- ray diffraction, scanning electron microscopy, and X-ray energy dispersive spectroscopy. The effect of carboxylic acid type, Pb{sup +} {sup 2} to carboxylic acid molar ratio, and calcination temperature was investigated on the morphology of the products and several experiments were carried out to obtain the optimal reaction conditions. It was found that the phase and the morphology of the products are influenced by the investigated parameters. Furthermore, vibrating sample magnetometer (VSM) was used to study the magnetic properties of PbFe{sub 12}O{sub 19} samples. - Graphical abstract: Display Omitted - Highlights: • PbFe{sub 12}O{sub 19} nanoceramics were synthesized from Fe(NO{sub 3}){sub 3} and Pb(NO{sub 3}){sub 2} via the sol–gel auto combustion method. • The maleic acid can be instead of common capping agent and fuel in auto-combustion sol–gel. • The synthesized PbFe{sub 12}O{sub 19} is a hard magnetic material. • The specific saturation magnetization and coercivity are 27 emu/g and 1900 Oe, respectively.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2015

Characterization of mechano-thermally synthesized Curie temperature-adjusted La{sub 0.8}Sr{sub 0.2}MnO{sub 3} nanoparticles coated with (3-aminopropyl) triethoxysilane

This research aimed to synthesize nanostructured strontium-doped lanthanum manganite, La{sub 0.8}Sr{sub 0.2}MnO{sub 3} (LSMO), with its Curie temperature (T{sub c}) adjusted to the therapeutic range, through a mechanothermal route. In order to investigate the effect of heat treatment temperature and duration on the resulting crystallite size, morphology, magnetic behavior and Curie temperature, the starting powder mixture was milled in a planetary ball mill before being subsequently heat treated at distinct temperatures for different time lengths. The composition, morphology, and magnetic behavior were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED) and vibrating sample magnetometer (VSM). In addition, magnetic properties were further investigated using an alternating current (AC) susceptometer and thermo-magnetic analyzer. 20 h of milling produced a crystallite size reduction leading to a decrease in the heat treatment temperature of LSMO synthesis to 800 °C. Moreover, SEM analysis has shown the morphology of a strong agglomeration of fine nanoparticles. HRTEM showed clear lattice fringes of high crystallinity. The mean crystallite and particle size of 20-hour milled sample heat treated at 1100 °C for 10 h are relatively 69 and 100 nm, respectively. The VSM data at room temperature, indicated a paramagnetic behavior for samples heat treated at 800 °C. However, by increasing heat treatment temperature to 1100 °C, LSMO indicates a ferromagnetic behavior with well-adjusted Curie temperature of 320 K, suitable for hyperthermia applications. Also, reentrant spin glass (RSG) behavior has been found in heat treated samples. The particles are coated with (3-aminopropyl) triethoxysilane (APTES) for biocompatibility purposes; Fourier transform infrared spectroscopy (FTIR) and thermo-gravimetric analysis (TGA) are used for further confirmation of APTES coating. - Highlights: • La{sub 0.8}Sr{sub 0.2}MnO{sub 3} nanoparticles were synthesized via a mechanothermal route. • We report a significant reduction in the heat treatment temperature. • The Curie temperature was tuned within the therapeutic range. • The particles were coated with (3-aminopropyl) triethoxysilane for biocompatibility purposes.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2015

Influence of pH on the physical and electromagnetic properties of Mg–Mn ferrite synthesized by a solution combustion method

The synthesis of nano-crystalline Mg–Mn ferrites by a solution combustion method using citric acid and ammonia was investigated by varying the pH of the precursor solution, which played an important role in controlling the morphology of the synthesized powders. The phase formation, microstructure and electromagnetic properties were studied using X-ray diffraction, scanning electron microscopy, impedance analyzer and vibrating sample magnetometer. Single phase pure spinel Mg–Mn ferrite powders were obtained for all the samples at different pH (< 1, 3, 5, 7, 9). The results showed that an increase of pH improves the crystallinity of the Mg–Mn ferrite nanoparticles. The average grain size of sintered samples was found to decrease from 2 μm to 0.5 μm with increasing pH values from pH < 1 to pH 9, respectively. The dielectric constant of the samples with different pH is in the range of 7–12 from frequencies of 1 MHz to 1 GHz. The highest saturation magnetization (30.04 emu/g) was obtained for the sample with pH < 1. - Highlights: • Mg–Mn ferrites were synthesized by a solution combustion method with different pH. • Auto-combustion process resulted in the formation of single phase spinel ferrite. • An increase of pH improves the crystallinity of the Mg–Mn ferrite nanoparticles. • pH variation has influence on phase formation and morphology of the ferrite.

