Design and fabrication of surface-enhanced Raman scattering substrate from DNA-gold nanoparticles assembly with 2-3 nm interparticle gap

被引:5
作者
Zhang, Li [1 ]
Ma, Hongwei [2 ]
Yang, Liangbao [3 ]
机构
[1] Suzhou Univ, Sch Biol & Chem Engn, Anhui Key Lab Spin Electron & Nanomat, Suzhou 234000, Peoples R China
[2] Anhui Univ, Sch Life Sci, Hefei 230039, Peoples R China
[3] Chinese Acad Sci, Inst Intelligent Machines, Hefei 230031, Peoples R China
基金
美国国家科学基金会;
关键词
THIN-FILM ASSEMBLIES; SERS; SPECTROSCOPY; ARRAYS; AGGREGATION; NANOSENSORS; DIMENSIONS; DEPENDENCE; NETWORK; SIZE;
D O I
10.1039/c4ra06947a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An ideal substrate for surface-enhanced Raman scattering (SERS) detection should induce a high signal enhancement and be easy to synthesize. Here, we showed that gold nanoparticles (Au NPs) were self-assembled onto DNA strands by electrostatic interactions and formed a well-defined DNA-Au hybrid structure with an interparticle gap of ca. 2-3 nm between two adjacent Au NPs, which could be used as active SERS substrates. Four different types of molecule, i.e. Rhodamine 6G, 4-aminothiophenol, pyridine and 2,4,6-trinitrotoluene, were studied on these substrates. All the detection limits for each analyte on the DNA-Au hybrid substrate were at least one order of magnitude higher than those on Au NPs alone without self-assembly on DNA. This phenomenon of assembly-induced signal enhancement has been experimentally and theoretically demonstrated in this study.
引用
收藏
页码:45207 / 45213
页数:7
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