In this paper, we theoretically investigate the coherent enhancement of resonance-mediated (2+2) four-photon absorption. It is found that by shaping the spectral phase with a π phase step, the resonance-mediated (2+2) four-photon transition probability can be enhanced. Furthermore, the coherent enhancement dependences on the detuning between the two two-photon absorptions, laser spectral bandwidth and laser centre frequency are explicitly discussed and analysed. We believe these theoretical results may play an important role in enhancing more complex resonance-mediated multiphoton absorption processes.
The dependence of the multiphoton absorption probability for an atomic system on the statistical properties of the incident light is investigated. It is shown, by means of
nth-order time-dependent perturbation theory, that the multiphoton absorption probability depends on the
(n,n)th normally ordered correlation functions of the electromagnetic field. For stationary fields, the transition probability per unit time is constant and is directly related to the reduced cross-spectral correlation function of the electromagnetic field. This expression for the transition probability is then analyzed under various conditions of coherence. Explicit calculations are carried out for thermal light and for laser light, and the transition rates are compared when each has a Lorentzian spectrum. In particular, when the width of the final atomic level is much larger than the bandwidth of the field, the transition rate for thermal light is
n! times higher than with laser light of the same mean intensity. The other extreme case, i.e., when the width of the final atomic level is much smaller than the bandwidth of the field, is also considered in detail. An equation for the density operator of the field is derived; this equation governs the change in the statistical properties of the photon system in
n-photon absorption processes. On the basis of this equation, the time-dependent properties of the photon system are then studied and some physical consequences of these equations are discussed. Some numerical solutions relating to the time dependence of the factorial moments in two-photon absorption processes are presented.
The resonantly enhanced multiphoton ionization of atomic hydrogen is studied for the case of four-photon ionization (three-photon resonant). The time-dependent probabilities, the shape of the resonance profile at different intensities, and the nonlinear index are computed for coherent light at frequencies around the resonance (365 nm). The systematic dependence of the cross section as a function of the principal quantum number of the resonant state (as this tends towards the Rydberg states) is investigated at zero detuning. The probabilities of absorption of one photon more than necessary for the four-photon ionization process (resonantly enhanced above-threshold ionization) is computed and the relevant branching ratios are examined. Then it is shown that the effect of the spatio-temporal structures of the laser pulse is to red shift the maximum of the resonance profile, whereas that of an ideal chaotic light is to blue shift and broaden the resonance peak. The shape, shift, and width of the profile resulting from both these effects are in very fair agreement with the experimental ones.