A durable surface-enhanced Raman scattering substrate: ultrathin carbon layer encapsulated Ag nanoparticle arrays on indium-tin-oxide glass

被引:7
|
作者
Bian, Juncao [1 ,2 ]
Li, Qian [3 ]
Huang, Chao [1 ,2 ]
Guo, Yao [1 ,2 ]
Zaw, Myowin [1 ,2 ]
Zhang, Rui-Qin [1 ,2 ]
机构
[1] City Univ Hong Kong, Dept Phys & Mat Sci, Hong Kong, Hong Kong, Peoples R China
[2] City Univ Hong Kong, CFP, Hong Kong, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Dept Phys, Hong Kong, Hong Kong, Peoples R China
关键词
SILVER NANOPARTICLES; SPECTROSCOPY; ELECTRODEPOSITION;
D O I
10.1039/c4cp05803h
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The application of Ag nanostructures to surface-enhanced Raman scattering (SERS) is hindered by their chemical instability. Fabrication of durable Ag-based SERS substrates is therefore of great significance in practical applications. In this work, ultrathin C-layer-encapsulated Ag nanoparticle arrays (UCL-Ag-NAs) are successfully fabricated on the surface of indium-tin-oxide (ITO) glass, using a hydrothermal method, for use as durable SERS substrates. The problem of Ag nanoparticles dissolving during the hydrothermal process is solved by using ZnO powder as a pH-buffering reagent. The SERS signal intensity of UCL-Ag-NAs decreases, accompanied by an improvement in Raman signal stability, as the C-layer thickness increases. Raman spectra show that the SERS signal intensities obtained from UCL-Ag-NAs with C-layers of 4.5 nm and 7.3 nm stored for 180 days are 64.9% and 77.8% of those obtained from as-prepared counterparts. The SERS intensity of the UCL-Ag-NA (C-layer of 4.5 nm) is 152.7% that of the bare Ag NA after 180 days of storage. XPS spectra confirm that the C-layer effectively suppresses the oxidation of the Ag NA. This methodology can be generalized to improve the durability of other dimensional Ag nanostructures for SERS applications.
引用
收藏
页码:14849 / 14855
页数:7
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