Large-Scale Hot Spot Engineering for Quantitative SERS at the Single-Molecule Scale

被引:354
作者
Chen, Hung-Ying [1 ]
Lin, Meng-Hsien [1 ]
Wang, Chun-Yuan [1 ]
Chang, Yu-Ming [2 ]
Gwo, Shangjr [1 ,3 ]
机构
[1] Natl Tsing Hua Univ, Dept Phys, Hsinchu 30013, Taiwan
[2] Natl Taiwan Univ, Ctr Condensed Matter Sci, Taipei 10617, Taiwan
[3] Natl Synchrotron Radiat Res Ctr, Hsinchu 30076, Taiwan
关键词
ENHANCED RAMAN-SCATTERING; PLASMONIC NANOPARTICLE; INTERNAL STANDARDS; SILVER ELECTRODE; NEAR-FIELD; SPECTROSCOPY; NANOSTRUCTURES; PROOF;
D O I
10.1021/jacs.5b09111
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Quantitative surface enhanced Raman spectroscopy (SERS) requires precise control of Raman enhancement factor and detection uniformity across the SERS substrate. Here, we show that alkanethiolate ligand-regulated silver (Ag) nanoparticle films can be used to achieve quantitative SERS measurements down to the single-molecule level. The two-dimensional hexagonal close-packed superlattices of Ag nanoparticles formed in these films allow for SERS detection over a large area with excellent uniformity and high Raman enhancement factor. In particular, the SERS signal from the thiolate ligands on Ag nanoparticle surfaces can be utilized as a stable internal calibration standard for reproducible quantitative measurements. We demonstrate the capability of quantitative SERS by measuring the areal densities of crystal violet molecules embedded in an ultrathin spin-on-glass detection "hot zone", which is a planar and uniformly enhanced region several nanometers above the Ag nanoparticles. The Raman measurement results exhibit a linear response over a wide dynamic range of analyte concentration.
引用
收藏
页码:13698 / 13705
页数:8
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