共查询到20条相似文献,搜索用时 140 毫秒
1.
2.
3.
为实现浸没式光刻照明系统掩模面上高均匀照明性和不同照明模式,对照明系统中的光束传输系统进行了研究。浸没式光刻照明系统中的激光光束传输系统是光刻机中的重要组成部分,直接影响光刻机性能。针对浸没式光刻照明系统特点,提出了采用球面镜和柱面镜组合的光学结构,进行了激光准直扩束系统的光学设计与仿真分析。此外,对设计的准直扩束系统进行了公差分析,以保证在加工和装调完成后光束的发散角和口径均满足设计要求。最后,在系统完成的基础上对不同位置处的光斑尺寸进行测量。设计结果表明,系统能够满足光束在5~20 m传输光路范围内,不需要进行透镜间隔的调节,实现光斑大小和发散角满足设计要求,保证目标光束口径在(28.5±0.5)mm范围内,X方向发散角为1.2 mrad,Y方向发散角为1.84 mrad。通过分析发现,设计结果能够很好地满足指标的精度要求,具有重要的应用价值和实用意义。 相似文献
4.
硬X射线微聚焦及应用光束线站(BL15U1)是上海光源工程首批光束线站中.第一条进行调试的真空波荡器光束线站。2月6日下午.科研人员完成了调束前准备工作,晚18:00开始正式调束,随即在光束线荧光靶和丝扫描探测器上分别观测到波荡器辐射光斑和光电流,21:30分在实验站铍窗出口处的电离室上探测到波荡器辐射的5.4keY单色光(3次谐波),并扫描获得该能量下单色器摇摆曲线,实现了首轮调束目标。 相似文献
5.
通过实验研究了大气湍流信道下中轨道角动量(OAM)光束与高斯光束的传输性能,并将两种光束的传输性能进行对比。实验以加载调制信号的OAM光束以及高斯光束为传输载波,分别测量了在大气湍流信道下两种光束的光束展宽、指向偏差、功率抖动以及误码率。实验结果表明:在大气湍流信道中传输后,OAM光束相比高斯光束,光束展宽减少10.5%,功率抖动的方差下降0.13,指向偏差的散布圆直径减小30.4%,并且光束中心更集中于接收面中心;OAM光束载波系统的最低探测灵敏度达到?28.97 dBm,相比高斯光束提升2.5 dB。实验结果证明了在大气湍流信道传输中,OAM光束比高斯光束受到湍流的影响更小,并且随着湍流强度的增加,OAM光束恶化程度远小于高斯光束。实验的结论为大气湍流信道下自由空间激光通信的发展和应用提供了参考。 相似文献
6.
7.
通过数值仿真研究了高斯光束在贝塞尔晶格中的传输特性,贝塞尔晶格是在光折变晶体中通过光诱导产生的。在有晶格和无晶格的情况下,高斯光束的传输特性有很大差别。高斯光束在均匀介质中传输时会呈现出线性衍射和自聚焦现象,当晶体中存在晶格时,光束可以克服光在均匀介质中的衍射和自聚焦效应,在不同的初始输入条件下,高斯光束在传输的过程中会演变成一个环形孤子或者圆形孤子。 相似文献
8.
为了研究厄米-高斯光束在光折变饱和非线性介质中的传输特性,采用有限差分方法数值求解了光波演化方程,理论分析了厄米-高斯光束的传输特性。结果表明,1维1阶、2阶和3阶厄米-高斯光束在光折变非线性介质中传输时,在合适的非线性条件下,均可以形成呼吸模式的孤子;随着非线性的加大,厄米-高斯光束的光场分量之间的相互分离趋势将逐渐变弱,同时,每个光场分量的振幅起伏效应会更加明显;改变厄米-高斯光束的入射位置、入射角度对其传输特性没有影响;2维厄米-高斯光束的传输特性和1维情况是类似的。厄米-高斯光束的这些特性在光开关领域有一定的应用前景。 相似文献
9.
10.