36 MATERIALS SCIENCE↗
DOE OSTI2013

Facile fabrication and characterization of amino-functionalized Fe{sub 3}O{sub 4} cluster@SiO{sub 2} core/shell nanocomposite spheres

Highlights: ► A method developed for the preparation of Fe{sub 3}O{sub 4} clusters@SiO{sub 2} nanocomposites. ► This method permits production of core/shell nanomaterials with high yields. ► Resultant superparamagnetic particles are monodisperse with high magnetizations. - Abstract: We developed a modified straightforward method for the fabrication of uniformly sized silica-coated magnetite clusters core/shell type nanocomposite particles. Proposed simple one-step processing method permits quick production of materials in high yield. The structural, surface, and magnetic characteristics of the nanocomposite particles were investigated by transmission electron microscopy (TEM), scanning electron microscope (SEM), powder X-ray diffraction (XRD), vibrating sample magnetometer (VSM), and Fourier-transform infrared (FTIR). The sphere-shaped particles almost have the average diameter of 120 nm, with a magnetic cluster core of 80 ± 15 nm, and a silica shell of 25 ± 10 nm thickness. The particles are superparamagnetic and present strong magnetization (18 emu/g) due to the fact that they possess core of the magnetic clusters. Subsequently, the silica surface of core/shell particles was amino-functionalized via N-(2-aminoethyl)-3-aminopropyltrimethoxysilane (EDS). Findings of the present work highlight the potential for using amino-functionalized magnetic silica core/shell nanocomposite particles in biological applications since they possess useful magnetic properties and proper structure.

36 MATERIALS SCIENCE↗
DOE OSTI2013

Multifunctional Fe{sub 3}O{sub 4}@C@Ag hybrid nanoparticles: Aqueous solution preparation, characterization and photocatalytic activity

Highlights: ► Ag-loaded Fe{sub 3}O{sub 4}@C magnetic-optical bifunctional materials have been investigated. ► The magnetism was studied at the room temperature. ► The photocatalytic activity was evaluated under visible light irradiation. ► Ag-loaded Fe{sub 3}O{sub 4}@C nanocomposites show superior magnetism and photocatalytic activity. ► A simple synthetic process was discussed. - Abstract: The paper describes a kind of multifunctional Fe{sub 3}O{sub 4}@C@Ag hybrid nanoparticles, which can be successfully synthesized using a simple route based on directly adsorption and spontaneous reduction of silver ions onto the surface shell of carbon-coated magnetic nanoparticles. The as-prepared samples have been characterized by transmission electron microscopy (TEM), X-ray powder diffraction (XRD), Fourier transform infrared (FT-IR) spectrum, vibrating sample magnetometer (VSM) and UV–vis spectrum (UV–vis). The Ag nanocrystals loaded on the surface shell of carbon-coated magnetic nanoparticles are nearly spherical with an average diameter of 10 nm. And the carbonaceous polysaccharides shell obtained using an glucose hydrothermal reaction act as a role of a bridge between magnetic Fe{sub 3}O{sub 4} core and noble metallic Ag nanocrystals. The as-prepared samples can be used as an effective catalyst for the photodegradation of organic dyes (neutral red) under the exposure of visible light. Results show that the as-prepared samples have a degradation rate of 93.7% for dyes within 30 min, which indicates their high-efficiency and rapid photocatalytic activity.

