Plasmonic waveplate: incident polarization modulation

Abstract We demonstrate that the rectangular nanohole arrays perforated in a 100 nm gold film can be used to tune the polarization direction of the transmitted light with maximum rotation angle of about 30 degrees. Theoretical analysis with the three-dimensional finite-difference time-domain simulations indicates that this phenomenon is attributed to the excitation of the surface plasmon wave on the gold film surface and the resonance of localized surface plasmon in the hole. With multiple plasmon resonances, the plasmonic waveplate can realize multi-wavelength polarization modulation. Our results may be useful to understanding the physical mechanism of enhanced plasmon mediated transmission and potential applications in plasmonic optical components.     

基于链状SemSn(2≤m+n≤4)小分子的硒硫碳复合正极材料的制备及其电化学性能

将Se固溶复合到链状小硫分子S_2~4中,利用超微孔碳(UMC)的空间限域效应,在UMC中成功构建了链状Se_mS_n(2≤m+n≤4)小分子,并用作锂硫(Li-S)电池正极材料。与链状S_2~4小分子相比,改性后的Se_mS_n(2≤m+n≤4)小分子电导率更高,锂化能更低,放电锂化过程更容易。所制得的UMC/Se_mS_n(2≤m+n≤4)复合正极材料的放电过程为一步固相转化反应,从而有效抑制了活性物质的穿梭流失。与UMC/S_2~4复合正极材料相比,UMC/Se_mS_n(2≤m+n≤4)复合正极材料的电荷传递阻抗更小,放电比容量更高。因此,UMC/Se_mS_n-40(2≤m+n≤4,w_SeS2∶w_UMC=4∶6)复合正极材料在0.1C时循环100次后,比容量依然保持有844 mAh·g^-1;在0.5C下长时间循环500次时,每次循环容量损失仅约为0.07%,表现出优异的循环稳定性。     

Fe-Pb合金凝固多相体系内偏析形成过程的三维数值模拟

基于Eulerian-Eulerian方法和流体体积技术,建立了三维多相流体动力学凝固模型,并将其与质量、动量、溶质和热焓守恒方程相耦合,对Fe-Pb合金侧向凝固过程进行了数值模拟.首先,分析了分布面积二次梯度((SPb))和浓度二次梯度((CPb))对偏析模式的影响,结果表明:液、气两相的流动相变使偏析模式表现为上端X形下端V形,X偏析由气相相变驱动力和多取向相变作用下的"散射"形成;ttc时,随(SPb)和(CPb)曲线降低,X偏析的下偏析角增大,上偏析角和V偏析角减小,Pb收得率增大,有利于获得含量稳定弥散的凝固组织.此外,还研究了液、气两相交互流动下通道偏析的形成机理,结果表明:通道偏析仅存在于流动-相变交互作用(ul·cl和ug·cg)为负值的区域,该区域的流动扰动抑制合金的局部凝固,促进偏析通道生长;流动-相变交互作用负值越小,偏析通道持续增长越稳定.模拟结果与实验结果相符合,验证了模型的准确性.     

Automated human frontal lobe identification in MR images based on fuzzy-logic encoded expert anatomic knowledge

Identification of human brain structures in MR images comprises an area of increasing interest, which also presents numerous methodological challenges. Here we describe a new knowledge-based automated method designed to identify several major brain sulci and then to define the frontal lobes by using the identified sulci as landmarks. To identify brain sulci, sulcal images were generated by morphologic operations and then separated into different components based on connectivity analysis. Subsequently, the individual anatomic features were evaluated by using fuzzy membership functions. The crisp decisions, i.e., the identification of sulci, were made by taking the maximum of the summation of all the membership functions. The identification was designed in a hierarchical order. The longitudinal fissure was extracted first. The left and right central sulci were then identified based on the left and right hemispheres. Next, the lateral sulci were identified based on the central sulci and hemispheres. Finally, the left and right frontal lobes were defined from the two hemispheres. The method was evaluated by visual inspection, comparison with manual segmentation, and comparison with manually volumetric results in references. The average Jaccard similarities of left and right frontal lobes between the automated and manual segmentation were 0.89 and 0.91, respectively. The average Kappa indices of left and right frontal lobes between the automated and manual segmentation were 0.94 and 0.95, respectively. These results show relatively high accuracy of using this novel method for human frontal lobe identification and segmentation.     

Spectra and structure of silicon containing compounds. XXXII. Raman and infrared spectra,conformational stability,vibrational assignment and ab initio calculations of n-propylsilane-d0 and Si-d3

