Hostname: page-component-586b7cd67f-2brh9 Total loading time: 0 Render date: 2024-11-29T03:34:25.016Z Has data issue: false hasContentIssue false

Analysis of Biological Structures by Electron Energy Loss Spectroscopy and Imaging

Published online by Cambridge University Press:  02 July 2020

R.D. Leapman
Affiliation:
Division of Bioengineering and Physical Science, ORS, MD20892
S.B. Andrews
Affiliation:
Laboratory of Neurobiology, NINDS, National Institutes of Health, Bethesda, MD20892
Get access

Abstract

As techniques for electron energy-loss spectroscopy (EELS) reach a higher degree of optimization, detection limits for analyzing biological structures are approaching those predicted by theory. in favorable specimens, single atom detection is predicted for elemental maps acquired by means of the scanning transmission electron microscope (STEM) equipped with a field emission source, paralleldetection EELS and a spectrum-imaging system. to obtain such results, the electron detector should have a detective quantum efficiency close to unity and a well behaved point-spread function; such design features are now available with a cooled charge-couple device (CCD) array. The energy-filtering transmission electron microscope (EFTEM) provides a complementary approach to mapping elements occurring at higher concentrations but distributed over larger regions of the specimen. Use of an optimized CCD detector in the EFTEM now enables accurate quantitation in addition to high analytical sensitivity, albeit not at the single atom level.

Type
EELS Microanalysis at High Sensitivity: Advances in Spectrum Imaging, Energy Filtering and Detection (Organized by R. Leapman and J. Bruley)
Copyright
Copyright © Microscopy Society of America 2001

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

References:

1.Shuman, H. and Somlyo, A.P., Ultramicroscopy 21 (1987) 23.CrossRefGoogle Scholar
2.Leapman, R.D. and Rizzo, N.W., Ultramicroscopy 78 (1999) 251.CrossRefGoogle Scholar
3.Jeanguillaume, C. & Colliex, C., Ultramicroscopy 28 (1989) 252.CrossRefGoogle Scholar
4.Hunt, J.A. and Williams, D.B., Ultramicroscopy 38 (1991) 47.CrossRefGoogle Scholar
5.Brink, H., Trevor, C., Hunt, J. and Mooney, P., Microsc. & Microanal. 6, suppl. 2 (2000) 212.CrossRefGoogle Scholar
6.Krivanek, O.L. et al., Ultramicroscopy 59 (1995) 267.CrossRefGoogle Scholar
7.Hunt, J.A. et al., Microsc. & Microanal. 5 (Suppl. 2) (1999) 616.CrossRefGoogle Scholar
8.Egerton, R.F., Ultramicroscopy 4 (1979) 169.CrossRefGoogle Scholar
9.Andrews, S.B. et al., Microsc. & Microanal. 6, suppl. 2 (2000) 162.CrossRefGoogle Scholar