The adsorption and thermal decomposition of C2N2 on Si(100)-2 x 1 have
been investigated with TPD, XPS, UPS, and HREELS. For the C2N2 specie
s, two desorption peaks at 160 and similar to 230 K were noted in the
TPD spectrum, deriving from the C2N2 adsorbed in overlayers and the su
bmonolayer, respectively.;The latter showed C-1s and N-1s XPS peaks at
similar to 1.8 eV lower in binding energy than those of the multilaye
r C2N2 The large energy shift in the XPS peaks is likely caused by the
strong interaction between the C2N2 adsorbed side-on and the surface
at lower coverages. Annealing the C2N2-doses Si(100) at similar to 600
K caused the breaking of the NC-CN bond, and the CN adspecies could b
e identified on the surface. At 700-800 K, CN bond scission occurred,
and thus a mixture of silicon carbide and silicon nitride was formed.
Similar results were found for C2N2 on Si(111)-7 x 7; however, the rel
ative signal intensities, e.g., C-1s and N-1s XPS and HREELS, are weak
er than those of the C2N2 On Si(100). This difference may be attributa
ble to the fact that there are fewer dangling bonds on Si(ll 1)-7 x 7
than on Si(100)-2 x 1.