36 MATERIALS SCIENCE↗
DOE OSTI2013

Microstructures, magnetic and electric properties of diluted magnetic semiconductors InTe{sub 1−x} Fe{sub x} (Co{sub x})

Highlights: ► The prepared InTe{sub 0.9}Fe{sub 0.1} was found to be ferromagnetic at room temperature and can be characterized as diluted magnetic semiconductors. ► The presence of staking faults, various types of defects, strained lattice, grain boundaries and the impurity of minor non-magnetic phase were suggested to participate in high temperature ferromagnetism. - Abstract: InTe compound doped by 10% of Fe or Co respectively was synthesized. X-ray diffraction (XRD), transmission electron microscope (TEM), scanning electron microscope (SEM), energy dispersive X-ray (EDX), vibrating sample magnetometer (VSM) and Kiethley electrometer were used for characterizing the prepared samples. XRD show the presence of InTe{sub 0.9}Fe{sub 0.1} or InTe{sub 0.9}Co{sub 0.1} together with minor In{sub 4}Te{sub 3} phase. InTe{sub 0.9}Fe{sub 0.1} is ferromagnetic with high Curie and high blocking temperature, while InTe{sub 0.9}Co{sub 0.1} is antiferromagnetic with two high Neels temperatures. σRT of InTe{sub 0.9}Fe{sub 0.1} and InTe{sub 0.9}Co{sub 0.1} are greater than those of InTe. The higher conductivity is due to the higher carrier's density obtained from the interaction of the sp-d orbitals, of the electric and magnetic system. The presence of In{sub 4}Te{sub 3} minor phase and different kinds of defects are taking major roles in the formation of high Tc ferromagnetism and antiferromagnetism.

36 MATERIALS SCIENCE↗
DOE OSTI2013

Synthesis of magnetite-porphyrin nanocomposite and its application as a novel magnetic adsorbent for removing heavy cations

Graphical abstract: Magnetite-porphyrin nanocomposite (MPNC) as a novel magnetic adsorbent for removing heavy cations was synthesized. - Highlights: • Nanosized Fe{sub 3}O{sub 4} was prepared by hydrothermal reaction of iron salt in alkaline media. • The synthesized magnetite and nanocomposite had soft ferromagnetic property. • Magnetic nanocomposite as a novel magnetic adsorbent for heavy cations was prepared. • Satisfactory separation from solutions in the order of Pb{sup 2+} > Cd{sup 2+} > Hg{sup 2+} was obtained. - Abstract: Magnetite-porphyrin nanocomposite (MPNC) was synthesized as a novel magnetic adsorbent for removing heavy cations. Firstly, we prepared nano-sized magnetite using a simple hydrothermal route. The synthesis of nanoscaled magnetite was carried out through reaction between iron source and various amines. In this paper, we studied effective parameters in controlling shape and size of nanoscaled magnetite. These parameters were presence of alkaline, reaction time, kind of amine and iron salt. Morphology, particle size and magnetic properties of the nanoscaled magnetite were obtained by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), Fourier transform infrared (FT-IR), diffuse reflectance spectra (DRS) and vibrating sample magnetometer (VSM). Our study showed that the synthesized magnetite from reaction between FeSO{sub 4} and hydrazinum hydrate has spherical shape. The synthesized magnetite was a nanosized compound and used for preparation of magnetite-porphyrin nanocomposite. The synthesized magnetite-porphyrin hybrid material had magnetic property and was used as magnetic adsorbent for removing heavy cations of water. Satisfactory separation from solutions in the order of Pb{sup 2+} > Cd{sup 2+} > Hg{sup 2+} was obtained.

36 MATERIALS SCIENCE↗
DOE OSTI2013

Synthesis of NiCuZn-ferrite powders by means of mechanochemical treatment

Graphical abstract: The peak intensity for the product calcined at 500 °C is relatively weak, but it gradually increases with increasing the temperature. This implies that the temperature up to 700 °C leads to well crystallization of the spinel type of Ni{sub 0.45}Cu{sub 0.05}Zn{sub 0.5}Fe{sub 2}O{sub 4} phase. - Highlights: • NiCuZn-ferrite powders were obtained at a low temperature by mechanochemical activation. • The effects of the mechanical and thermal treatments on the mixtures were analyzed. • The mechanochemical method benefited achieving the lower M{sub s} and μ{sub i}. - Abstract: NiCuZn-ferrite powders were synthesized by mechanochemical treatments using NiCO{sub 3}⋅2Ni(OH){sub 2}⋅4H{sub 2}O, CuO, ZnO and Fe{sub 2}O{sub 3} as raw materials. Scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and vibrating sample magnetometer (VSM) were employed to evaluate the morphologies and structures of samples. The results indicated that the mechanochemical treatment produced several structural and chemical effects on reactants of the powder mixtures, and single phase Ni{sub 0.45}Cu{sub 0.05}Zn{sub 0.5}Fe{sub 2}O{sub 4} could be obtained after annealed at 700 °C for 2 h. In comparison with the traditional firing method, the mechanochemical method benefited achieving the lower M{sub s} and μ{sub i}, which indicated that the sample had better magnetic properties.

