Fluorescence-Detected Two-Quantum and One-Quantum-Two-Quantum 2D Electronic Spectroscopy

被引:37
作者
Mueller, Stefan [1 ]
Draeger, Simon [1 ]
Ma, Xiaonan [1 ]
Hensen, Matthias [1 ]
Kenneweg, Tristan [2 ]
Pfeiffer, Walter [2 ]
Brixner, Tobias [1 ,3 ]
机构
[1] Univ Wurzburg, Inst Phys & Theoret Chem, D-97074 Wurzburg, Germany
[2] Univ Bielefeld, Fac Phys, Univ Str 25, D-33615 Bielefeld, Germany
[3] Univ Wurzburg, CNC, Theodor Boveri Weg, D-97074 Wurzburg, Germany
基金
欧洲研究理事会;
关键词
MULTIDIMENSIONAL COHERENT SPECTROSCOPY; 2-DIMENSIONAL INFRARED-SPECTROSCOPY; ASSEMBLED PORPHYRIN DIMERS; PHOTOCURRENT SPECTROSCOPY; VIBRATIONAL SPECTROSCOPY; SOLVATION DYNAMICS; CONFORMATION; RELAXATION; SINGLE;
D O I
10.1021/acs.jpclett.8b00541
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
We demonstrate two-quantum (2Q) coherent two-dimensional (2D) electronic spectroscopy using a shot-to-shot-modulated pulse shaper and fluorescence detection. Broadband collinear excitation is realized with the supercontinuum output of an argon-filled hollow-core fiber, enabling us to excite multiple transitions simultaneously in the visible range. The 2Q contribution is extracted via a three-pulse sequence with 16 fold phase cycling and simulated employing cresyl violet as a model system. Furthermore, we report the first experimental realization of one-quantum two-quantum (1Q-2Q) 2D spectroscopy, offering less congested spectra as compared with the 2Q implementation. We avoid scattering artifacts and nonresonant solvent contributions by using fluorescence as the observable. This allows us to extract quantitative information about doubly excited states that agree with literature expectations. The high sensitivity and background-free nature of fluorescence detection allow for a general applicability of this method to many other systems.
引用
收藏
页码:1964 / 1969
页数:11
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