激发
红外线的
光谱学
光学
二维红外光谱
红外光谱学
材料科学
信号(编程语言)
核磁共振
物理
计算机科学
量子力学
程序设计语言
作者
Abhijit Maity,Wolfgang Schweinberge,Christina Höfer,Sarah R. Hutter,Sebastian Gröbmeyer,Dionysios Potamianos,Michael K. Trubetskov,Hojjat Heydarian,Marinus Huber,Maciej Kowalczyk,Philipp Steinleitne,Zheng Wei,Alfred Leitenstorfer,Ioachim Pupeza,Ferenc Krausz,Alexander Weigel
标识
DOI:10.1109/cleo/europe-eqec57999.2023.10232750
摘要
Field-resolved infrared spectroscopy (FRS) with electro-optic sampling (EOS) has evolved as a powerful alternative to conventional intensity-based infrared absorption measurements [1]. It allows to capture the response field of a molecular sample emitted upon vibrational excitation with an ultrashort infrared pulse, directly in the time domain. The temporal separation of excitation and molecular response enables background-free detection of the sample-specific signal via temporal filtering. In order to additionally reduce the influence of low- frequency noise of the mid-infrared (mid-IR) excitation, ultra-rapid EOS detection at multi-kHz scan rates has been implemented with mechanical [2] and dual-oscillator [3] approaches. Here, we present a dual-oscillator FRS instrument, recording broadband mid- IR EOS traces simultaneously in sample and reference channels, at a scan rate of 4.2 kHz. With full spectroscopic referencing on the individual-scan basis, the system can correct sample measurements for fast fluctuations and long-term drifts of the mid- IR excitation pulses.
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