SELF-ASSEMBLY OF N-ALKANETHIOLATE MONOLAYERS ON SILVER NANOSTRUCTURES- PROTECTIVE ENCAPSULATION

Electrochemically synthesized silver nanostructures having dimensions 200-1000 Angstrom in diameter and 20-50 Angstrom high were prepared on graphite surfaces using the scanning tunneling microscope (STM). Thes e nanostructures were stable while immersed in aqueous solutions conta ining small(0.5 mM) concentrations of Ag+ during repeated STM imaging at small sample-negative biases for at least Ih. Upon exchange of the silver plating-solution for pure water, dissolution of the nanostructu re occurred within 30 min, irrespective of the applied imaging bias up to +/-200 mV. The anodic dissolution of silver nanostructures in pure water was strongly inhibited following the formation of an n-alkaneth iolate self-assembled monolayer (SAM) on the silver surface, demonstra ting that molecular self-assembly provides a method for the protective , and chemically selective, encapsulation of reactive nanometer-scale structures on solid surfaces. In contrast, self-assembly was not obser ved following the exposure of silver nanostructures to long-chain n-al kylamines or carboxylic acids and these prospective ligands provided n o protection from dissolution of the nanostructure in pure water.