空潜信道中基于多光束阵列的二维图案传输 总被引:1,自引:0,他引:1
提出了一种利用多光束阵列在复杂散射信道中进行二维图案传输的理论模型。与传统多光束传输方案思路不同,该模型有效利用信道的强散射特性,使各光束充分扩散,在接收面形成交迭区域,成像光学系统在该区域内接收光信号并恢复各发射光束的空间位置信息,完成二维图案信息在空潜信道中的多通道传输。视在参数的引入使光束原本在两个不同折射率介质中的传输简化为仅在一种介质中传输的简单问题。实验采用直径为15 mm的微透镜阵列以及长为12.65 m的海水、大气信道来模拟实际信道中的强散射作用,结果表明该模型具有较好的可行性。 相似文献
11.
12.
A soft X ray lithographic technique capable of contactless replication of submicrometre linewidth planar-device patterns is described. Special soft X ray exposure masks have been developed for the 4?14 ? wavelength region. Elastic-surface-wave-transducer patterns with 1.3 ?m electrode spacings were fabricated onto such masks using electron-beam techniques, and were successfully replicated. 相似文献
13.
Mesostructured Arrays of Nanometer‐spaced Gold Nanoparticles for Ultrahigh Number Density of SERS Hot Spots 下载免费PDF全文
Ying‐Huang Lai Shiaw‐Woei Chen Michitoshi Hayashi Ying‐Jen Shiu Chiao‐Cheng Huang Wei‐Tsung Chuang Chun‐Jen Su Hu‐Cin Jeng Jhe‐Wei Chang Yao‐Chang Lee An‐Chung Su Chung‐Yuan Mou U‐Ser Jeng 《Advanced functional materials》2014,24(17):2544-2552
A novel one‐trough synthesis via an air‐water interface is demonstrated to provide hexagonally packed arrays of densely spaced metallic nanoparticles (NPs). In the synthesis, a mesostructured polyoxometalate (POM)‐silicatropic template (PSS) is first self‐assembled at the air‐water interface; upon UV irradiation, anion exchange cycles enable the free‐floating PSS film to continuously uptake gold precursors from the solution subphase for diffusion‐controlled and POM‐site‐directed photoreduction inside the silica channels. NPs ≈ 2 nm can hence be homogeneously formed inside the silica‐surfactant channels until saturation. As revealed via X‐ray diffraction, small‐angle X‐ray scattering (SAXS), grazing incidence SAXS, and transmission electron microscopy, the Au NPs directed by the PSS template are arrayed into a 2D hexagonal lattice with inter‐channel spacing of 3.2 nm and a mean along‐channel NP spacing of 2.8 nm. This corresponds to an ultra‐high number density (≈1019 NPs cm?3) of narrowly spaced Au NPs in the Au‐NP@PSS composite, leading to 3D densely deployed hot‐spots along and across the mesostructured POM‐silica channels for surface‐enhanced Raman scattering (SERS). Consequently, the Au‐NP@PSS composite exhibits prominent SERS with 4‐mercaptobenzoic acid (4‐MBA) adsorbed onto Au NPs. The best 4‐MBA detection limit is 5 nm , with corresponding SERS enhancement factors above 108. 相似文献
14.
用准分子激光扫描原位淀积法制备了极薄膜BIT/p-Si(100)和PZT/p-Si(100),借助于X-射线衍射(XRD)和扫描电镜(SEM)研究了薄膜的显微结构,并对这两种极薄铁电薄膜Au/BIT/p-Si(100)和Au/PZT/p-Si(100)的J-V曲线温度特性进行了拟合分析讨论。模拟分析结果表明,在负温区,电流密度J对温度T有较强的依赖关系,但与通常欧姆电流温度关系不同。而在正温区,服从J=KV^2关系,ε和SCLC电流密度J则与温度T无关。 相似文献
15.
