AVS 56th International Symposium & Exhibition | |
Applied Surface Science | Thursday Sessions |
Session AS-ThA |
Session: | Chemical State Depth Profiling |
Presenter: | A.G. Shard, National Physical Laboratory, UK |
Authors: | A.G. Shard, National Physical Laboratory, UK A. Rafati, University of Nottingham, UK J.L.S. Lee, National Physical Laboratory, UK M.R. Alexander, University of Nottingham, UK M.C. Davies, University of Nottingham, UK |
Correspondent: | Click to Email |
We show that these samples possess an overlayer of almost pure poly(lactide), which fortuitously allows the direct comparison of different samples in terms of secondary ion yield behaviour. By comparing between data obtained from samples with different concentrations, it is found that secondary ion intensities do not scale linearly with composition. However, it is possible to relate secondary ion intensities to local concentrations for a binary system. The dependence of secondary ion yield on composition is described in terms of a model based on the kinetically limited transfer of charge between secondary ions and secondary neutrals. In this case, secondary ions from codeine, which contain a basic amine group, have an enhanced yield when dilute in poly(lactide). The enhancement diminishes with increasing concentration. The suppression in secondary ion yield for ions arising from poly(lactide) has the same functional form as the enhancement for secondary ions from codeine. The model is found to describe the data very well and has some wider implications for the interpretation of SIMS data from organic systems.
[1] A.G. Shard, F.M. Green, P.J. Brewer, M.P. Seah, I.S. Gilmore, Journal of Physical Chemistry B 112 (2008) 2596-2605.