Scouting for strong light-matter coupling signatures in Raman spectra

被引:20
作者
Takele, Wassie Mersha [1 ,2 ]
Piatkowski, Lukasz [3 ]
Wackenhut, Frank [2 ]
Gawinkowski, Sylwester [1 ]
Meixner, Alfred J. [2 ]
Waluk, Jacek [1 ,4 ]
机构
[1] Polish Acad Sci, Inst Phys Chem, Kasprzaka 44-52, PL-01224 Warsaw, Poland
[2] Univ Tubingen, Inst Phys & Theoret Chem, Morgenstelle 18, D-72076 Tubingen, Germany
[3] Poznan Univ Tech, Fac Mat Engn & Tech Phys, Piotrowo 3, PL-60965 Poznan, Poland
[4] Cardinal Stefan Wyszynski Univ, Fac Math & Sci, Dewajtis 5, PL-01815 Warsaw, Poland
关键词
SPECTROSCOPY; SURFACE; STATES; SCATTERING; CHEMISTRY; DEPENDENCE; EXCITONS; CAVITY; SERS;
D O I
10.1039/d1cp01863a
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
Strong coupling between vibrational transitions and a vacuum field of a cavity mode leads to the formation of vibrational polaritons. These hybrid light-matter states have been widely explored because of their potential to control chemical reactivity. However, the possibility of altering Raman scattering through the formation of vibrational polaritons has been rarely reported. Here, we present the Raman scattering properties of different molecules under vibrational strong coupling conditions. The polariton states are clearly observed in the IR transmission spectra of the coupled system for benzonitrile and methyl salicylate in liquid phase and for polyvinyl acetate in a solid polymer film. However, none of the studied systems exhibits a signature of the polariton states in the Raman spectra. For the solid polymer film, we have used cavities with different layer structures to investigate the influence of vibrational strong coupling on the Raman spectra. The only scenario where alterations of the Raman spectra are observed is for a thin Ag layer being in direct contact with the polymer film. This shows that, even though the system is in the vibrational strong coupling regime, changes in the Raman spectra do not necessarily result from the strong coupling, but are caused by the surface enhancement effects.
引用
收藏
页码:16837 / 16846
页数:10
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