Anomalous Hall effect in perpendicular CoFeB thin films

Our recent research achievements in the perpendicular magnetic anisotropy （PMA） properties of the CoFeB sand- wiched by MgO and tantalum layers are summarized. We found that the PMA behaviors of Ta/CoFeB/MgO and MgO/CoFeB/Ta thin films are different. The larger PMA in the latter film is related to the lower magnetization of CoFeB deposited on MgO. Furthermore, we have demonstrated a large anomalous Hall effect in perpendicular CoFeB thin fihn. Our results show large anomalous Hall resistivity, large longitudinal resistivity, and low switching field can be achieved, all at the same time, in the perpendicular CoFeB thin film. Anomalous Hall effect with high and linear sensitivity is also found in an MgO/CoFeBFFa thin film with a thick MgO layer, which opens a door tbr future device applications of perpendicular ferromagnetic thin films.     

耦合势有限体积法高效模拟各向异性地层中海洋可控源的三维电磁响应

本文基于电场矢势与标势分解的耦合势有限体积法研究建立一套各向异性地层中海洋可控源电磁法的三维响应的高效数值模拟技术.首先引入电场的矢势和标势,将电场分解为无散场和无旋场之和,Maxwell方程转换为关于矢势与标势的混合Helmholtz方程,克服低感应数问题.在此基础上,借助Yee氏交错网格和有限体积法以及非均质单元中等效电导率公式,建立混合Helmholtz方程的离散方程.并采用直接法求解器PARDISO求解离散方程,有效保证在大的求解空间中仍然能够获得电磁场稳定可靠的数值解.此外,在数值模拟中利用差异场技术,克服源的奇异性问题,尽可能提高近场的计算精度.与解析解的对比证明了该算法的有效性.数值模拟结果表明,海洋可控源电磁法沿测线方向的电场,对油气藏的纵向电阻率敏感,对横向电阻率不敏感;对油气藏上方的覆盖层的纵向电阻率和横向电阻率都敏感.     

晶体锥折射空心光束的位相差及偏振特性

根据双轴晶体内锥折射效应产生空心光环的基本原理,推导出空心光环上各点相对于光环最低点的位相差分布规律解析式.通过模拟得到了位相差分布规律,证明了光环上各点的偏振方向变化具有连续性.实验采用非偏振的He-Ne激光准直后经小孔光阑垂直照射KNbO3晶体获得了空心光束,对其偏振特性进行了测试,结果与理论分析相吻合,很好的验证了理论分析的正确性.     

Synthesis,Characterization, and Directional Binding of Anisotropic Biohybrid Microparticles for Multiplexed Biosensing

Anisotropic microarchitectures with different physicochemical properties have been developed as advanced materials for challenging industrial and biomedical applications including switchable displays, multiplexed biosensors and bioassays, spatially‐controlled drug delivery systems, and tissue engineering scaffolds. In this study, anisotropic biohybrid microparticles (MPs) spatio‐selectively conjugated with two different antibodies (Abs) are first developed for fluorescence‐based, multiplexed sensing of biological molecules. Poly(acrylamide‐co‐acrylic acid) is chemically modified with maleimide‐ or acetylene groups to introduce different targeting biological moieties into each compartment of anisotropic MPs. Modified polymer solutions containing two different fluorescent dyes are separately used for electrohydrodynamic co‐jetting with side‐by‐side needle geometry. The anisotropic MPs are chemically stabilized by thermal imidization, followed by bioconjugation of two different sets of polyclonal Abs with two individual compartments via maleimide‐thiol coupling reaction and Huisgen 1,3‐dipolar cycloaddition. Finally, two compartments of the anisotropic biohybrid MPs are spatio‐selectively associated with the respective monoclonal Ab‐immobilized substrate in the presence of the antigen by sandwich‐type immunocomplex formation, resulting in their ordered orientation due to the spatio‐specific molecular interaction, as confirmed by confocal laser scanning microscopy. In conclusion, anisotropic biohybrid MPs capable of directional binding have great potential as a new fluorescence‐based multiplexing biosensing system.

