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In this study, the attosecond transient absorption (ATA) spectrum below the excited states of the helium atom was investigated by numerically solving the fully three-dimensional time-dependent Schrödinger equation. Under single-active electron approximation, the helium atom was illuminated by a combined field comprising of extreme ultraviolet (XUV) and delayed infrared (IR) fields. The response function demonstrates that the absorption near the central frequency ( ω X ) of the XUV field is periodically modulated during the overlapping between the XUV and IR pulses. Using the time-dependent perturbation, the absorption near ω X is attributed to the wavepacket excited by the XUV pulse. The wave function oscillating at the frequency of the XUV pulse was obtained. Furthermore, the chirp-dependent absorption spectrum near ω X potentially provides an all-optical method for characterizing the attosecond pulse duration. Finally, these results can extend to other systems, such as solids or liquids, indicating a potential for application in photonic devices, and they may be meaningful for quantum manipulation. [ABSTRACT FROM AUTHOR]

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 Schrödinger 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. [ABSTRACT FROM AUTHOR]

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 Schrödinger 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.

In this study, the attosecond transient absorption (ATA) spectrum below the excited states of the helium atom was investigated by numerically solving the fully three-dimensional time-dependent Schrödinger equation. Under single-active electron approximation, the helium atom was illuminated by a combined field comprising of extreme ultraviolet (XUV) and delayed infrared (IR) fields. The response function demonstrates that the absorption near the central frequency (ωX) of the XUV field is periodically modulated during the overlapping between the XUV and IR pulses. Using the time-dependent perturbation, the absorption near ωX is attributed to the wavepacket excited by the XUV pulse. The wave function oscillating at the frequency of the XUV pulse was obtained. Furthermore, the chirp-dependent absorption spectrum near ωX potentially provides an all-optical method for characterizing the attosecond pulse duration. Finally, these results can extend to other systems, such as solids or liquids, indicating a potential for application in photonic devices, and they may be meaningful for quantum manipulation.