Multidimensional resonance Raman spectroscopy by six-wave mixing in the deep UV

• Published in: The Journal of chemical physics 2014-09, Vol.141 (11), p.114202-114202
• Main Authors: Molesky, Brian P, Giokas, Paul G, Guo, Zhenkun, Moran, Andrew M
• Format: Article
• Language: English
• Subjects: Anharmonicity; Cascades; DATA ACQUISITION; Delay time; EMISSION; FOURIER TRANSFORMATION; Fourier transforms; GROUND STATES; INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; IODINE COMPOUNDS; Laser beams; LASERS; MOLECULES; NEON; Physics; PULSES; RAMAN SPECTRA; RAMAN SPECTROSCOPY; RELAXATION; Representations; SAPPHIRE; SENSITIVITY; SIGNALS; Spectrum analysis; TITANIUM; Titanium-Sapphire; WAVE PACKETS
• ISSN: 0021-9606; 1089-7690
• DOI: 10.1063/1.4894846

Two-dimensional (2D) resonance Raman spectroscopies hold great potential for uncovering photoinduced relaxation processes in molecules but are not yet widely applied because of technical challenges. Here, we describe a newly developed 2D resonance Raman experiment operational at the third-harmonic of a Titanium-Sapphire laser. High-sensitivity and rapid data acquisition are achieved by combining spectral interferometry with a background-free (six-pulse) laser beam geometry. The third-harmonic laser pulses are generated in a filament produced by the fundamental and second-harmonic pulses in neon gas at pressures up to 35 atm. The capabilities of the setup are demonstrated by probing ground-state wavepacket motions in triiodide. The information provided by the experiment is explored with two different representations of the signal. In one representation, Fourier transforms are carried out with respect to the two experimentally controlled delay times to obtain a 2D Raman spectrum. Further insights are derived in a second representation by dispersing the signal pulse in a spectrometer. It is shown that, as in traditional pump-probe experiments, the six-wave mixing signal spectrum encodes the wavepacket's position by way of the (time-evolving) emission frequency. Anharmonicity additionally induces dynamics in the vibrational resonance frequency. In all cases, the experimental signals are compared to model calculations based on a cumulant expansion approach. This study suggests that multi-dimensional resonance Raman spectroscopies conducted on systems with Franck-Condon active modes are fairly immune to many of the technical issues that challenge off-resonant 2D Raman spectroscopies (e.g., third-order cascades) and photon-echo experiments in the deep UV (e.g., coherence spikes). The development of higher-order nonlinear spectroscopies operational in the deep UV is motivated by studies of biological systems and elementary organic photochemistries.