The infrared (3100-40 cm(-1)) and Raman (3100-20 cm(-1)) spectra of gaseous and solid n-propylsilane, CH(3)CH(2)CH(2)SiH(3) and the Si-d(3) isotopomer, CH(3)CH(2)CH(2)SiD(3), have been recorded. Additionally, the Raman spectra of the liquids have been recorded and qualitative depolarization values obtained. Both the anti and gauche conformers have been identified in the fluid phases but only the anti conformer remains in the solid. Variable temperature (-105 to -150 degrees C) studies of the infrared spectra of n-propylsilane dissolved in liquid krypton have been recorded and the enthalpy difference has been determined to be 220+/-22 cm(-1) (2.63+/-0.26 kJ mol(-1)) with the anti conformer the more stable form. A similar value of 234+/-23 cm(-1) (2.80+/-0.28 kJ mol(-1)) was obtained for deltaH for the Si-d(3) isotopomer. At ambient temperature it is estimated that there is 30+/-2% of the gauche conformer present. The potential function governing the conformation interchange has been estimated from the far infrared spectral data, the enthalpy difference, and the dihedral angle of the gauche conformer, which is compared to the one predicted from ab initio MP2/6-31G(d) calculations. The barriers to conformational interchange are: 942, 970 and 716 cm(-1) for the anti to gauche, gauche to gauche, and gauche to anti conformers, respectively. Relatively complete vibrational assignments are proposed for both the n-propylsilane-d(0) and Si-d(3) molecules based on the relative infrared and Raman spectral intensities, infrared band contours, depolarization ratios, and normal coordinate calculations. The geometrical parameters, harmonic force constants, vibrational frequencies, infrared intensities, Raman activities and depolarization ratios, and energy differences have been obtained for the anti and gauche conformers from ab initio MP2/6-31G(d) calculations. Structural parameters and energy differences have also been obtained utilizing the larger 6-311 + G(d,p) and 6-311 + G(2d,2p) basis sets. From the isolated Si-H stretching frequency from the Si-d(2) isotopomer the r(0) distances of 1.484 and 1.485 A have been determined for the SiH(s) and SiH(a) bonds, respectively, for the anti conformer, and 1.486 A for the SiH bond for the gauche conformer. Utilizing previously reported microwave rotational constants for the anti conformer and the determined SiH distances along with ab initio predicted parameters 'adjusted r(0)' parameters have been obtained for the anti conformer. The results are discussed and compared to those obtained for some similar molecules.     

基于半导体量子点的片上手性纳米光子器件

手性量子光学在量子信息技术研究领域中受到了广泛的关注,其主要研究光在微纳结构中自旋依赖的手性耦合及传输行为。利用手性光与物质的相互作用可以增强光子与量子发射器的耦合,赋予纳米光子器件新的功能和应用,从而推动手性量子光学在量子信息领域中的大规模应用。主要对基于半导体量子点的片上手性纳米光子器件进行了综述,重点讨论了半导体量子点的光学性质和手性光与物质相互作用的物理机制,在此基础上对近年来应用手性耦合原理实现的多功能手性光子器件进行了总结,并对手性量子光学的未来应用场景进行了展望。     

基于组态软件和多串口通讯的真空检漏监测系统设计与开发

许 婕,蔡立君,卢 勇,罗 山,张 龙,田培红     

基于UMAP辅助的模糊C聚类方法进行太赫兹光谱识别

太赫兹(THz)具有低能性、瞬态性、波谱分析能力强的优点,在物质鉴别方面具有广阔的应用前景。现有的基于THz的物质鉴别方法,虽然取得了一定的效果,但是存在容易陷入局部最优的问题,从而导致识别精度不高。均匀流形逼近与投影(UMAP)作为一种非线性降维方法,其假设数据均匀分布在黎曼流形上,可以对具有模糊拓扑结构的流形进行建模。UMAP降维的过程是通过最小化两个拓扑表示之间的交叉熵,从而实现低维空间中数据表示的布局优化。传统的模糊C聚类方法（FCM）在聚类时,初始聚类中心往往随机给定,当初始聚类中心选择不恰当时,容易导致错误的聚类。为此,提出一种基于UMAP辅助的模糊C聚类算法,首先运用UMAP对输入的THz样本矩阵进行降维;再根据类与类之间距离最大化的原则,选择合适的初始聚类中心;最后利用模糊C均值聚类的方法进行聚类。所提出的方法不仅能够解决聚类过程中类与类之间过度拥挤的现象,而且能够反映出类别间的距离信息以便于给样本选择合适的初始聚类中心。为了验证提出的聚类方法的可靠性,运用太赫兹时域光谱技术对鲁棉研28、鲁棉研29、鲁棉研36、中棉28四种不同类型的转基因棉花种子进行了探测,利用基于UMAP辅助的模糊C聚类算法对转基因棉花种子的吸光度光谱数据进行聚类分析,成功地将四种不同类型的转基因棉花种子区分开,得到了总正确率为0.983 3的聚类效果,说明提出的基于UMAP辅助的模糊C聚类算法在物质太赫兹光谱识别方面具有良好的应用前景。     

基于阻尼LSQR-LMBC的火焰三维温度场重建

光场相机可以解决辐射测温多相机系统光路复杂、同步触发难等问题,在辐射成像三维温度重建时有其独特优势. LSQR是求解基于大型稀疏矩阵最小二乘问题的经典算法,该算法用于重建三维温度场时对温度初值依赖较大,在信噪比较低的情况下重建精度不理想.本文提出阻尼LSQR-LMBC重建算法,通过在LSQR方法中添加阻尼正则化项,提高火焰三维温度场重建的抗噪性能,并结合LMBC算法,实现吸收系数和三维温度场同时求解.在数值模拟部分,随着信噪比逐渐降低,阻尼LSQR的重建效果比LSQR更加稳定,在信噪比达到13.86 d B时,重建精度大约提高30%.阻尼LSQR-LMBC的平均重建误差为6.63%.用丁烷火焰进行了实验,重建的丁烷火焰三维温度场分布符合辐射火焰燃烧的特征,和热电偶的测温数据结果进行对比,相对误差在6.8%左右.