posted on 2007-08-07, 00:00authored byDirk Burdinski, Martin H. Blees
The transcription of microcontact-printed self-assembled monolayer patterns into gold substrates requires
a wet chemical etch process that selectively dissolves unprotected metal without attacking SAM-covered
gold regions. Gold dissolution in a standard thiosulfate−ferricyanide etch solution, the most commonly
used etchant containing sulfur-based ligands, shows a complex kinetic behavior. Etch-rate-determining
under most conditions are the concentrations of thiosulfate, ferricyanide, and hydroxide. The etch process
is accelerated under high ionic strength conditions, in particular in the presence of potassium ions. This
is ascribed to the formation of potassium−reagent ion pairs, which reduce the Coulomb repulsion between
the negatively charged reaction partners. The thiosulfate−ferricyanide etchant is intrinsically unstable
due to the reduction of the ferricyanide oxidant during thiosulfate decomposition. The gold ligand
thiosulfate was therefore substituted with benzenethiosulfonate, which was expected to be less oxidation
sensitive. The new bath decomposed in the course of days instead of several hours. Since the etch efficiency
was also reduced, a significantly higher concentration of the gold ligand was required to achieve a
sufficiently high etch rate. The somewhat lower etch quality of the new bath could be compensated for
by introducing a new defect healing additive, 1-decanesulfonamide, which was found to be more effective
than 1-octanol in the new etchant.