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Journal ArticleDOI

Is Scanning Electron Microscopy/Energy Dispersive X-ray Spectrometry (SEM/EDS) Quantitative?

01 May 2013-Scanning (Scanning)-Vol. 35, Iss: 3, pp 141-168
TL;DR: Scanning electron microscopy/energy dispersive X-ray spectrometry (SEM/EDS) is a widely applied elemental microanalysis method capable of identifying and quantifying all elements in the periodic table except H, He, and Li, but measurement issues continue to diminish the impact.
Abstract: Scanning electron microscopy/energy dispersive X-ray spectrometry (SEM/EDS) is a widely applied elemental microanalysis method capable of identifying and quantifying all elements in the periodic table except H, He, and Li. By following the "k-ratio" (unknown/standard) measurement protocol development for electron-excited wavelength dispersive spectrometry (WDS), SEM/EDS can achieve accuracy and precision equivalent to WDS and at substantially lower electron dose, even when severe X-ray peak overlaps occur, provided sufficient counts are recorded. Achieving this level of performance is now much more practical with the advent of the high-throughput silicon drift detector energy dispersive X-ray spectrometer (SDD-EDS). However, three measurement issues continue to diminish the impact of SEM/EDS: (1) In the qualitative analysis (i.e., element identification) that must precede quantitative analysis, at least some current and many legacy software systems are vulnerable to occasional misidentification of major constituent peaks, with the frequency of misidentifications rising significantly for minor and trace constituents. (2) The use of standardless analysis, which is subject to much broader systematic errors, leads to quantitative results that, while useful, do not have sufficient accuracy to solve critical problems, e.g. determining the formula of a compound. (3) EDS spectrometers have such a large volume of acceptance that apparently credible spectra can be obtained from specimens with complex topography that introduce uncontrolled geometric factors that modify X-ray generation and propagation, resulting in very large systematic errors, often a factor of ten or more.
Citations
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Journal ArticleDOI
TL;DR: This review focuses on the toolbox of available methods for the preparation of polymeric nanoparticles and highlights some recent examples from the literature that demonstrate the influence of the preparation method on the physicochemical characteristics of the nanoparticles.

357 citations

Journal ArticleDOI
TL;DR: Accurate analyses of low atomic number elements, C, N, O, and F, are demonstrated and measurement of trace constituents with limits of detection below 0.001 mass fraction is possible within a practical measurement time of 500 s.
Abstract: Electron-excited X-ray microanalysis performed in the scanning electron microscope with energy-dispersive X-ray spectrometry (EDS) is a core technique for characterization of the microstructure of materials. The recent advances in EDS performance with the silicon drift detector (SDD) enable accuracy and precision equivalent to that of the high spectral resolution wavelength-dispersive spectrometer employed on the electron probe microanalyzer platform. SDD-EDS throughput, resolution, and stability provide practical operating conditions for measurement of high-count spectra that form the basis for peak fitting procedures that recover the characteristic peak intensities even for elemental combination where severe peak overlaps occur, such PbS, MoS2, BaTiO3, SrWO4, and WSi2. Accurate analyses are also demonstrated for interferences involving large concentration ratios: a major constituent on a minor constituent (Ba at 0.4299 mass fraction on Ti at 0.0180) and a major constituent on a trace constituent (Ba at 0.2194 on Ce at 0.00407; Si at 0.1145 on Ta at 0.0041). Accurate analyses of low atomic number elements, C, N, O, and F, are demonstrated. Measurement of trace constituents with limits of detection below 0.001 mass fraction (1000 ppm) is possible within a practical measurement time of 500 s.

256 citations


Cites background from "Is Scanning Electron Microscopy/Ene..."

  • ...This situation has developed because of three contributing factors: (1) the rise of standardless analysis which now dominates EDS quantitative analysis [14]; (2) the severe effects of specimen geometry on the accuracy of X-ray microanalysis which occur no matter which analytical protocol is followed, standards-based or standardless [15]; and (3) the occasional but significant failures in qualitative analysis, i....

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Journal ArticleDOI
TL;DR: In this paper, a review of the use of X-ray diffraction, Raman spectroscopy, electron microscopy/spectroscopy and a number of other techniques to understand if the precursor is suitable for MXene synthesis, confirm successful synthesis of MXene, and finally determine its composition, structure and properties.

