Ion-surface interactions on c-Si(001) at the radiofrequency-powered electrode in low-pressure plasmas:: Ex situ spectroscopic ellipsometry and Monte Carlo simulation study

We use variable-angle spectroscopic ellipsometry (VASE) to investigate oxide and interface formation during plasma-oxidation of monocrystalline Si(001) at the radio frequency (rf) powered electrode of a plasma-enhanced chemical vapor deposition reactor. HF-etched c-Si(001) wafers were exposed to an oxygen plasma under conditions similar to those used in optical coatings deposition in order to ascertain the effects of plasma-bulk interactions, and to gauge to what depth O-2(+) and O+ ions interact with and alter the structure and composition of the target in the presence of negative self-bias, V-B From VASE analyses, modifications are best described using a two-layer model: A top layer consisting of SiO2 and a defective interfacial layer (DL) composed of a mixture of c-Si, a-Si, and SiO2. The saturation value of the modification depth (oxide and DL thickness) increases from 3.4 +/- 0.4 to 9.6 +/- 0.4 nm, for V-B ranging from -60 to -600 V-B respectively, and scales with E-max(1/2) where E-max is the maximum energy of ions from an rf discharge. These results are in agreement with nuclear ion-bulk interactions leading to atornic displacements and defect accumulation. The interfacial layer broadens with increasing vertical bar V-B vertical bar while the fraction of a-Si detected increases from similar to 1% up to similar to 55% over the investigated V-B range, indicative of ballistic and thus depth-dependent oxygen transport to the SiO2-Si interface. Monte Carlo simulations in the binary collision approximation predict significant surface recession due to sputtering, therefore resulting in an apparent self-limiting oxidation mechanism. The surface layers reach their steady-state thicknesses within the first 2 min of plasma exposure and subsequently move into the bulk of the c-Si substrate as a result of oxide sputtering and oxygen transport. (c) 2006 American Vacuum Society.