Yu Fan Wenzhi Tu Mingwu Shen Xuming Chen Yuesheng Ning Junjun Li Tingfeng Chen Han Wang Fangfang Yin Yong Liu Xiangyang Shi 《Advanced functional materials》2020,30(13)
The efficacy of radiation therapy (RT) is often limited by the poor response of hypoxia inside most solid tumors. The development of a theranostic nanoplatform for precision‐imaging‐guided sensitized RT for tumor hypoxia is still challenging. Herein, the creation of hypoxia‐targeted dendrimer‐entrapped gold nanoparticles complexed with gadolinium(III) (Gd‐Au DENPs‐Nit) for dual‐mode CT/MR imaging and sensitized RT of hypoxic tumors is reported. In this work, generation 5 poly(amidoamine) dendrimers are partially conjugated with Gd(III) chelator, entrapped with Au nanoparticles, and conjugated with hypoxia‐targeting agent nitroimidazole via a polyethylene glycol linker, and ending with chelation of Gd(III) and conversion of their leftover amine termini to acetamides. The designed dendrimer‐based nanohybrids with 3.2 nm Au cores exhibit an excellent X‐ray attenuation effect, acceptable r1 relaxivity (1.32 mM?1 s?1), and enhanced cellular uptake in hypoxic cancer cells, affording efficient dual‐mode CT/MR imaging of tumor hypoxia. Under X‐ray irradiation, the Gd‐Au DENPs‐Nit nanohybrids can produce reactive oxygen species, promote DNA damage, and prevent DNA repair, facilitating sensitized RT of hypoxic cancer cells in vitro and tumor hypoxia in vivo. The developed hypoxia‐targeted dendrimer‐based nanohybrids may be employed as both contrast agents and nanosensitizers for precision tumor hypoxia imaging and sensitized tumor RT. 相似文献
16.
17.
Alan K. Mo Victoria L. Brown Brandon K. Rugg Thomas C. DeVore Harry M. Meyer Xiaofeng Hu W. Christopher Hughes Brian H. Augustine 《Advanced functional materials》2013,23(11):1431-1439
The adhesion of vapor deposited Au and Pt thin films onto poly(methyl methacrylate) (PMMA) substrates can be significantly enhanced by either spin‐casting or vapor‐exposure to hydrohalocarbon solvents prior to metal deposition. X‐ray photoelectron spectroscopy (XPS) and evolved gas analysis Fourier transform infrared spectroscopy detect residual halogenated solvent at the PMMA surface which chemically activates the surface. Density functional theory (DFT) calculations show that the solvent molecules form a Lewis acid‐base adduct with the ester oxygens in PMMA. DFT predicts that the deposited metal atom (M) inserts into the C–halogen (X) bond on either CHCl3 or CHBr3 to form a O–M–X interaction. This is consistent with M–X bonding observed in high resolution XPS. A model is proposed in which the bond energy of the C–X bond of the solvent must be weak enough so that it can be cleaved by the metal atom to form a M–X bond. A negative control of PMMA exposed to CHF3 is shown to have no effect on Au or Pt adhesion since the bond dissociation energy of the C–F bond is stronger than the C–Cl and C–Br bond energy compared to the metal halide bond energies. 相似文献
18.
Z. Zhong J. Lin S.‐P. Teh J. Teo F. M. Dautzenberg 《Advanced functional materials》2007,17(8):1402-1408
A rapid, simple, and efficient method for the preparation of highly dispersed supported Au catalysts has been developed. In the preparation, NaBH4 is used to reduce the Au precursor, lysine is employed to cap the formed Au colloids, and a short sonication time is applied to facilitate dispersion and deposition of the Au colloids onto the catalyst support, which has been mixed with the precursor beforehand. The end‐point pH value of the solution and the isoelectric points (IEPs) of the catalyst supports have an influence on the size of the Au particles and their deposition. The optimum value for the end‐point pH is 7.5–10.0, and the IEP should be 5–10. The amino acid capping agent is easily removed at the catalyst activation stage at 200 °C, and the Au particles are thermally stable against sintering, even at 500 °C for 3 h. It is also proven that the method is applicable to the preparation of supported Pt catalysts. The catalytic activity of the prepared Au catalysts for CO oxidation in the absence/presence of H2 is comparable to that of a Au catalyst prepared by the co‐precipitation (CP) method, and to that of the standard catalyst from the World Gold Council (WGC). X‐ray photoelectron spectroscopy (XPS) results show that only metallic Au exists in the catalysts before and after activation, and also after the catalysis reaction. 相似文献
19.
20.
同步辐射X射线光刻实验研究 总被引:4,自引:0,他引:4
同步辐射X射线光刻是一种很好的深亚微米图形复制技术。本文报道了北京同步辐射装置3BlA光刻束线上的曝光结果,并对X射线掩模的制作工艺作了简要介绍。 相似文献