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Tracking Ultrafast Structural Dynamics by Time-Domain Raman Spectroscopy

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 143, 期 26, 页码 9699-9717

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AMER CHEMICAL SOC
DOI: 10.1021/jacs.1c02545

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  1. JST, PRESTO, Japan [JPMJPR17P4]

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Traditional Raman spectroscopy detects inelastic scattering of narrow-band light on a sample to provide rich information about molecular-level properties. Utilizing ultrashort optical pulses allows for real-time observation of molecular vibrations through inducing Raman-active coherent nuclear motion. Time-resolved impulsive stimulated Raman spectroscopy with stable, ultrashort laser pulse sources has successfully revealed molecular mechanisms underlying efficient functions of complex molecular systems.
In traditional Raman spectroscopy, narrow-band light is irradiated on a sample, and its inelastic scattering, i.e., Raman scattering, is detected. The energy difference between the Raman scattering and the incident light corresponds to the vibrational energy of the molecule, providing the Raman spectrum that contains rich information about the molecular-level properties of the materials. On the other hand, by using ultrashort optical pulses, it is possible to induce Raman-active coherent nuclear motion of the molecule and to observe the molecular vibration in real time. Moreover, this time-domain Raman measurement can be combined with femtosecond photoexcitation, triggering chemical changes, which enables tracking ultrafast structural dynamics in a form of time-resolved time-domain Raman spectroscopy, also known as time-resolved impulsive stimulated Raman spectroscopy. With the advent of stable, ultrashort laser pulse sources, time-resolved impulsive stimulated Raman spectroscopy now realizes high sensitivity and a wide detection frequency window from THz to 3000 cm(-1), and has seen success in unveiling the molecular mechanisms underlying the efficient functions of complex molecular systems. In this Perspective, we overview the present status of time-domain Raman spectroscopy, particularly focusing on its application to the study of femtosecond structural dynamics. We first explain the principle and a brief history of time-domain Raman spectroscopy and then describe the apparatus and recent applications to the femtosecond dynamics of complex molecular systems, including proteins, molecular assemblies, and functional materials. We also discuss future directions for time-domain Raman spectroscopy, which has reached a status allowing a wide range of applications.

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