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Volumn 16, Issue 4, 1998, Pages 2595-2603

Characteristic losses in metals: Al, Be, and Ni

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EID: 0032337535     PISSN: 07342101     EISSN: None     Source Type: Journal    
DOI: 10.1116/1.581388     Document Type: Article
Times cited : (3)

References (57)
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    • edited by D. C. Konigsberger and R. Prins Wiley, New York
    • For a short overview of SXAS, and of related techniques for CB DOS studies see: J. C. Fuggle and J. E. Inglesfield, Topics in Applied Physics, (Springer, Berlin, 1992), Vol. 69, pp. 1-24; and for a discussion of the theoretical approach(es) to understanding that part of the SXAS data, the near-edge structure, of relevance to our results, see P. J. Durham, in X-Ray Adsorption: Principles, Applications, Techniques of EXAFS, SEX-AFS and XANES, edited by D. C. Konigsberger and R. Prins (Wiley, New York, 1988), pp. 53-84.
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    • note
    • Because of a potassium impurity in our Al source material, the W substrate was held at T=600-675 K during the deposition of Al. This allowed Al films to be deposited while keeping K levels below AES detection limits. For the results presented here, the Ni films were deposited onto oxidized Al films. Deposition of clean Ni was continued until there was no AES evidence of the underlying aluminum or oxygen.
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    • note
    • For a discussion of loss deconvolution see Ref. 21. The "proper" amount of losstail scaling for processing AES data is guided by the criterion that Auger signals should be finite in energy width, so that they should approach zero intensity smoothly around 10-15 eV below the high energy thresholds. Such behavior reduces the average upward slope in the loss-corrected spectrum after the threshold region. For Ni, this required that we increase the strength of the loss tail of the experimentally measured system response function (see Fig. 3). The system response functions for Be and Al loss deconvolution in Fig. 3 were found to satisfy this criterion as measured, so that no scaling of the loss tail was done in either of these two cases. We should note that the shape of the final N(E) spectrum is sensitive to the scaling used for the loss tail of the response function (e.g., for Ni, utilizing no scaling produces a step at threshold, in contrast to the peak in Fig. 5).
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    • edited by M. W. Roberts and J. M. Thomas Chemical Society, Burlinghouse, London
    • See review articles: R. L. Park and J. E. Houston, J. Vac. Sci. Technol. 11, 1 (1974); A. M. Bradshaw, in Surface and Defect Properties of Solids, edited by M. W. Roberts and J. M. Thomas (Chemical Society, Burlinghouse, London, 1974), Vol. 3, pp. 153-183.
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    • In Ref. 24, see Figs. 10.9 and 10.10
    • In Ref. 24, see Figs. 10.9 and 10.10.
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    • see also Fig. 6.24 (p. 248) in Ref. 22 above
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    • note
    • 23)-SXAS results for solid Al.


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