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Investigation of element distribution and homogeneity of TXRF samples using SR-micro-XRF to validate the use of an internal standard and improve external standard quantification

机译:使用SR-micro-XRF研究TXRF样品的元素分布和同质性,以验证内标的使用并改善外标定量

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摘要

Total reflection X-ray fluorescence analysis (TXRF) offers a nondestructive qualitative and quantitative analysis of trace elements. Due to its outstanding properties TXRF is widely used in the semiconductor industry for the analysis of silicon wafer surfaces and in the chemical analysis of liquid samples. Two problems occur in quantification: the large statistical uncertainty in wafer surface analysis and the validity of using an internal standard in chemical analysis. In general TXRF is known to allow for linear calibration. For small sample amounts (low nanogram (ng) region) the thin film approximation is valid neglecting absorption effects of the exciting and the detected radiation. For higher total amounts of samples deviations from the linear relation between fluorescence intensity and sample amount can be observed. This could be caused by the sample itself because inhomogeneities and different sample shapes can lead to differences of the emitted fluorescence intensities and high statistical errors. The aim of the study was to investigate the elemental distribution inside a sample. Single and multi-element samples were investigated with Synchrotron-radiation-induced micro X-ray Fluorescence Analysis (SR-μ-XRF) and with an optical microscope. It could be proven that the microscope images are all based on the investigated elements. This allows the determination of the sample shape and potential inhomogeneities using only light microscope images. For the multi-element samples, it was furthermore shown that the elemental distribution inside the samples is homogeneous. This justifies internal standard quantification.
机译:全反射X射线荧光分析(TXRF)提供了痕量元素的无损定性和定量分析。由于其出色的性能,TXRF被广泛用于半导体行业中的硅晶片表面分析和液体样品的化学分析。量化中存在两个问题:晶圆表面分析中的统计不确定性很大,以及在化学分析中使用内标的有效性。通常,已知TXRF允许进行线性校准。对于少量样品(低纳克(ng)区域),薄膜近似有效地忽略了激发和检测到的辐射的吸收效应。对于更高的样品总量,可以观察到荧光强度和样品量之间线性关系的偏离。这可能是由于样品本身引起的,因为不均匀性和不同的样品形状会导致发射的荧光强度差异和高统计误差。该研究的目的是调查样品内部的元素分布。通过同步辐射诱导的微量X射线荧光分析(SR-μ-XRF)和光学显微镜研究了单元素和多元素样品。可以证明显微镜图像都是基于所研究的元素。这使得仅使用光学显微镜图像即可确定样品的形状和潜在的不均匀性。对于多元素样品,还表明样品内部的元素分布是均匀的。这证明了内标定量的合理性。

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