复合外场中磁光材料(BiTm)_3(FeGa)_5O_(12)薄膜畴壁运动特性的研究

通过对 (BiTm) 3 (FeGa) 5O12 膜施工加低频交变磁场 ,匀速率增加的直流磁场和同时对该膜施加这两种磁场 (复合外场 ) ,用照相划线读数方法和通过电荷耦合器件 (CCD) 计算机作数字化处理获得磁畴壁 (DW)的相对百分数。结果表明 :( 1 )复合外场下DW运动规律中存在交互作用项 ;( 2 )低频交变磁场幅值 ( 1 4 0A/m)远低于等效阻力场 ( 1 0 3 A/m)时 ,DW可以运动 ,但不同步 ,频率大于 1Hz时明显滞后 ,( 3 )利用图像转换有利于提高实验结果的分辨率。     

复合外场中磁光材料(BiTm)3(FeGa)5O12薄膜畴壁运动特性的研究

通过对BiTm)₃(FeGa)₅O₁₂膜施工加低频交变磁场,匀速率增加的直流磁场和同时对该膜施加这两种磁场(复合外场),用照相划线读数方法和通过电荷耦合器件(CCD)-计算机作数字化处理获得磁畴壁(DW)的相对百分数。结果表明:(1)复合外场下DW运动规律中存在交互作用项;(2)低频交变磁场幅值(140A/m)远低于等效阻力场(10³A/m)时,DW可以运动,但不同步,频率大于1Hz时明显滞后,(3)利用图像转换有利于提高实验结果的分辨率。     

磁畴和畴壁的实验演示

利用透射光法进行磁畴和畴壁的实验演示，在磁性材料中的薄膜中，若无外加磁场时，可以观察到很多蜿蜒曲折的条状磁畴，当垂直薄膜面上加一个磁场（磁化场）时，这些条状磁畴就会产生变化，凡与外加磁场方向一致的磁畴体积扩大，与加外磁场方向相反的磁畴体积会缩小。     

消磁场对纳米铁磁线磁畴壁动力学行为的影响

为了实现基于磁畴壁运动的自旋电子学装置, 掌握磁畴壁动力学行为是重要争论之一.研究了在外磁场驱动下L-型纳米铁磁线磁畴壁的动力学行为. 通过微磁学模拟,在各种外磁场的驱动下考察了纳米铁磁线磁畴壁的动力学特性; 在较强外磁场的驱动下, 在不同厚度纳米线上考察了纳米线表面消磁场对磁畴壁动力学行为的影响. 为了进一步证实消磁场对磁畴壁动力学的影响, 在垂直于纳米线表面的外磁场辅助下分析了磁畴壁的动力学行为变化. 结果表明, 随着纳米线厚度和外驱动磁场强度的增加, 增强了纳米线表面的消磁场的形成, 使得磁畴壁内部自旋结构发生周期性变化, 导致磁畴壁在纳米线上传播时出现Walker崩溃现象. 在垂直于纳米线表面的外磁场辅助下, 发现辅助磁场可以调节消磁场的强度和方向. 这意味着利用辅助磁场可以有效地控制纳米铁磁线磁畴壁的动力学行为.     

微磁动力学的新进展

本文介绍微磁动力学领域的一个最新进展,我们的研究发现在磁场驱动下且保持畴结构不变地沿着纳米磁线运动的磁畴壁,其运动源于能量耗散,磁畴壁运动速度正比于能量耗散率。与此同时,我们根据能量守恒原则,给出了磁畴壁速度的一个合理定义,该定义适用于任意的磁畴壁结构。在此定义下,即使磁畴壁没有做刚性运动,我们也能得到磁畴壁运动的瞬时速度和平均速度。我们的结果不仅能重复低磁场下的沃克（Walker）解,还能反映出当磁场高于沃克极限（Walker limit）时速度{磁场的依赖关系,该结果跟数值模拟和实验数据都符合得很好。我们根据微磁动力学研究的这一新进展,最终澄清了一个事实即“磁畴壁质量”这个概念是错误的。     

交变磁场下磁光薄膜动态法拉第效应特性的测量

论述了在交变磁场下测量磁光薄膜动态法拉第效应的原理和方法，利用此方法，在不同的调制磁场强度和频率下测量磁光薄膜的动态法拉第旋转特性，获得了较好的测量结果，并对测量误差进行了分析。     

