部分偏振部分相干光光栅衍射场的偏振特性和角相关研究

为了研究部分偏振部分相干光光栅衍射场的衍射特性.利用部分偏振部分相干光的光束相干-偏振(BCP)矩阵,推导出了部分偏振部分相干光通过任意偏振光栅后,衍射场的偏振度及场中衍射级次角相关的一般解析表达式.以部分偏振的高斯-谢尔模型光束(PGSM)为例,数值分析了偏振光栅TE和TM波的复振幅透过率、入射光束的光学参量对衍射场偏振度和场中各衍射级次的角相关的影响.计算结果表明,部分相干光透过偏振光栅后的其衍射光场是一非均匀、周期变化的部分偏振相干光场;场中对称级次的角相干值对应相等,且随衍射级次序数的增大而缓慢递减至零.     

衍射效应诱导涡旋光束的偏振度变化

基于惠更斯-菲涅耳衍射原理以及部分相干光的相干与偏振的统一理论,研究了衍射效应诱导部分相干涡旋光束的偏振度变化.通过理论分析与数值计算表明,部分相干涡旋光束经圆孔衍射后偏振度将发生变化,在衍射场中光束的偏振度分布情况与入射光束的相干度、入射光束的拓扑电荷数、衍射孔径的大小等因素有关.     

上海光源硬X射线相干衍射成像实验方法初探

相干X射线衍射成像方法是一种先进的成像技术,分辨率可达纳米量级.国际上大多数的同步辐射装置和自由电子激光装置都建立了该成像方法,并有将其作为主要成像技术的趋势.上海光源作为目前国内唯一的一台第三代同步辐射光源,尚未建立基于硬X射线的相干衍射成像实验平台.随着一批以波荡器为光源的光束线站投入使用,使得该方法的建立成为了可能.本文基于上海光源BL19U2生物小角散射线站,通过有效的光路设计,搭建了相干衍射实验平台,在12 keV和13.5 keV能量点均获得了硬X射线相干光束,并基于小孔衍射测量了入射光束的空间相干长度.该平台支持常规和扫描相干衍射实验模式,对小孔衍射图样及波带片扫描衍射图样实现了正确的相位重建,证明了该平台初步具备开展硬X射线相干衍射成像实验的能力.硬X射线相干衍射成像实验平台为国内首次建立,将为国内该实验方法的发展和应用提供有效的软硬件支持.     

X射线双晶衍射摇摆曲线本征半峰宽的理论计算

本文应用X射线衍射动力学理论,推导出Bragg衍射几何X射线双晶衍射反射率的数学表达式。多种晶体、不同衍射的摇摆曲线计算结果表明,σ偏振的摇摆曲线的峰值和积分强度均比π偏振的高。而且半峰宽较宽。同时指出,对圆偏振X射线入射或者A,B两晶体不同类或者两者的衍射级数不相同时,很多文献给出的双晶衍射摇摆曲线半峰宽的近似表达式2^1/2∞不再适用。 关键词：     

KTP(001)晶体分光性能研究

根据同步辐射光源对软X射线分光晶体的性能要求,分析了软X射线能区常用分光晶体的性能优劣,指出对于晶格常数值大的分光晶体,KTP(KTiOPO₄)(011)是该能区比较理想的分光晶体. 同时提出了一种利用同步辐射光源测量晶体衍射效率的实验方法,指出光源的发散度与晶体的衍射效率密切相关. 测量了KTP(011)晶体的晶格常数,给出了KTP(011)晶体的实测衍射效率. 关键词： 同步辐射 KTP(011)晶体 衍射效率 光源发散度     

部分相干平顶光束经光阑衍射的偏振特性

根据光束的相干-偏振矩阵和传输理论，对部分相干平顶光束经正多边形光阑衍射的偏振特性进行了系统的研究.给出了部分相干平顶光束偏振度传输公式，并将高斯-谢尔模型光束以及部分相干平顶光束在自由空间传输的偏振度作为特例统一于一般表达式中.研究表明：部分相干平顶光束经光阑衍射的偏振特性与光阑截断参数、光束的空间相干性、衍射角、传输距离、平顶光束的阶数有关.     

