Multiphoton Resonance in Attosecond Transient Absorption

被引:1
作者
Xue, Jinxing [1 ,2 ]
Wang, Meng [3 ]
Zhou, Cangtao [1 ]
Ruan, Shuangchen [1 ]
机构
[1] Shenzhen Technol Univ, Ctr Adv Mat Diagnost Technol, Shenzhen Key Lab Ultraintense Laser & Adv Mat Tec, Shenzhen 518118, Peoples R China
[2] Shenzhen Univ, Coll Phys & Optoelect Engn, Shenzhen 518060, Peoples R China
[3] Shenzhen Technol Univ, Sino German Coll Intelligent Mfg, Shenzhen 518118, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
attosecond pulse; attosecond transient absorption; high order harmonics; HARMONIC-GENERATION; MOLECULAR NITROGEN; ULTRAVIOLET LIGHT; DEEP-ULTRAVIOLET; DYNAMICS; STATES; NM; SPECTRUM; CRYSTAL; LINE;
D O I
10.3390/photonics9040257
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
We present the theory and simulation of attosecond transient absorption in helium atoms under the single-active-electron approximation. This study investigates the attosecond dynamics of intrinsic atomic states that interact with a field comprising vacuum ultraviolet (VUV) and extreme ultraviolet (XUV) fields. The absorption spectrum of the helium atom is obtained from the response function, which is constructed by numerically solving the three-dimensional time-dependent Schrodinger equation. We observe a fine structure near the intrinsic atomic level, which is modulated with a 0.2 fs period. Based on high-order time-dependent perturbation theory, the frequency-dependent phase of the dipole response induced by the VUV and XUV fields is analytically obtained, and the fine structure is well explained by the phase difference. In addition, the absorption fringes are dependent on the chirp of the VUV field. This study investigates the features of the attosecond transient absorption in the VUV region, which may have valuable applications in the study of ultrafast phenomena in atoms, molecules, and solids.
引用
收藏
页数:12
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