草酸铕颗粒微米层状颗粒的合成及其光学性能

在室温条件下, 以柠檬酸钠为辅助剂, 通过简单沉淀法合成了草酸铕Eu₂(C₂O₄)₃·10H₂O微米层状颗粒. 应用X射线衍射、X射线电子能谱、场发射扫描电子显微镜、光致发光光谱对Eu₂(C₂O₄)₃·10H₂O结构与性能进行了表征. 讨论了草酸铕微米层状颗粒可能的形成机理.     

Ni70Co30/Cu磁性金属多层膜界面元素分布的X射线异常散射研究

应用X射线异常散射技术研究了[Ni₇₀Co₃₀(25A)/Cu(20A)]₂₀多层膜的界面结构, 结果表明, 退火前后Cu/Ni₇₀Co₃₀和Ni₇₀Co₃₀/Cu界面的温度行为不同.对于制备态样品, 界面结构是非对称的, 在Cu/Ni₇₀Co₃₀界面, 存在一个8A厚的CuNi₃过渡层和一个4A厚的NiCo层. 然而, Ni₇₀Co₃₀/Cu界面却不存在任何扩散. 285\textcelsius 2h退火后,Ni₇₀Co₃₀/Cu界面开始发生扩散, 产生了一个12A厚的CuNi₂Co过渡层. X射线能量分别在Co, Ni, Cu K吸收边附近的X射线漫散射实验, 揭示了在Ni₇₀Co₃₀/Cu多层膜的界面处, Cu与Ni和Co具有不同的横向关联长度, 显示了不均匀的横向分布.     

C3N4的高温高压同步辐射研究

利用激光加热金刚石对顶砧技术在高温高压条件下合成了纯beta相和立方相C₃N₄beta相C₃N₄所属对称群为P63/M (176).对石墨相与beta相C₃N₄的X射线衍射结果进行了精确分析, 得到优化晶胞参数.原位高压同步辐射X射线衍射分析表明, 在6GPa时由beta相到立方相C₃N₄的相转变已经发生, 之后两相共存直到19GPa时相变结束得到纯立方相C₃N₄.     

高空核爆炸下大气的X射线电离及演化过程数值模拟

利用数值模拟程序模拟了不同高度核爆炸下大气的X射线电离及演化过程.结果表明: X射线电离产生的电子数密度在射线到达后约100 ns时刻达到峰值, 峰值数密度随着到裸核区距离的增加而减小;电子具有较长的寿命, 电子寿命随着到裸核区距离的增加而增大; X射线电离空气产生正离子O⁺, O₂⁺, N₂⁺,爆高为120 km情况下 O⁺的峰值数密度与O₂⁺的相近,能维持约1 s. X射线对空气的电离影响范围在数十千米以内,在距裸核区较近的区域, 爆高为80 km时产生的电子峰值数密度比爆高为120 km时的电子峰值数密度高, 在距裸核区较远的区域则相反.     

飞秒激光-物质相互作用产生Kα X射线

 用无色散X射线谱仪分别在靶前后测量了飞秒激光辐照铜箔产生的Kα X射线,获得了能量转换效率。入射激光脉冲宽度33 fs,能量在50 mJ～5 J,强度10₁₇～10₁₉ W/cm₂。靶后发射的Kα X射线强度随入射激光能量的增加而增加,其单色性较靶前好。采用100 μm厚靶,其能量转换率为2.2×10_-5。     

Cr4+:Ca2GeO4激光晶体生长及结构表征

采用助熔剂法,以CaCl₂为助熔剂,生长Cr⁴⁺ :Ca₂GeO₄新型近红外可调谐激光晶体.通过X射线衍射(XRD)、激光Raman光谱、X射线光电子能谱(XPS)等方法对晶体进行结构表征.结果表明,得到的晶体为单斜晶系镁橄榄石结构的低温γ-Cr⁴⁺ :Ca₂GeO₄单晶,晶格参数为a=5.3209 (1 =0.1 nm)     

YBCO薄膜微结构的表征

用X射线衍射技术和扫描电镜详细表征了生长在Y-ZrO₂(YSZ)衬底上YBa₂Cu₃O_7-σ(YBCO)薄膜的微结构.结果发现,采用Eu₂CuO₄(ECO)做缓冲层,可以提高YBCO薄膜的质量,而不改变其超导性能.     

有机金属化学气相沉积法制备的Ni/Al2O3纳米复合材料的氢吸附

研究了通过有机金属化学气相沉积技术及单源分子前躯体方法制备的Ni/Al₂O₃纳米复合材料的氢吸附(存储). 在冷壁的有机金属化学气相沉积反应器中,通过降解Ni(acac)₂粉末基底上的[H₂Al(OtBu)]₂制备的Ni/Al₂O₃纳米复合材料. 通过X射线粉末衍射、扫描电镜、透射电镜以及能量色散型X射线荧光光谱等技术表征该复合材料. 采用自制Sievert's设备研究该复合材料的氢吸附(存储),可以储存约2.9%(重量比)的氢.     

