Metal film adhesion to polymers can be improved by pretreatment with U
V-laser radiation before metal deposition. Chemical changes associated
with irradiation are investigated for polyimide (PI) and polybutylene
terephthalate (PET) surfaces. Irradiated surfaces are coated with alu
minum films less than or equal to 10 nm in thickness, enabling the eff
ects of irradiation on the metal/polymer interface to be studied. Irra
diation is done in air with KrF-excimer laser radiation(lambda = 248 n
m) at fluences per pulse less than or equal to 600 mJ/cm(2). The thres
hold fluence epsilon(t) for material removal is determined by profilom
etry measurements of etched features, and the chemical properties of t
he polymer and the metal/polymer interface are studied with X-ray phot
oelectron spectroscopy (XPS). Aluminum films are thermally evaporated
in situ in the XPS spectrometer. Irradiation of PI at fluences near ep
silon(t) (41 mJ/cm(2)) results in loss of oxygen and opening of the im
ide ring, resulting in doubly bonded nitrogen species. After evaporati
on of aluminum the carbonyl (C = O) Cls XPS signal is reduced in inten
sity, and both Al-0 and Al3+ are found, the latter being located at th
e interface. In comparison to unirradiated areas, irradiated areas hav
e more aluminum in total and a higher proportion of interfacial Al3+ s
pecies, indicating an increase in the concentration of metal binding s
ites. Although for PET the O to C ratio also decreases with irradiatio
n at fluences near epsilon(t) (38 mJ/cm(2)), changes in the amounts of
Al-0 or Al3+ for irradiated areas in comparison to unirradiated areas
are much smaller than for PI and consist mainly of a slight enhanceme
nt of Al-0 for films deposited on irradiated surfaces.