In situ spectroelectrochemical surface-enhanced Raman scattering (SERS) investigations on composite Ag/TiO2-nanotubes/Ti substrates

被引:45
作者
Roguska, A. [1 ,2 ]
Kudelski, A. [3 ]
Pisarek, M. [1 ,2 ]
Lewandowska, M. [2 ]
Kurzydlowski, K. J. [2 ]
Janik-Czachor, M. [1 ]
机构
[1] Polish Acad Sci, Inst Phys Chem, PL-01224 Warsaw, Poland
[2] Warsaw Univ Technol, Fac Mat Sci & Engn, PL-02507 Warsaw, Poland
[3] Univ Warsaw, Dept Chem, PL-02093 Warsaw, Poland
关键词
Silver clusters; TiO2-nanotubes; Surface-enhanced Raman scattering (SERS); SEM morphological examinations; AES surface analysis; TIO2; NANOTUBES; SPECTROSCOPY; MOLECULES; SILVER; PYRIDINE; FILMS; IONS; GOLD; AG;
D O I
10.1016/j.susc.2009.07.028
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
A tubular array of TiO2-nanotubes on a Ti substrate was used as a support for an Ag sputter-deposited layer intended for surface-enhanced Raman scattering (SERS) investigations. Composite samples of Ag/TiO2-nanotube/Ti were studied with the aid of scanning electron microscopy (SEM) and Auger electron spectroscopy (AES) to reveal their characteristic morphological and chemical features. Raman spectra of pyridine (as a probe molecule) were measured at different cathodic potentials ranging from -0.2 down to -1.2 V after the pyridine had been adsorbed on the TiO2-nanotube/Ti substrates covered with the Ag deposit. In addition, SERS spectra on a bulk electrochemically-roughened Ag reference substrate, were also measured. The SERS activity of the composite samples was strongly dependent on the amount of Ag deposit and, in some cases, was even higher than that for the Ag reference substrate. The SERS intensity vs. electrode potential dependences measured were interpreted in terms of the modified electronic structure of the Ag deposits due to the interaction of the Ag clusters with the TiO2-nanotube/Ti substrate. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:2820 / 2824
页数:5
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