二维红外光谱
红外线的
光谱学
傅里叶变换
红外光谱学
激发
傅里叶变换光谱学
傅里叶变换红外光谱
分子振动
化学
分子物理学
材料科学
光学
物理
拉曼光谱
有机化学
量子力学
作者
Joseph N. Mastron,Andrei Tokmakoff
标识
DOI:10.1021/acs.jpca.7b10305
摘要
While time-resolved infrared (IR) vibrational spectroscopy provides insight on structural dynamics of solution-phase systems, current techniques are limited to high concentrations. Fluorescence-encoded infrared spectroscopy (FEIR) can be used to encode IR-driven vibrational excitations into excited electronic states that fluoresce, which can be detected at lower concentrations than a coherently detected IR signal. Here, we report on the development of Fourier transform FEIR as an alternate approach for high-sensitivity IR spectroscopy. Upon driving vibrational excitation with a pair of IR fields with a variable time delay, an interferometric component was observed in the encoded fluorescence. This signal can be Fourier transformed to obtain a vibrational spectrum. By additionally varying the time delay of the encoding pulse following the second IR pulse, we observed frequency-difference oscillations, allowing us to construct a 2D correlation spectrum of coupled vibrations. Response functions for this experiment have been modeled, which reproduce the observed spectral features and relate them to excitation pathways using diagrammatic perturbation theory. The pathways observed in a 2D FEIR spectrum arise from the excitation of vibrational populations and coherences between coupled vibrations.
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