Surface-Enhanced Raman and Surface-Enhanced Hyper-Raman Scattering of Thiol-Functionalized Carotene

被引:21
|
作者
Guehlke, Marina [1 ]
Heiner, Zsuzsanna [1 ,2 ]
Kneipp, Janina [1 ,2 ]
机构
[1] Humboldt Univ, Dept Chem, Brook Taylor Str 2, D-12489 Berlin, Germany
[2] Humboldt Univ, Sch Analyt Sci Adlershof SALSA, Albert Einstein Str 5-9, D-12489 Berlin, Germany
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2016年 / 120卷 / 37期
关键词
RESONANCE RAMAN; BETA-CAROTENE; SELECTION-RULES; EXCITATION PROFILE; SINGLE-MOLECULE; SILVER; SPECTROSCOPY; SERS; SPECTRA; ABSORPTION;
D O I
10.1021/acs.jpcc.6b01895
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 thiol-modified carotene, 7'-apo-7'-(4-mercaptomethylphenyl)-beta-carotene, was used to obtain nonresonant surface-enhanced Raman scattering (SERS) spectra of carotene at an excitation wavelength of 1064 nm, which were compared with resonant SERS spectra at an excitation wavelength of 532 nm. These spectra and surface-enhanced hyper-Raman scattering (SEHRS) spectra of the functionalized carotene were compared with the spectra of nonmodified beta-carotene. Using SERS, normal Raman, and SEHRS spectra, all obtained for the resonant case, the interaction of the carotene molecules with silver nanoparticles, as well as the influence of the resonance enhancement and the SERS enhancement on the spectra, were investigated. The interaction with the silver surface occurs for both functionalized and nonfunctionalized beta-carotene, but only the stronger functionalization-induced interaction enables the acquisition of nonresonant SERS spectra of beta-carotene at low concentrations. The resonant SEHRS and SERS spectra are very similar. Nevertheless, the SEHRS spectra contain additional bands of infrared-active modes of carotene. Increased contributions from bands that experience low resonance enhancement point to a strong interaction between silver nanoparticles and electronic levels of the molecules, thereby giving rise to a decrease in the resonance enhancement in SERS and SEHRS.
引用
收藏
页码:20702 / 20709
页数:8
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