Abstract

The migration behavior of Li, K, and F during secondary ion mass spectrometry (SIMS) depth profiling was investigated in both n- and p-type Si using different oxygen bombardment conditions. The presence of an electric field across the surface oxide is shown to be the major driving force for both the segregation of Li and K at the SiO2/Si interface and the antisegregation of F into the oxide. Room temperature SIMS measurements revealed that K segregates at the oxide side of the SiO2/Si interface, whereas Li segregates at the silicon side of the interface. We have also found that the field-induced segregation of Li and antisegregation of F are less pronounced in high resistivity (11 000–16 000 Ω cm) p-type Si than in low resistivity (∼0.011 Ω cm) n-type Si. Although Li segregates at the Si side of the interface in both types of Si, some Li, however, remains at the oxide side in the high resistivity p-type Si. The high solid solubility of Li in amorphous Si is also considered as a driving force for its segregation.

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