We
employ time-dependent photoluminescence (PL) and steady-state
PL excitation (PLE) measurements to study the size-dependent optical
properties of ultrasmall silicon carbide (SiC) nanoparticles (NPs).
We find that the nature of the optical transition transforms from
solid-state indirect gap to molecular-like as the diameter of spherical
SiC NPs is reduced from 4–6 to 1–3 nm with a smooth
transition in between. We deduce the radiative lifetimes of SiC NPs
that are well supported by ab initio time-dependent density functional
theory calculations on realistically large SiC NPs with realistic
surface terminations, including the solvation effects.
Carbon diffusion in a SiO 2 /Si system was investigated. The source was provided by chemical vapor deposition of a hydrogenated amorphous carbon layer onto the oxide at low temperature. From layers with low oxygen content, no carbon outdiffusion was detected up to 1190 • C. If the O content was high, the diffusion would start suddenly at 1140 • C, and carbon accumulation would be found on the Si side of the SiO 2 /Si interface in the form of SiC precipitates. These results are interpreted by assuming oxygen-assisted dissociation of carbon atoms from the carbon layer in form of CO molecules, fast CO diffusion through SiO 2 and an exothermic reaction of CO with Si. No carbon segregation was found in SiO 2 . Consequences of carbon island formation during SiC oxidation are pointed out.
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