Ultrafast Picometer-Resolved Molecular Structure Imaging by Laser-Induced High-Order Harmonics

被引:1
|
作者
He, Lixin [1 ,2 ]
Yuen, C. H. [4 ]
He, Yanqing [1 ,2 ]
Sun, Siqi [1 ,2 ]
Goetz, E. [5 ]
Le, Anh-Thu
Deng, Yu [1 ]
Xu, Chengqing [1 ,2 ]
Lan, Pengfei [1 ,2 ,6 ]
Lu, Peixiang [1 ,2 ,3 ,6 ]
Lin, C. D. [4 ]
机构
[1] Huazhong Univ Sci & Technol, Wuhan Natl Lab Optoelect, Wuhan, Peoples R China
[2] Huazhong Univ Sci & Technol, Sch Phys, Wuhan, Peoples R China
[3] Wuhan Inst Technol, Hubei Key Lab Opt Informat & Pattern Recognit, Wuhan 430205, Peoples R China
[4] Kansas State Univ, Dept Phys, Manhattan, KS 66506 USA
[5] Univ Connecticut, Dept Phys, Storrs, CT 06269 USA
[6] Hubei Opt Fundamental Res Ctr, Wuhan 430074, Peoples R China
基金
中国国家自然科学基金;
关键词
X-RAY-DIFFRACTION; AMMONIA CATION; DYNAMICS; GENERATION;
D O I
10.1103/PhysRevLett.133.023201
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Real-time visualization of molecular transformations is a captivating yet challenging frontier of ultrafast optical science and physical chemistry. While ultrafast x-ray and electron diffraction methods can achieve the needed subangstrom spatial resolution, their temporal resolution is still limited to hundreds of femtoseconds, much longer than the few femtoseconds required to probe real-time molecular dynamics. Here, we show that high-order harmonics generated by intense femtosecond lasers can be used to image molecules with few-ten-attosecond temporal resolution and few-picometer spatial resolution. This is achieved by exploiting the sensitive dependence of molecular recombination dipole moment to the geometry of the molecule at the time of harmonic emission. In a proof-of-principle experiment, we have applied this high-harmonic structure imaging (HHSI) method to monitor the structural rearrangement in NH3, ND3, and N-2 from one to a few femtoseconds after the molecule is ionized by an intense laser. Our findings establish HHSI as an effective approach to resolve molecular dynamics with unprecedented spatiotemporal resolution, which can be extended to trace photochemical reactions in the future.
引用
收藏
页数:7
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