Based on numerical solutions of the time-dependent Schr ¨odinger equation, we theoretically investigate the photoelectron spectrum of hydrogen atoms ionized by a pair of ultrashort, intense, and orthogonally pola...Based on numerical solutions of the time-dependent Schr ¨odinger equation, we theoretically investigate the photoelectron spectrum of hydrogen atoms ionized by a pair of ultrashort, intense, and orthogonally polarized laser pulses with a relative time delay in a pump–probe configuration. The pump pulse resonantly excites electrons from the 1s and 2p levels,inducing Rabi oscillations. The resulting dynamically enhanced Autler–Townes(AT) splitting is observed in the photoelectron energy spectrum upon interaction with the second probe pulse. In contrast to the previous parallel-polarization scheme, the proposed orthogonal-polarization configuration enables the resolution of dynamically enhanced AT splitting over a considerably wider range of probe photon energies.展开更多
We present an efficient method to generate an ultrashort wavelength-tunable XUV pulse by using the harmonic selec- tive enhancement scheme. The results show that by properly controlling the delay times of a two-color ...We present an efficient method to generate an ultrashort wavelength-tunable XUV pulse by using the harmonic selec- tive enhancement scheme. The results show that by properly controlling the delay times of a two-color field or a three-color field, selective enhancement of the harmonics with photon energies between 80 eV and 315 eV can be obtained. Fur- ther, a wavelength-tunable and bandwidth-controllable XUV radiation can be obtained by Fourier transformation of these enhanced harmonics.展开更多
The direct above-threshold ionization(ATI) of diatomic molecules in linearly-polarized infrared and extreme ultraviolet(IR+XUV) laser fields is investigated by the frequency–domain theory based on the nonperturbative...The direct above-threshold ionization(ATI) of diatomic molecules in linearly-polarized infrared and extreme ultraviolet(IR+XUV) laser fields is investigated by the frequency–domain theory based on the nonperturbative quantum electrodynamics. The destructive interference fringes on the angle-resolved ATI spectra, which are closely related to the molecular structure, can be well fitted by a simple predictive formula for any alignment of the molecular axis. By comparing the direct ATI spectra for monochromatic and two-color laser fields, we found that the XUV laser field can both raise the ionization probability and the kinetic energy of the ionized electron, while the infrared(IR) laser field can broaden the energy distribution of the ionized electron. Our results demonstrate that, by using IR+XUV two-color laser fields, the angle-resolved spectra of the direct ATI can image the structural information of molecules without considering the recollision process of the ionized electron.展开更多
We theoretically study the dependence of photoelectron angular distribution on laser polarization direction in nitrogen molecules. The approach is based on the time-dependent density functional theory at the level of ...We theoretically study the dependence of photoelectron angular distribution on laser polarization direction in nitrogen molecules. The approach is based on the time-dependent density functional theory at the level of local density approximation complemented by self-interaction correction. It is found that photoelectron emission in one photon regime could be considered as a probing tool for the main character of different types of molecular orbitals （σ or π）. The pattern of emitted photoelectrons strongly depends on the polarized angle of the laser, for σ orbital, the number of photoelectron decreases with increasing the polarized angle, while for π orbital, it has the inverse relation to the polarized angle, which reveals the multi-electron effect in molecules. On the other hand, concerning the total photoelectron emission, one should take into account a few occupied orbitals instead of only the outmost one.展开更多
Attosecond transient absorption(ATA)has been developed as an all-optical technique for probing electron dynamics in matter.Here we present a scheme that can modify the laserinduced state and the corresponding ATA spec...Attosecond transient absorption(ATA)has been developed as an all-optical technique for probing electron dynamics in matter.Here we present a scheme that can modify the laserinduced state and the corresponding ATA spectrum via excitation by a pair of XUV attosecond pulses and by a time-delayed mid-infrared(MIR)laser probe.Different from the scheme of the electronic excitation by a single XUV attosecond pulse,the application of a pair of XUV pulses provides extra degrees of freedom,such as the time delay and the intensity ratio between two XUV pulses,which make it possible to adjust the pump process,resulting in the modification of the ATA spectrum.We show that by varying the time delay between the two XUV pulses,the population of the dark state and the ATA spectrum of the laser-induced state have periodic modulations.We also demonstrate that the peak of the ATA spectrum of the laser-induced state appears at a fixed time delay between the XUV pair and the MIR laser when the intensity ratio is large,and it changes with the time delay when the intensity ratio is small,which can be related to either one of two peaks in the population of the dark state.展开更多
We investigate the above-threshold ionization of an atom in a combined infrared （IR） and extreme ultraviolet （XUV） two-color laser field and focus on the role of XUV field in the high-order above-threshold ionizat...We investigate the above-threshold ionization of an atom in a combined infrared （IR） and extreme ultraviolet （XUV） two-color laser field and focus on the role of XUV field in the high-order above-threshold ionization （HATI） process. It is demonstrated that, in stark contrast to previous studies, the XUV laser may play a significant role in atomic HATI process, and in particular, the XUV laser can accelerate the ionized electron in a quantized way during the collision between the electron and its parent ion. This process cannot be explained by the elassical three-step model Our results indicate that the previously well-established concept that HATI is an elastic recollision process is broken down.展开更多
基金supported by the National Natural Science Foundation of China(Grant Nos.12074265,12234002,and 92250303)the Guangdong Basic and Applied Basic Research Foundation(Grant No.2022A1515010329)。
文摘Based on numerical solutions of the time-dependent Schr ¨odinger equation, we theoretically investigate the photoelectron spectrum of hydrogen atoms ionized by a pair of ultrashort, intense, and orthogonally polarized laser pulses with a relative time delay in a pump–probe configuration. The pump pulse resonantly excites electrons from the 1s and 2p levels,inducing Rabi oscillations. The resulting dynamically enhanced Autler–Townes(AT) splitting is observed in the photoelectron energy spectrum upon interaction with the second probe pulse. In contrast to the previous parallel-polarization scheme, the proposed orthogonal-polarization configuration enables the resolution of dynamically enhanced AT splitting over a considerably wider range of probe photon energies.
