Abstract

Thermal desorption of surface oxide from silicon wafers has been studied in ultrahigh vacuum and in hydrogen by secondary-ion mass spectrometry. Heating in 132 Pa hydrogen virtually eliminates residual boron contamination which creates a p-type surface layer on vacuum-annealed wafers. Lower pressures of hydrogen and substitution of nitrogen have proved less efficient in reducing surface boron concentration. In-situ ellipsometry indicates differences in reaction kinetics for oxide desorption in vacuum and in hydrogen.

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