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Applications of Nuclear Techniques, Computer Simulation and Microscopy to Surface Analysis of Materials

Published online by Cambridge University Press:  06 August 2013

J. Pacheco de Carvalho
Affiliation:
Departamento de Física, Universidade da Beira Interior, Rua Marquês d’Ávila e Bolama, 6201-001 Covilhã, Portugal Unidade de Detecção Remota, Universidade da Beira Interior, Rua Marquês d’Ávila e Bolama, 6201-001 Covilhã, Portugal
C.F.R. Pacheco
Affiliation:
Unidade de Detecção Remota, Universidade da Beira Interior, Rua Marquês d’Ávila e Bolama, 6201-001 Covilhã, Portugal
A.D. Reis
Affiliation:
Departamento de Física, Universidade da Beira Interior, Rua Marquês d’Ávila e Bolama, 6201-001 Covilhã, Portugal Unidade de Detecção Remota, Universidade da Beira Interior, Rua Marquês d’Ávila e Bolama, 6201-001 Covilhã, Portugal

Abstract

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There is a wide range of surface analysis techniques which are, generally, complementary. Nuclear and non-nuclear techniques have been available. Nuclear techniques, which are non-destructive, provide for analysis over a few microns close to the surface of the sample, giving absolute values of concentrations of isotopes and elements. They have been applied in areas such as scientific, technologic, industry, arts and medicine, using MeV ion beams. Nuclear reactions permit tracing of isotopes with high sensitivities. We use ion-ion nuclear reactions, elastic scattering and the energy analysis method where, at a chosen energy of the incident ion beam, an energy spectrum is recorded of ions from nuclear events, coming from several depths in the target. Such spectra are computationally predicted, giving target composition and concentration profile information. A computer program has been developed in this context, mainly for flat targets. The non-flat target situation arises as an extension. Successful applications of the method are given using the 18O(p,α0)15N reaction and elastic scattering of (4He)+ ions. SEM and TEM are used as useful complementary techniques.

Two types of samples were prepared containing thick and thin oxides, respectively. The first sample (S1) was obtained by high temperature oxidation of austenitic steel in C 18O2 gas. Weight gain measurements had given a 4.2 μm thick oxide. SEM has shown a reasonably flat oxide (Figure 1 (a)). The second sample (S2, also labelled Al/Al2O3) was obtained by anodization of high purity aluminium at 100V in an aqueous solution of ammonium citrate. An oxide thickness of 0.1370 μm was expected. TEM has given an oxide film thickness of 0.1340 μm (Figure 1 (b)). The 18O(p,α0)15N reaction at Ep=1.78 MeV and 165º was used to analyse sample S1. Figure 2 (a) shows a good computed fit to data. A 18O step concentration profile was found, corresponding to a thick 18O oxide with thickness X1=4.4 μm. Sample S2 was analysed by elastic scattering of α particles at Eα=2.0 MeV and 165º. Figure 2 (b) shows a good computed fit to data. A thin oxide film thickness of X1=0.1350 μm was found, close to the TEM value. The fit also shows a ratio of atomic densities of O and Al slightly above 1.5. The combined use of nuclear techniques, SEM and TEM microscopy has proved to be very important for surface analysis of materials. The reported results would be difficult to obtain by other techniques.

Supports from University of Beira Interior and FCT (Fundação para a Ciência e a Tecnologia)/PEst-OE/FIS/UI0524/2011 (Projecto Estratégico-UI524-2011-2012) are acknowledged.

Type
Materials Sciences
Copyright
Copyright © Microscopy Society of America 2013