Nonlinear Fourier transformation spectroscopy of small molecules with intense attosecond pulse train

被引:11
|
作者
Okino, T. [1 ,2 ]
Furukawa, Y. [1 ,2 ]
Shimizu, T. [2 ]
Nabekawa, Y. [1 ,2 ]
Yamanouchi, K. [2 ,3 ]
Midorikawa, K. [1 ,2 ]
机构
[1] RIKEN, Ctr Adv Photon, Wako, Saitama 3510198, Japan
[2] RIKEN, Laser Technol Lab, Wako, Saitama 3510198, Japan
[3] Univ Tokyo, Sch Sci, Dept Chem, Bunkyo Ku, Tokyo 1130033, Japan
关键词
nonlinear spectroscopy; attosecond; Fourier transformation spectroscopy; PHOTOIONIZATION CROSS-SECTIONS; ABSOLUTE OSCILLATOR-STRENGTHS; REAL-TIME OBSERVATION; HIGH-ORDER HARMONICS; DISSOCIATIVE PHOTOIONIZATION; CONFIGURATION-INTERACTION; ELECTRON LOCALIZATION; IONIC FRAGMENTATION; CHARGE MIGRATION; DYNAMICS;
D O I
10.1088/0953-4075/47/12/124007
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
We have developed an attosecond nonlinear molecular spectroscopic method called nonlinear Fourier transformation spectroscopy (NFTS) that uses an intense attosecond pulse train (APT) to induce multiphoton ionization processes. In the NFTS method, in addition to characterization of the temporal profile of attosecond pulses, the nonlinear molecular responses are encoded in the interferometric autocorrelation traces depending on the molecular species, their fragment ions and their kinetic energy distributions. The principle and applicability of the NFTS method are described in this paper along with the numerical simulations. The method is applied to diatomic molecules (N-2, D-2 and O-2) and polyatomic molecules (CO2, CH4 and SF6). Our results highlight the fact that nonlinear spectroscopic information of molecules in the short wavelength region can be obtained through the irradiation of intense APT by taking advantage of the broad spectral bandwidth of attosecond pulses. The development of the nonlinear spectroscopic method in attoseconds is expected to pave the way to investigate the ultrafast intramolecular electron motion such as ultrafast charge migration and electron correlation.
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页数:23
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