Solvothermal synthesis of CoFe<Subscript>2</Subscript>O<Subscript>4</Subscript> hollow spheres

Hollow CoFe₂O₄ spheres consisted of CoFe₂O₄ nanoparticles were synthesized by a facile solvothermal treatment of an ethylene glycol solution of FeCl₃ · 6H₂O, CoCl₂ · 6H₂O, and NaAc at 200 °C in the presence of polyethylene glycol and oleic acid. The products were characterized by powder X-ray diffraction, transmission electron microscopy, selected area electron diffraction, high-resolution transmission microscopy, scanning electron microscopy. The magnetic properties were evaluated using a vibrating sample magnetometer. The probable mechanism of the formation of Hollow CoFe₂O₄ spheres was discussed. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Room temperature magnetic exchange coupling in multiferroic BaTiO<Subscript>3</Subscript>/CoFe<Subscript>2</Subscript>O<Subscript>4</Subscript> magnetoelectric superlattice

Multiferroic BaTiO₃/CoFe₂O₄ superlattice films are deposited by laser molecular beam epitaxy. The film growth modes are studied by in situ reflection high energy electron diffraction and the film structures are revealed by high resolution transmission electron microscopy study. Ferroelectric switching behavior was studied by piezoresponse force microscopy, and it shows that good ferroelectricity was retained in the superlattice. Such a multiferroic superlattice also shows a magnetic exchange coupling under room temperature. Detailed analysis reveals that different growth modes and the substrate strain effect may be responsible for the magnetic exchange coupling.     

Preparation and magnetic properties of the CoFe<Subscript>2</Subscript>O<Subscript>4</Subscript> thin films on Si substrate by sol-gel technique

A stable precursor for CoFe₂O₄ thin film was prepared by sol-gel technique from the aqueous solution of FeCl₃·6H₂O and CoCl₂·6H₂O. Sol was deposited on a naturally oxidized silicon-substrate by spinning technique (2000 rpm) and heat treated at different temperatures ranging from 700 to 1100 °C. Thickness of the films was controlled in the range of 400–500 nm and all the films were characterized by using XRD and SEM. The effects of temperature and the composition on the formation of CoFe₂O₄ thin film were also studied. Films obtained at relatively lower temperature showed multi-phases of α-Fe₂O₃, CoFe₂O₄ and CoO while the formation of CoFe₂O₄ phase increases with increasing temperature. Furthermore, the composition of the solution in mol% has great role on the formation of CoFe₂O₄ films and the film containing 50 mol% of Co²⁺ exhibited CoFe₂O₄ mono-phase. Surface morphology of the films was studied by scanning electron microscope (SEM). Magnetic properties of the films, studied by using vibrating sample magnetometer (VSM), showed relatively high saturation magnetization (8.04–22.21 kWb/m²) as well as high coercivity (44.59–63.30 kA/m). Saturation magnetization also increases with increasing heat treatment temperature.     

Ordered mesoporous carbon-supported CoFe<Subscript>2</Subscript>O<Subscript>4</Subscript> composite with enhanced lithium storage properties

A high and stable reversible specific capacity (1277.7 mAh g^?1) was successfully achieved by the CoFe₂O₄/ordered mesoporous carbon nanohybrids (CFO/CMK-3) composite anode at the current density of 0.1 A g^?1 after 100 cycles. CFO/CMK-3 electrode also exhibited a stable capacity up to 733.2 and 482.6 mAh g^?1 at the current densities of 0.5 and 1 A g^?1 after 500 cycles, respectively. The CFO particles were found to be uniformly distributed inside the pore channels of CMK-3. Structure characterization before and after 100 tests revealed that the specific CMK-3 mesoporous structure and CFO crystallites remained unchanged. The stability of the anode composite stability and the rapid redox capability of CFO gave rise to superior lithium storage capacity and excellent cycling stability. CFO/CMK-3 showed a great promise to serve as anode for high-performance lithium-ion battery.     

Synthesis,phase formation study and magnetic properties of CoFe<Subscript>2</Subscript>O<Subscript>4</Subscript> nanopowder prepared by mechanical milling

In this work we report the phase formation and magnetic properties of CoFe₂O₄ nanopowder prepared by mechanical alloying technique using metallic cobalt and hematite powder (1:1 molar ratio) as the initial raw material in ambient air atmosphere. The formation of single phase cobalt ferrite of (Co _0.18 ²⁺ Fe _0.82 ³⁺ )[Co _0.82 ²⁺ Fe _1.18 ³⁺ ]O₄ stoichiometry was confirmed for the samples milled above 15 h without any heat-treatment by XRD and Mössbauer techniques. The average crystallite size of the sample milled for 30 h was ～13 nm. The highest room temperature value of the magnetization measured at 1.5 T was 51 e.m.u/g for the sample milled for 25 h which was much lower than the corresponding value of the bulk cobalt ferrite (80.8 e.m.u/g at 300 K) due to the size effect.     

