Ultrafast continuum mid-infrared spectroscopy: probing the entire vibrational spectrum in a single laser shot with femtosecond time resolution

被引:64
作者
Calabrese, Carmella [1 ]
Stingel, Ashley M. [1 ]
Shen, Lei [1 ]
Petersen, Poul B. [1 ]
机构
[1] Cornell Univ, Dept Chem & Chem Biol, Ithaca, NY 14853 USA
基金
美国国家科学基金会;
关键词
IR SPECTROSCOPY; MU-M; GENERATION; PULSES; AIR; DYNAMICS;
D O I
10.1364/OL.37.002265
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Until now, ultrafast IR spectroscopy has been limited by the bandwidth of optical parametric amplifiers, typically 100-400 cm(-1). Here we present the first example of transient IR spectroscopy using a continuum laser source to probe the entire mid-IR region with ultrafast time resolution. The continuum source is based on focusing the fundamental, second harmonic, and third harmonic of 1 mJ, 25 fs, 800 nm pulses in air, generating similar to 150 fs continuum mid-IR pulses that span the frequency range of <400 to >5000 cm(-1) or, conversely, <2 to >25 mu m. We characterize the spectral and temporal properties of dicarbonylacetonato rhodium(I) in hexane. We further demonstrate the versatility of the method by measuring the very fast and broad (>1500 cm(-1)) spectral changes following IR excitation associated with the 7-azaindole-acetic acid heterodimer in carbon tetrachloride. (C) 2012 Optical Society of America
引用
收藏
页码:2265 / 2267
页数:3
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