From micro to nano: Analysis of surface-enhanced resonance Raman spectroscopy active sites via multiscale correlations

被引:34
作者
Khan, I [1 ]
Cunningham, D
Littleford, RE
Graham, D
Smith, WE
McComb, DW
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Mat, London SW7 2AZ, England
[2] Univ Strathclyde, Dept Pure & Appl Chem, Glasgow G1 1XL, Lanark, Scotland
关键词
D O I
10.1021/ac051158a
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Effective correlation of data from a number of analytical techniques over length scales spanning several orders of magnitude is required to more fully investigate the active sites on silver nanoparticles that are responsible for surface-enhanced resonance Raman scattering (SERRS). In this paper, a method is presented that uses fluorescent beads as optical markers to allow direct correlation between a SERRS/fluorescence map and a transmission electron microscope (TEM) collage of the same area. Factors influencing the accuracy of the technique include the flatness of the substrate, the size of the fluorescent beads, and the strength of the signal from the fluorescent beads. When the effect of each of these factors on the technique is addressed, a simple and accurate correlation between the optical spectroscopy and the electron microscopy is achieved. A statistically significant number of particles can then be easily and reliably located and characterized at both optical limits, by SERRS, and with subnanometer resolution in the high-resolution TEM. Examples of HRTEM images and the locations of these particles within the SERRS map/TEM collage are presented. Our findings reveal that the relative SERRS activity of single particles is very low compared to dimers and larger aggregates of particles. The relative activity of dimers is estimated to be 12.4 times greater than single particles, and as the number of particles in the aggregate increase, the relative SERRS activity also increases. The relative SERRS activities of single particles/dimers/trimers/aggregates of 4-9 particles/aggregates of 10-20 are estimated to be 1/12.4/15.6/23.2/43.
引用
收藏
页码:224 / 230
页数:7
相关论文
共 29 条
[1]   Surface-enhanced Raman scattering [J].
Campion, A ;
Kambhampati, P .
CHEMICAL SOCIETY REVIEWS, 1998, 27 (04) :241-250
[2]   Nanoparticles with Raman spectroscopic fingerprints for DNA and RNA detection [J].
Cao, YWC ;
Jin, RC ;
Mirkin, CA .
SCIENCE, 2002, 297 (5586) :1536-1540
[3]   The first SERRS multiplexing from labelled oligonucleotides in a microfluidics lab-on-a-chip [J].
Docherty, FT ;
Monaghan, PB ;
Keir, R ;
Graham, D ;
Smith, WE ;
Cooper, JM .
CHEMICAL COMMUNICATIONS, 2004, (01) :118-119
[4]   SERRS as a more sensitive technique for the detection of labelled oligonucleotides compared to fluorescence [J].
Faulds, K ;
Barbagallo, RP ;
Keer, JT ;
Smith, WE ;
Graham, D .
ANALYST, 2004, 129 (07) :567-568
[5]   Electromagnetic fields around silver nanoparticles and dimers [J].
Hao, E ;
Schatz, GC .
JOURNAL OF CHEMICAL PHYSICS, 2004, 120 (01) :357-366
[6]   Plasmon-sampled surface-enhanced Raman excitation spectroscopy [J].
Haynes, CL ;
Van Duyne, RP .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (30) :7426-7433
[7]   SURFACE-ENHANCED RESONANCE RAMAN-SPECTROSCOPY OF RHODAMINE-6G ADSORBED ON COLLOIDAL SILVER [J].
HILDEBRANDT, P ;
STOCKBURGER, M .
JOURNAL OF PHYSICAL CHEMISTRY, 1984, 88 (24) :5935-5944
[8]   Nanosphere lithography: Tunable localized surface plasmon resonance spectra of silver nanoparticles [J].
Jensen, TR ;
Malinsky, MD ;
Haynes, CL ;
Van Duyne, RP .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (45) :10549-10556
[9]   The optical properties of metal nanoparticles: The influence of size, shape, and dielectric environment [J].
Kelly, KL ;
Coronado, E ;
Zhao, LL ;
Schatz, GC .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (03) :668-677
[10]   Identification and characterization of active and inactive species for surface-enhanced resonance Raman scattering [J].
Khan, I ;
Cunningham, D ;
Graham, D ;
McComb, DW ;
Smith, WE .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (08) :3454-3459