     

Active and Passive LC Based Polarization Elements

Passive and active polarization elements were created by surface and bulk photo-alignment of LCs, reactive LCs, photo-sensitive LCP and photo-curable monomer/LC composites. The use of different photo­sensitive liquid crystalline materials for the development of highly anisotropic elements with high spatial resolution and stability or, alternatively, fast switch ability will be discussed. Photo-active and voltage tunable polarization and diffraction elements are presented. For active micro-optic application a photo-addressed patterned retarder was created. Electrically switchable diffraction gratings were generated by interference exposure of photo-curable LC composites at room temperature characterized by droplet free morphology. These polarization sensitive diffraction elements are characterized be excellent optical properties and low switching times.     

C60 adsorption on Cu(110) studied by optical spectroscopy

The formation of the interface between C₆₀ thin films and the Cu(110) surface has been investigated in situ using reflectance difference spectroscopy (RDS). The electronic interaction between C₆₀ molecules in the first monolayer and the substrate inhibits low‐energy intramolecular transitions, whereas the C₆₀ molecules above the first monolayer are effectively decoupled from the substrate. The morphology of C₆₀ thin films prepared at room temperature is thermally stable up to 500 K. Above this threshold, optical spectroscopy and low energy electron diffraction (LEED) indicate the formation of rather large three dimensional C₆₀ islands on a one monolayer thick wetting layer. (© 2014 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

SIMPRE: A software package to calculate crystal field parameters,energy levels,and magnetic properties on mononuclear lanthanoid complexes based on charge distributions

This work presents a fortran77 code based on an effective electrostatic model of point charges around a rare earth ion. The program calculates the full set of crystal field parameters, energy levels spectrum, and wave functions, as well as the magnetic properties such as the magnetization, the temperature dependence of the magnetic susceptibility, and the Schottky contribution to the specific heat. It is designed for real systems that need not bear ideal symmetry and it is able to determine the easy axis of magnetization. Its systematic application to different coordination environments allows magneto‐structural studies. The package has already been successfully applied to several mononuclear systems with single‐molecule magnetic behavior. The determination of effective point charge parameters in these studies facilitates its application to new systems. In this article, we illustrate its usage with two example studies: (a) an ideal cubic structure coordinating a lanthanoid ion and (b) a system with slow relaxation of the magnetization, LiHo_xY_(1‐x)F₄. © 2013 Wiley Periodicals, Inc.     

Dielectric properties of three‐ring fluorinated compounds

Four three‐ring compounds, consisting of two cyclohexyl rings and one mono‐ or difluorinated phenyl ring, were studied using dielectric spectroscopy methods over a broad frequency range (1 kHz–3 GHz). They exhibit a nematic phase in a broad temperature interval, enriched by a smectic B phase in one case. The static and dynamic dielectric properties were analysed. It was established that the bridging CH₂CH₂ group placed between cyclohexyl and phenyl rings considerably changes the reference frame of the molecule, unlike the situation when it links two cyclohexyl rings. In the nematic and smectic B phases the motion around the short axis is a Debye process, whereas the rotation around the long axis is split into two processes: independent rotation of the whole molecule and its fluorophenyl part.     

The effect of inversion of the ester group on the mesophase behaviour of some azo/ester compounds

Five homologous series of 4-substituted phenyl 4′-(4″-alkoxy phenylazo) benzoates (In_a–?e) were prepared in which, within each homologous series, the length of the terminal alkoxy group varies between 8, 10, 12, 14 and 16 carbons, while the other terminal substituent, X, is a polar group that alternatively changed from CH₃O, CH₃, H, Br, and CN groups. Compounds prepared were characterised by infrared, mass, and H¹-NMR spectroscopy and their mesophase behaviour investigated by differential scanning calorimetry (DSC) and polarised light microscopy (PLM). The results were discussed in terms of mesomeric and polarisability effects. Only for the lower group of compounds, I8_a-e, that showed a nematic phase, the nematic-to-isotropic transition temperatures (T_N–I) were successfully correlated to the polarisability anisotropy of bonds to the substituent X. A comparative study was made between the investigated compounds and two previously prepared isomeric groups. In the first group of isomers, 4-(4′alkoxy phenylazo) phenyl 4″-substituted benzoates (IIn_a–e), the ester groups are inverted. While in the second, 4-(4′-substituted phenylazo) phenyl 4″-alkoxy benzoates (IIIn_a–e), two modifications were made, inversion of the COO group, and exchange of the two wing substituents