磁畴壁拓扑结构研究进展

拓扑磁性斯格明子作为信息载体单元具备高可靠性、高集成度、低能耗等优势,有望提高数据读写精度、降低功耗,从而研发新型拓扑自旋电子学材料与原理型器件,为信息技术、5G通信和大数据等的高速发展提供材料与技术支持.但磁性斯格明子同时存在需要磁场稳定以及电流驱动下斯格明子霍尔效应引起偏转等缺点,严重阻碍了其在实际器件中的应用,因此探索新型拓扑磁畴结构和适宜应用的材料体系成为研究的关键.本文将重点介绍自2013年理论预言磁畴壁斯格明子以来,利用高分辨率洛伦兹透射电子显微镜原位实空间发现并研究磁畴壁拓扑麦纫和磁畴壁斯格明子的实验工作.首次在范德瓦耳斯Fe_5–xGeTe₂二维磁性材料中发现温度诱发的180°磁畴壁转变为拓扑麦韧链,研究了磁畴壁麦纫态在外界电场、磁场作用下的集体运动行为,揭示了基于自旋重取向、磁畴壁限域效应以及弱相互作用下生成磁畴壁拓扑态的机制.在该机制指导下,设计制备了具有自旋重取向的GdFeCo非晶亚铁磁薄膜,不仅获得了磁畴壁麦纫,验证了生成机制的普适性,还成功实现了畴壁麦韧对到畴壁斯格明子的可逆拓扑转变,开辟了基于磁畴壁等内禀限域效应开展...     

具有条纹磁畴结构的NiFe薄膜的制备与磁各向异性研究

具有条纹磁畴结构的磁性薄膜表现出面内转动磁各向异性,对于解决高频电子器件的方向性问题起着至关重要的作用.本文采用射频磁控溅射的方法,研究了NiFe薄膜的厚度、溅射功率密度、溅射气压等制备工艺参数对条纹磁畴结构、面内静态磁各向异性、面内转动磁各向异性、垂直磁各向异性的影响规律.研究发现,在功率密度15.6 W/cm~2与溅射气压2 mTorr(1 Torr=1.33322×102Pa)下生长的NiFe薄膜,表现出条纹磁畴的临界厚度在250 nm到300 nm之间.厚度为300 nm的薄膜比250 nm薄膜的垂直磁各向异性场增大近一倍,从而磁矩偏离膜面形成条纹磁畴结构,并表现出面内转动磁各向异性.高溅射功率密度可以降低薄膜出现条纹磁畴的临界厚度.在相同功率密度15.6 W/cm~2下生长300 nm的NiFe薄膜,随着溅射气压由2 mTorr增大到9 mTorr,NiFe薄膜的垂直磁各向异性场逐渐由1247.8 Oe(1 Oe=79.5775 A/m)增大到3248.0 Oe,面内转动磁各向异性场由72.5 Oe增大到141.9 Oe,条纹磁畴周期从0.53μm单调减小到0.24μm.NiFe薄膜的断面结构表明柱状晶的形成是表现出条纹磁畴结构的本质原因,高功率密度下低溅射气压有利于柱状晶结构的形成,表现出规整的条纹磁畴结构,高溅射气压会导致柱状晶纤细化,面内转动磁各向异性与面外垂直磁各向异性增强,条纹磁畴结构变得混乱.     

面内场对三类硬磁畴的影响

采用直流偏场整形的方法,研究了面内场对石榴石磁泡薄膜中三类硬磁畴的影响.得到面内场作用下三类硬磁畴畴壁中垂直布洛赫线(VBL)是逐步解体的,而且三类硬磁畴具有相同的临界面内场范围［H¹_ip,H²_ip］,其中H¹_ip是硬磁畴中VBL开始丢失时的临界面内场,H²_ip是VBL完全丢失 关键词： 硬磁畴 整形 垂直布洛赫线     

不均匀磁化薄膜中静磁波对导波光的Bragg衍射

研究了横向不均匀偏置磁场作用下掺Bi的YIG薄膜中微波静磁波的激发和传播特性；采用变分方法计算了静磁正向体波的色散关系和交变磁化强度，分析了不均匀场对静磁波－导波光耦合的影响理论计算得到的衍射效率曲线与实验结果基本一致，表明适当不均匀场可以大大提高磁光Bragg器件的衍射性能.     

