采用曲率传感器测量热透镜焦距

分析了用光栅型波前曲率传感器测量热透镜焦距的基本原理,针对高功率固体激光器的工作特点,结合实验现象推导了在热透镜效应较强时热透镜焦距变化的计算公式。对半导体二极管(LD)侧面泵浦的百W级Nd:YAG激光棒在泵浦电流为15~25 A时的热透镜焦距值进行了测量,讨论了可能存在的误差。实验现象和理论分析一致,测量的热透镜焦距值与理论值符合得较好。     

无线传感器网络多跳路由协议研究

目的：无线传感器网络发展迅速,但传感器的高能耗问题成为制约其发展的主要瓶颈,高效节能的路由协议设计成为研究热点。方法：针对目前无线传感器网络常用的LEACH路由协议存在的簇首能耗过分集中、簇首分布不均衡问题,提出了改进的路由协议EEACRA,在总结、分析LEACH路由协议现有问题的基础上,给出了EEACRA路由协议的簇首选取门限值、簇首位置调整算法和基于能量代价最小的簇间多跳路由算法的实现方法,同时给出了具体的实现EEACRA协议的工作流程和关键算法。在MATLAB环境下对LEACH路由协议和EEACRA路由协议进行了仿真,对比了不同能耗降低措施对网络能耗降低的贡献。结果：仿真结果表明EEACRA路由协议的网络稳定期较LEACH路由协议有较大的改善。结论：证明了改进的路由协议EEACRA可以有效地提高网络的稳定期。     

基于敦煌辐射校正场的FY3B/VIRR反射太阳波段衰减分析

VIRR是搭载在我国最新一代极轨气象卫星FY-3B上的可见光红外扫描辐射计,发射后的遥感器需要进行不断的辐射定标校准以提高数据质量,更好的满足用户需求。为了研究FY3B/VIRR入轨后辐射响应的衰变规律,利用2011年—2015年敦煌辐射校正场同步试验数据,采用反射率基法计算其反射太阳波段的辐射定标系数,除受水汽吸收影响的波段10,其余各波段定标系数相对标准差均小于1.5%。以Aqua/MODIS为辐射基准验证了该方法的精度,结果表明,正演大气顶辐射与卫星观测值的平均偏差均小于2.5%。基于上述五年的VIRR定标结果,结合发射前定标系数,计算了遥感器的年际衰变率,结果表明:仪器衰减显示出一定的波长依赖性,波长越短的波段衰减越大;与发射前定标系数相比,入轨第一年的仪器定标系数有较大程度的变化;随着在轨运行时间变长,仪器衰减趋势开始减缓,在轨运行的第二和第三年衰减均大幅减小;从第四年开始波长0.8μm的波段,有衰减增大的趋势;在轨运行两年后,波长0.8μm的波段部分年份出现了响应增加的现象;与孙凌等的FY3A/MERSI衰减变化规律相比,衰减率和波长的相关性是一致的,但MERSI在0.65μm的波段3和13均出现相应增加的现象,而VIRR在该波长处的波段1却有衰减增大的趋势;综合历年的衰减率可以看出,波长较短的波段7,8和9年衰减率基本大于5%。     

大型望远镜设计与研究

介绍一种４．３ｍ红外望远镜。它与２．１６ｍ望远镜用真空管道联机用于ＣＣＤ照相和光干涉测量，可使集光能力达４．８ｍ口径，分辨率达１０１ｍ口径。     

等高线图分析技术在GC／FTIR联用数据处理中的应用

在三种高聚物的裂解大口径毛细管气相色谱－傅里叶变换红外光谱联用分析（ＰｙＷＢＣＧＣ／ＦＴＩＲ）数据获得的基础上，介绍应用等高线图（ＣＴＤ）分析技术处理色谱重叠峰，并在该分析提供的信息指导下进行红外光谱累加及差减技术，获得了重叠峰中各纯物质较好信噪比的气相红外谱图并予以定性，显著了等高线图分析技术在联用数据中的优点，充分发挥了ＧＣ／ＦＴＩＲ联用特有的光谱分离离度优势。     

红外系统后向反射光的光强研究

根据衍射光学理论分析了红外系统后向反射光强的分布,反射区域可以分成近场传输区域、菲涅耳衍射区域和夫琅和费衍射区域。在菲涅耳衍射区域内,反射光斑中心光强是呈明暗变化的,反射光斑中心光强在0～1km内剧烈振荡,1～3km之间达到峰值,然后随传输距离的继续增加,反射光斑中心光强逐渐减小。在夫琅和费衍射区域内,光斑图像中央是亮光斑,周围环绕着明暗交替的圆环。     

