首页> 外文会议>Conference on scanning microscopies >Scanning Electron Microscopy/Energy Dispersive Spectrometry Fixed-beam or Overscan X-ray Microanalysis of Particles Can Miss the Real Structure: X-ray Spectrum Image Mapping Reveals the True Nature
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Scanning Electron Microscopy/Energy Dispersive Spectrometry Fixed-beam or Overscan X-ray Microanalysis of Particles Can Miss the Real Structure: X-ray Spectrum Image Mapping Reveals the True Nature

机译:扫描电子显微镜/能谱仪对粒子的固定束或过扫描X射线显微分析会错过真实结构:X射线光谱图像映射揭示了真实的性质

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The typical strategy for analysis of a microscopic particle by scanning electron microscopy/energy dispersive spectrometry x-ray microanalysis (SEM/EDS) is to use a fixed beam placed at the particle center or to continuously overscan to gather an "averaged" x-ray spectrum. While useful, such strategies inevitably concede any possibility of recognizing microstructure within the particle, and such fine scale structure is often critical for understanding the origins, behavior, and fate of particles. Elemental imaging by x-ray mapping has been a mainstay of SEM/EDS analytical practice for many years, but the time penalty associated with mapping with older EDS technology has discouraged its general use and reserved it more for detailed studies that justified the time investment. The emergence of the high throughput, high peak stability silicon drift detector (SDD-EDS) has enabled a more effective particle mapping strategy: "flash" x-ray spectrum image maps can now be recorded in seconds that capture the spatial distribution of major (concentration, C > 0.1 mass fraction) and minor (0.01 ≤ C ≤ 0.1) constituents. Ne0w SEM/SDD-EDS instrument configurations feature multiple SDDs that view the specimen from widely spaced azimuthal angles. Multiple, simultaneous measurements from different angles enable x-ray spectrometry and mapping that can minimize the strong geometric effects of particles. The N1ST DTSA-Ⅱ software engine is a powerful aid for quantitatively analyzing EDS spectra measured individually as well as for mapping information.
机译:通过扫描电子显微镜/能量分散光谱X射线微分析(SEM / EDS)分析微观粒子的典型策略是使用放置在粒子中心的固定光束或连续过扫描以收集“平均”X射线光谱。虽然有用,但这些策略不可避免地承认识别粒子内的微观结构的可能性,并且这种微量规模结构通常对于了解粒子的起源,行为和命运通常是至关重要的。 X射线映射的元素成像是多年来的SEM / EDS分析实践的主干,但与旧EDS技术的映射相关的时间惩罚已经阻止了其一般使用,并保留了更多的详细研究,详细研究了合理的时间投资。高吞吐量的出现,高峰稳定性硅漂移探测器(SDD-EDS)已经启用了更有效的粒子映射策略:现在可以在捕获主要空间分布的秒内以几秒钟记录“闪光”X射线谱图像图(浓度,C> 0.1质量分数)和次要(0.01≤C≤0.1)成分。 NE0W SEM / SDD-EDS仪器配置具有多个SDD,可从广泛间隔的方位角查看样本。多个,来自不同角度的同步测量使X射线光谱和映射能够最小化粒子的强几何效果。第N1ST DTSA-Ⅱ软件引擎是一种强大的辅助辅助,用于定量分析IDS光谱,单独测量以及映射信息。

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