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Surface-enhanced Raman scattering (SERS) of riboflavin on nanostructured Ag surfaces: The role of excitation wavelength, plasmon resonance and molecular resonance
被引:10
作者:

Subr, Martin
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Charles Univ Prague, Inst Phys, Fac Math & Phys, Ke Karlovu 5, Prague 12116, Czech Republic Charles Univ Prague, Inst Phys, Fac Math & Phys, Ke Karlovu 5, Prague 12116, Czech Republic

Kuzminova, Anna
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Charles Univ Prague, Dept Macromol Phys, Fac Math & Phys, V Holesovickach 2, Prague 18000, Czech Republic Charles Univ Prague, Inst Phys, Fac Math & Phys, Ke Karlovu 5, Prague 12116, Czech Republic

Kylian, Ondrej
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Charles Univ Prague, Dept Macromol Phys, Fac Math & Phys, V Holesovickach 2, Prague 18000, Czech Republic Charles Univ Prague, Inst Phys, Fac Math & Phys, Ke Karlovu 5, Prague 12116, Czech Republic

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机构:
[1] Charles Univ Prague, Inst Phys, Fac Math & Phys, Ke Karlovu 5, Prague 12116, Czech Republic
[2] Charles Univ Prague, Dept Macromol Phys, Fac Math & Phys, V Holesovickach 2, Prague 18000, Czech Republic
关键词:
SERS;
Riboflavin;
Ag nanoislands;
Excitation profile;
LSPR;
SIZE;
NANOPARTICLES;
DEPENDENCE;
SHAPE;
D O I:
10.1016/j.saa.2018.01.055
中图分类号:
O433 [光谱学];
学科分类号:
0703 ;
070302 ;
摘要:
Optimization of surface-enhanced Raman scattering (SERS)-based sensors for (bio)analytical applications has received much attention in recent years. For optimum sensitivity, both the nanostructure fabrication process and the choice of the excitation wavelength used with respect to the specific analyte studied are of crucial importance. In this contribution, detailed SERS intensity profiles were measured using gradient nanostructures with the localized surface-plasmon resonance (LSPR) condition varying across the sample length and using riboflavin as the model biomolecule. Three different excitation wavelengths (633 nm, 515 nm and 488 nm) corresponding to non-resonance, pre-resonance and resonance excitation with respect to the studied molecule, respectively, were tested. Results were interpreted in terms of a superposition of the enhancement provided by the electromagnetic mechanism and intrinsic properties of the SERS probe molecule. The first effect was dictated mainly by the degree of spectral overlap between the LSPR band, the excitation wavelength along with the scattering cross-section of the nanostructures, while the latter was influenced by the position of the molecular resonance with respect to the excitation wavelength. Our experimental findings contribute to a better understanding of the SERS enhancement mechanism. (C) 2018 Published by Elsevier B.V.
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页码:202 / 207
页数:6
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