Phase transitions in the superionic protonic conductor CsHSeO4 investigated by Brillouin spectroscopy

A Brillouin investigation in CsHSeO₄ has been performed over the temperature range 20–165 °C which includes two phase transitions, in particular the transition to the superionic phase near T_s = 129 °C. We observed strong discontinuities for elastic constants C₁₁, C₂₂ and C₃₃ at T_s and a broadening of the Brillouin lines above T_s. The results are discussed on the basis of a linear coupling between strains and mobile protons.     

The origin of the redshift in Brillouin spectra of silica films containing tin nanoparticles

The abrupt change of velocity in surface acoustic waves in thin films of amorphous SiO_x containing nanometre scale -Sn crystals is shown to be directly associated with the size-dependent melting of the nanoparticles, confirming preliminary experiments. High resolution thin film powder diffraction using synchrotron radiation shows that the abrupt redshift in the Brillouin spectra satellites occurs at the same temperature as the melting of the nanoparticles, evident for the loss of the Bragg peaks. Effective medium theory is used to explain the origin of the anomaly. A central peak in the Brillouin spectrum, the intensity of which shows a maximum at the melting temperature, can be interpreted in terms of overdamped fluctuations in the dielectric function. The melting temperature as a function of particle size is in agreement with theoretical predictions. No evidence for strain could be found on the X-ray diffraction profiles; the a- and c-axis thermal expansion coefficients are the same as those in bulk tin. Received 30 March 2000 and Received in final form 24 July 2000     

含咔唑与偶氮分散红共聚物的表面增强共振拉曼光谱研究

借助于表面增强共振拉曼光谱散射(SERRS)技术,研究了一种新型的偶氮聚合物材料侧链含咔唑与偶氮分散红共聚物(CAP)在化学沉积法制备的银膜表面的拉曼峰增强和吸附行为。实验结果显示,CAP在银表面的状态为: 聚合物通过咔唑单体中咔唑基团和偶氮单体中硝基与银膜衬底发生物理吸附,而聚合物的主链与衬底相距较远没有相互作用。可以推测,聚合物在衬底表面的这种状态将对偶氮光存储器件的稳定性和工作效率产生不良影响。     

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.     

高层大气风场四强度测量法误差分析与计算

利用干涉成像光谱技术和电磁波的多普勒效应,通过测量高层大气(80—300km)中的气辉(极光)辐射线的四个干涉强度值而获知高层大气的速度和温度信息.采用四强度干涉测量法,分别对基于Michelson干涉仪的动镜扫描和基于无动镜四分区镀膜的干涉图获取模式所引起的测量误差进行了深入的理论分析与研究.给出了由于此测量误差所导致的相位误差所引起的高层大气风场速度、温度的误差数值;采用计算机模拟得出了在不同相位误差条件下,两种模式计算得到的风场速度和温度的误差分布图;给出了风速误差、温度误差与相位步进误差的关系曲线 关键词： 高层大气风场测量 四强度测量法 模拟计算     

基于LED的非相干宽带腔增强吸收光谱技术

介绍了基于可见光波段高功率LED作为光源的高灵敏度宽带腔增强吸收光谱技术,该系统的探测灵敏度通过测量NO₂在472.3～479.3 nm范围内的吸收得到验证。将中心波长为457 nm的高功率LED发出的宽带非相干光耦合进入92.5 cm长、由两片高反射率透镜组成的高精度光学谐振腔内,使用CCD光谱仪(HR2000)测量透过光学腔的光强信号。腔镜在472.3～479.3 nm波长范围内的反射率通过O₂-O₂聚合物的吸收确定,实验测量了一系列低浓度NO₂气体样品,采用差分光谱拟合技术在80 s的平均时间内NO₂浓度反演的统计不确定性约为3.1 ppb(ng·mL-1)。     

Study of multipacting effect in superconducting cavity

A number of superconducting cavities of axis-symmetric geometry have been considered to study the effect in order to achieve the desired performance. It is shown that the multipacting effect is strongly dependent on the condition of the RF surface and can be suppressed with reconsideration of the geometry. The simulation result is compared with the result of the semi-analytical model in the end.     

X射线衍射增强成像中的定量测量

提出了一种基于X射线衍射增强成像(DEI)断层计算机X射线层析术(CT)图像的物体尺寸精确测量方法.X射线衍射增强成像是一种基于相位衬度的成像技术.通过建立DEI的简化模型,研究衍射成像过程中品体转角、投影图像谷点位置、成像系统等效模糊等因素之间关系,由此具体探讨了系统模糊效应对圆物体边界成像带来的位置偏移,并以圆形被测样品为例.提出可精确测定直径的简单有效算法.通过理论仿真模型数据和北京同步辐射装置上的实测数据验证了该算法的精度.该方法实现了利用DEI图像对被测物体几何尺寸的精确测量,可用于对牛物组织样品等物体内部微小结构的尺寸的精确测量.     

Self‐Assembled Silver–Gold Nanoisland Films on Glass for SERS Applications

We present a study of resonant optical properties of gold‐protected silver nanoisland films. Silver nanoislands were grown on a glass substrate using out‐diffusion technique, the growth was followed by the deposition of nanometer‐thick gold coatings. Scanning electron microscopy and optical spectroscopy were used to characterize morphology and extinction spectra of the grown combined silver–gold nanostructures. Micro Raman spectroscopy of the combined nanoislands has demonstrated their signal enhancement factor exceeding that one of the initial silver nanoislands.     

水流损失和热补偿共同作用对增强型地热系统(EGS)产能影响的研究

基于青海共和盆地-3705m地热田实测数据,结合流固耦合传热理论并运用Comsol软件,建立了离散型裂隙岩体流体传热模型。考虑水流损失和热补偿共同作用,模拟得到了开采过程中上、下岩层(盖层和垫层)为绝热不渗透、传热不渗透、渗透传热时,储层(上、下岩层和压裂层)温度场的变化特征,分析了产出流量、水流损失、产出温度、产热速率的变化规律。研究结果表明:采热过程中产出流量始终小于注入流量;产出流量增幅速率先增大后减小,最后趋于稳定,前3a产出流量增幅超过总增幅量的3/4;忽略水流损失,将高估产热速率,采热初期甚至达到考虑水流损失时产热速率的3倍以上;考虑水流损失,产热速率呈先快速上升再趋于稳定后逐渐下降的趋势,最优开采时间为3a^11a;研究上、下岩层对产出温度的影响,仅考虑传热,采热寿命延长5.43%,同时考虑渗流传热时,采热寿命延长2.71%;采热前9a,水流损失占主导作用,即流入上、下岩层水流损失对产热速率的影响高于热补偿效应,开采10a后,热补偿效应占主导作用;同时考虑水流损失和热补偿效应得到的产热速率变化规律与实际工程更为符合,建议选择低渗透能力的上、下岩层延长增强型地热系统(EGS)运行时间。