First Observation of the nu(17)-nu(4) Difference Bands of Diborane (10)B(2)H(6) and (11)B(2)H(6)

An analysis of the nu(17)-nu(4) difference bands near 800 cm(-1) of two isotopic species, (10)B(2)H(6) and (11)B(2)H(6), of diborane has been carried out using infrared spectra recorded with a resolution of ca. 0.003 cm(-1). In addition, the nu(17) band of (10)B(2)H(6) has been recorded and assigned. Since this band in (11)B(2)H(6) had already been studied (R. L. Sams, T. A. Blake, S. W. Sharpe, J.-M. Flaud, and W. J. Lafferty, J. Mol. Spectrosc. 191, 331-342 (1998)), it was possible to derive precise energy levels and Hamiltonian constants for the 4(1) vibrational states of both isotopic species. Copyright 2000 Academic Press.     

The Perturbation between the G(1)Pi(g) and 2(1)Delta(g) States of (7)Li(2)

We have observed the rotational levels in the v = 2, 3, 5, 6, 7, and 8 vibrational manifolds of the 2(1)Delta(g) state of (7)Li(2) via the A(1)Sigma(+)(u) intermediate levels by DeltaLambda = 2 transitions. This violation of the DeltaLambda = 0, +/-1 selection rule is due to the interaction with the G(1)Pi(g) state. Band-by-band deperturbations of the G(1)Pi(g) approximately 2(1)Delta(g) (v(Pi), v(Delta)) = (11, 2), (12, 3), (15, 5), (16, 6), (18, 7), and (19, 8) bands have been performed. Deperturbed molecular constants and rotational-electronic interaction parameters are reported here. Copyright 2000 Academic Press.     

Generalization of the N(p)N(n)N(p)N(n) scheme and the structure of the valence space

The N(p)N(n) scheme, which has been extensively applied to even-even nuclei, is found to be a very good benchmark for odd-even, even-odd, and doubly-odd nuclei as well. There are no apparent shifts in the correlations for these four classes of nuclei. The compact correlations highlight the deviant behavior of the Z = 78 nuclei and are used to deduce effective valence proton numbers near Z = 64 as well as to study the evolution of the Z = 64 subshell gap.     

N(2)-Broadening Coefficients in the nu(1) Band of (35)Cl(12)C(14)N

N(2)-broadening coefficients have been measured for 30 lines of cyanogen chloride ((35)Cl(12)C(14)N) at room temperature in the P and R branches of the nu(1) band, using a tunable diode-laser spectrometer. These lines, with J values ranging from 0 to 55, are located in the spectral range 694-736 cm(-1). The collisional widths are obtained by fitting the spectral lines with a Voigt and a Rautian profile. The broadenings coefficients of (35)ClCN-N(2) have also been calculated from a semiclassical theory involving the atom-atom Lennard-Jones model for the intermolecular potential in addition to electrostatic interaction. Copyright 2000 Academic Press.     

Theoretical Study of the Collision-Induced Double Transition CO(2) (nu(3) = 1) + N(2) (nu(1) = 1) <-- CO(2) (nu(3) = 0) + N(2) (nu(1) = 0) at 296 K

A procedure is presented for the calculation of the double vibrational collision-induced absorption CO(2) (nu(3) = 1) + N(2) (nu(1) = 1) <-- CO(2) (nu(3) = 0) + N(2) (nu(1) = 0) on the basis of quantum lineshapes computed using an isotropic potential and dipole-induced dipole functions. The linestrengths and energies of the vibration-rotation transitions are treated explicitly for N(2), utilizing the HITRAN database for CO(2). The theoretical absorption profile is compared to recent experimental results. By narrowing the width of the individual lines contributing to the overall absorption profile relative to their values determined for N(2)-N(2) collision-induced absorption, excellent agreement between theory and experiment is obtained. Copyright 2000 Academic Press.     

Rovibrational Intensities of the (00(0)3) <-- (10(0)0) Dyad Absorption Bands of (12)C(16)O(2)

Absolute line intensities of (12)C(16)O(2) are experimentally measured for the first time for the (00(0)3)(I) <-- (10(0)0)(II) band at 5687.17 cm(-1) and the (00(0)3)(I) <-- (10(0)0)(I) band at 5584.39 cm(-1). The spectra were obtained using a Bomem DA8 Fourier transform spectrometer and a 25-m base-path White cell at NASA-Ames Research Center. The rotationless bandstrengths at a temperature of 296 K and the Herman-Wallis parameters are S(0)(vib) = 6.68(30) x 10(-25) cm(-1)/(molecule/cm(2)); A(1) = 1.4(9) x 10(-4), and A(2) = -1.1(5) x 10(-5) for the (00(0)3)(I) <-- (10(0)0)(II) band and S(0)(vib) = 6.07(22) x 10(-25) cm(-1)/(molecule/cm(2)); A(1) = 5.2(1.5) x 10(-4) and A(2) = -4.0(7) x 10(-5) for the (00(0)3)(I) <-- (10(0)0)(I) band.     

