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

被引:29
作者
LI, WJ [1 ]
VIRTANEN, JA [1 ]
PENNER, RM [1 ]
机构
[1] UNIV CALIF IRVINE,DEPT CHEM,ISIS,IRVINE,CA 92717
关键词
D O I
10.1021/la00011a031
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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). These nanostructures were stable while immersed in aqueous solutions containing 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 nanostructure 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-alkanethiolate self-assembled monolayer (SAM) on the silver surface, demonstrating 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 observed following the exposure of silver nanostructures to long-chain n-alkylamines or carboxylic acids and these prospective ligands provided no protection from dissolution of the nanostructure in pure water.
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页码:4361 / 4365
页数:5
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