一种在二步相移数字全息中实现准确相移的方法

相移数字全息中的相移准确性决定了重建结果的质量,本文提出了在二步相移数字全息中.实现准确相移的方法.该方法使用数字电压源开环控制普通的压电陶瓷微位移器,通过连续以微小的间隔来改变施加在压电陶瓷微位移器上的电压,可以获得一系列对应于不同相移角的全息图像,进而可以利用这些全息图像重建出来物光波在全息面上的强度分布.实验中采...     

关于超音速多普勒效应的思考

超音速多普勒效应由于其不便于测量,基本停留在纯理论分析阶段,导致人们产生了一些错误的观点.本文通过逻辑分析、计算机软件模拟等手段,对超音速多普勒效应的音频时序进行了分析研究,找出了错误观点产生的原因,作出了相应的解释,并对错误观点进行了修正,提供了解决方案.     

一种离轴计算全息图在凹非球面检测中的应用

为了精确检测大口径非球面面型质量,将CGH作为补偿器应用于凹非球面的离轴全息检测系统中.根据计算全息图的离轴全息检测系统检测凹非球面的基本原理,分析了离轴CGH的计算、制作过程,实现了对口径为150 mm,近轴半径为1499.7 mm,非球面系数为-1的凹非球面镜的检测.实验结果与轮廓仪检测结果吻合得很好.     

Shift‐invert Lanczos method for the symmetric positive semidefinite Toeplitz matrix exponential

The Lanczos method with shift‐invert technique is exploited to approximate the symmetric positive semidefinite Toeplitz matrix exponential. The complexity is lowered by the Gohberg–Semencul formula and the fast Fourier transform. Application to the numerical solution of an integral equation is studied. Numerical experiments are carried out to demonstrate the effectiveness of the proposed method. Copyright © 2010 John Wiley & Sons, Ltd.     

Two-body threshold spectral analysis, the critical case

We study in dimension d?2 low-energy spectral and scattering asymptotics for two-body d-dimensional Schrödinger operators with a radially symmetric potential falling off like −γr−2, γ>0. We consider angular momentum sectors, labelled by l=0,1,…, for which γ>²(l+d/2−1). In each such sector the reduced Schrödinger operator has infinitely many negative eigenvalues accumulating at zero. We show that the resolvent has a non-trivial oscillatory behaviour as the spectral parameter approaches zero in cones bounded away from the negative half-axis, and we derive an asymptotic formula for the phase shift.     

有限重数的Dirichlet移位

In this paper, we show that a multiplication operator on the Dirichlet space D is unitarily equivalent to Dirichlet shift of multiplicity n ＋ 1 （n ≥ 0） if and only if its symbol is c zn＋1 for some constant c. The result is very different from the cases of both the Bergman space and the Hardy space.     

Red top-emitting organic light-emitting device with improved efficiency and saturated color

In this work, characteristics of microcavity top-emitting red organic light-emitting device (TEROLED) having metallic electrodes had been examined. The TEOLED shows the higher efficiency in comparison with that of the bottom OLED. However, color variation with the increasing view angles is also observed. For the purpose of diminishing the blue-shift of resonant wavelength (RW) in the device with increasing view angle, the effect of out-coupling layer on the emission properties of the TEOLED is discussed in detail. Finally, the out-coupling layer was introduced in theory without sacrificing the efficiency through precise optical simulation.     

INS/Doppler组合导航中安装偏角的在线估计

INS和Doppler在载机上安装时存在安装偏角,会对组合导航精度产生影响.为此,提出了一种新的INS/Doppler组合导航算法,将标度因数和安装偏角作为状态变量进行估计.在分析Doppler输出误差模型的基础上,详细推导了组合导航算法模型,并进行了仿真.仿真结果表明,在载机正常飞行并适当机动的情况下,该组合导航算法能够准确对标度因数和安装偏角进行估计,标度因数的估计精度为0.4‰,安装偏角的估计精度为0.1′-0.3′,从而提高了导航精度.     

一种基于分子内质子转移发色团的硫化氢荧光探针的合成及其生物成像研究

硫化氢在许多生理过程中扮演十分重要的角色,因此检测和成像生物体内的硫化氢具有十分重要的意义。该研究成功制备了一种基于分子内质子转移发色团的硫化氢荧光探针(DHCD)。在PBS-DMSO(磷酸盐-二甲基亚砜,99∶1,体积比,pH 7.45)缓冲溶液中,DHCD的荧光强度与NaHS的浓度在0～10μmol/L范围内呈现良好的线性关系,检出限为0.84μmol/L。该探针对硫化氢的响应具有较大的Stokes位移(～165 nm)、高灵敏度和选择性。此外,合成的探针拥有良好的细胞渗透性和低的毒性,可用于HeLa细胞中硫化氢的荧光成像,在生物分析中具有潜在应用价值。     

Dual Metal Active Sites in an Ir1/FeOx Single‐Atom Catalyst: A Redox Mechanism for the Water‐Gas Shift Reaction

Herein, we report a theoretical and experimental study of the water‐gas shift (WGS) reaction on Ir₁/FeO_x single‐atom catalysts. Water dissociates to OH* on the Ir₁ single atom and H* on the first‐neighbour O atom bonded with a Fe site. The adsorbed CO on Ir₁ reacts with another adjacent O atom to produce CO₂, yielding an oxygen vacancy (O_vac). Then, the formation of H₂ becomes feasible due to migration of H from adsorbed OH* toward Ir₁ and its subsequent reaction with another H*. The interaction of Ir₁ and the second‐neighbouring Fe species demonstrates a new WGS pathway featured by electron transfer at the active site from Fe³⁺?O???Ir²⁺?O_vac to Fe²⁺?O_vac???Ir³⁺?O with the involvement of O_vac. The redox mechanism for WGS reaction through a dual metal active site (DMAS) is different from the conventional associative mechanism with the formation of formate or carboxyl intermediates. The proposed new reaction mechanism is corroborated by the experimental results with Ir₁/FeO_x for sequential production of CO₂ and H₂.