Synthesis of carbon nanotube,graphene, CoFe<Subscript>2</Subscript>O<Subscript>4</Subscript>, and NiFe<Subscript>2</Subscript>O<Subscript>4</Subscript> polypyrrole nanocomposites and study their microwave absorption

In this experimental work, different conductive polymer nanocomposites were synthesized using polypyrrole as conductive polymer and CoFe₂O₄, NiFe₂O₄, CNT and graphene as fillers. X-ray diffraction pattern was used to study the crystallinity of the products and it was found CoFe₂O₄, NiFe₂O₄, CNT, and graphene were successfully embedded in the polymer matrix. To further approve the synthesis of the nanocomposites, energy dispersive X-ray spectroscopy was served. Surface groups of the synthesized nanocomposites were studied by Fourier transform infrared and Raman spectroscopy. The morphology of the products was examined by scanning electron microscopy and transmission electron microscopy. It was found the fillers were successfully embedded in the polymer matrix and they were in nanometer scales. To investigate the magnetic properties and conductivity of the polymer nanocomposites, alternating gradient force magnetometer and four-point probe were used, respectively. Finally, the microwave absorption properties of the polymer nanocomposites were studied and it was found the fillers have different effects on the polymer microwave absorption value.     

One-step accurate synthesis of shell controllable CoFe<Subscript>2</Subscript>O<Subscript>4</Subscript> hollow microspheres as high-performance electrode materials in supercapacitor

Multi-shelled CoFe₂O₄ hollow microspheres with a tunable number of layers (1–4) were successfully synthesized via a facile one-step method using cyclodextrin as a template, followed by calcination. The structural features, including the shell number and shell porosity, were controlled by adjusting the synthesis parameters to produce hollow spheres with excellent capacity and durability. This is a straightforward and general strategy for fabricating metal oxide or bimetallic metal oxide hollow microspheres with a tunable number of shells.

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Cu doping effect on the resistive switching behaviors of CoFe<Subscript>2</Subscript>O<Subscript>4</Subscript> thin films

Spin-coated Cu_xCo_1?xFe₂O₄ (x = 0, 0.2, 0.4, 0.6, and 0.8) thin films were prepared on Pt/TiO₂/SiO₂/Si substrates. Pt/Cu_xCo_1?xFe₂O₄/Pt structures were fabricated to investigate the effect of Cu doping concentration on the resistive switching behaviors. Structural and morphology characterizations revealed that Cu doping improved the crystallization of the thin films as compared to undoped CoFe₂O₄. Current–voltage characterization showed that all Cu_xCo_1?xFe₂O₄ thin films showed unipolar resistance switching, but the distribution range of the set voltage, reset voltage, and resistances were much reduced by Cu doping. Clear improvement in the stability of these parameters started to appear with x = 0.4, and the optimized performance was observed in the Pt/Cu_0.6Co_0.4Fe₂O₄/Pt structure. The improved stability of the switching parameters was attributed to the enhancement of hopping process between the Fe ions and the Cu ions in the spinel lattice. Our results indicated that appropriate adjustment of the doping elements in oxides can be a feasible approach in achieving stable resistance switching memory devices.     

Synthesis and microwave absorption property of ternary composites: polyaniline/CoFe<Subscript>2</Subscript>O<Subscript>4</Subscript>/Ba<Subscript>3</Subscript>Co<Subscript>2</Subscript>Fe<Subscript>24</Subscript>O<Subscript>41</Subscript>

Polyaniline (PANI)/CoFe₂O₄/Ba₃Co₂Fe₂₄O₄₁ composite was prepared by an in-situ polymerization method. The phase structure, morphology and magnetic properties of the as-prepared PANI/CoFe₂O₄/Ba₃Co₂Fe₂₄O₄₁ composite were characterized by XRD, FT-IR, SEM, TEM, and VSM, respectively. The microwave absorption properties of the composite were investigated by using a vector network analyzer in the 2–18 GHz frequency range. The results show that the maximum reflection loss value of the PANI/CoFe₂O₄/Ba₃Co₂Fe₂₄O₄₁ composite reaches ?30.5 dB at 10.5 GHz with a thickness of 3 mm and the bandwidth of reflection loss below ?10 dB reaches up to 1.2 GHz. The excellent microwave absorption properties of the as-prepared PANI/CoFe₂O₄/Ba₃Co₂Fe₂₄O₄₁ composite due to the enhanced impedance match between dielectric loss and magnetic loss.     

