Ag@SiO2 core-shell nanoparticles on silicon nanowire arrays as ultrasensitive and ultrastable substrates for surface-enhanced Raman scattering

被引:34
|
作者
Zhang, Chang Xing [1 ,2 ]
Su, Lei [1 ,2 ]
Chan, Yu Fei [1 ,2 ]
Wu, Zheng Long [3 ]
Zhao, Yong Mei [4 ]
Xu, Hai Jun [1 ,2 ]
Sun, Xiao Ming [1 ,2 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[2] Beijing Univ Chem Technol, Sch Sci, Beijing 100029, Peoples R China
[3] Beijing Normal Univ, Analyt & Testing Ctr, Beijing 100875, Peoples R China
[4] Chinese Acad Sci, Inst Semicond, Engn Res Ctr Semicond Integrated Technol, Beijing 100083, Peoples R China
关键词
AG NANOPARTICLES; RAPID DETECTION; NANOROD ARRAYS; SERS; FABRICATION; SPECTROSCOPY; MOLECULES; MECHANISM;
D O I
10.1088/0957-4484/24/33/335501
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Ag nanoparticles (NPs) coated with silica nanolayers were decorated onto a large-scale and uniform silicon nanowire array (SiNWA) by simple chemical etching and metal reduction processes. The three-dimensional Ag/SiNWAs thus formed are employed as a substrate for surface-enhanced Raman scattering (SERS), and a detection limit for rhodamine 6G as low as 10(-16) M and a Raman enhancement factor as large as 10(14) were obtained. Simulation results show that two kinds of inter-Ag-NP nanogaps in three-dimensional geometry create a huge number of SERS 'hot spots' where electromagnetic fields are substantially amplified, contributing to the higher SERS sensitivity and lower detection limit. The excellent SERS stability of Ag/SiNWAs is attributed to the presence of the SiO2 nanolayer around Ag NPs that prevented the Ag NP surface from being oxidized. The calibration of the Raman peak intensities of rhodamine 6G and thiram allowed their quantitative detection. Our finding is a significant advance in developing SERS substrates for the fast and quantitative detection of trace organic molecules.
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页数:9
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