High detection sensitivity in bulk analysis or depth profiling by secondary ion mass spectrom etry (SIMS) can only be achieved, for positively charged ions, if the near surface regions of the sputter eroded sample are fully oxidized. Using oxygen prim ary ions, a stationary oxidation state is established after some tim e of bom bardm ent during which period the sputtering yield decreases and the ionization probability increases. The physical and chemical processes occurring during the transient period are reviewed w ith emphasis on the results for im purity analysis in silicon, i.e. the m atrix m aterial th a t has been studied most thoroughly in the past. The transient de crease in sputtering yield gives rise to a depth scale offset and an associated apparent shift of im purity profiles towards the surface. The effect is largest at normal beam incidence, ca. 1 nm/keVXOf), in which case silicon is fully oxidized. The transition depth, i.e. the depth sputtered before achieving a stable ion yield is about twice as large and increases as the im pact angle is turned away from normal. The shift and the depth scale offset can be measured safely using thin (delta) layers of isotopically pure tracers, for example 30Si in 28Si. Boron delta layers can serve as secondary standards because this im purity behaves almost the same as the host silicon atoms. The profile shift observed w ith other common dopants may contain contributions due to unidirectional relocation, often driven by segregation away from the surface. At O j energies below about 0.7 keV the transition depths fall below the thickness of typical native oxides, so th a t the transient changes in sputtering yield and ionization probability can disappear. The transient phenomena may be described by a simple sputtering-oxidation model th a t connects the depth scale offset to other observable param eters like the initial and final sputtering yield, the transition fluence and the oxide thickness.
I n tr o d u c tio nOver the past 20 years secondary ion mass spectrom etry (SIMS) has been used quite successfully for depth profiling im purity distributions in solids. Most of the previous work has been done on semiconductor samples which constitute the m ajor challenge to the SIMS technique because of the need for high sensitivity in combination with high precision (Wilson et al. 1989). The excellent sensitivity reported for many ele ments is based on two characteristic features of SIMS: first, the absence of an inherent