Combinations of spectroscopic analysis and microscopic techniques are used across many disciplines of scientific research, including material science, chemistry and biology. X-ray spectromicroscopy, in particular, is a powerful tool used for studying chemical state distributions at the micro and nano scales. With the beam fixed, a specimen is typically rastered through the probe with continuous motion and a range of multimodal data is collected at fixed time intervals. The application of this technique is limited in some areas due to: long scanning times to collect the data, either because of the area/volume under study or the compositional properties of the specimen; and material degradation due to the dose absorbed during the measurement. In this work, we propose a novel approach for reducing the dose and scanning times by undersampling the raster data. This is achieved by skipping rows within scans and reconstructing the x-ray spectromicroscopic measurements using low-rank matrix completion. The new method is robust and allows for x 5-6 reduction in sampling. Experimental results obtained on real data are illustrated.
翻译:在科学研究的许多学科,包括材料科学、化学和生物学,都采用光谱分析和微显微技术的结合。特别是X射线光谱显微镜分析是研究微观和纳米尺度化学状态分布的有力工具。光束固定后,典型的标本是通过连续运动通过探针对试样进行研磨,并在固定时间间隔内收集一系列多式数据。由于下列原因,这种技术在某些地区的应用有限:由于研究中的面积/体积或标本的构成特性,收集数据的扫描时间很长;由于测量过程中吸收的剂量造成物质降解。在这项工作中,我们建议采用一种新颖的办法,通过对RAST数据进行下取样来减少剂量和扫描时间。这是通过在扫描中跳行和重新利用低层矩阵完成的X射线谱微微微微测量而实现的。新的方法是稳健的,可以减少X 5-6的采样。在实际数据上取得的实验结果得到了说明。