Torsional Splitting in the nu(5) Fundamental Infrared Band of CH(3)CD(3) and (13)CH(3)CD(3)

The nu(5) fundamental (C-C stretching) of CH(3)CD(3) shows a resolved torsional structure, caused by perturbations due mainly to the linear dependence of the torsional potential barrier on the normal coordinate Q(5). We were able to analyze this structure and to assign vibration-rotation transition wavenumbers for all five torsional components, classified according to the symmetry species of the G(18)((3)) extended molecular group. The torsional splitting pattern is qualitatively similar to that of a nondegenerate vibrational state with an even number of excited torsional quanta v(6). Explorative calculations show that the main perturber system should consist of the torsional components of the vibrational ground state correlating with v(6)=4 in the high barrier limit. The strength of the perturbation on the E(r0) torsional components of nu(5) increases rapidly with r, the E(40) component being the most affected. The observed transition wavenumbers can be reasonably fitted by a simplified model containing independent effective vibration-rotation parameters for the five different torsional components of nu(5), for both CH(3)CD(3) and (13)CH(3)CD(3). The trend of the determined values of the effective vibrational wavenumbers and rotational parameters over the torsional components supports the proposed vibration-torsion interaction mechanism, responsible for the observed torsional splittings. A strong anomaly observed in the rotational intensity distribution of nu(5) is discussed. Copyright 2001 Academic Press.     

Absolute Intensities of the nu(1) and nu(3) Bands of (16)O(3)

New experimental data on the nu(1) and nu(3) bands of (16)O(3) improving the value of absolute line intensities have been obtained. The intensities of 295 lines have been measured with an average accuracy between 2.5% and 3% and the rotational expansion of the transition moment operators for the nu(1) and nu(3) bands has been deduced. Finally, a complete listing of line intensities has been computed with an intensity cutoff of 1x10(-25) cm(-1)/molecule cm(-2). Copyright 2001 Academic Press.     

Giant enhancement of the thermal Hall conductivity kappa(xy) in the superconductor YBa(2)Cu(3)O(7)

In high-purity YBa(2)Cu(3)O(7), the (weak-field) thermal Hall conductivity kappa(xy) is observed to increase a thousand-fold between 90 and 30 K. The inferred quasiparticle lifetime tau increases a hundred-fold starting below 90 K, in disagreement with a recent photoemission experiment. We show that kappa(xy) exhibits a specific scaling behavior below approximately 30 K. This scaling may bear on the issue of whether Landau quantization of the quasiparticle states occurs.     

The v(1)+v(3) Bands of the (16)O(17)O(16)O and (16)O(16)O(17)O Isotopomers of Ozone

Using 0.002 cm(-1) resolution Fourier transform absorption spectra of an (17)O enriched ozone sample, an extensive analysis of the v(1)+v(3) bands of the (16)O(17)O(16)O and (16)O(16)O(17)O isotopomers of ozone has been performed for the first time. The experimental rotational levels of the (101) vibrational states were satisfactorily reproduced using a Hamiltonian matrix that takes into account the observed rovibrational resonances. More precisely, for (16)O(17)O(16)O, as for the other C(2v)-type ozone isotopomers, it was necessary to account for the Coriolis type resonances linking the (101) rotational levels with the levels of the (200) and (002) vibrational states and the Darling-Dennison interaction coupling the levels of (200) with those of (002). For the C(s)-type isotopomer, namely (16)O(16)O(17)O, as for (16)O(16)O(18)O and (16)O(18)O(18)O, it proved necessary to also account for an additional DeltaK(a)&equals+/-2 resonance involving the rotational levels from (101) and (002) (J.-M. Flaud and R. Bacis, Spectrochimica Acta Part A 54, 3-16 (1998)). Using a Hamiltonian matrix which takes these resonances explicitly into account, precise vibrational energies and rotational and coupling constants were deduced, leading to the following band centers: v(0)(v(1)+v(3))=2078.3496 cm(-1) for (16)O(17)O(16)O and v(0)(v(1)+v(3))=2098.8631 cm(-1) for (16)O(16)O(17)O. Copyright 2001 Academic Press.