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Merging single-shot XFEL diffraction data from inorganic nanoparticles: a new approach to size and orientation determination

机译:合并来自无机纳米粒子的单次XFEL衍射数据:确定尺寸和方向的新方法

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摘要

X-ray free-electron lasers (XFELs) provide new opportunities for structure determination of biomolecules, viruses and nanomaterials. With unprecedented peak brilliance and ultra-short pulse duration, XFELs can tolerate higher X-ray doses by exploiting the femtosecond-scale exposure time, and can thus go beyond the resolution limits achieved with conventional X-ray diffraction imaging techniques. Using XFELs, it is possible to collect scattering information from single particles at high resolution, however particle heterogeneity and unknown orientations complicate data merging in three-dimensional space. Using the Linac Coherent Light Source (LCLS), synthetic inorganic nanocrystals with a core–shell architecture were used as a model system for proof-of-principle coherent diffractive single-particle imaging experiments. To deal with the heterogeneity of the core–shell particles, new computational methods have been developed to extract the particle size and orientation from the scattering data to assist data merging. The size distribution agrees with that obtained by electron microscopy and the merged data support a model with a core–shell architecture.
机译:X射线自由电子激光器(XFEL)为确定生物分子,病毒和纳米材料的结构提供了新的机会。凭借前所未有的峰值亮度和超短脉冲持续时间,XFEL可以通过利用飞秒级的曝光时间来承受更高的X射线剂量,因此可以超越传统X射线衍射成像技术所达到的分辨率极限。使用XFEL,可以以高分辨率从单个粒子收集散射信息,但是粒子异质性和未知方向会使在三维空间中合并数据变得复杂。使用直线加速器相干光源(LCLS),具有核-壳结构的合成无机纳米晶体被用作原理证明相干衍射单粒子成像实验的模型系统。为了处理核-壳粒子的异质性,已经开发了新的计算方法来从散射数据中提取粒径和方向,以帮助数据合并。尺寸分布与通过电子显微镜获得的分布一致,合并后的数据支持具有核-壳结构的模型。

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