Atominstitut, Vienna University of Technology, Wien, Austria.
Anal Bioanal Chem. 2011 Jun;400(8):2649-54. doi: 10.1007/s00216-010-4592-9. Epub 2010 Dec 29.
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.
全反射 X 射线荧光分析(TXRF)可对微量元素进行非破坏性定性和定量分析。由于其出色的性能,TXRF 在半导体行业中被广泛用于硅片表面分析和液体样品的化学分析。在定量分析中存在两个问题:晶圆表面分析中统计不确定性大,以及在化学分析中使用内标法的有效性。一般来说,TXRF 被认为允许线性校准。对于小样本量(低纳克(ng)区域),可以忽略激发和检测辐射的吸收效应,采用薄膜近似法。对于更高的总样品量,可以观察到荧光强度与样品量之间的线性关系发生偏离。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可能导致发射荧光强度的差异和高统计误差。本研究的目的是调查样品内部的元素分布。使用同步辐射诱导微 X 射线荧光分析(SR-μ-XRF)和光学显微镜对单元素和多元素样品进行了研究。可以证明显微镜图像均基于所研究的元素。这允许仅使用光学显微镜图像确定样品形状和潜在的不均匀性。对于多元素样品,进一步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。