Spectroelectrochemistry of Silver Deposition on Single Gold Nanocrystals

被引:54
作者
Chirea, Mariana [1 ]
Collins, Sean S. E. [2 ,3 ]
Wei, Xingzhan [2 ,3 ]
Mulvaney, Paul [2 ,3 ]
机构
[1] Univ Porto, Fac Ciencias, CIQ L4, P-4169007 Oporto, Portugal
[2] Univ Melbourne, Sch Chem, Parkville, Vic 3010, Australia
[3] Univ Melbourne, Inst Bio21, Parkville, Vic 3010, Australia
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2014年 / 5卷 / 24期
关键词
DEPENDENT ELECTROCHEMICAL PROPERTIES; UNDERPOTENTIAL DEPOSITION; AU NANOPARTICLES; SIZE; MONOLAYERS; AG; ASSEMBLIES; ELECTRODES; NANOSTARS; NANORODS;
D O I
10.1021/jz502349x
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report the electrodeposition of metallic silver onto gold nanostars adsorbed to ITO electrodes. The electrochemical process was studied at the single particle level by correlated in situ dark field spectroscopy and scanning electron microscopy (SEM). Underpotential deposition avoids bulk silver formation on the ITO substrates. SEM proves that deposition occurs on all surfaces of the gold nanostars when polyvinylpyrrolidone (PVP) is stabilizing the nanostars or preferentially at the nanostar tips when the ligand is removed. The surface plasmon resonance blue-shifts by more than 100 nm following the formation of a 5 nm Ag film on PVP stabilized gold nanostars, moving the scattered color from the near-infrared to red or orange. The spectral shifts can be accurately modeled using finite element simulations. These results demonstrate that the morphology and composition of individual bimetallic nanocrystals can be engineered electrochemically.
引用
收藏
页码:4331 / 4335
页数:5
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