We have developed and tested an efficient mathematical model for calculating a coherent population trapping (CPT) resonance in a periodically modulated laser field when the modulation frequency $f$ is close to the fractional part of the hyperfine splitting frequency (HFS) in the ground state ${\mathrm{\Delta }}_{\mathrm{HFS}}/N$ (where $N=1,2,3,\dots$). In such a polychromatic light, only two frequency components that are most resonant with the working optical transitions in the atom are taken into account exactly, while all other off-resonant frequency components are taken into account by using the second-order perturbation theory in the field magnitude. Within the framework of our concept, an equation for the atomic density matrix is obtained, in which all off-resonant frequency components are described by two operators (which are nondiagonal in the general case): a shift operator and a relaxation operator. This model has been verified by numerical calculations for various dependencies, in which we have not found visual differences from the results of exact calculations. Thus, in our bichromatic model, the infinite variety of periodically modulated fields in CPT spectroscopy can be uniformly described by only five parameters. In addition to a significant mathematical simplification, our model provides a clear physical picture of the various features of CPT spectroscopy in a periodically modulated laser field, including some effects that have not yet been discussed in the scientific literature. In particular, we show a widespread viewpoint that the CPT resonance shift is determined by standard ac Stark shifts of the lower levels is, in general, fundamentally incorrect, since the contribution to the light shift due to beats at the frequency ${\mathrm{\Delta }}_{\mathrm{HFS}}$ between different off-resonant frequency components can be comparable to the value of standard ac Stark shift (or even dominate it). Therefore, even if we have detailed information on the spectral composition of the modulated field (e.g., using a spectrum analyzer), this is, in general, absolutely insufficient for determining the light shift of the CPT resonance.

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• Atomic, optical & lattice clocks
• Coherent population trapping
• Quantum optics