Ag60纳米颗粒[{Cl@Ag12}@Ag48(dppm)12]的结构(其中dppm=双(二苯基膦基)甲烷

本文合成一种新的双膦连接Ag₆₀纳米团簇[{Cl@Ag₁₂}@Ag₄₈(dppm)₁₂],并通过X射线晶体学进行表征. 二十面体的银处于核心位置,里面是中心氯化物组成,外面有48 个银原子/离子的包裹,顶端是12个双(二苯基膦基)甲烷(dppm)配体. 同时利用密度泛函理论对阳离子[{Cl@Ag₁₂}@Ag₄₈(dppm)₁₂]⁺进行计算,以确定该结构是否对应于核心数n=58的超原子. DFT计算的优化结构与X射线一致,但是HOMO-LUMO的能差并不能保证其超级稳定性.     

用云母弯晶谱仪探测Z箍缩等离子体X射线光谱

 为了研究Z箍缩等离子体辐射的X射线光谱,研制了可用于“阳”加速器上探测宽频谱范围的X射线椭圆弯曲晶体谱仪。该谱仪晶体分析器采用云母材料,椭圆焦距为1 350 mm,离心率为0.948 5,覆盖布拉格范围为30°~60°,可探测X射线波长范围为0.10~1.73 nm(0.86~1.00 nm除外),用X射线胶片接收光谱信号。探测实验在中国工程物理研究院“阳”加速器上进行,实验结果表明:谱仪获取了氩的类氢共振线L_ya及其伴线、类氦共振线(1s2p¹P₁-1s2¹S₀)w线及磁四级M₂2跃迁(1s2p³P₂-1s²¹S₀)x线、互组合跃迁(1s2p³P₁-1s²¹S­₀)y线、禁戒谱线(1s2p³S₁-1s²¹S₀)z线和K­_-a线,谱线分辨率达到564。实验证明弯晶谱仪适合于Z箍缩等离子体X射线光谱学诊断。     

微型X射线管出射谱特征研究及Be窗厚度确定

微型X射线管已广泛应用于现场元素分析、放射性医疗等领域,对于微型X射线管铍窗,普遍认为除保证管内真空外,应越薄越好。采用蒙特卡洛方法,模拟了从50～500 μm范围内共13个Be窗厚度的微型X射线管出射X射线谱。按照在应用中的作用,将出射X射线划分为不同能量段进行分析。通过分析谱线特征,发现Be窗厚度应依据其应用要求合理选择。因此,提出了K系特征X射线与轫致辐射强度的比值和低能射线与激发射线计数比值等参量作为评价Be窗厚度最优化的判断依据。除上述评判指标外,铍窗的厚度最优化选择还应考虑Be窗对不同能量X射线的屏蔽效果。依据模拟结果分析,原位(现场)X射线能量色散荧光分析应用中,Be窗厚度约250 μm的微型X射线管最为合适。与50 μm铍窗厚度出射射线相比,71.66%低能原级X射线被屏蔽,5~50 keV能量原级X射线仅有21.31%被屏蔽,低能射线强度占总X射线比值小于10%,且K系X射线占激发射线的比例仍保持较高的水平。因此,采用250 μm铍窗厚度的微型X射线管作为能量色散激发源,能保证探测器探测的有效信号比值较高,低能X射线对探测器的能量分辨率的影响最小,而且能量色散分析谱线的散射本底相对强度处于较低的水平,从而保证元素分析结果精准度。对于放射性治疗的应用中,则铍窗厚度越薄越好,此时,低能X射线具有较高的通量,能保证辐射剂量在治疗组织中剂量的集中。     

同轴X射线相位衬度计算机X射线断层摄影术研究

基于北京同步辐射装置(BSRF)开展了同轴X射线相位衬度计算机X射线断层摄影术(CT)研究.利用北京同步辐射的14 keV单色X射线作为光源,以高分辨能力的X射线胶片作为探测器,分别开展吸收衬度和同轴相位衬度成像的比较研究以及相位衬度计算机X射线断层摄影术研究.相位衬度计算机X射线断层摄影术重建采用Bronnikov提出的算法.结果显示,与传统的吸收衬度图像相比,相位衬度图像具有更好的衬度和更高的空间分辨力;实验获得人工样品和蝗虫的相位衬度计算机X射线断层摄影术重建图像.重建图像中可见样品的一些结构细节.实验结果表明,相位衬度X射线成像更适合于研究弱吸收或吸收差异很小的材料;利用北京同步辐射开展同轴X射线相位衬度计算机X射线断层摄影术研究是可行的.     

