The chemical modification of the surfaces of polycarbonate films by mi
crowave-induced argon plasma treatment has been followed by X-ray abso
rption spectroscopy (XAFS) and core level photoemission spectroscopy (
XPS). Measurements have been made on thin films of both ex-situ spin-c
oated bis-phenol-A polycarbonate with phenol endgroups and the model c
ompound bis-phenol-A polycarbonate (n = 1) with tert-butyl phenyl endg
roups evaporated in-situ in UHV on single crystal surfaces. A preferen
tial orientation of a monolayer of the model compound on a Ag{111} sur
face was determined from the angular dependence of the XAFS spectra. S
pectral features were assigned to contributing transitions within diff
erent moieties. Relatively mild microwave Ar plasma activation of the
surfaces of both types of films led to a decrease in intensity of carb
onyl features in both XAFS and XPS. Combined with the observation of n
ew spectral features in XPS the data can be interpreted in terms of a
formation of ester and ether groups in the near-surface region with po
ssible cross-linking after desorption of CO or CO2. (C) 1998 Elsevier
Science B.V.