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In this paper, ZnFe2O4 spinel ferrite nanoparticles with different grain sizes at different annealing temperatures have been synthesized using the starch-assisted sol–gel auto-combustion method. The synthesized nanoparticles were characterized by conventional powder X-ray diffraction, Raman spectroscopy, Fourier transform infrared spectroscopy, field emission scanning electron microscopy, and vibrating sample magnetometer. The X-ray diffraction (XRD) patterns demonstrated that the ZnFe2O4 nanoparticles consist of single-phase spinel structure with crystallite sizes 4.81, 8.72, 12.06, 29.32, and 72.60 nm annealed at 400, 600, 800, 1000, and 1200 °C, respectively. Field emission scanning electron microscopy reveals that particles are of spherical morphology at lower annealing temperature and hexagonal-like morphology at higher temperature. An infrared spectroscopy study shows the presence of two principal absorption bands in the frequency range around 525 cm?1 (ν 1) and around 350 cm?1 (ν 2), which indicate the presence of tetrahedral and octahedral group complexes, respectively, within the spinel ferrite nanoparticles. Raman spectroscopy study also indicated the change in octahedral and tetrahedral site-related Raman modes in zinc ferrite nanoparticles with change of particle size. The nanocrystalline ZnFe2O4 samples (4.81, 8.72, 12.06, 29.32 nm) show ferrimagnetic behavior, and bulk sample (72.60 nm) shows paramagnetic behavior. This change in magnetic behavior is due to change of cation distribution in ZnFe2O4 nanoparticles with decrease of particle size.  相似文献   

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Journal of Superconductivity and Novel Magnetism - La0.5Ag0.1Ca0.4MnO3 manganite nanoparticles are synthesized via two different ways, namely, a solid-state reaction (S1) and the sol–gel...  相似文献   

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In this work, Fe3O4–ZnO core–shell nanoparticles have been successfully synthesized using a simple two-step co-precipitation method. In this regard, Fe3O4 (magnetite) and ZnO (zincite) nanoparticles (NPs) were synthesized separately. Then, the surface of the Fe3O4 NPs was modified with trisodium citrate in order to improve the attachment of ZnO NPs to the surface of Fe3O4 NPs. Afterwards, the modified magnetite NPs were coated with ZnO NPs. Moreover, the influence of the core to shell molar ratio on the structural and magnetic properties of the core–shell NPs has been investigated. The prepared nanoparticles have been characterized utilizing transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy and vibrating sample magnetometer (VSM). The results of XRD indicate that Fe3O4 NPs with inverse spinel phase were formed. The results of VSM imply that the Fe3O4–ZnO core–shell NPs are superparamagnetic. The saturation magnetization of prepared Fe3O4 NPs is 54.24 emu/g and it decreases intensively down to 29.88, 10.51 and 5.75 emu/g, after ZnO coating with various ratios of core to shell as 1:1, 1:10 and 1:20, respectively. This reduction is attributed to core–shell interface effects and shielding. TEM images and XRD results imply that ZnO-coated magnetite NPs are formed. According to the TEM images, the estimated average size for most of core–shell NPs is about 12 nm.  相似文献   

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A series of nanostructured Zr-doped anatase TiO_2 tubes with the Zr/Ti molar ratio of 0.01, 0.02, 0.03, and0.09 were prepared by a sol–gel technology on a carbon fiber template. The electrochemical performance of Zr-doped anatase TiO_2 as anodes for rechargeable lithium batteries was investigated and compared with undoped titania. Tests represented that after 35-fold charge/discharge cycling at C/10 the reversible capacity of Zr-doped titania(Zr/Ti = 0.03) reaches 135 m A h g~(-1), while the capacity of undoped titania(Zr/Ti = 0) yielded only 50 m A h g~(-1). Based on the results of the physicochemical investigation, three reasons of improving electrochemical performance of Zr-doped titania were suggested. According to the scanning electron microscopy and transmission electron microscopy, Zr~(4+) doping induces a decrease in nanoparticle size, which facilitates the Li+diffusion. The Raman investigations show the more open structure of Zr-doped TiO_2 as compared to undoped titania due to changing of the unit cell parameters, that significantly affects on the reversibility of the insertion/extraction process. The electrochemical impedance spectroscopy results indicate that substitution of Zr~(4+) for Ti~(4+) into anatase TiO_2 has favorable effects on the conductivity.  相似文献   

