V. Bertagna et al., ELECTROCHEMICAL AND RADIOCHEMICAL STUDY OF COPPER CONTAMINATION MECHANISM FROM HF SOLUTIONS ONTO SILICON SUBSTRATES, Journal of the Electrochemical Society, 144(12), 1997, pp. 4175-4182
The mechanism of copper contamination of silicon wafers from dilute HF
solutions containing ultratrace levels of metallic ion impurities, wa
s investigated using a new electrochemical cell, which proved to act a
s a very efficient sensor for in situ characterization. Upon copper co
ntamination, the open-circuit potential was observed to shift rapidly
toward more positive values at a rate nearly proportional to the coppe
r concentration. All potential/time curves tend to reach a plateau, wh
ile quantitative measurements using radioactive tracers revealed that
during a few tens of minutes, copper ions were continuously reduced on
the silicon surface. Results are interpreted in terms of the mixed-po
tential theory and lead to the conclusion that copper nuclei act as a
catalyst which enhances the cathodic activity for proton reduction. Th
e model was supported by atomic force microscopy observations which sh
owed the initiation of corrosion pits around the nuclei.