Bulk magnetic properties of CdFe<Subscript>2</Subscript>O<Subscript>4</Subscript> in nano-regime

Cadmium ferrite particles have been synthesized using co-precipitation technique followed by a low temperature (600°C) annealing in a time scale much shorter than reported in literature. Incorporation of sodium chloride during annealing helps to form a single phase spinel structure with a final particle size of around 50 nm. Even at such a short length scale we observe the overall magnetic properties to be similar to those of the bulk. The observed magnetic properties can be explained on the basis of an anti-ferromagnetic core with a shell containing ‘ferromagnetic-like’, but canted spin structure.     

Synthesis and Characterization of CoFe<Subscript>2</Subscript><Emphasis Type="Italic">O</Emphasis><Subscript>4</Subscript>/BaTiO<Subscript>3</Subscript> Multiferroic Composites

Three composite modes of CoFe₂ O ₄/BaTiO₃ (CFO/BTO) were created with appropriate stoichiometric proportion. They are nitrate solution of CFO mixed with BTO (SCB), self-propagating precursor of CFO mixed with BTO (PCB), and the made-up CFO mixed with BTO (MCB) separately. The microstructural, ferroelectric, and ferromagnetic properties of SCB, PCB, and MCB bulk composites were investigated. SCB, PCB, and MCB bulk composites with a molar ratio of 2:8 were calcined at 1020, 1120, and 1160 ^°C, respectively. And X-ray diffraction (XRD) analysis showed that they all correspond to the CFO with cubic spinel structure and the BTO with tetragonal perovskite structure. The formation temperature of BTO with hexagonal structure is related to the distance of inter-diffusion and Co ²⁺ concentration in the CFO/BTO bulk composite. The wet chemical routing is of benefit to inhibit the agglomeration of the BTO in the CFO/BTO bulk composite. The maximum polarization of 5.24 μC/cm ² was received in the MCB bulk composite sintered at 1160 ^°C with a molar ratio of 1:9. The maximum saturation magnetization of 31.609 emu/g and the remnant magnetization of 10.336 emu/g were obtained in the MCB bulk composite sintered at 1160 ^°C with a molar ratio of 4:6. The threshold ferromagnetic phase content of percolation which has an effect on the MCB bulk composite is less than 40 mol %.     

Fast microwave synthesis of Fe<Subscript>3</Subscript>O<Subscript>4</Subscript> and Fe<Subscript>3</Subscript>O<Subscript>4</Subscript>/Ag magnetic nanoparticles using Fe<Superscript>2+</Superscript> as precursor

A simple and quick microwave method to prepare high performance magnetite nanoparticles (Fe₃O₄ NPs) directly from Fe has been developed. The as-prepared Fe₃O₄ NPs product was fully characterized by X-ray diffraction, transmission electron microscopy and scanning electron microscopy. The results show that the as-prepared Fe₃O₄ NPs are quite monodisperse with an average core size of 80 × 5 nm. The microwave synthesis technique can be easily modified to prepare Fe₃O₄/Ag NPs and these NPs possess good magnetic properties. The formation mechanisms of the NPs are also discussed. Our proposed synthesis procedure is quick and simple, and shows potential for large-scale production and applications for catalysis and biomedical/biological uses.     

Preparation of magnetic composites through SrO-Fe<Subscript>2</Subscript>O<Subscript>3</Subscript>-Al<Subscript>2</Subscript>O<Subscript>3</Subscript>-B<Subscript>2</Subscript>O<Subscript>3</Subscript> glass crystallization

Glasses with nominal compositions 11SrO · 5.5Fe₂O₃ · 4.5Al₂O₃ · 4B₂O₃ (1) and 15SrO · 5.5Fe₂O₃ · 4.5Al₂O₃ · 4B₂O₃ (2) were prepared by rapidly quenching oxide melts between counterrotating steel rollers. The glasses were then heat-treated in the range 650–950°C to produce glass-ceramic samples. The samples were characterized by X-ray diffraction, electron microscopy, and magnetic measurements. The phase composition of the glass-ceramics was determined, and their microstructure and magnetic properties were studied. The annealing temperature was shown to have a strong effect on the coercivity of the materials, which reaches 650 and 570 kA/m for compositions 1 and 2, respectively.     

Er-Doped LiMn<Subscript>2</Subscript>O<Subscript>4</Subscript>

LiMn_2-x Er_xO₄ (x ≤ 0.02) materials were synthesized by a rheological phase reaction method. The thermal behavior of the materials was examined by thermogravimetric and differential scanning calorimetry. X-ray diffraction showed that the samples (x ≤ 0.02 ) exhibited the same phase as the pure spinel. The lattice parameter of the Er-doped spinel was smaller than that of the undoped one and decreased with increasing doping level. Cyclic voltammograms showed two reversible processes corresponding to the typical response of spinel LiMn₂O₄ and revealed an insertion-extraction reaction occurring at two stages in the 4-V region. The electrochemical performances of the samples were studied and displayed a better reversibility and cyclability.__________From Neorganicheskie Materialy, Vol. 41, No. 6, 2005, pp. 740–743.Original English Text Copyright © 2005 by Haowen Liu, Li Song, Kelli Zhang.This article was submitted by the authors in English.     

