Pole placement controllers for linear time-delay systems with commensurate point delays

This paper investigates the exact and approximate spectrum assignment properties associated with realizable output-feedback pole-placement type controllers for single-input single-output linear time-invariant time-delay systems with commensurate point delays. The controller synthesis problem is discussed through the solvability of a set of coupled diophantine equations of polynomials. An extra complexity is incorporated to the above design to cancel extra unsuitable dynamics being generated when solving the above diophantine equations. Thus, the complete controller tracks any arbitrary prefixed (either finite or delaydependent) closed-loop spectrum. However, if the controller is simplified by deleting the above mentioned extra complexity, then the robust stability and approximated spectrum assignment are still achievable for a certain sufficiently small amount of delayed dynamics. Finally, the approximate spectrum assignment and robust stability problems are revisited under plant disturbances if the nominal controller is maintained. In the current approach, the finite spectrum assignment is only considered as a particular case to the designer‘s choice of a (delay-dependent) arbitrary spectrum assignment objective.     

Surface morphologies of anthracene single crystals grown from vapor phase

The morphologies and lattice structures of anthracene single crystals grown from the vapor phase were investigated using optical microscopy, phase contrast microscopy, atomic force microscopy (AFM), and X-ray diffraction analysis. Common morphologies with hexagonal large planes were observed irrespective of crystal size. The observation of certain surface morphologies with a phase contrast microscopy revealed that the spiral steps originated from screw dislocations present on the (0 0 1) planes. Moreover, the center and edge of the (0 0 1) planes had large curvatures, similar to hills. Resultantly, quarter-monolayer (ML) steps were observed on the large and flat planes between both hills.     

春季南黄海表层海水中二氧化碳的分布特征及其影响因素

根据2007年4月南黄海区块(SYS)表层海水中二氧化碳分压(pCO₂)的连续走航数据,结合水温(T)、盐度(S)、叶绿素 (Chla)以及pH的同步观测资料,对该海域pCO₂分布特征及其主要影响因素进行了初步探讨。分析结果表明：春季南黄海pCO₂的范围在365.2~734.9 μatm之间,平均值为548.0 μatm;最高值出现在121.5°E,33.4°N海域,最低值出现在123°E,32.3°N海域。受海水中物理、化学和生物因素的综合影响,pCO₂的分布存在较大的不均匀性,总体上表现为西部高于东部,中间高于南北两边;在苏北浅滩和鲁南海区,pCO₂与水温的变化呈正相关关系,与盐度的大小呈明显的负相关关系,而在长江入海口变化趋势则相反;此外,在整个调查海区pCO₂与叶绿素、pH基本上呈负相关关系。研究将两台检测器串联进行互校,同时利用二氧化碳标准气体对其中一台仪器进行全程校准,可连续不间断观测海水和大气中的pCO₂。该方法操作简单,获得的数据准确可靠,可为节能减排能力建设提供技术支持。     

航空偏振遥感数据反演陆地上空气溶胶光学厚度

在陆地上空气溶胶遥感中,地表多样性会导致地表反射率计算误差增加,降低地气解耦精度,进而影响气溶胶反演精度。多角度、多光谱和偏振观测数据的引入有利于解决地气解耦精度和气溶胶参数的提取精度受限的问题。基于多角度偏振辐射计(AMPR)航空多光谱遥感数据,结合气溶胶散射和地表偏振反射规律,提出了在1 640 nm波段对AMPR观测偏振反射率进行连续大气辐射校正,实现地气解耦的方法。在此基础上,构建了陆地上空气溶胶偏振反演算法。运算过程中使用665和865 nm波段观测数据进行气溶胶参数提取,使用1 640 nm波段观测数据结合提取的气溶胶参数进行大气偏振辐射校正,重新获取地表偏振反射率。在反演过程中引入迭代,逐步逼近大气与地表真实辐射值,实现地气解耦,并利用查找表的方法实现气溶胶光学厚度反演。通过AMPR在京津唐地区5个架次的航空观测实验数据对反演算法进行了验证,结果与地基CE318观测数据一致性较好,在气溶胶光学厚度小于0.5的情况下,反演平均误差为约0.03。     

基于集合卡尔曼变换的东中国海声学 敏感区判定方法*

为改善海洋与水声环境预报质量,针对常规观测成本高、资料利用率低等问题,将适应性观测方法应用于海洋声学领域。结合海洋-声学耦合模式与集合卡尔曼转换敏感区诊断方法,以东中国海宫古海峡北部区域为验证区,计算并分析不同条件下海洋环境敏感区与声学敏感区分布,通过观测系统模拟试验验证适应性观测对验证区预报的提升效果。结果表明,两种敏感区位置随时间间隔增加均向验证区上游移动,海洋环境敏感区相比于声学敏感区分布更为集中,且平移特征更明显;对海洋环境敏感区和声学敏感区添加适应性观测均能提升海洋与水声环境的预报质量,提升效果随时间间隔增加而减小,在某种类型敏感区的适应性观测对相对应参数的预报质量提升效果优于对其他类型敏感区进行观测的效果。     

