To formulate a description of nonlinear polarization spectroscopy that is valid over a wide range of pump intensities, we present an approach that considers any order of the external fields. The Liouville von Neumann equation governing the dynamics of a multilevel molecular system is made tractable by expansion of the particular density matrix into powers of the carrier waves of the external fields. For a two-level system a solution of the resulting set of equations to first order of the probe field but to all orders of pump field is demonstrated. A remarkable change in the homogeneously broadened line shape is obtained at high pump intensities, caused by the optical Stark effect among others. Improvements over results derived by other authors are discussed.
To formulate a description of nonlinear polarization spectroscopy that is valid over a wide range of pump intensities, we present an approach that considers any order of the external fields. The Liouville von Neumann equation governing the dynamics of a multilevel molecular system is made tractable by expansion of the particular density matrix into powers of the carrier waves of the external fields. For a two-level system a solution of the resulting set of equations to first order of the probe field but to all orders of pump field is demonstrated. A remarkable change in the homogeneously broadened line shape is obtained at high pump intensities, caused by the optical Stark effect among others. Improvements over results derived by other authors are discussed.
A nonperturbative theoretical study of four-wave-mixing processes in four-level systems is presented. Using the density-matrix formalism, numerical results are obtained for two arbitrarily intense pump fields with the third field a weak probe. The fourth wave, radiated by the system, is obtained analytically for some special cases. We find, for different frequency detunings, Rabi frequencies, and relaxation rates that the line shapes exhibit: (i) dynamic Stark splitting and shifting, and merging of resonances; (ii) power broadening with two-photon antiresonance behavior resulting from a destructive interference between different contributions to the optical polarization; and (iii) extra resonances induced by field intensities and saturation processes.
The influence of the high-pump-field intensity saturation and dynamic Stark effects on the resonant nearly degenerate four-wave-mixing signal (${\mathrm{\ensuremath{\omega}}}_{3}$=2${\mathrm{\ensuremath{\omega}}}_{1}$-${\mathrm{\ensuremath{\omega}}}_{2}$) is studied in a frequency space defined by the pump- and probe-field frequencies, ${\mathrm{\ensuremath{\omega}}}_{1}$ and ${\mathrm{\ensuremath{\omega}}}_{2}$, respectively. Variable inhomogeneous widths have been considered ranging from extremely narrow (homogeneous distribution) to extremely wide. Remarkable differences between nearly homogeneously broadened systems and extreme inhomogeneous ones are exhibited. It is shown, for the situation of homogeneous broadening, that the spectra carried on with fixed probe and fixed pump frequency values have substantial differences in shape. These differences disappear in the situation of extreme inhomogeneous broadening. Fixed-pump-frequency resonant and fixed-probe-frequency nonresonant spectra are proposed as very convenient tools to yield useful evidence about the width of the inhomogeneous molecular distribution.
For the interaction of coherent radiation with a nondegenerate, homogeneously broadened multilevel system the nonlinear susceptibilities and excitations and their time dependence are evaluated using a perturbation approach to the density matrix up to fourth order. This is done for the "off-resonance" case, ${(\ensuremath{\Delta}{\ensuremath{\omega}}^{2}+{\ensuremath{\Gamma}}^{2})}^{\frac{1}{2}}\ensuremath{\gg}\frac{1}{\ensuremath{\tau}}$, as well as for the "on-resonance" case, ${(\ensuremath{\Delta}{\ensuremath{\omega}}^{2}+{\ensuremath{\Gamma}}^{2})}^{\frac{1}{2}}\ensuremath{\ll}\frac{1}{\ensuremath{\tau}}$, with $\ensuremath{\tau}$ being the pulse duration, by taking into account the temporal change of the electric field amplitude and the phase and energy relaxation times, T2 and T1. It is shown that the transient one-photon excitation known as adiabatic following, is not only important for a pulse duration $\ensuremath{\tau}<{T}_{2}$, but may also be important for ${T}_{2}\ensuremath{\lesssim}\ensuremath{\tau}<{T}_{1}$. In addition, expressions for the transient two-photon excitation in a multilevel system are derived. Finally, the two-level limit is evaluated to all orders of the perturbation including damping effects, which gives results valid also for large incident light intensities. For the "off-resonance" case an expression is obtained which describes not only the transient adiabatic following process, but also the usual one-photon absorption including saturation effects giving rise to power broadening.
