同时实现OR及XOR逻辑运算的多功能计算全息光学元件

本文提出了一种在光学上同时实现两图像间的OR及XOR运算的方法,利用计算全息制成了同时进行上述两种基本逻辑运算的光学元件,并给出了实验结果。     

超短激光脉冲技术及其研究进展

首先阐述超短激光脉冲发展的几个历史阶段及其特点．并介绍了飞秒激光器的类型及飞秒脉冲的产生、放大与测量，最后介绍了飞秒激光技术的相关学科。     

飞秒激光诱导掺锰玻璃长磷光和光激励长磷光

报道了掺锰氟铝磷酸盐玻璃在聚焦的800nm飞秒激光作用后产生明显的黄绿色长磷光以及当长磷光完全衰减后，再用365nm的紫外光激发时，飞秒激光照射处的光激励长磷光现象。讨论了该现象产生的机理和在三维超高密度光贮存中的应用。     

一种新型的实验地震学光学模拟系统

介绍了一种新型的实验地震学光学模拟系统。它将实时全息技术与声发射源测定技术相结合应用于实验地震学研究 ,前者检测和记录试件内应力场及其变化 ,后者检测和记录微破裂所激发的超声波 ,借以确定试件内微破裂发生的时间、位置和强度。综合两种方法所获数据 ,从微破裂丛集成核过程与应力场之间的关系来寻求破裂形成、扩展的某些规律性。试验观察到一些极有研究价值的现象 ,特别是系统能将破裂的形成和扩展 ,从微破裂丛集成核直至整个试件碎裂的过程 ,以较高的分辨率记录下来 ,初步获得微破裂成核过程与应力场关系的某些规律性。     

实现CLOS变换网络与蝶形变换网络的光学方法

本文介绍了实现CLOS变换网络与蝶形变换网络的光学方法,它是通过利用计算全息原理制作的光学元件来完成的。给出了一维16个元素的CLOS变换和一维8个元素的蝶形变换的计算全息光学元件的制作方法,并给出了实验结果,整个实验光路简单,该方法亦可很方便地推广到其它光学互连网络。     

Electron holography and AFM studies on styrenic block copolymers and a high impact polystyrene

Many of the artifacts of conventional electron microscopy can be avoided if the unstained polymers are studied by electron holography and atomic force microscopy (AFM). Holograms of thin sections (50–70 nm) of organic block copolymers were recorded, and the corresponding phase images were reconstructed. In this way, typical structures such as lamellae and cylinders could be imaged without any staining. In addition, we successfully recorded holograms and performed Lorentz microscopy of an impact‐modified polystyrene (high‐impact polystyrene). The results were compared with the tapping mode AFM phase images. Electron holography and AFM have been demonstrated as suitable tools to image unstained heterogeneous polymers, leading to the understanding of their structure. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 1573–1583, 2005     

Correlative High‐Resolution Mapping of Strain and Charge Density in a Strained Piezoelectric Multilayer

A key to strain engineering of piezoelectric semiconductor devices is the quantitative assessment of the strain‐charge relationship. This is particularly demanding in current InGaN/GaN‐based light‐emitting diode (LED) designs as piezoelectric effects are known to degrade the device performance. Using the state‐of‐the‐art inline electron holography, we have obtained fully quantitative maps of the two‐dimensional strain tensor and total charge density in conventional blue LEDs and correlated these with sub‐nanometer spatial resolution. We show that the In_0.15Ga_0.85N quantum wells are compressively strained and elongated along the polar growth direction, exerting compressive stress/strain on the GaN quantum barriers. Interface sheet charges arising from a polarization gradient are obtained directly from the strain data and compared with the total charge density map, quantitatively verifying only 60% of the polarization charges are screened by electrons, leaving a substantial piezoelectric field in each In_0.15Ga_0.85N quantum well. The demonstrated capability of inline electron holography provides a technical breakthrough for future strain engineering of piezoelectric optoelectronic devices.     

反射式离轴数字全息再现像中的噪声抑制

为了抑制反射式离轴数字全息再现像中的零级像和散斑噪声对再现像的影响,利用高斯核函数在空域对数字全息图进行低通滤波,再用原数字全息图减去滤波后的低频信息来抑制零级像,采用非局部均值滤波来抑制散斑噪声。实验结果表明空域高斯核函数处理法能有效地抑制零级像,非局部均值滤波可以抑制散斑噪声但对部分细节的保持能力不强,改进后的非局部均值滤波在抑制散斑噪声的同时能很好地保护细节信息,提高了离轴数字全息再现像的质量。     

Design of a Microchannel‐Nanochannel‐Microchannel Array Based Nanoelectroporation System for Precise Gene Transfection

A micro/nano‐fabrication process of a nanochannel electroporation (NEP) array and its application for precise delivery of plasmid for non‐viral gene transfection is described. A dip‐combing device is optimized to produce DNA nanowires across a microridge array patterned on the polydimethylsiloxane (PDMS) surface with a yield up to 95%. Molecular imprinting based on a low viscosity resin, 1,4‐butanediol diacrylate (1,4‐BDDA), adopted to convert the microridge‐nanowire‐microridge array into a microchannel‐nanochannel‐microchannel (MNM) array. Secondary machining by femtosecond laser ablation is applied to shorten one side of microchannels from 3000 to 50 μm to facilitate cell loading and unloading. The biochip is then sealed in a packaging case with reservoirs and microfluidic channels to enable cell and plasmid loading, and to protect the biochip from leakage and contamination. The package case can be opened for cell unloading after NEP to allow for the follow‐up cell culture and analysis. These NEP cases can be placed in a spinning disc and up to ten discs can be piled together for spinning. The resulting centrifugal force can simultaneously manipulate hundreds or thousands of cells into microchannels of NEP arrays within 3 minutes. To demonstrate its application, a 13 kbp OSKM plasmid of induced pluripotent stem cell (iPSC) is injected into mouse embryonic fibroblasts cells (MEFCs). Fluorescence detection of transfected cells within the NEP biochips shows that the delivered dosage is high and much more uniform compared with similar gene transfection carried out by the conventional bulk electroporation (BEP) method.