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

被引:371
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
相关论文
共 38 条
[1]   Rationally designed nanostructures for surface-enhanced Raman spectroscopy [J].
Banholzer, Matthew J. ;
Millstone, Jill E. ;
Qin, Lidong ;
Mirkin, Chad A. .
CHEMICAL SOCIETY REVIEWS, 2008, 37 (05) :885-897
[2]   Quantitative surface-enhanced Raman spectroscopy [J].
Bell, Steven E. J. ;
Sirimuthu, Narayana M. S. .
CHEMICAL SOCIETY REVIEWS, 2008, 37 (05) :1012-1024
[3]   Controlled Plasmonic Nanostructures for Surface-Enhanced Spectroscopy and Sensing [J].
Camden, Jon P. ;
Dieringer, Jon A. ;
Zhao, Jing ;
Van Duyne, Richard P. .
ACCOUNTS OF CHEMICAL RESEARCH, 2008, 41 (12) :1653-1661
[4]   Tunable plasmonic response from alkanethiolate-stabilized gold nanoparticle superlattices: Evidence of near-field coupling [J].
Chen, Chi-Fan ;
Tzeng, Shien-Der ;
Chen, Hung-Ying ;
Lin, Kuan-Jiuh ;
Gwo, Shangjr .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (03) :824-+
[5]   SOFT MATTER [J].
DEGENNES, PG .
REVIEWS OF MODERN PHYSICS, 1992, 64 (03) :645-648
[6]   A frequency domain existence proof of single-molecule surface-enhanced Raman Spectroscopy [J].
Dieringer, Jon A. ;
Lettan, Robert B., II ;
Scheidt, Karl A. ;
Van Duyne, Richard P. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (51) :16249-16256
[7]   Silver nanoparticles self assembly as SERS substrates with near single molecule detection limit [J].
Fan, Meikun ;
Brolo, Alexandre G. .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2009, 11 (34) :7381-7389
[8]   Measurement of the distribution of site enhancements in surface-enhanced Raman scattering [J].
Fang, Ying ;
Seong, Nak-Hyun ;
Dlott, Dana D. .
SCIENCE, 2008, 321 (5887) :388-392
[9]   RAMAN-SPECTRA OF PYRIDINE ADSORBED AT A SILVER ELECTRODE [J].
FLEISCHMANN, M ;
HENDRA, PJ ;
MCQUILLAN, AJ .
CHEMICAL PHYSICS LETTERS, 1974, 26 (02) :163-166
[10]   SELF-ASSEMBLED METAL COLLOID MONOLAYERS - AN APPROACH TO SERS SUBSTRATES [J].
FREEMAN, RG ;
GRABAR, KC ;
ALLISON, KJ ;
BRIGHT, RM ;
DAVIS, JA ;
GUTHRIE, AP ;
HOMMER, MB ;
JACKSON, MA ;
SMITH, PC ;
WALTER, DG ;
NATAN, MJ .
SCIENCE, 1995, 267 (5204) :1629-1632