Nature Publishing Group, publisher of Nature, and other science journals and reference works
Nature
my account e-alerts subscribe register
   
Sunday 05 July 2009
Journal Home
Current Issue
AOP
Archive
Download PDF
References
Export citation
Export references
Send to a friend
More articles like this

Letters to Nature
Nature 366, 143 - 146 (11 November 1993); doi:10.1038/366143a0

Atomic-resolution chemical analysis using a scanning transmission electron microscope

N. D. Browning, M. F. Chisholm & S. J. Pennycook

Solid State Division, Oak Ridge National Laboratory, PO Box 2008, Oak Ridge, Tennessee 37831-6030, USA

THE high angle elastic scattering of electrons in scanning transmission electron microscopy depends strongly on the atomic number Z, of the sample atoms, through the Z 2 dependence of the Rutherford scattering cross-section1. The detection of scattered electrons at high angles and over a large angular range (75& ndash;150 milliradians) removes the coherent effects of diffraction, and the resulting incoherent image provides a compositional map of the sample with high atomic-number contrast1. If a fine electron probe is used, and the sample is a crystalline material oriented along one of its principal axes, individual columns of atoms can be imaged in this way2. Electrons scattered at low angles are not used in this detection scheme, and are thus available for simultaneous electron energy-loss spectroscopy3; in principle, this combination of techniques should allow the direct chemical analysis of single atomic columns in crystalline materials. Here we present electron energy-loss spectra from expitaxial interfaces between cobalt silicide and silicon, which confirm that atomic resolution can be achieved by this approach. The ability to correlate structure and chemistry with atomic resolution holds great promise for the detailed study of defects and interfaces.

------------------

References
1. Pennycook, S. J. & Boatner, L. A. Nature 336, 565−567 (1988).
2. Pennycook, S. J. & Jesson, D. E. Phys. Rev. Lett. 64, 938−941 (1990); Acta Metall. Mater. 40, S149−S159 (1992).
3. Crewe, A. V., Wall, J. & Langmore, J. Science 168, 1338−1340 (1970).
4. Jesson, D. E. & Pennycook, S. J. in 51st A. Proc. Microsc. Soc. Am. (eds Bailey, G. W. & Rieder, C. L.) 978−979 (San Francisco Press, California, 1993).
5. Loane, R. F., Xu, P. & Silcox, J. Ultramicroscopy 40, 121−138 (1992).
6. Browning, N. D. & Pennycook, S. J. Microbeam Analysis 2, 81−89 (1993).
7. Browning, N. D., McGibbon, M. M., Chisholm, M. F. & Pennycook, S. J. in 51st A. Proc. Microsc. Soc. Am. (eds Bailey, G. W. & Rieder, C. L.) 576−577 (San Francisco Press, California, 1993).
8. Pennycook, S. J. Contemp. Phys. 23, 371−400 (1982).
9. Kohl, H. & Rose, H. Adv. Electron. Electron Phys. 65, 175−200 (1985).
10. Ritchie, R. H. & Howie, A. Phil. Mag. A58, 753−767 (1988).
11. Allen, L. J. & Rossouw, C. J. Phys. Rev. B42, 11644−11654 (1990).
12. Scheinfein, M. R. & Isaacson, M. S. J. Vac. Sci. Technol. B4, 326−332 (1986).
13. Batson, P. E. Phys. Rev. B44, 5556−5561 (1991).
14. Browning, N. D., Yuan, J. & Brown, L. M. Phil. Mag. A67, 261−271 (1993).
15. Browning, N. D., Chisholm, M. F., Pennycook, S. J., Norton, D. P. & Lowndes, D. H. Physica C212, 185−190 (1993).
16. Batson, P. E. Ultramicroscopy 47, 133−144 (1992).
17. de Jong, A. F. & Bulle-Liewma, C. W. T. Phil. Mag. A62, 183−201 (1990).
18. Chisholm, M. F., Jesson, D. E., Pennycook, S. J. & Mantl, S. in 51st A. Proc. Microsc. Soc. Am. (eds Bailey, G. W. & Rieder, C. L.) 802−803 (San Francisco Press, California, 1993).
19. De Crescenzi, M., Derrien, J., Chainet, E. & Orumchian, K. Phys. Rev. B39, 5520−5523 (1989).



© 1993 Nature Publishing Group
Privacy Policy