一类不确定延迟神经网络的自适应投影同步

研究了一类参数不确定的延迟神经网络的投影同步,基于Lyapunov稳定性理论,设计了一种新型的自适应控制方法.该方法能同时实现一类参数不确定延迟神经网络的参数识别和投影同步.数值模拟证明了该方法的有效性. 关键词： 延迟神经网络 Lyapunov稳定性理论 参数识别 投影同步     

激光靶心冲击波观测镜折反式光学系统设计

设计了一种激光靶心冲击波观测镜的光学系统.用反射式光学系统代替折射式光学系统,解决了普通玻璃在200 nm端透过率较低的问题.反射镜不引入色差,有利于系统在200~800 nm谱段消色差.为消系统轴外像差,反射系统选型为对称式.反射镜全部采用球面镜,为消反射镜以及平板玻璃窗带入的球差,引入校正镜(材料JGS1),在满足要求的条件下,控制折射镜的厚度,使系统色差满足瑞利判据的色差允差,得到了良好的成像质量.     

Intermolecular Vibrational Relaxation in Mixtures of Excited Benzophenone and Anthraquinone Molecules with Water Vapor

The intermolecular vibrational energy transfer from triplet molecules of benzophenone and anthraquinone to H₂O molecules has been investigated. To determine the rates of establishment of vibrational (V-V) and thermal (V-T) equilibrium in a vibrational quasi-continuum of mixed singlet-triplet levels, the dependences of the decay rates and intensities of the fast and slow components of delayed fluorescence on the H₂O vapor pressure have been investigated. For V-V relaxation, the efficiencies ₁ and the mean energies E transferred per collision in mixtures with H₂O and other polyatomic foreign gases have been compared. It has been established that the efficiencies ₁ for quasi-resonant vibrational energy transfer (V-V) from benzophenone and anthraquinone to H₂O are an order of magnitude lower than the gas-kinetic ones and lower than those obtained under the same experimental conditions for such foreign gases as C₅H₁₂, SF₆, and CCl₄, and decrease with increasing temperature in the 433–513 K range. It has been concluded that the mechanism of V-V relaxation in mixtures with H₂O are determined by long-range attractive forces. In mixtures with H₂O, no acceleration of V-T relaxation due to the formation of hydrogen bonds has been revealed. The low-efficiency thermalization process (V-T relaxation) is controlled by short-range repulsive forces, and the differences between the intensities ₂ for mixtures of benzophenone and anthraquinone with H₂O and other polyatomic gases are determined by the change in the reduced mass of interacting molecules.     

Mechanochromic Delayed Fluorescence Switching in Propeller-Shaped Carbazole–Isophthalonitrile Luminogens with Stimuli-Responsive Intramolecular Charge-Transfer Excited States

Herein, the universal design of high-efficiency stimuli-responsive luminous materials endowed with mechanochromic luminescence (MCL) and thermally activated delayed fluorescence (TADF) functions is reported. The origin of the unique stimuli-triggered TADF switching for a series of carbazole–isophthalonitrile-based donor–acceptor (D–A) luminogens is demonstrated based on systematic photophysical and X-ray analysis, coupled with theoretical calculations. It was revealed that a tiny alteration of the intramolecular D–A twisting in the excited-state structures governed by the solid morphologies is responsible for this dynamic TADF switching behavior. This concept is applicable to the fabrication of bicolor emissive organic light-emitting diodes using a single TADF emitter.     

Molecular Engineering of Isomeric Benzofurocarbazole Donors for Photophysical Management of Thermally Activated Delayed Fluorescence Emitters

Benzofurocarbazole moieties are commonly used donor structures in the design of thermally activated delayed fluorescence (TADF) emitters. However, only 5 H-benzofuro[3,2-c]carbazole (34BFCz) has been reported and, to the best of our knowledge, no other benzofurocarbazole derivatives have been covered in the literature. In the present study, two further benzofurocarbazole moieties, 12 H-benzofuro[3,2-a]carbazole (12BFCz) and 7 H-benzofuro[2,3-b]carbazole (23BFCz), have been synthesized to investigate the effect of the donor structure on the photophysics and device parameters of TADF emitters. Two benzofurocarbazole-derived TADF emitters, 12-(2-(4,6-diphenyl-1,3,5-triazin-2-yl)phenyl)-12 H-benzofuro[3,2-a]carbazole (o12BFCzTrz) and 7-(2-(4,6-diphenyl-1,3,5-triazin-2-yl)phenyl)-7 H-benzofuro[2,3-b]carbazole (o23BFCzTrz), have been compared with 5-(2-(4,6-diphenyl-1,3,5-triazin-2-yl)phenyl)-5 H-benzofuro[3,2-c]carbazole (oBFCzTrz). The benzofurocarbazole donor structure governs the TADF characteristics, such as charge-transfer property and emission color. The 12BFCz donor has proved to be effective in blue-shifting the emission color, and 34BFCz has proven useful for improving the external quantum efficiency (EQE). The 12BFCz-derived o12BFCzTrz showed blue-shifted color coordinates of (0.159, 0.288), compared to (0.178, 0388) for o23BFCzTrz and (0.169, 0.341) for oBFCzTrz. The 34BFCz-derived oBFCzTrz exhibited an EQE of 22.9 %, compared to 19.2 % for o12BFCzTrz and 21.1 % for o23BFCzTrz.