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991.
SmCoxTi0.4 (x=6.6, 7.1, 7.6, 8.1) ribbons have been prepared by melt spinning at a wheel speed of 42 m/s, followed by annealing at 750 °C for 2 h. Both as-spun and as-annealed ribbons possess the disordered TbCu7-type (1:7) phase even when the Sm/(Co,Ti) atomic ratio deviates from 1/7. The c/a ratio increases with increasing Co concentration x, but the unit cell volume decreases. The Curie temperatures show above 700 °C, increasing from 707 °C for x=6.6 to 782 °C for x=8.1. The saturation magnetizations increase almost linearly with increasing Co content. The observed magnetic hardening is believed to arise from the high magnetocrystalline anisotropy of the 1:7 phase and the fine nanograin structure. The intrinsic coercivity of 9797 Oe has been obtained in the melt-spun SmCo7.1Ti0.4 ribbons. 相似文献
992.
Polyaniline/Zn0.5Cu0.5Fe2O4 nanocomposite was synthesized by a simple, general and inexpensive in-situ polymerization method in w/o microemulsion. The
effects of polyaniline coating on the magnetic properties of Zn0.5Cu0.5Fe2O4 nanoparticles were investigated. The structural, morphological and magnetic properties of as-prepared samples were characterized
by X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectra, scanning electron microscopy (SEM) and magnetic measurements.
The morphology analysis confirmed that polyaniline was deposited on the porous surface of magnetic Zn0.5Cu0.5Fe2O4. It was shown that the saturation magnetization and coercivity of Zn0.5Cu0.5Fe2O4 decreased after polyaniline coating, which can be interpreted by the interparticle dipole–dipole interactions that contributed
to magnetic anisotropy and changed the magnetic properties of the nanoparticles.
PACS 74.25.Ha; 81.05.-t; 81.05.Lg 相似文献
993.
In this paper, we propose a physical scheme to realize quantum SWAP
gate by using a large-detuned single-mode cavity field and two
identical Rydberg atoms. It is shown that the scheme can also be used
to create multi-atom cluster state. During the interaction between
atom and cavity, the cavity is only virtually excited and thus the
scheme is insensitive to the cavity field states and cavity decay.
With the help of our scheme it is very simple to prepare the $N$-atom
cluster state with perfect fidelity and probability. The practical
feasibility of this method is also discussed. 相似文献
994.
Triangular, truncated triangular, quadrangular, hexagonal, and net-structured silver nanoplates as well as decahedral silver nanoparticles were manipulatively prepared starting from silver nitrate and silver seeds in the presence of poly(ethylene glycol) (PEG), poly(N-vinyl pyrrolidone) (PVP), and Tween 80 at room temperature, respectively. UV-vis spectroscopy, XRD, HRTEM, SAED, and FTIR were used to illustrate the crystal growth process and to characterize the resultant silver nanoparticles. It was found that the silver seeds and organic modifiers synergistically affected the morphology evolution of the silver nanoparticles. The co-presence of silver seeds and PEG was beneficial to the formation of triangular and truncated triangular silver nanoplates; the silver seeds and PVP favored the formation of polygonal silver nanoplates; the silver seeds and Tween 80 preferred to the formation of net-structured silver plates. The morphology evolution of the resultant silver nanoparticles was correlated with the crystallinity of the silver seeds and the adsorption ability of the organic modifiers on the crystal surfaces. 相似文献
995.
Perfect epitaxial growth of La0.67Ca0.33MnO3 (LCMO) thin film has been achieved on (1 0 0) LaAlO3 (LAO) single crystal substrate by radio frequency sputtering method. X-ray diffraction (XRD) and electron diffraction analysis indicates that La0.67Ca0.33MnO3 film grows epitaxially on LaAlO3 along [1 0 0] direction of the substrate. The resistivity variation with temperature of the film shows a sharp metal to semiconductor transition peak around 253 K, which is close to that of the target. The magnetoresistance (MR) also reveals high quality epitaxy film characteristic at low temperatures and near the metal to semiconductor transition temperature. 相似文献
996.
Wenmeng Duan Xianwu Jing Jiang Tan Minmin Tao Lu Wang 《Journal of Dispersion Science and Technology》2018,39(9):1309-1315
A series of amphiphilic triblock polymers based on poly(ethylene glycol) (PEG) and two symmetrical poly(2-(dimethylamino)ethyl methacrylate) (PDMAEMA) blocks was synthesized via the Atom Transfer Radical Polymerization (ATRP) method. Conductivity, pH, and viscosity tests demonstrated the CO2-switchability jointly; Cryogenic transmission electron microscopy (Cryo-TEM), Dynamic light scattering (DLS) revealed the self-assembly morphology transformation from unilamellar vesicle to network structure when bubbling CO2. These changes were all attributed to the protonation of tertiary amine groups in PDMAEMA blocks and the mechanism was proved by ?H NMR. The vesicles have a relatively low release rate of drug; once stimulated by CO2, the release rate will be accelerated. The polymeric vesicle has the possibility to find potential applications in drug delivery and release domains. 相似文献
997.
998.
In this study, bis(diphenylphosphinemethyl)dimethyl silane ( L1 ) and its palladium(II) halide complex, L1 /PdCl2 ( C1 ), were synthesized and characterized. Single‐crystal X‐ray analysis of the complex revealed bidentate coordination at the Pd center. In combination with methylaluminoxane (MAO) as co‐catalyst, C1 exhibited excellent catalytic activity and selectivity for ethylene dimerization toward butene. The maximum catalytic activity obtained from the C1 /MAO system for ethylene dimerization to yield butenes was 7.33 × 105 g/(molPd · h). The selectivity toward butene remained stable and high (> 96%) over the various conditions. 相似文献
999.
Gao Pei‐Sen Zhang Jin‐Lei Li Ning Zheng Zhan Jiang Yuan Yang Gao Zi‐Wei Zhang Weiqiang Xu Li‐Wen 《应用有机金属化学》2018,32(3)
Catalytic allylic γ‐substitution with Morita‐Baylis‐Hillman (MBH) adducts for creating a new family of unsymmetrical dicarbonyl compounds was presented in this work, in which a variety of allylated amide products were achieved in good yields and high regioselectivity with excellent linear‐to‐branched ratios. Especially, it was found that the Pd/HZNU‐Phos complex exhibited remarkably high activity (with a TON up to 16800) in this transformation between dicarbonyl amides and MBH adducts. In addition, the possibly multisite interaction between multifunctional Pd/HZNU‐Phos catalyst system and substrates might responsible for its exceptionally high efficiency in this reaction. 相似文献
1000.