Surface-enhanced Raman scattering-active gold nanoparticles modified with a monolayer of silver film

被引:16
|
作者
Chang, Chun-Chao [2 ,3 ,4 ]
Yang, Kuang-Hsuan [7 ]
Liu, Yu-Chuan [1 ,4 ]
Yu, Chung-Chin [6 ]
Wu, Yi-Hao [5 ]
机构
[1] Taipei Med Univ, Dept Biochem, Sch Med, Coll Med, Taipei 11031, Taiwan
[2] Taipei Med Univ Hosp, Div Gastroenterol & Hepatol, Dept Internal Med, Taipei 11031, Taiwan
[3] Taipei Med Univ, Dept Internal Med, Sch Med, Coll Med, Taipei 11031, Taiwan
[4] Taipei Med Univ, Biomed Mass Imaging Res Ctr, Taipei 11031, Taiwan
[5] Taipei Med Univ, Dept Pharmacognosy Sci, Taipei 11031, Taiwan
[6] Vanung Univ, Dept Environm Engn, Chung Li City, Taiwan
[7] Vanung Univ, Dept Mat Sci & Engn, Chung Li City, Taiwan
关键词
SELF-ASSEMBLED MONOLAYERS; UNDERPOTENTIAL DEPOSITION; THERMAL-STABILITY; ARGON PLASMA; SERS; AG; NANOSTRUCTURES; SPECTROSCOPY; TIO2; SUBSTRATE;
D O I
10.1039/c2an35912j
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
As shown in the literature, electrochemical underpotential deposition (UPD) offers the ability to deposit up to a monolayer of one metal onto a more noble metal with a flat surface. In this work, we develop an electrochemical pathway to prepare more surface-enhanced Raman scattering (SERS)active substrates with Ag UPD-modified Au nanoparticles (NPs) by using sonoelectrochemical deposition-dissolution cycles (SEDDCs). Encouragingly, the SERS of Rhodamine 6G (R6G) adsorbed on these Ag UPD-modified Au NPs exhibits a higher intensity by ca. 12-fold magnitude, as compared with that of R6G adsorbed on unmodified Au NPs. The prepared SERS-active substrate demonstrates a large Raman scattering enhancement for R6G with a detection limit of 2 x 10(-14) M and an enhancement factor of 5.0 x 10(8). Also, the strategy proposed in this work to improve the SERS effects by using UPD Ag based on SEDDCs has an effect on the smaller probe molecules of 2,2'-bipyridine (BPy).
引用
收藏
页码:4943 / 4950
页数:8
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