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In the present work TiO2 nanoparticles were prepared by sol–gel method and both small-sized nanoparticles and proper crystals were delivered by simultaneous use of surfactant, which was applied for the purpose of size reduction of nanoparticles, and acid ions that were used so that the formation of crystalline structures occurs appropriately. Photocatalytic activity of samples was measured by degrading RO dye, and photoelectrochemical properties were assayed using anodic photocurrent responses under Xe lamp light irradiation. The synthesized nanoparticles exhibit great photoelectrochemical and photocatalytic activity compared to that of commercial photocatalyst, Degussa P-25, which demonstrates that the method can be applied in the synthesis of other semiconductor oxides nanoparticles.  相似文献   

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CoFe2?x Al x O4 (x = 0.0,0.5,1.0, and 1.5) ferrite nanoparticles have been synthesized by the sol–gel auto-combustion method. The effect of non-magnetic Al content on their structural, morphological, optical, and magnetic properties was also investigated. X-ray diffraction (XRD) diffraction analysis was applied and indicated that the synthesized nanopowders of samples with x<1.5 and calcined at 800 °C have single-phase spinel structure. It has shown also by increasing Al content, the particle size, lattice parameter, unit cell volume, coercivity, anisotropy constant, and magnetization decrease, while the energy band gap increases. The size of particles was measured by TEM being in the range of 65–75 nm (for x = 0.0) and 9–10 nm (for x = 1.0). For sample with x = 1.5, the minimum calcination temperature for obtaining a single-phase spinel structure was 1000 °C. By increasing the calcination temperature from 1000 to 1100 °C, the mean crystallite size and crystallinity increase, while the lattice parameter, coercivity, anisotropy constant, and magnetization decrease. The average grain size evaluated by SEM analysis was found to be \(\tilde 91\) and 166 nm for samples calcined at 1000 and 1100 °C, respectively.  相似文献   

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Transparent conductive ZnO : Al : Mo films with a molar ratio of Zn : Al : Mo = 99 : 0·99 : 0·01 were deposited on quartz glass substrate by a template-assisted sol-gel process and characterized by X-ray diffraction, atomic force microscopy, scanning electron microscopy, and UV–Vis and luminescent spectrophotometries. The four types of organic template have induced nanowire morphology with varying aspect ratio. Dip coating in one constant positive and reverse direction causes the parallel array of ZnO : Al : Mo nanowires on the quartz glass substrate. Long and parallel arrayed nanowire films show obviously blue shifts and enhanced transmittances in the UV-Vis light range. The PEG-1000 and PEG-2000 have optimal effects among four templates as constant weight content is used. The films show strong ultraviolet, violet and bluish violet emissions. The templates also lead to overall thicker film and more native defect and thereby remarkably enhancing photoluminescence of the films. Long chain organic template can be used to optimize the optical properties of the doped ZnO film.  相似文献   

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《工程(英文)》2020,6(2):132-140
Nanoscale permanent magnetic materials, which possess excellent magnetic and mechanical properties, thermal stability, and corrosion resistance, have become a research hotspot for permanent magnets. In reality, however, the obtained maximum energy product, (BH)max, is not satisfactory in comparison with the theory limit, especially for exchange-coupled nanocomposite magnets. The construction of an ideal microstructure still remains a challenge in the synthesis and preparation of nanoscale permanent magnets. This work reported the impact of rapid thermal process (RTP) with electron-beam heating on the microstructures of Nd12.5-xFe80.8+xB6.2Nb0.2Ga0.3 (x = 0, 2.5) nanocomposites. It was found that the crystallization time was greatly reduced, from 15 min under the conventional annealing conditions to 0.1 s under the RTP. For Nd2Fe14B single-phase materials, the crystallization temperature of the RTP ribbons decreased by about 248 °C compared with that of the ribbons produced by the conventional annealing method. A synergetic crystallization of the Nd2Fe14B and α-Fe phases was observed under the RTP, which restrained not only the shape, size distribution, and compositions of the hard and the soft phases, but also the interface between them. This modification effect became more obvious as the fraction of Fe increased. Due to the improvement in the uniformity of the Nd2Fe14B and α-Fe phases, and their grain size distribution, better magnetic properties were achieved using RTP in comparison with the conventional annealing method.  相似文献   

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