Amorphous hydrogenated carbon deposited from acetylene in a dc glow di
scharge has been studied using solid-state C-13 NMR and FTIR spectrosc
opies. The fraction of sp2 carbon and the fraction of sp2 carbons that
bear a proton increase from 0.39 and 0.33, respectively, for the as-d
eposited material to approximately 1.0 and 0.44, respectively, after a
nnealing at 500-degrees-C. The loss of aliphatic carbon with increasin
g temperature arises not from aromatization but from outgassing of hyd
rocarbons or evolution of CO and CO2 formed by reactions between oxyge
n and the film. Infrared spectra are presented which show absorption f
eatures not previously seen for this material. The changing structure
with heat treatment and the role of oxygen in the formation and modifi
cation of the material are discussed.