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Is scanning electron microscopy/energy dispersive x-ray spectroscopy (SEM/EDS) quantitative? Effect of specimen shape

机译:扫描电子显微镜/能量分散X射线光谱(SEM / EDS)定量吗?样品形状的影响

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The extraordinary throughput of the silicon drift detector energy dispersive x-ray spectrometer (SDD-EDS) enables collection of EDS spectra with much higher integrated counts within practical time periods, e.g., 100 s or less, compared to past experience with the Si(Li)-EDS. Such high count SDD spectra, containing one million to ten million counts, yield characteristic peak intensities with relative standard deviation below 0.25%, a precision similar to that achieved with wavelength dispersive spectrometry (WDS), the "gold standard" of microprobe analysis, but at lower dose because of the greater solid angle of the SDD-EDS. Such high count SDD-EDS spectra also enable more accurate quantification, nearly indistinguishable from WDS for major and minor constituents when the WDS unknown-to-standard intensity ratio ("k-value") protocol is followed. A critical requirement to satisfy this measurement protocol is that the specimen must be a highly polished bulk target. The geometric character of specimens examined in the scanning electron microscope (SEM) often deviates greatly from the ideal flat bulk target but EDS spectra can still be readily obtained and analyzed. The influence of geometric factors such as local inclination and surface topography on the accuracy of quantitative EDS analysis is examined. Normalized concentration values are subject to very large errors, as high as a factor of 10, as a result of deviation of the specimen geometry from the ideal flat bulk target.
机译:硅漂移探测器能量分散X射线光谱仪(SDD-EDS)的非凡吞吐量使得在实际期间内具有更高的集成计数,例如100 S或更少,与SI的过去经验相比(LI )的。这种高计数SDD光谱,含有一百万到百万计数,产生特征峰强度,相对标准偏差低于0.25%,这是一种与波长分散光谱(WDS)相似的精度,微探针分析的“金标准”,但是由于SDD-EDS的较大直角,较低剂量。这种高计数SDD-EDS光谱还能使更准确的量化,几乎无法区分,几乎无法从WDS中遵守主要和次要成分时,当遵循WDS未知标准强度比(“k值”)协议时。满足该测量方案的关键要求是样品必须是高度抛光的散装目标。在扫描电子显微镜(SEM)中检查的样本的几何特征通常从理想的扁平散装靶偏离,但仍然可以容易地获得并分析EDS光谱。研究了几何因子等局部倾斜和表面形貌对定量EDS分析精度的影响。归一化浓度值受到非常大的误差,高度为10,由于样本几何形状从理想的扁平散块靶的偏差导致。

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