36 MATERIALS SCIENCE↗
DOE OSTI2013

Single source preparation of superparamagnetic Fe{sub 3}O{sub 4} nanoparticles by simple cyclic microwave approach

Graphical abstract: - Highlights: • Superparamagnetic Fe{sub 3}O{sub 4} nanoparticles were synthesized in high yield. • PEG-200 was applied as both solvent and reductive agent. • Single source synthesis of Fe{sub 3}O{sub 4} was performed. • Nontoxic materials and surfactant were used in current investigation. • Reaction time and temperature significantly decreased in current experiment. - Abstract: Polyol mediated process was applied for the synthesis of Fe{sub 3}O{sub 4} nanoparticles under microwave irradiation. By combination of polyol medium and microwave irradiation different advantages including low reaction time, low consumption of energy, and simplicity were achieved. Different parameters affecting on products including microwave irradiation power, reaction time, reactants concentration, and solvent were changed to reach the optimum condition for synthesis of Fe{sub 3}O{sub 4} nanoparticles. The products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), Fourier transform infrared (FT-IR) spectra, and vibrating sample magnetometer (VSM). 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 Fe{sub 3}O{sub 4} nanoparticles in nonaqueous solution, which will be important for inorganic synthesis methodology.

36 MATERIALS SCIENCE↗
DOE OSTI2013

High coercivity sized controlled cobalt–gold core–shell nano-crystals prepared by reverse microemulsion

Graphical abstract: - Highlights: • Calculating the crystallinity percentage and percentage of phases presented in Co–Au core–shell nanoparticles. • Magnetic properties of four groups nanogarin: 5, 10, 15, 20 nm. • Single domain ferromagnetic materials with high coercivity at room temperature. • Intrinsic blocking temperature measured in zero field cooled-warmed (ZFC-W). - Abstract: Size-controlled cobalt–gold core–shell nanoparticles were synthesized via the reverse-micelle microemulsion method. In order to control the size of the nanoparticles, the nucleation and growth process were performed within a confined space by adjusting the water to surfactant ratio of reverse micelles solution during synthesis. The crystallinity percentage and percentage of phases presented in Co–Au core–shell nanoparticles were calculated using X-ray diffraction data. The results from transmission electron microscopy provide direct evidence for core–shell structure nanomaterials. Magnetic properties of the samples were investigated using a vibrating sample magnetometer. The as-prepared samples showed significant coercivity at room temperature. The intrinsic blocking temperature was experimentally deduced from zero-field-cooled warmed (ZFC-W) curves by a simple method without employing an external magnetic field. The B-field dependence temperature data of Co–Au nanoparticles exhibited an intrinsic blocking temperature at 45 K. Annealing these samples at 400 °C caused an increase in particle size, crystallinity percentage and further enhanced their magnetic properties.

36 MATERIALS SCIENCE↗
DOE OSTI2013

Structural, optical and magnetic properties of gadolinium sesquioxide nanobars synthesized via thermal decomposition of gadolinium oxalate

Graphical abstract: - Highlights: • The cubic Gd{sub 2}O{sub 3} nanobars are synthesized by decomposition of C{sub 6}H{sub 20}Gd{sub 2}O{sub 22}. • The nanoparticles are rectangular bar shape with high porous surface. • The combination of magnetic and optical properties within a single particle. • The Gd{sub 2}O{sub 3} nanobars have tailorable nanostructure, wide bandgap and are paramagnetic. - Abstract: Gadolinium oxide nanobars were obtained by thermal decomposition of gadolinium oxalate, which was synthesized by the chemical precipitation method along with glycerol. The functional group analysis and formation of gadolinium oxide from gadolinium oxalate were characterized by the Fourier transform infrared spectroscopy and thermo gravimetric analyzer. The crystal structure, average crystallite size, and lattice parameter were analyzed by X-ray diffraction technique. Moreover, Raman shifts, elemental composition and morphology of the gadolinium oxide was widely investigated by the laser Raman microscope, X-ray photoelectron spectroscopy, FE-SEM-EDAX and HR-TEM, respectively. Furthermore, the optical properties like band gap, absorbance measurement of the gadolinium oxide were extensively examined. In addition, the paramagnetic property of gadolinium oxide nanobars was explored by the vibrating sample magnetometer.

