Real-Time Observation of Molecular Spinning with Angular High-Harmonic Spectroscopy

被引:71
作者
He, Lixin [1 ,2 ]
Lan, Pengfei [1 ,2 ]
Anh-Thu Le [3 ]
Wang, Baoning [1 ,2 ]
Wang, Bincheng [1 ,2 ]
Zhu, Xiaosong [1 ,2 ]
Lu, Peixiang [1 ,2 ,4 ]
Lin, C. D. [3 ]
机构
[1] Huazhong Univ Sci & Technol, Wuhan Natl Lab Optoelect, Wuhan 430074, Hubei, Peoples R China
[2] Huazhong Univ Sci & Technol, Sch Phys, Wuhan 430074, Hubei, Peoples R China
[3] Kansas State Univ, Dept Phys, Cardwell Hall, Manhattan, KS 66506 USA
[4] Wuhan Inst Technol, Lab Opt Informat Technol, Wuhan 430205, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
OPTICAL CENTRIFUGE; GENERATION; DYNAMICS; ORBITALS;
D O I
10.1103/PhysRevLett.121.163201
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
We demonstrate an angular high-harmonic spectroscopy method to probe the spinning dynamics of a molecular rotation wave packet in real time. With the excitation of two time-delayed, polarization-skewed pump pulses, the molecular ensemble is impulsively kicked to rotate unidirectionally, which is subsequently irradiated by another delayed probe pulse for high-order harmonic generation (HHG). The spatiotemporal evolution of the molecular rotation wave packet is visualized from the time-dependent angular distributions of the HHG yields and frequency shift measured at various polarization directions and time delays of the probe pulse. The observed frequency shift in HHG is demonstrated to arise from the nonadiabatic effect induced by molecular spinning. Different from the previous spectroscopic and Coulomb explosion imaging techniques, the angular high-harmonic spectroscopy method can reveal additionally the electronic structure and multiple orbitals of the sampled molecule. All the experimental findings are well reproduced by numerical simulations. Further extension of this method would provide a powerful tool for probing complex polyatomic molecules with HHG spectroscopy.
引用
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页数:6
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