部分相干平顶光束经光阑衍射的偏振特性

根据光束的相干-偏振矩阵和传输理论,对部分相干平顶光束经正多边形光阑衍射的偏振特性进行了系统的研究.给出了部分相干平顶光束偏振度传输公式,并将高斯-谢尔模型光束以及部分相干平顶光束在自由空间传输的偏振度作为特例统一于一般表达式中.研究表明：部分相干平顶光束经光阑衍射的偏振特性与光阑截断参数、光束的空间相干性、衍射角、传输距离、平顶光束的阶数有关. 关键词： 部分相干平顶光束 偏振特性 相干-偏振矩阵 正多边形光阑 光阑衍射     

冲击加载下LiF晶格形变的闪光X射线衍射测量

在轻气炮加载实验平台上,利用小型闪光X射线源建立了一套脉冲X射线衍射测量系统。利用该测量系统对平面冲击加载条件下LiF晶体微观结构变化进行了研究,得到了不同冲击加载压力下LiF晶体的单次脉冲X射线衍射图像。实验结果表明:沿[100]晶向加载,LiF晶体晶格发生了压缩,压缩量与衍射峰偏移量相关;基于小型闪光X射线源的脉冲X射线衍射测量系统可实现冲击压缩下材料微观结构变化的定量化测量,同时具有体积小、操作简单等优点,为研究弹塑性形变微观机理提供了一种有效手段。     

冲击加载下LiF晶格形变的闪光X射线衍射测量EI北大核心CSCD

在轻气炮加载实验平台上,利用小型闪光X射线源建立了一套脉冲X射线衍射测量系统。利用该测量系统对平面冲击加载条件下LiF晶体微观结构变化进行了研究,得到了不同冲击加载压力下LiF晶体的单次脉冲X射线衍射图像。实验结果表明:沿[100]晶向加载,LiF晶体晶格发生了压缩,压缩量与衍射峰偏移量相关;基于小型闪光X射线源的脉冲X射线衍射测量系统可实现冲击压缩下材料微观结构变化的定量化测量,同时具有体积小、操作简单等优点,为研究弹塑性形变微观机理提供了一种有效手段。     

合肥扭摆器光源的特性和利用

国家同步辐射实验室正在设计和制造一台６Ｔ单周期超导扭摆器，把合肥同步辐射光源的可用范围延伸到Ｘ射线，满足部分Ｘ射线用户的要求，利用扭摆器光源装备四条光束线，分别用于Ｘ射线吸收精细结构，生物大分子晶体多波长反常衍射，Ｘ射线深度光刻和高分辩Ｘ射线衍射的研究。     

Large‐surface‐area diamond (111) crystal plates for applications in high‐heat‐load wavefront‐preserving X‐ray crystal optics

Fabrication and results of high‐resolution X‐ray topography characterization of diamond single‐crystal plates with large surface area (10 mm × 10 mm) and (111) crystal surface orientation for applications in high‐heat‐load X‐ray crystal optics are reported. The plates were fabricated by laser‐cutting of the (111) facets of diamond crystals grown using high‐pressure high‐temperature methods. The intrinsic crystal quality of a selected 3 mm × 7 mm crystal region of one of the studied samples was found to be suitable for applications in wavefront‐preserving high‐heat‐load crystal optics. Wavefront characterization was performed using sequential X‐ray diffraction topography in the pseudo plane wave configuration and data analysis using rocking‐curve topography. The variations of the rocking‐curve width and peak position measured with a spatial resolution of 13 µm × 13 µm over the selected region were found to be less than 1 µrad.     