A Novel Acoustic Emission Fiber Optic Sensor Based on a Single Mode Optical Fiber Coupler

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Position magnifying sensor

This paper describes the application of multiple beam shearing interferometry to a position magnifying sensor. A multiple beam shearing interferometer (MBSI) with a shear plate wedged in the vertical direction produces sharp multiple beam fringes. When the lateral displacement of a point source (which gives rise to the input beam of the MBSI) or its image occurs in the horizontal direction, these fringes move vertically in a magnified manner. This characteristic was used in a position magnifying sensor to detect the displacement of a point image. The advantages of the sensor include a large displacement magnification (more than a hundred times) and a large working distance.     

Si／SiNx／SiO2多层膜的光致发光

采用射频磁控溅射法,制备了具有强光致可见发光的纳米Si/SiNx/SiO2多层膜,利用傅立叶红外吸收(FTIR)谱,光致发光(PL)谱对其进行了研究。用260nm光激发得到的PL谱中观察到高强度的392nm(3.2eV)和670nm(1.9eV)光致发光峰,分析认为它们分别来自于缺陷态≡Si-到价带顶和从导带底到缺陷态≡Si-的辐射跃迁而产生的光致激发辐射复合发光。PL谱中只有370nm(3.4eV)处发光峰的峰位会受退火温度的影响,结合FTIR谱认为370nm发光与低价氧化物—SiOx(x<2.0)结合体有密不可分的关系。当SiO2层的厚度增大时,发光强度有所增强,800℃退火后出现最强发光,认为具有较大SiO2层厚度的Si/SiNx/SiO2结构多层膜更有利于退火后形成Si—N网络,能够得到更高效的光致发光。用量子限制-发光中心(QCLC)模型解释了可能的发光机制,并建立了发光的能隙态(EGS)模型。     

Effect of an aliphatic spacer group on the adsorption mechanism on the colloidal silver surface of L‐proline phosphonodipeptides

A comparative study of molecular structures of five L ‐proline (L ‐Pro) phosphonodipeptides: L ‐Pro‐NH‐C(Me,Me)‐PO₃H₂ (P1), L ‐Pro‐NH‐C(Me,iPr)‐PO₃H₂ (P2), L ‐Pro‐L ‐NH‐CH(iBu)‐PO₃H₂ (P3), L ‐Pro‐L ‐NH‐CH(PA)‐PO₃H₂ (P4) and L ‐Pro‐L ‐NH‐CH(BA)‐PO₃H₂ (P5) has been carried out using Raman and absorption infrared techniques of molecular spectroscopy. The interpretation of the obtained spectra has been supported by density functional theory calculations (DFT) at the B3LYP; 6–31 + + G** level using Gaussian 2003 software. The surface‐enhanced Raman scattering (SERS) on Ag‐sol in aqueous solutions of these phosphonopeptides has also been investigated. The surface geometry of these molecules on a silver colloidal surface has been determined by observing the position and relative intensity changes of the Pro ring, amide, phosphonate and so‐called spacer (−R) groups vibrations of the enhanced bands in their SERS spectra. Results show that P4 and P5 adsorb onto the silver as anionic molecules mainly via the amide bond (∼1630, ∼1533, ∼1248, ∼800 and ∼565 cm⁻¹), Pro ring (∼956, ∼907 and ∼876 cm⁻¹) and carboxylate group (∼1395 and ∼909 cm⁻¹). Coadsorption of the imine nitrogen atom and PO group with the silver surface, possibly by formation of a weaker interaction with the metal, is also suggested by the enhancement of the bands at 1158 and 1248 cm⁻¹. P1, P2 and P3 show two orientations of their main chain on the silver surface resulting from different interactions of the  C CH₃,  NH and  CONH fragments with this surface. Bonding to the Ag surface occurs mainly through the imino atom (1166 cm⁻¹) for P2, while for P1 and P3 it occurs via the methyl group(s) (1194–1208 cm⁻¹). The amide group functionality (CONH) is practically not involved in the adsorption process for P1 and P2, whereas the C_s P bonds do assist in the adsorption. Copyright © 2008 John Wiley & Sons, Ltd.