36 MATERIALS SCIENCE↗
DOE OSTI2014

Magnetic properties of high Li doped ZnO sol–gel thin films

Highlights: • Ferromagnetism in high Li doped ZnO films. • Magnetic properties observed by Guoy's and VSM method. • The rod and wrinkle like structures are observed from the surface of the films. • Band gap of ZnO does not get altered by high Li doping. - Abstract: Undoped and Li doped ZnO thin films were deposited on a glass substrate using the sol–gel dip coating method. The films were prepared at 5 mol.% and 10 mol.% of Li doped ZnO at 550 °C annealing temperature and the deposited films were characterized by X-ray diffraction (XRD), microscopic studies, Gouy's method, vibrating sample magnetometer (VSM) and UV–visible spectroscopy. All the deposited thin films had a hexagonal wurtzite structure with polycrystalline grains at random. Primarily magnetic properties of pure and Li doped ZnO films were observed by Guoy's method which depicted Dia and Para magnetic behavior at room temperature. VSM measurement reveals a coercivity of 97.7 Oe in the films. An inverse relative ferromagnetism was perceived in Li doped ZnO films which had an average transmission of <90%.

36 MATERIALS SCIENCE↗
DOE OSTI2014

Synthesis and electromagnetic properties of BaFe{sub 11.92}(LaNd){sub 0.04}O{sub 19}/titanium dioxide composites

Graphical abstract: Due to combining different functions and characteristics of individual materials, hybrid nanocomposite materials can strengthen their applications. Magnetic-conductive nanocomposites are the promising materials with electromagnetic loss, which have synergetic behavior between magnetic and conductive materials. It is the first time to report the synthesis of BaFe{sub 11.92}(LaNd){sub 0.04}O{sub 19}/titanium dioxide (BF/TD) composites by the gel-precursor self-propagating combustion process. The influence of mass ratio of BF and TD on the electromagnetic properties of BaFe{sub 11.92}(LaNd){sub 0.04}O{sub 19}/titanium dioxide composites was studied. The tgδ{sub μ} and tgδ{sub ε} of BF–TD composites. - Highlights: • It is the first time to report BaFe{sub 11.92}(LaNd){sub 0.04}O{sub 19}/titanium dioxide composites. • The composites are prepared by the gel-precursor self-propagating combustion. • The electromagnetic properties could be adjusted by the mass ratio of BF and TD. • The introduction of TD enhances the dielectric loss and widens the frequency bands. • BF/TD composites will be microwave absorption materials with wide frequency band. - Abstract: Doped BaFe{sub 11.92}(LaNd){sub 0.04}O{sub 19}/titanium dioxide composites have been prepared by the gel-precursor self-propagating combustion process. The characterization of the composites are performed by Fourier transform infrared (FT-IR), X-ray diffraction (XRD), Differential thermal analysis-thermo gravimetry (DTA–TG), scanning electron microscopy (SEM), vibrating sample magnetometer (VSM) and network analyzer. Both XRD and FT-IR indicate that the doped BaFe{sub 11.92}(LaNd){sub 0.04}O{sub 19}/titanium dioxide composites are successfully synthesized and there are some interactions between BaFe{sub 11.92}(LaNd){sub 0.04}O{sub 19} and titanium dioxide. DTA–TG analysis of BaFe{sub 11.92}(LaNd){sub 0.04}O{sub 19}/titanium dioxide composites shows that the composite gel decomposition process mainly includes two stages: the first stage is the crystallized water and the residual moisture evaporation; the second stage is the nitrate and citric acid decomposition reaction. SEM demonstrates that the doped BaFe{sub 11.92}(LaNd){sub 0.04}O{sub 19}/titanium dioxide solid solution has formed. The magnetic parameters indicate that the electromagnetic properties of the composites could be well adjusted by the mass ratio of BaFe{sub 11.92}(LaNd){sub 0.04}O{sub 19} and titanium dioxide. When the mass ratio of BaFe{sub 11.92}(LaNd){sub 0.04}O{sub 19} and titanium dioxide is 4:5, the composites have the best magnetic loss. The composites with the mass ratio 6:5 of BaFe{sub 11.92}(LaNd){sub 0.04}O{sub 19} and titanium dioxide. BaFe{sub 11.92}(LaNd){sub 0.04}O{sub 19} and titanium dioxide possess good dielectric loss. The introduction of titanium dioxide enhances the dielectric loss and widens the frequency bands. The composites will be promising microwave absorption materials with wide frequency band.