Pressure study of monoclinic ReO2 up to 1.2 GPa using X‐ray absorption spectroscopy and X‐ray diffraction

The crystal and local atomic structure of monoclinic ReO₂ (α‐ReO₂) under hydrostatic pressure up to 1.2 GPa was investigated for the first time using both X‐ray absorption spectroscopy and high‐resolution synchrotron X‐ray powder diffraction and a home‐built B₄C anvil pressure cell developed for this purpose. Extended X‐ray absorption fine‐structure (EXAFS) data analysis at pressures from ambient up to 1.2 GPa indicates that there are two distinct Re—Re distances and a distorted ReO₆ octahedron in the α‐ReO₂ structure. X‐ray diffraction analysis at ambient pressure revealed an unambiguous solution for the crystal structure of the α‐phase, demonstrating a modulation of the Re—Re distances. The relatively small portion of the diffraction pattern accessed in the pressure‐dependent measurements does not allow for a detailed study of the crystal structure of α‐ReO₂ under pressure. Nonetheless, a shift and reduction in the (011) Bragg peak intensity between 0.4 and 1.2 GPa is observed, with correlation to a decrease in Re—Re distance modulation, as confirmed by EXAFS analysis in the same pressure range. This behavior reveals that α‐ReO₂ is a possible inner pressure gauge for future experiments up to 1.2 GPa.     

Sound velocities of compressed Fe3C from simultaneous synchrotron X‐ray diffraction and nuclear resonant scattering measurements

The applications of nuclear resonant scattering in laser‐heated diamond anvil cells have provided an important probe for the magnetic and vibrational properties of ⁵⁷Fe‐bearing materials under high pressure and high temperature. Synchrotron X‐ray diffraction is one of the most powerful tools for studying phase stability and equation of state over a wide range of pressure and temperature conditions. Recently an experimental capability has been developed for simultaneous nuclear resonant scattering and X‐ray diffraction measurements using synchrotron radiation. Here the application of this method to determine the sound velocities of compressed Fe₃C is shown. The X‐ray diffraction measurements allow detection of microscale impurities, phase transitions and chemical reactions upon compression or heating. They also provide information on sample pressure, grain size distribution and unit cell volume. By combining the Debye velocity extracted from the nuclear resonant inelastic X‐ray scattering measurements and the structure, density and elasticity data from the X‐ray diffraction measurements simultaneously obtained, more accurate sound velocity data can be derived. Our results on few‐crystal and powder samples indicate strong anisotropy in the sound velocities of Fe₃C under ambient conditions.     

X光高分辨探测用CsI(Tl)晶体的蒙特卡罗模拟研究

提出了一种基于CsI(Tl)闪烁晶体和面阵CCD器件、采用光纤和光纤面板进行光耦合及传输、以扇形束线阵扫描方式实现对X光高分辨探测的方案。CsI(Tl)晶体的尺寸大小将直接影响到晶体的发光效率及X光的高分辨探测,据此开展了蒙特卡罗模拟研究。模拟研究了X射线能量、X射线源到探测晶体的距离(源距)、CsI(Tl)晶体的厚度与X射线能量分布、全能峰效率与CsI(Tl)闪烁晶体转换效率之间的关系。结果表明,当X射线能量为120~450 keV,CsI(Tl)晶体尺寸厚度为0~1.5 cm变化时,全能峰效率的变化范围为31.34~96.74%,CsI(Tl)闪烁晶体的转换效率的变化范围为12.8~97.43%。可见,X射线的能量及CsI(Tl)闪烁晶体尺寸的厚度,是决定X光高分辨探测的重要参量,这对优化X光高分辨探测用CsI(Tl)晶体的尺寸设计具有一定的参考价值。     

A new ultra‐high‐vacuum variable temperature and high‐magnetic‐field X‐ray magnetic circular dichroism facility at LNLS

X‐ray magnetic circular dichroism (XMCD) is one of the most powerful tools for investigating the magnetic properties of different types of materials that display ferromagnetic behavior. Compared with other magnetic‐sensitive techniques, XMCD has the advantage of being element specific and is capable of separating the spin and magnetic moment contributions associated with each element in the sample. In samples involving, for example, buried atoms, clusters on surfaces or at interfaces, ultrathin films, nanoparticles and nanostructures, three experimental conditions must be present to perform state‐of‐the‐art XMCD measurements: high magnetic fields, low temperatures and an ultra‐high‐vacuum environment. This paper describes a new apparatus that can be easily installed at different X‐ray and UV beamlines at the Brazilian Synchrotron Light Laboratory (LNLS). The apparatus combines the three characteristics described above and different methods to measure the absorption signal. It also permits in situ sample preparation and transfer to another chamber for measurement by conventional surface science techniques such as low‐energy electron diffraction (LEED), reflection high‐energy electron diffraction (RHEED), X‐ray photoelectron spectroscopy (XPS) and X‐ray photoelectron diffraction (XPD). Examples are given of XMCD measurements performed with this set‐up on different materials.     

