Although the time-dependent buildup processes of Autler-Townes splitting in attosecond transient absorption spectra have been observed in plenty of experiments, there still exists an open question of when the splitting is maximized, which tells us how fast the system responds to the pump field and how well the adiabatic following is in a slowly varying few-cycle laser pulse. In this Letter we work out a compact formula to quantify the buildup time of the Autler-Townes splitting, which is related to multiple timescales of the laser-atom system, e.g., the Rabi period, the laser cycle, and the pulse duration, according to a universal power law. This scaling law applies not only to singly excited states, but also to doubly excited states in which complex electron-electron interaction gets involved. Our findings have potential applications in calibrating the zero delay in a transient absorption spectroscopy.

Close

PrevNext

View figure in article

• Nonlinear optics
• Optical transient phenomena
• Stark effect
• Ultrafast optics
• Ultrafast phenomena
• Adiabatic approximation
• Rotating wave approximation
• Schroedinger equation
• Two-level models