Ultrafast infrared plasmonics advances vibrational spectroscopy
Ultrafast infrared plasmonics advances vibrational spectroscopy
复制标题
超快红外等离子体激元推进振动光谱学
DOI:
10.11470/photo.220204
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发表时间:
2022
期刊:
影响因子:
--
通讯作者:
S. Ashihara
中科院分区:
文献类型:
--
作者:
I. Morichika;S. Ashihara
Absorption and scattering in the mid-infrared (mid-IR) range represent the vibrational spectrum of matter. The vibrational spectrum, or the fingerprint of matter, provides information on its microscopic structure at the molecular level. Nowadays, anyone can easily measure vibrational spectra using a commercially available Fourier transform infrared spectrometer (FT-IR), and vibrational spectroscopy has become one of the indispensable methods for instrumental analysis in materials and life sciences.Since the discovery of Kerr-lens mode-locking in the 1990s, ultrashort laser technology has made great progress in vibrational spectroscopy. In particular, ultrafast spectroscopy has enabled time-resolved observation of chemical reaction processes on femtosecond time scales and greatly contributed to elucidation of reaction mechanisms 1). In addition, the characteristics of ultrashort lasers are being utilized to higherorder structural analysis via two-dimensional infrared spectroscopy 2), and high-resolution and short-time measurement via dual-comb spectroscopy 3). The broadband, short-pulsed, and high-intensity properties of ultrashort lasers are useful not only for vibrational spectroscopy, but also for vibrational control of chemical reactions. Strong excitation of molecular vibration with mid-IR pulses is expected to selectively induce chemical reactions in which the vibrational mode participates. This approach, called “bond-selective chemistry,” holds great promise as one of the ultimate methods of controlling chemical reactions at the molecular level 4).