The hoard of Beçin—non-destructive analysis of the silver coins

We report the results of an analytical investigation on 416 silver-copper coins stemming from the Ottoman Empire (end of 16th and beginning of 17th centuries), using synchrotron micro X-ray fluorescence analysis (SRXRF). In the past, analyses had already been conducted with energy dispersive X-ray fluorescence analysis (EDXRF), scanning electron microscopy with energy dispersive X-ray spectrometry (SEM/EDX) and proton induced X-ray emission spectroscopy (PIXE). With this combination of techniques it was possible to confirm the fineness of the coinage as well as to study the provenance of the alloy used for the coins.     

Diagnostics of gold-containing surgical-dressing materials with X-ray and synchrotron radiation

An analysis of biocompatible and antibacterial Au-gauze nanocomposites for medical purposes using X-ray and synchrotron radiation is conducted. The samples are produced by the modification of medical cotton gauze by Au organosol in isopropanol, which is synthesized via the metal-vapor method. The nanocomposites are examined with X-ray photoelectron spectroscopy, as well as with X-ray adsorption diffraction spectroscopy (EXAFS/XANES) and small-angle X-ray scattering using synchrotron radiation.     

X-ray microbeams based on Kumakhov polycapillary optics and its applications: Analytical consideration

Kumakhov polycapillary optics is based on the effective passage of X-ray radiation through bundles of monocapillaries of various configurations. The passage of radiation takes place because of the total external reflection of X-rays from the inner capillary walls. In this work, the basic characteristics of intense quasi-parallel X-ray polycapillary microbeams from a laboratory source with microfocus X-ray tube/polycapillary cylindrical structure are investigated theoretically (analytical consideration). The data generated from theoretical estimations are compared with the experimental results. Several new generations of X-ray analytical devices like, laboratory synchrotron, fluorescent spectrometers, reflectometers/refractometers, diffractometers, X-ray microscopes and combinations of several such devices, are developed based on polycapillary optics. Besides, a number of devices can be developed for the most modern research problems such as nanomateriology, namely, X-ray nanoscanner, portable X-ray nanothickness indicator etc. X-ray tubes and the radiators, specially developed for polycapillary optics as efficiently as possible, are used in all the devices mentioned above.     

EXAFS and diffraction

We discuss advantages and limitations of X-ray absorption fine structure (EXAFS), X-ray diffraction and anomalous X-ray diffraction as structural tools for ordered and (chemically and structurally) disordered solids.     

Review on applications of synchrotron-based X-ray techniques in materials characterization

Synchrotron radiation (SR), as a result of its high-intensity, brilliant, monochromatic, and collimated beams, is becoming one of the most crucial components of research in various fields of materials science such as nanomaterials, biomaterials, and energy materials. SR-based characterization methods can be employed to analyze different systems such as powders, thin films, and bulk forms having complex crystalline or amorphous structures. In this review, peculiarities of SR are briefly explained. Moreover, various techniques carried out utilizing this instrument for material characterization such as X-ray powder diffraction, grazing-incidence X-ray diffraction, small/wide-angle X-ray scattering, X-ray absorption spectroscopy, different techniques of X-ray imaging, X-ray photoelectron spectroscopy, and X-ray microprobes/nanoprobes are presented. As a result, by shedding light on the advantages of SR and its superiority to the equivalent laboratory experiments, researchers are recommended to exploit the capabilities of this invaluable tool in their materials characterization.     

ZnO:Ga晶体对硬X射线的时间及能量响应

 介绍了ZnO:Ga晶体对重复频率快脉冲硬X 射线的时间响应,利用X射线荧光分析仪测量了ZnO:Ga晶体对10～100 keV硬X射线的能量响应。结果表明:ZnO:Ga晶体对硬X射线响应的上升时间为316 ps,半高宽为440 ps;对40 keV以上的X射线的能量响应很平坦。该晶体可以作为一种新颖的硬X射线探测元件。     

On the state of iron in a clinoptilolite

The characterization of an iron-containing natural zeolitic sample from the deposit of Tasajeras (Cuba) has been carried out by means of X-ray powder diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX), X-ray photoelectron spectroscopy (XPS),⁵⁷Fe Mössbauer spectroscopy and Fe K-edge X-ray absorption near-edge structure (XANES) and extended X-ray absorption fine structure (EXAFS). The results show that iron is mainly located (ca. 96%) as Fe³⁺ in an octahedral site of the clinoptilolite framework. No evidence of tetrahedrally coordinated Fe³⁺ was found. The remaining 4% Fe is located as Fe²⁺ in an extraframework octahedral site, probably as a solvated ion, within the clinoptilolite structure.     

高电荷态离子129Xe29+与不同金属表面作用产生的X射线谱

研究了高电荷态离子129Xe29+入射金属Au、Mo、Be表面产生的特征X射线谱。实验结果表明,在入射离子的动能相同时,Au的Mα1-X射线产额比Mo的Lα1-X、Lα2-X、Lβ 1-X射线总产额高,特征X射线的产额随入射离子动能的增加而显著增加;不同动能的Xe29+入射金属Au、Mo、Be表面均未产生Xe的特征X射线。