Kalkan A Kaan, Fonash Stephen J
Center for Nanotechnology Education and Utilization, The Pennsylvania State University, University Park, PA 16802, USA.
J Phys Chem B. 2005 Nov 10;109(44):20779-85. doi: 10.1021/jp052958s.
Two and three-dimensional Ag nanoparticle ensembles were synthesized on deposited nanostructured column-void Si films simply by film immersion into pure Ag(2)SO(4) or AgNO(3) solutions. In addition to functioning as a reducer, this nanostructured material provides immobilization and monodispersion of the Ag nanoparticles due to its systematic nanoscale topography. This is accomplished without the requirement of a surfactant, capping agent, or linker. Kinetics, as monitored from plasmon optical extinction, and infrared spectroscopy suggest accompanying oxide growth limits and finally inhibits synthesis enabling nanoparticle size control. Kinetics is also limited by Ag+ transport through the voids unless the Si film is ultrathin. Our synthesis approach offers significant advantages for surface-enhanced molecular detection, including the absence of any agents on the nanoparticle surfaces and the ability to obtain nanoparticle ensembles on any substrate.
通过将沉积有纳米结构柱状孔隙硅薄膜浸入纯硫酸银或硝酸银溶液中,在其上合成了二维和三维银纳米颗粒聚集体。除了作为还原剂外,这种纳米结构材料因其系统的纳米级形貌,还能实现银纳米颗粒的固定和单分散。这一过程无需表面活性剂、封端剂或连接剂。通过等离子体光消光监测的动力学以及红外光谱表明,伴随的氧化物生长会限制并最终抑制合成,从而实现纳米颗粒尺寸的控制。动力学还受到银离子通过孔隙传输的限制,除非硅薄膜超薄。我们的合成方法为表面增强分子检测提供了显著优势,包括纳米颗粒表面不存在任何试剂以及能够在任何基底上获得纳米颗粒聚集体。