脉搏的效果 A 上的时间的侧面 utler-Townes (在) 在光电子系列切开被为一个旋转 Na-2 分子采用时间依赖者波浪包方法理论上学习。切开源于足够的 Rabi 摆动的 AT 被脉搏侧面和分子的排列影响。切开的 AT 可以仅仅由与某个紧张利用合适...脉搏的效果 A 上的时间的侧面 utler-Townes (在) 在光电子系列切开被为一个旋转 Na-2 分子采用时间依赖者波浪包方法理论上学习。切开源于足够的 Rabi 摆动的 AT 被脉搏侧面和分子的排列影响。切开的 AT 可以仅仅由与某个紧张利用合适的脉搏 proliles 被观察。展开更多
The method of time-dependent quantum wave packet dynamics is used to calculate the femtosecond pump-probe photoelectron spectra and study the wave packet dynamic processes of the double-minimum potential state 6^1∑^...The method of time-dependent quantum wave packet dynamics is used to calculate the femtosecond pump-probe photoelectron spectra and study the wave packet dynamic processes of the double-minimum potential state 6^1∑^＋ of NaK in intense laser fields. The evolutions of the wave packet and the photoelectron energy spectra with time and internuclear distance are described in detail. The wave packet dynamic information of the 6^1∑^＋ state can be extracted from the photoelectron energy spectra.展开更多
We present the photoelectron momentum distributions(PMDs) and the photoelectron angular distributions(PADs) of He+ ions, aligned H2+ molecules and N2 molecules by intense orthogonally polarized laser pulses. Simulatio...We present the photoelectron momentum distributions(PMDs) and the photoelectron angular distributions(PADs) of He+ ions, aligned H2+ molecules and N2 molecules by intense orthogonally polarized laser pulses. Simulations are performed by numerically solving the corresponding two-dimensional time-dependent Schr?dinger equations(TDSEs) within the single-electron approximation frame. Photoelectron momentum distributions and photoelectron angular distributions present different patterns with the time delays Td, illustrating the dependences of the PMDs and PADs on the time delays by orthogonally polarized laser pulses. The evolution of the electron wavepackets can be employed to describe the intensity of the PADs from the TDSE simulations for N2 molecules.展开更多
The laser-induced vibrational state-selectivity of product HF in photoassociation reaction H＋F→HF is theoret- ically investigated by using the time-dependent quantum wave packet method. The population transfer proce...The laser-induced vibrational state-selectivity of product HF in photoassociation reaction H＋F→HF is theoret- ically investigated by using the time-dependent quantum wave packet method. The population transfer process from the continuum state down to the bound vibrational states can be controlled by the driving laser. The effects of laser pulse parameters and the initial momentum of the two collision atoms on the vibrational population of the product HF are discussed in detail. Photodissociation accompanied with the photoassociation process is also described.展开更多
The ultrafast photoionization dynamics of N_(2) molecules by x-ray/XUV laser pulses is investigated.The molecular frame photoelectron momentum distributions(MF-PMDs) and the molecular frame photoelectron angular distr...The ultrafast photoionization dynamics of N_(2) molecules by x-ray/XUV laser pulses is investigated.The molecular frame photoelectron momentum distributions(MF-PMDs) and the molecular frame photoelectron angular distributions(MF-PADs) are obtained by numerically solving 2D time-dependent Schrodinger equations within the single-electron approximation(SEA) frame.The results show that the molecular photoionization diffraction appears in 5 nm laser fields.However,when the laser wavelength is 30 nm,the molecular photoionization diffraction disappears and the MF-PMDs show four-lobe pattern.The ultrafast photoionization model can be employed to describe the MF-PMDs and MF-PADs of N_(2) molecules.展开更多
基金This work was supported by the National Natural Science Foundation of China （No.21222308, No.21103187, and No.21133006）, the Chinese Academy of Sciences, and the National Basic Research Program of China （No. 2013CB922200）.
基金Project supported by the National Natural Science Foundation of China （Grant No 10374012）,
文摘The method of time-dependent quantum wave packet dynamics is used to calculate the femtosecond pump-probe photoelectron spectra and study the wave packet dynamic processes of the double-minimum potential state 6^1∑^＋ of NaK in intense laser fields. The evolutions of the wave packet and the photoelectron energy spectra with time and internuclear distance are described in detail. The wave packet dynamic information of the 6^1∑^＋ state can be extracted from the photoelectron energy spectra.
基金Project supported by the National Natural Science Foundation of China(Grant Nos.12074146,21827805,11974007,and 12074142)the Natural Science Foundation of Jilin Province of China(Grant No.20180101225JC)。
文摘We present the photoelectron momentum distributions(PMDs) and the photoelectron angular distributions(PADs) of He+ ions, aligned H2+ molecules and N2 molecules by intense orthogonally polarized laser pulses. Simulations are performed by numerically solving the corresponding two-dimensional time-dependent Schr?dinger equations(TDSEs) within the single-electron approximation frame. Photoelectron momentum distributions and photoelectron angular distributions present different patterns with the time delays Td, illustrating the dependences of the PMDs and PADs on the time delays by orthogonally polarized laser pulses. The evolution of the electron wavepackets can be employed to describe the intensity of the PADs from the TDSE simulations for N2 molecules.
基金Project supported by the National Natural Science Foundation of China （Grant Nos 10674022 and 20633070）.
文摘The laser-induced vibrational state-selectivity of product HF in photoassociation reaction H＋F→HF is theoret- ically investigated by using the time-dependent quantum wave packet method. The population transfer process from the continuum state down to the bound vibrational states can be controlled by the driving laser. The effects of laser pulse parameters and the initial momentum of the two collision atoms on the vibrational population of the product HF are discussed in detail. Photodissociation accompanied with the photoassociation process is also described.
基金Project supported by the National Natural Science Foundation of China(Grant Nos.12074146,11974007,12074142,11904122,91850114,and 11774131)the Natural Science Foundation of Jilin Province of China(Grant No.20180101225JC)。
文摘The ultrafast photoionization dynamics of N_(2) molecules by x-ray/XUV laser pulses is investigated.The molecular frame photoelectron momentum distributions(MF-PMDs) and the molecular frame photoelectron angular distributions(MF-PADs) are obtained by numerically solving 2D time-dependent Schrodinger equations within the single-electron approximation(SEA) frame.The results show that the molecular photoionization diffraction appears in 5 nm laser fields.However,when the laser wavelength is 30 nm,the molecular photoionization diffraction disappears and the MF-PMDs show four-lobe pattern.The ultrafast photoionization model can be employed to describe the MF-PMDs and MF-PADs of N_(2) molecules.
