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Microcalorimeter EDS Measurements of Chemical Shifts in Fe Compounds

Published online by Cambridge University Press:  02 July 2020

D. A. Wollman
Affiliation:
National Institute of Standards and Technology, Boulder, CO, 80303
Dale E. Newbury
Affiliation:
National Institute of Standards and Technology, Gaithersburg, MD, 20899
G. C. Hilton
Affiliation:
National Institute of Standards and Technology, Boulder, CO, 80303
K. D. Irwin
Affiliation:
National Institute of Standards and Technology, Boulder, CO, 80303
L. L. Dulcie
Affiliation:
National Institute of Standards and Technology, Boulder, CO, 80303
N. F. Bergren
Affiliation:
National Institute of Standards and Technology, Boulder, CO, 80303
John M. Martinis
Affiliation:
National Institute of Standards and Technology, Boulder, CO, 80303
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Extract

We report measurements of chemical shifts in the Fe-L x-ray lines of different Fe compounds from xray emission spectra acquired using a microcalorimeter energy dispersive spectrometer (EDS). The observed changes in peak position and relative intensity of the Fe-L x-ray lines are in agreement with measurements obtained using a wavelength dispersive spectrometer (WDS), demonstrating the usefulness of microcalorimeter EDS for high-energy-resolution x-ray microanalysis.

Chemical shifts result from changes in electron binding energies with the chemical environment of atoms. In x-ray spectra, chemical shifts lead to changes in x-ray peak positions, relative peak intensities, and peak shapes. These chemical bonding effects can be significant (with x-ray peak shifts on the order of 1 eV), particularly for x-ray lines resulting from transitions involving valence electrons of light elements such as B and C.

Type
30 Years of Energy Dispersive Spectrometry in Microanalysis
Copyright
Copyright © Microscopy Society of America

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References

1.Holliday, J. E., J. Appl. Phys., 38 (1967) 4720.CrossRefGoogle Scholar
2.Wollman, D. A. et al., J. Microscopy, 188 (1997) 196.CrossRefGoogle Scholar
3.Martinis, J. M. et al., these proceedings.Google Scholar
4.Fisher, D. W., J. Appl. Phys., 36 (1965) 2048.CrossRefGoogle Scholar
5.Smith, D. G. W. and O'Nions, R. K., J. Phys. D, 4 (1971) 147.CrossRefGoogle Scholar
6. Contribution of the U.S. Government; not subject to copyright.Google Scholar