Monomolecular Langmuir-Blodgett films at electrodes. Formation of passivating monolayers and incorporation of electroactive reagents
Monomolecular Langmuir-Blodgett films at electrodes. Formation of passivating monolayers and incorporation of electroactive reagents
复制标题
电极上的单分子 Langmuir-Blodgett 薄膜。
作者:
R. Bilewicz;M. Majda
Langmuir-Blodgett (LB) transfer of mixed octadecanethiol (Ci8SH)-octadecanol (CigOH) monlayers onto vapor-deposited gold films on glass slides leads to the formationof stable, densely packed mono-molecular films when the composition of the mixed monolayers involves 60-80 mol% octadecanethiol. This composition of the mixed LB films is a result of a trade-off between the mole fraction of CigOH, whose increasing magnitude allows one to increase surface pressure of a mixed monolayer during an LB transfer, and the mole fraction of CigSH, whose increasingmagnitude enhances stability of themixed monolayer on the gold surface following the LB transfer. The passivating properties of CigSH/CigOH LB monolayers were investigated electrochemically. Determinationof interfacial capacitance and measurements of the extent of permeability of the surface monolayers by cyclic voltammetry demonstrated that the passivating characteristics of the CigSH/CigOH LB monlayers are essentially identical to the best self-assembled octadecanethiol monolayers described in the literature. LB transfer of monolayers containing small quantities of an electroactive reagent can be used as a general technique of reagent immobilization at the electrode surface. Unlike self-assembly methods, reagent incorporation in Langmuir-Blodgett monolayers offers precise control of their composition in a broad range of concentrations. Comparison of the surface concentrations of ubiquinone incorporated in CigSH/CigOH monolayers at the air/water interface before LB transfer and at the electrode surface following LB transfer gave 1: 1 correlations in the concentration range 1.0 X 10~ 12-1.0 X 10~ 10 mol/cm* 12.