193 citations

Journal ArticleDOI
TL;DR: In this paper, the authors reported the design and synthesis of high surface area photocatalysts by coating TiO2 on fibrous nanosilica (KCC-1) using atomic layer deposition (ALD).
Abstract: In this work we report the design and synthesis of high-surface-area photocatalysts by coating TiO2 on fibrous nanosilica (KCC-1) using atomic layer deposition (ALD). Our developed catalyst showed enhanced photocatalytic activity, better than that of the well-known MCM-41- and SBA-15-supported TiO2 catalysts using ALD as well as that of other silica-supported TiO2 catalysts reported in the literature to date. This work shows how one can tune the photocatalytic activity of supported TiO2 catalysts by simply tuning the morphology of the support. In addition to extensive characterization of materials using various techniques, comprehensive mechanistic insight into ALD TiO2 coating on KCC-1 fibers was gained using solid-state NMR and UV-DRS. For the first time, we also observed the formation of small and monodispersed TiO2 nanoparticles after heat treatment of these ALD-coated samples of KCC-1. Notably, we observed size quantization effects in these TiO2 nanoparticles, which was confirmed by band gap shift me...

130 citations

References
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Journal ArticleDOI

3,871 citations


"Is Scanning Electron Microscopy/Ene..." refers background in this paper

  • ...The minimum level for quantitative analysis, the so-called determination limit, is defined as a level that exceeds the standard deviation of the background by at least a factor of ten (Currie, ’68)....

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Book
01 Jan 1987
TL;DR: SEM-Instrumentation: Introduction Principles of Operation Specimen/Electron Interactions Detectors Operating Conditions and Limitations Specimen Preparation: Specimen Characteristics Drying Techniques Coating Cryo-SEM SEM X-Ray Microanalysis Instrumentation as mentioned in this paper.
Abstract: SEM-Instrumentation: Introduction Principles of Operation Specimen/Electron Interactions Detectors Operating Conditions and Limitations Specimen Preparation: Specimen Characteristics Drying Techniques Coating Cryo-SEM SEM X-Ray Microanalysis-Instrumentation: Introduction X-Ray Production in the SEM Wavelength Dispersive Systems (WDS) Energy Dispersive Systems (EDX) Operating Conditions and Limitations Data Handling Other Surface Analytical Techniques.

2,084 citations


"Is Scanning Electron Microscopy/Ene..." refers background in this paper

  • ...Scanning electron microscopy with energy dispersive X-ray spectrometry (SEM/EDS) is an elemental microanalysis technique widely applied across a broad range of the physical and biological sciences, engineering, technology, and forensic investigations (Goldstein et al., 2003)....

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  • ...Geometrical structures such as scratches with dimensions on the micrometer scale similar to the electron interaction volume can significantly modify the generation and/or propagation of X-rays and introduce a large and unpredictable error component (Yakowitz, ’68; Goldstein et al., 2003)....

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  • ...and unpredictable error component (Yakowitz, ’68; Goldstein et al., 2003)....

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  • ...Goldstein et al. (2003) provide an explicit calculation of the standard deviation of the concentration value, σ C, taking into account the four sources of variance in the k-ratio measurement (the characteristic peak count and the background count for both the unknown in the numerator of the k-ratio…...

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  • ...…Division, National Institute of Standards and Technology, Gaithersburg, MD 20899 E-mail: dale.newbury@nist.gov Received 10 May 2012; Accepted with revision 29 June 2012 DOI 10.1002/sca.21041 Published online 9 August 2012 in Wiley Online Library (wileyonlinelibrary.com) (Goldstein et al., 2003)....

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Book ChapterDOI
01 Jan 1991
TL;DR: For about 20 years, quantitative analysis of homogeneous microvolumes has been performed with the aid of correction models which transform into mass concentrations C A the ratio k A between the emerging intensities from the specimen and a standard obtained for a characteristic line of element A.
Abstract: For about 20 years, quantitative analysis of homogeneous microvolumes has been performed with the aid of correction models which transform into mass concentrations C A the ratio k A between the emerging intensities from the specimen and a standard obtained for a characteristic line of element A:

1,138 citations

BookDOI
TL;DR: Practical scanning electron microscopy as discussed by the authors, a practical approach for the practical use of electron microscopes in the field of computer vision, is another example of such a technique, and
Abstract: Practical scanning electron microscopy , Practical scanning electron microscopy , کتابخانه مرکزی دانشگاه علوم پزشکی تهران

455 citations