Silatrane Anchors for Metal Oxide Surfaces: Optimization for Potential Photocatalytic and Electrocatalytic Applications

Silatrane surface anchors are protected siloxanes that are known to bond firmly (from pH 2–11) to metal oxide electrodes under heating. However, these conditions are not always compatible with the other functionality present. A silatrane-containing porphyrin molecule and a silatrane-containing ruthenium complex have now been designed, synthesized and optimized conditions have been identified for surface binding. Two mild, room-temperature surface binding methods were explored: binding with or without an acidic pretreatment; these methods were compared to the traditional, harsher binding conditions involving strong heating. We find that a preacidified electrode gave comparable surface loadings at room temperature compared to sensitization by using the previous strong heating method. This was also true on TiO₂, SnO₂, and <i>nano</i>ITO electrodes and thus may be generalizable. The new, milder binding methods also resulted in excellent aqueous and electrochemical stability from pH 2–11. Using a water-insoluble porphyrin with a silatrane anchor further increased the aqueous stability of the deposit, aided by the insolubility of the porphyrin. Finally, X-ray photoelectron spectroscopy (XPS) data confirmed for the first time that the triethanolamine released from the silatrane on deprotection/binding in turn binds to TiO₂, SnO₂, and <i>nano</i>ITO electrodes. This undesired triethanolamine deposit was easily removed from the surface by electrochemical voltage cycling or with an aqueous acidic wash for 1 h