Diamond and diamond-like carbon have properties which in principle mak
e them ideally suited to a wide variety of thin-film applications. The
widespread use of diamond thin films, however, has been limited for a
number of reasons related largely to the lack of understanding and co
ntrol of the nucleation and growth processes. Real-time, in-situ studi
es of the surface of the growing diamond film are experimentally diffi
cult because these films are normally grown under a relatively high pr
essure of hydrogen, and conventional surface analytical methods requir
e an ultrahigh vacuum environment. Pulsed ion beam based analytical me
thods with differentially pumped ion sources and particle detectors ar
e able to characterize the uppermost atomic layer of a film during gro
wth at ambient pressures in the range 0.7-27 Pa (4-6 orders of magnitu
de higher than other surface-specific analytical methods). We describe
here a system which has been developed for the purpose of determining
the hydrogen concentration and bonding sites on diamond surfaces as a
function of sample temperature and ambient hydrogen pressure under ho
t-filament chemical vapor deposition (CVD) growth conditions. It is de
monstrated that as the hydrogen partial pressure increases the saturat
ion hydrogen coverage of the surface of a CVD diamond film increases,
but that the saturation level depends on the atomic hydrogen concentra
tion and substrate temperature. At the highest temperatures studied (7
00 degrees C), it was found that the surface hydrogen concentration di
d not exceed 1/4 monolayer.