1. Introduction 2. Quantum Dynamics in Hilbert Space 3. The Density Operator and Quantum Dynamics in Liouville Space 4. Quantum Electrodynamics, Optical Polarization, and Nonlinear Spectroscopy 5. Nonlinear Response Functions and Optical Susceptibilities 6. The Optical Response Functions of a Multilevel System with Relaxation 7. Semiclassical Simulation of the Optical Response Functions 8. The Cumulant Expansion and the Multimode Brownian Oscillator Model 9. Fluorescence, Spontaneous-Raman and Coherent-Raman Spectroscopy 10. Selective Elimination of Inhomogeneous Broadening Photon Echoes 11. Resonant Gratings, Pump-Probe, and Hole Burning Spectroscopy 12. Wavepacket Dynamics in Liouville Space The Wigner Representation 13. Wavepacket Analysis of Nonimpulsive Measurements 14. Off-Resonance Raman Scattering 15. Polarization Spectroscopy Birefringence and Dichroism 16. Nonlinear Response of Molecular Assemblies The Local-Field Approximation 17. Many Body and Cooperative Effects in the Nonlinear Response
In earlier chapters we have considered in detail the susceptibility formalism of nonlinear optics, which is perhaps the most familiar approach and has a wide range of application. Starting from the constitutive relations of Chapter 2, the susceptibility formalism is quite general. In many practical applications, a particular phenomenon can be described accurately by a single order of nonlinearity, and the susceptibility then provides a useful and convenient description. However, this is not always the case. Some of the most interesting phenomena in nonlinear optics involve close resonance with the transition frequencies of the medium, and perhaps also the use of very intense optical fields. As remarked in §4.5, in these circumstances the resonant susceptibilities display mathematical divergences which are clearly unphysical. Strictly, these divergences occur only because higher-order nonlinearities have been neglected. Successive orders of nonlinearity take into account such effects as saturation, power broadening and level shifts (optical Stark effect). For intense fields or very close resonance, the contributions from several orders of nonlinearity may be comparable in magnitude. Therefore, despite its generality, the susceptibility formalism does not necessarily provide the most practical approach for the description of resonant processes. This chapter is concerned with the problem of deriving alternative and more manageable descriptions of resonant nonlinear processes, illustrated by examples. For much of the chapter, the nonlinear medium is treated as a two-level system (described in §6.2).
This paper presents a theory of lineshapes for molecular Optical-Optical Double Resonance (DR) Spectroscopy with arbitrary strength for both pump and probe fields using the steady-state solutions for the 3-level density matrix. When Doppler broadening can be neglected, the results are analytical, and the probe spectrum is a pair of Lorentzian lines that display Autler-Townes splitting, each with an angular frequency half-width half maximum equal to the relaxation rates, which are assumed to be equal. When Doppler broadening is introduced, one must resort to numerical integration except for the limit of weak pump and probe fields. When the Doppler width is assumed to be much larger than the pump and probe Rabi frequencies and the probe frequency is higher than that of the pump, the calculated DR lineshapes are found to be Lorentzian with a strong pump field limit width that is proportional to the pump Rabi frequency, which is commonly known as power broadening. However, the width does not equal that Rabi frequency and is different for co- and counter-propagating pump and probe fields. Furthermore, that broadening is largely inhomogeneous, despite the Lorentzian shape. The saturation power is found to be about 4 times higher than for the bare probe transition with the same relaxation rate, dramatically lower than that expected if the width is interpreted as homogeneous.