Diffraction‐based automated crystal centering

A fully automated procedure for detecting and centering protein crystals in the X‐ray beam of a macromolecular crystallography beamline has been developed. A cryo‐loop centering routine that analyzes video images with an edge detection algorithm is first used to determine the dimensions of the loop holding the sample; then low‐dose X‐rays are used to record diffraction images in a grid over the edge and face plane of the loop. A three‐dimensional profile of the crystal based on the number of diffraction spots in each image is constructed. The derived center of mass is then used to align the crystal to the X‐ray beam. Typical samples can be accurately aligned in ～2–3 min. Because the procedure is based on the number of `good' spots as determined by the program Spotfinder, the best diffracting part of the crystal is aligned to the X‐ray beam.     

A method to stabilize the incident X‐ray energy for anomalous diffraction measurements

A method to calibrate and stabilize the incident X‐ray energy for anomalous diffraction data collection is provided and has been successfully used at the single‐crystal diffraction beamline 1W2B at the Beijing Synchrotron Radiation Facilities. Employing a feedback loop to control the movement of the double‐crystal monochromator, this new method enables the incident X‐ray energy to be kept within a 0.2 eV range at the inflection point of the absorption edge.     

Crystallization Behavior and Crystal Morphology of PTT/PBT Blends

The crystallization behavior and crystal morphology of the poly(trimethyl terephthalate) (PTT)/poly(butylene terephthalate) (PBT) blends were investigated by means of differential scanning calorimetry (DSC), wide angle X‐ray diffraction (WAXD) and polarized light microscopy (PLM) techniques. It was found that the two components crystallized simultaneously in the crystalline regions. The degree of crystallinity changed with PTT content. Crystalline properties were worse when the ratio of PBT and PTT contents was close to 50:50, but were better when PBT content was greatly different from PTT content.     

Polarization control of an X‐ray free‐electron laser with a diamond phase retarder

A diamond phase retarder was applied to control the polarization states of a hard X‐ray free‐electron laser (XFEL) in the photon energy range 5–20 keV. The horizontal polarization of the XFEL beam generated from the planar undulators of the SPring‐8 Angstrom Compact Free‐Electron Laser (SACLA) was converted into vertical or circular polarization of either helicity by adjusting the angular offset of the diamond crystal from the exact Bragg condition. Using a 1.5 mm‐thick crystal, a high degree of circular polarization, 97%, was obtained for 11.56 keV monochromatic X‐rays, whereas the degree of vertical polarization was 67%, both of which agreed with the estimations including the energy bandwidth of the Si 111 beamline monochromator.     

Energy resolution of the CdTe‐XPAD detector: calibration and potential for Laue diffraction measurements on protein crystals

The XPAD3S‐CdTe, a CdTe photon‐counting pixel array detector, has been used to measure the energy and the intensity of the white‐beam diffraction from a lysozyme crystal. A method was developed to calibrate the detector in terms of energy, allowing incident photon energy measurement to high resolution (approximately 140 eV), opening up new possibilities in energy‐resolved X‐ray diffraction. In order to demonstrate this, Laue diffraction experiments were performed on the bending‐magnet beamline METROLOGIE at Synchrotron SOLEIL. The X‐ray energy spectra of diffracted spots were deduced from the indexed Laue patterns collected with an imaging‐plate detector and then measured with both the XPAD3S‐CdTe and the XPAD3S‐Si, a silicon photon‐counting pixel array detector. The predicted and measured energy of selected diffraction spots are in good agreement, demonstrating the reliability of the calibration method. These results open up the way to direct unit‐cell parameter determination and the measurement of high‐quality Laue data even at low resolution. Based on the success of these measurements, potential applications in X‐ray diffraction opened up by this type of technology are discussed.