Abstract

The thermal stability of end-of-range (EOR) defects formed in a CH4N-molecular-ion-implanted epitaxial silicon (Si) wafer was studied by transmission electron microscopy (TEM) observation. By plan-view TEM observation, we found that the density and size of the CH4N-ion-implantation-induced EOR defects negligibly changed upon heat treatment at temperatures below 1000 °C, whereas the EOR defect density was drastically reduced by heating at 1100 °C. This result suggests that almost all CH4N-ion-implantation-induced EOR defects were sufficiently thermally stable to maintain their size at temperatures below 1000 °C, and that above 1100 °C, most of the EOR defects lost their stability, shrank and finally dissolved. Additionally, by in situ cross-sectional TEM observation during heat treatment, we found a large difference in the shrinkage rates of the EOR defects between at the beginning of heat treatment and the last minute of just before defect disappearance. We found that the EOR defects began to gradually shrank at the beginning of heat treatment (1st stage), and then the shrinkage rate rapidly increased (2nd stage), finally resulting in the dissolution of the defects. The activation energies for the shrinkage of EOR defects in the 1st and 2nd stages (E D-1 and E D-2) were found to be 7.55 ± 1.03 and 4.57 ± 0.32 eV, respectively. The shrinkage behavior in the 1st stage is likely to be due to the thermally activated desorption of C and N species that segregated along the edge of an EOR defect. On the other hand, from the E D-2 value, the shrinkage behavior in the 2nd stage is deduced to be due to the desorption of interstitial Si atoms. These findings suggest that this two-stage shrinkage behavior is peculiar to the EOR defects formed in the CH4N-ion-implanted epitaxial Si wafer, and that the interaction between the EOR defect and the impurities segregated at the edge of the defect affects the thermal robustness of the molecular-ion-implantation-induced EOR defects.

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