基金supported by the Scientific Research Fund of Liaoning Provincial Education Department,China(Grant No.L2012223)the Scientific Research Fund of Liaoning University of Technology,China(Grant Nos.X201319 and X201312)
文摘We present an efficient method to generate an ultrashort wavelength-tunable XUV pulse by using the harmonic selec- tive enhancement scheme. The results show that by properly controlling the delay times of a two-color field or a three-color field, selective enhancement of the harmonics with photon energies between 80 eV and 315 eV can be obtained. Fur- ther, a wavelength-tunable and bandwidth-controllable XUV radiation can be obtained by Fourier transformation of these enhanced harmonics.
基金Project supported by the National Natural Science Foundation of China(Grant Nos.11334009,11425414,11474348,and 11774411)
文摘The direct above-threshold ionization(ATI) of diatomic molecules in linearly-polarized infrared and extreme ultraviolet(IR+XUV) laser fields is investigated by the frequency–domain theory based on the nonperturbative quantum electrodynamics. The destructive interference fringes on the angle-resolved ATI spectra, which are closely related to the molecular structure, can be well fitted by a simple predictive formula for any alignment of the molecular axis. By comparing the direct ATI spectra for monochromatic and two-color laser fields, we found that the XUV laser field can both raise the ionization probability and the kinetic energy of the ionized electron, while the infrared(IR) laser field can broaden the energy distribution of the ionized electron. Our results demonstrate that, by using IR+XUV two-color laser fields, the angle-resolved spectra of the direct ATI can image the structural information of molecules without considering the recollision process of the ionized electron.
文摘We theoretically study the dependence of photoelectron angular distribution on laser polarization direction in nitrogen molecules. The approach is based on the time-dependent density functional theory at the level of local density approximation complemented by self-interaction correction. It is found that photoelectron emission in one photon regime could be considered as a probing tool for the main character of different types of molecular orbitals （σ or π）. The pattern of emitted photoelectrons strongly depends on the polarized angle of the laser, for σ orbital, the number of photoelectron decreases with increasing the polarized angle, while for π orbital, it has the inverse relation to the polarized angle, which reveals the multi-electron effect in molecules. On the other hand, concerning the total photoelectron emission, one should take into account a few occupied orbitals instead of only the outmost one.
基金supported by the National Natural Science Foundation of China(Grant Nos.91950102 and 11834004)the Natural Science Foundation of Jiangsu Province(Grant No.BK20220925)the Funding of Nanjing University of Science and Technology(NJUST)(Grant No.TSXK2022D005)
文摘Attosecond transient absorption(ATA)has been developed as an all-optical technique for probing electron dynamics in matter.Here we present a scheme that can modify the laserinduced state and the corresponding ATA spectrum via excitation by a pair of XUV attosecond pulses and by a time-delayed mid-infrared(MIR)laser probe.Different from the scheme of the electronic excitation by a single XUV attosecond pulse,the application of a pair of XUV pulses provides extra degrees of freedom,such as the time delay and the intensity ratio between two XUV pulses,which make it possible to adjust the pump process,resulting in the modification of the ATA spectrum.We show that by varying the time delay between the two XUV pulses,the population of the dark state and the ATA spectrum of the laser-induced state have periodic modulations.We also demonstrate that the peak of the ATA spectrum of the laser-induced state appears at a fixed time delay between the XUV pair and the MIR laser when the intensity ratio is large,and it changes with the time delay when the intensity ratio is small,which can be related to either one of two peaks in the population of the dark state.
基金Supported by the National Natural Science Foundation of China under Grant Nos 11474348,61275128,11274050,11334009and 11425414the NSERC of Canada+1 种基金the Canadian Computing Facilities of SHARCnet and ACEnetthe National Basic Research Program of China under Grant No 2013CB922200
文摘We investigate the above-threshold ionization of an atom in a combined infrared （IR） and extreme ultraviolet （XUV） two-color laser field and focus on the role of XUV field in the high-order above-threshold ionization （HATI） process. It is demonstrated that, in stark contrast to previous studies, the XUV laser may play a significant role in atomic HATI process, and in particular, the XUV laser can accelerate the ionized electron in a quantized way during the collision between the electron and its parent ion. This process cannot be explained by the elassical three-step model Our results indicate that the previously well-established concept that HATI is an elastic recollision process is broken down.