36 MATERIALS SCIENCE↗
DOE OSTI2014

Magnetic force microscopy study of domain walls in Co{sub 2}Z ferrite

Graphical abstract: - Highlights: • Hexaferrite Co{sub 2}Z is synthesized through the modified Pechini method. • Magnetic domains are observed in anisotropic Co{sub 2}Z single grain using MFM. • Observed single grain domain thickness is in good agreement with Dotsh model. - Abstract: Hexaferrite Co{sub 2}Z was synthesized through the modified Pechini method. Partially oriented samples were obtained after consolidation with uniaxial pressing and calcination/sintering at 1300 °C/1330 °C. The sample composition and morphology was identified with X-ray diffractometry (XRD) and scanning electron microscopy (SEM) with energy-dispersive X-ray spectrometry (EDS). MFM studies of the single grains revealed a domain structure with 0.7 μm wide. The Co{sub 2}Z static magnetization was measured with a vibrating sample magnetometer (VSM), and was used to calculate a single grain domain with a thickness of 4.8 μm. This result is in good agreement with SEM observations of the single grain thickness.

36 MATERIALS SCIENCE↗
DOE OSTI2014

Uniform hollow magnetite spheres: Facile synthesis, growth mechanism, and their magnetic properties

Highlights: • Uniform Fe{sub 3}O{sub 4} hollow spheres with high saturation magnetization were synthesized through a simple solvothermal process. • Without using any hard templates or external magnetic field. • The as-prepared magnetite hollow spheres exhibit a ferromagnetic behavior with high Ms of ca. 85.9 emu/g at room temperature. • The morphology of Fe{sub 3}O{sub 4} with nanoparticles, hollow, and irregular structures could be adjusted by changing the reactive conditions. - Abstract: Hierarchical porous Fe{sub 3}O{sub 4} hollow spheres with high saturation magnetization were synthesized through a simple solvothermal process in ethylene glycol (EG) in the presence of Tetrabutylammonium chloride (TBAC) and urea. By investigating the effect of reaction temperature, time, the amount of urea, and concentration of iron ion on the formation of hollow spheres, it was proposed that the main formation mechanism of hollow spheres is Ostwald ripening process combined with assembly-then-inside-out evacuation process. Additionally, it is found that the morphology of Fe{sub 3}O{sub 4} with nanoparticles, hollow, and irregular structures could be adjusted by changing the above factors. The resulting products were characterized by means of scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray powder diffraction (XRD), high resolution transmission electron microscopy (HRTEM), energy dispersive X-ray spectroscopy (EDX), and vibrating sample magnetometer (VSM). The hierarchical porous Fe{sub 3}O{sub 4} hollow spheres exhibited enhanced saturation magnetization as compared with Fe{sub 3}O{sub 4} nanoparticles.

36 MATERIALS SCIENCE↗
DOE OSTI2014

One-step synthesis of homogeneous BaFe{sub 12}O{sub 19}/Y{sub 3}Fe{sub 5}O{sub 12} composite powders

Highlights: • A simple one-step sol–gel method was used to synthesize composite magnets. • The composite powders show good homogeneity and exchange coupling. • The M{sub r}/M{sub s} value increases with the BaM concentration. - Abstract: BaFe{sub 12}O{sub 19}/Y{sub 3}Fe{sub 5}O{sub 12} (BaM/YIG) composite powders were synthesized via a simple one-step sol–gel method. The phase composition and morphology of the as-synthesized composite powders were characterized using an X-ray diffractometer and a scanning electron microscopy equipped with energy dispersive X-ray spectroscopy. The magnetic properties of the composite powders were investigated by a vibrating sample magnetometer. Compared with the composite powders prepared by the conventional physical mixing method, the BaM/YIG composite powders show better homogeneity and exchange coupling.

36 MATERIALS SCIENCE↗