Fabrication and magnetic properties of NiFe<Subscript>2</Subscript>O<Subscript>4</Subscript> nanocrystalline nanotubes

Aligned NiFe₂O₄ polycrystalline nanotubes have been successfully fabricated inside the nanochannels of porous anodic aluminum oxide (AAO) templates by wetting chemical deposition. A mixture of Fe nitrate and Ni nitrate, which was thermally decomposed at no less than 400 °C, was used to yield NiFe₂O₄ tubes. By varying the deposition conditions and the parameters of the templates, we could tailor the lengths and the outer as well as the inner diameters of the tubes. Transmission electron microscopy (TEM) images reveal that the nanotubes are uniform and well isolated. X-ray diffraction (XRD) and selected area electron diffraction (SAED) demonstrate that the as-obtained nanotubes can be indexed to polycrystalline cubic spinel. The Mössbauer spectra show that the magnetic hyperfine field is reduced with the decrease of the metrical temperature as well as the decrease of the size of nanoparticles.     

Characterization and electrical properties of semiconducting Fe<Subscript>2</Subscript>O<Subscript>3</Subscript>-Bi<Subscript>2</Subscript>O<Subscript>3</Subscript>-K<Subscript>2</Subscript>B<Subscript>4</Subscript>O<Subscript>7</Subscript> glasses

Semiconducting glasses of the Fe₂O₃-Bi₂O₃-K₂B₄O₇ system were prepared by the press-quenching method and their dc conductivity in the temperature range 223–393 K was measured. The glass transition temperature values (T_g) of the present glasses were larger than those of tellurite glasses. This indicates a higher thermal stability of the glass in the present system. The density for these glasses was consistent with the ionic size, atomic weight and amount of different elements in the glasses. Mössbauer results revealed that the relative fraction of Fe increases with increasing Fe₂O₃ content. Electrical conductivity showed a similar composition dependency as the fraction of Fe. The glasses had conductivities ranging from 10 to 10 Scm at temperatures from 223 to 393 K. Electrical conduction of the glasses was confirmed to be due to non-adiabatic small polaron hopping and the conduction was primarily determined by hopping carrier mobility.     

Electrical conductivity of Bi<Subscript>2</Subscript>O<Subscript>3</Subscript>-Tm<Subscript>2</Subscript>O<Subscript>3</Subscript>-Nb<Subscript>2</Subscript>O<Subscript>5</Subscript> solid solutions

New solid solutions, Bi_2?x?y Tm _x Nb _y O_3+δ, with tetragonal and cubic structures have been synthesized in the Bi₂O₃-Tm₂O₃-Nb₂O₅ system, and their electrical conductivity has been measured at temperatures from 670 to 1020 K. The 1020-K conductivity of the tetragonal solid solution Bi_1.8Tm_0.15Nb_0.05O_3+δ is comparable to that of Bi_1.75Tm_0.25O₃, the best conductor in the Bi₂O₃-Tm₂O₃ system.     

Reactions of V<Subscript>2</Subscript>O<Subscript>5</Subscript>, Nb<Subscript>2</Subscript>O<Subscript>5</Subscript>, and Ta<Subscript>2</Subscript>O<Subscript>5</Subscript> with AlN

Reactions of vanadium, niobium, and tantalum pentoxides with aluminum nitride have been studied using X-ray diffraction. At temperatures from 1000 to 1600°C, we have identified various V, Nb, and Ta nitrides. The composition of the niobium and tantalum nitrides depends on the reaction temperature. The tendency toward nitride formation becomes stronger in the order V₂O₅ < Ta₂O₅ < Nb₂O₅.     

Growth and properties of LiCu<Subscript>2</Subscript>O<Subscript>2</Subscript>-NaCu<Subscript>2</Subscript>O<Subscript>2</Subscript> crystals

Platelike Li_{1 ? x} Na _x Cu₂O₂ single crystals up to 2 × 10 × 10 mm in dimensions have been grown by slowly cooling (1 ? x)Li₂CO₃·xNa₂O₂·4CuO melts in alundum crucibles in air. Li_{1 ? x} Na _x Cu₂O₂ solid solutions in the LiCu₂O₂-NaCu₂O₂ system have been shown to exist in the composition range 0.78 < x < 1. The temperature stability ranges of NaCu₂O₂ and LiCu₂O₂ are 780–930 and 890–1050°C, respectively. The Mössbauer spectra and electrical conductivity of the crystals have been measured.