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IN SITU COMPOSITION ANALYSIS BY EDS AT ELEVATED TEMPERATURES IN SEM AND STEM

机译:在SEM和茎的升高温度下,EDS原位成分分析

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We discuss possibilities and challenges of energy-dispersive X-ray spectroscopy (EDS) and EDS element mapping at elevated temperatures in SEM and STEM. An electron transparent Pd-Au-nanoparticle test structure on carbon film is one example. The agglomeration and evaporation of nanoparticle material during heating from room temperature up to 1,000 °C [1] in a conventional STEM were studied. Chemical phase analysis and simple statistical methods were applied to quantify the areal coverage of different species and its change with rising temperature. Heat radiation at elevated temperatures changes the low energy part of EDS spectra. We demonstrate, that element identification below 2 kV and chemical phase analysis are still possible within certain limits. For example, nitrogen can be detected up to 900 °C (Fig. 1). The results of phase and particle analysis (Fig. 2) demonstrate the capabilities of in-situ EDS in combination with statistical methods. Material agglomeration and evaporation of one involved species during heating could be quantified by areal coverage. The stability of the heating holder during temperature change ensured very low drift and successful element mapping and tracking [1].
机译:我们讨论能量分散X射线光谱(EDS)和EDS元素映射在SEM和茎的升高温度下的可能性和挑战。碳膜上的电子透明PD-Au-纳米粒子测试结构是一个实例。研究了在常规茎中加热至1,000℃[1]期间纳米颗粒材料的凝聚和蒸发。应用化学相分析和简单的统计方法来量化不同物种的面积覆盖及其随着温度上升的变化。升高温度下的热辐射改变了EDS光谱的低能量部分。我们证明,在一定限度内仍有以下2 kV和化学相分析的元素鉴定。例如,可以检测到氮气高达900℃(图1)。阶段和颗粒分析的结果(图2)展示了原位EDS与统计方法的能力。通过在加热过程中涉及一个涉及的物质的材料凝聚和蒸发可以通过区域覆盖量化。温度变化期间加热保持器的稳定性确保了非常低的漂移和成功的元素映射和跟踪[1]。

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