DNA origami based assembly of gold nanoparticle dimers for surface-enhanced Raman scattering

被引:379
|
作者
Thacker, Vivek V. [1 ,2 ]
Herrmann, Lars O. [1 ,2 ]
Sigle, Daniel O. [1 ,2 ]
Zhang, Tao [3 ]
Liedl, Tim [3 ]
Baumberg, Jeremy J. [1 ,2 ]
Keyser, Ulrich F. [1 ,2 ]
机构
[1] Univ Cambridge, Cavendish Lab, Cambridge CB3 0HE, England
[2] Univ Munich, Ctr NanoSci, D-80539 Munich, Germany
[3] Univ Munich, Dept Phys, D-80539 Munich, Germany
来源
NATURE COMMUNICATIONS | 2014年 / 5卷
基金
英国工程与自然科学研究理事会;
关键词
PLASMONIC NANOSTRUCTURES; SINGLE NANOPARTICLES; FOLDING DNA; MOLECULE; FLUORESCENCE; SHAPES; SPECTROSCOPY; NANOPORES; RULER; MOTOR;
D O I
10.1038/ncomms4448
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Plasmonic sensors are extremely promising candidates for label-free single-molecule analysis but require exquisite control over the physical arrangement of metallic nanostructures. Here we employ self-assembly based on the DNA origami technique for accurate positioning of individual gold nanoparticles. Our innovative design leads to strong plasmonic coupling between two 40 nm gold nanoparticles reproducibly held with gaps of 3.3 +/- 1 nm. This is confirmed through far field scattering measurements on individual dimers which reveal a significant red shift in the plasmonic resonance peaks, consistent with the high dielectric environment due to the surrounding DNA. We use surface-enhanced Raman scattering (SERS) to demonstrate local field enhancements of several orders of magnitude through detection of a small number of dye molecules as well as short single-stranded DNA oligonucleotides. This demonstrates that DNA origami is a powerful tool for the high-yield creation of SERS-active nanoparticle assemblies with reliable sub-5 nm gap sizes.
引用
收藏
页数:7
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