Vibronic coupling of Rhodamine 6G molecules studied by doubly resonant sum frequency generation spectroscopy with narrowband infrared and broadband visible

被引:3
|
作者
Zeng, Wei-Wang [1 ,2 ]
Luo, Ting [1 ,3 ,4 ]
Xu, Peng [1 ,5 ]
Zhou, Chuanyao [1 ]
Yang, Xueming [1 ,6 ]
Ren, Zefeng [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Mol React Dynam, 457 Zhongshan Rd, Dalian 116023, Peoples R China
[2] Univ Chinese Acad Sci, 19A Yuquan Rd, Beijing 100049, Peoples R China
[3] Westlake Univ, Res Ctr Ind Future, Hangzhou 310030, Peoples R China
[4] Westlake Univ, Sch Engn, Hangzhou 310030, Peoples R China
[5] Univ Sci & Technol China, Dept Chem Phys, Hefei 230026, Peoples R China
[6] Southern Univ Sci & Technol, Dept Chem, 1088 Xueyuan Rd, Shenzhen 518055, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
PULSE-FRONT TILT; VIBRATIONAL SPECTROSCOPY; ELECTRONIC-STRUCTURE; UNIFIED TREATMENT; RAMAN-SCATTERING; SPECTRA; SURFACE; FILMS; INTERFACES; INTERFERENCE;
D O I
10.1063/5.0179871
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
Doubly resonant sum frequency generation (DR-SFG) serves as a potent characteristic technique for probing the electronic spectra and vibronic coupling of molecules on surfaces. In this study, we successfully developed a novel infrared (IR)-white light (WL) DR-SFG spectroscopy based on narrowband IR and tunable broadband WL. This novel method was employed to explore the excitation spectrum and vibronic couplings of sub-monolayer Rhodamine 6G molecules. Our findings elucidate that the xanthene skeleton vibrational modes exhibit strong coupling with the S-0-S-1 electronic transition. Notably, we observed not only the 0-0 transition of the S-0-S-1 electronic continuum but also the 0-1 transition, a first time observation in the realm of DR-SFG spectroscopy. This advanced DR-SFG spectroscopy methodology facilitates a more sensitive examination of electronic spectra and the coupling between electronic transitions and vibrational modes, heralding a significant advancement in the understanding of molecular interactions on surfaces.
引用
收藏
页数:9
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