Theoretical auger electron spectra of polymers by density functional theory calculations using model dimers

Abstract

We propose a new approach for analysis of Auger electron spectra (AES) of polymers by density functional theory (DFT) calculations with the Slater's transition-state concept. Simulated AES and X-ray photoelectron spectra (XPS) of four polymers [(CH2CH2)n (PE), (CH2CH(CH3))n (PP), (CH2CH(OCH3))n (PVME), and (CH2CH(COCH3))n (PVMK)] by DFT calculations using model dimers are in a good accordance with the experimental ones. The experimental AES of the polymers can be classified in each range of 1s–2p2p, 1s–2s2p, and 1s–2s2s transitions for C KVV and O KVV spectra, and in individual contributions of the functional groups from the theoretical analysis. © 2002 Wiley Periodicals, Inc. J Comput Chem 23: 394–401, 2002