This paper calculates quantum-mechanically the photoelectron energy spectra excited by attosecond x-rays in the presence of a few-cycle laser. A photoelectron laser phase determination method is used for precise measu...This paper calculates quantum-mechanically the photoelectron energy spectra excited by attosecond x-rays in the presence of a few-cycle laser. A photoelectron laser phase determination method is used for precise measurements of the pulse natural properties of x-ray intensity and the instantaneous frequency profiles. As a direct procedure without any previous pulse profile assumptions and time-resolved measurements as well as data fitting analysis, this method can be used to improve the time resolutions of attosecond timing and measurements with metrological precision. The measurement range is half of a laser optical cycle.展开更多
To measure and control the electron motion in atoms and molecules by the strong laser field on the attosecond time scale is one of the research frontiers of atomic and molecular photophysics. It involves many new phen...To measure and control the electron motion in atoms and molecules by the strong laser field on the attosecond time scale is one of the research frontiers of atomic and molecular photophysics. It involves many new phenomena and processes and raises a series of questions of concepts, theories, and methods. Recent studies show that the Coulomb potential can cause the ionization time lag(about 100 attoseconds) between instants of the field maximum and the ionization-rate maximum. This lag can be understood as the response time of the electronic wave function to the strong-field-induced ionization event. It has a profound influence on the subsequent ultrafast dynamics of the ionized electron and can significantly change the time–frequency properties of electron trajectory(an important theoretical tool for attosecond measurement). Here, the research progress of response time and its implications on attosecond measurement are briefly introduced.展开更多
The photoelectron energy spectra （PESs） excited by narrow bandwidth attosecond x-ray pulses in the presence of a few-cycle laser are quantum-mechanically calculated. Transfer equations are used to reconstruct the de...The photoelectron energy spectra （PESs） excited by narrow bandwidth attosecond x-ray pulses in the presence of a few-cycle laser are quantum-mechanically calculated. Transfer equations are used to reconstruct the detailed temporal structure of an attosecond x-ray pulse directly from a measured PES. Theoretical analysis shows that the temporal uncertainties of the pulse reconstruction depend on the x-ray bandwidth. The procedure of pulse reconstruction is direct and simple without making any previous pulse assumption, data fitting analysis and time-resolved measurement of PESs. The temporal measurement range is half of a laser optical cycle.展开更多
文摘This paper calculates quantum-mechanically the photoelectron energy spectra excited by attosecond x-rays in the presence of a few-cycle laser. A photoelectron laser phase determination method is used for precise measurements of the pulse natural properties of x-ray intensity and the instantaneous frequency profiles. As a direct procedure without any previous pulse profile assumptions and time-resolved measurements as well as data fitting analysis, this method can be used to improve the time resolutions of attosecond timing and measurements with metrological precision. The measurement range is half of a laser optical cycle.
基金Project supported by the National Natural Science Foundation of China(Grant No.91750111)the National Key Research and Development Program of China(Grant No.2018YFB0504400)。
文摘To measure and control the electron motion in atoms and molecules by the strong laser field on the attosecond time scale is one of the research frontiers of atomic and molecular photophysics. It involves many new phenomena and processes and raises a series of questions of concepts, theories, and methods. Recent studies show that the Coulomb potential can cause the ionization time lag(about 100 attoseconds) between instants of the field maximum and the ionization-rate maximum. This lag can be understood as the response time of the electronic wave function to the strong-field-induced ionization event. It has a profound influence on the subsequent ultrafast dynamics of the ionized electron and can significantly change the time–frequency properties of electron trajectory(an important theoretical tool for attosecond measurement). Here, the research progress of response time and its implications on attosecond measurement are briefly introduced.
基金Project supported by the National Natural Science Foundation of China (Grant No 10675014)
文摘The photoelectron energy spectra （PESs） excited by narrow bandwidth attosecond x-ray pulses in the presence of a few-cycle laser are quantum-mechanically calculated. Transfer equations are used to reconstruct the detailed temporal structure of an attosecond x-ray pulse directly from a measured PES. Theoretical analysis shows that the temporal uncertainties of the pulse reconstruction depend on the x-ray bandwidth. The procedure of pulse reconstruction is direct and simple without making any previous pulse assumption, data fitting analysis and time-resolved measurement of PESs. The temporal measurement range is half of a laser optical cycle.
