基于激光诱导相位模型，研究了周期性相位调控的He原子体系的光谱响应。研究发现，周期性的相位调控会导致He原子吸收谱由单个孤立的洛伦兹线型转化为等间隔的“梳状”结构。“梳状”光谱的性质主要由原子系统和控制脉冲链的性质决定，并给出了表征“梳状”光谱的理论公式。该机理具有普遍适用性，它可以应用到任意原子体系，进而推广到任意波段，并且为任意波段的脉冲整形提供了可能。%Based on the laser-induced-phase model, periodic quantum phase modulation of the dipole response in atomic He is studied theoretically. The two-level system of the transition 1s2 →1s2p with a delay width of 1.8 × 109 s−1 and an energy difference of 21.2 eV between the excited state and the ground state is used in the calculation. The system is excited by attosecond laser pulse from high harmonic generator, and the spectral response of the system is of single isolated symmetric Lorentzian absorption line. After the excitation, near infrared (NIR) femtosecond laser pulse train with a repetition rate of 5 GHz, central frequency 780 nm, and pulse duration of 100 fs, is utilized to periodically modify the spontaneous decay of the excited 1s2p level. The incremental phase step ∆ϕ depends on the intensity of the NIR laser pulse, while the initial offset phase ϕ can be controlled independently by partially overlapping the first NIR pulse with the excitation. Simulated results show that the Lorentzian absorption line is transformed into comb-like spectral structure with equal gap depending on the repetition rate of the NIR pulse train. The line shape of each comb tooth is symmetric Lorentzian line by setting ϕ = ∆ϕ/2 = π/2, while it is Fano line by setting ϕ = ∆ϕ = π. The location of the comb structure is mainly dependent on the energy difference between the excited state and the ground state, while it can be slightly tuned by controlling the incremental phase step ∆ϕ. We develop an analytic description of the comb-like spectral structure by Fourier analysis, depending on both the atomic and the phase-control properties. The analytical expressions can be readily used to estimate the exact experimental parameters. The universality of this mechanism allows the spectral modulation in arbitrary atomic system at arbitrary frequency, including the hard X-ray regime, by using reference transitions in highly charged ions. The generalization of this approach should thus not only enable relative frequency measurement and relevant applications at extremely high frequencies, but also open the way for pulse shaping at arbitrary frequencies.
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