Stimulated Raman scattering (SRS) is experimentally investigated for solid hydrogen in the context of the strong coupling. Coherence decay behaviors are measured for the Raman transition of
Q(0) $(\ensuremath{\nu}=1\ensuremath{-}0)$ using the time-resolved coherent anti-Stokes Raman-scattering method. We show that the coherence decay for the Raman transition changes with the evolution of the SRS from the weak-coupling regime to the strong-coupling regime.
Saturation effects in coherent anti-Stokes Raman scattering (CARS) spectroscopy are discussed. The discussion is limited to Raman-resonant CARS (${\ensuremath{\omega}}_{l}\ensuremath{-}{\ensuremath{\omega}}_{s}\ensuremath{\simeq}{\ensuremath{\omega}}_{21}$, where ${\ensuremath{\omega}}_{l,s}$ are the frequencies of the pump fields with powers
Pl,s, and ${\ensuremath{\omega}}_{21}$ is the frequency of the Raman transition $|1〉\ensuremath{\rightarrow}|2〉$) with the possible addition of a one-photon resonance (${\ensuremath{\omega}}_{l}\ensuremath{\simeq}{\ensuremath{\omega}}_{31}$ is the frequency of the electronic transition $|1〉\ensuremath{\rightarrow}|3〉$). For these cases we show that the CARS polarization
pCARS is proportional to the off-diagonal density-matrix element ${\ensuremath{\rho}}_{21}$. In order to determine ${\ensuremath{\rho}}_{21}$, we use Laplace transforms to solve the Bloch equations for the effective two-level system
∣1〉 and
∣2〉 when ${\ensuremath{\omega}}_{l}$ is far from resonance, or for the three-level system
∣1〉,∣2〉, and
∣3〉, when ${\ensuremath{\omega}}_{l}\ensuremath{\simeq}{\ensuremath{\omega}}_{31}$. The steady-state expression for
pCARS in the former case gives ${\mathcal{p}}_{\mathrm{CARS}}\ensuremath{\propto}{P}_{l}{P}_{s}^{\frac{1}{2}}$ at low powers and ${\mathcal{p}}_{\mathrm{CARS}}\ensuremath{\propto}{P}_{l}^{0}{P}_{s}^{\frac{\ensuremath{-}1}{2}}$ at high powers. In the three-level system, we show that when the pressure is low and at least one field is weak, the slow time dependence of ${\ensuremath{\rho}}_{21}$ must be considered. When one field is strong and the other weak, the CARS spectrum is Stark split. When
Pl is high, for example, ${\mathcal{p}}_{\mathrm{CARS}}\ensuremath{\propto}{P}_{l}^{0}{P}_{s}^{\frac{1}{2}}$ for ${\ensuremath{\omega}}_{s}\ensuremath{\simeq}{\ensuremath{\omega}}_{32}$ and ${\mathcal{p}}_{\mathrm{CARS}}\ensuremath{\propto}{({P}_{l}{P}_{s})}^{\frac{1}{2}}$ when ${\ensuremath{\omega}}_{s}\ensuremath{\simeq}{\ensuremath{\omega}}_{32}\ifmmode\pm\else\textpm\fi{}{V}_{13}$ where
V13 is the one-photon Rabi frequency for the $|1〉\ensuremath{\rightarrow}|3〉$ transition. The Wilcox-Lamb approximation is used to reduce the three-level Bloch equations to rate equations containing one- and two-photon terms. When the fields are so weak that both one- and two-photon terms are small compared to the decay terms, the usual expression for
pCARS is reproduced. If only the direct two-photon processes are important, the effective-two-system results are reproduced. When both fields are intense and nearly resonant, the steady state is rapidly achieved. The results for the case where one field is much stronger than the other are essentially the same as those for one strong and one weak field. When the fields are of comparable strength, ${\mathcal{p}}_{\mathrm{CARS}}\ensuremath{\propto}{P}_{l}^{\frac{1}{2}}{P}_{s}^{0}$ for ${\ensuremath{\omega}}_{l}\ensuremath{\simeq}{\ensuremath{\omega}}_{31}$ and ${\ensuremath{\omega}}_{s}\ensuremath{\simeq}{\ensuremath{\omega}}_{32}$, and the CARS spectrum is split into five components.
The traditional Raman process alluded to in Chap. 13 is a three-state sequence of transitions in which radiative excitation (induced by a pump field) is followed by spontaneous emission that produces a final state differing from the initial state [Her50b] [Sho90, § 17.5]. When the final state of the sequence is more energetic than the initial state the resulting emission line (to the red of the pump wavelength) is known as a Stokes spectral line. The difference between the pump frequency and the Stokes frequency, the Raman frequency , defines the excitation energy of the final state relative to the initial state. When, instead, the final state has lower energy than the initial state, as can occur when the initial quantum state is already excited, then the emission is an anti-Stokes line, at a bluer wavelength than the pump field. The overall Raman scattering is a two-photon process. Typically Raman spectroscopy deals with molecules; the two-photon transitions are then between vibrational-rotational states, through electronically excited intermediate states, that are characterized in part by vibrational quantum number v and rotational angular momentum quantum numbers J, M . From any given excited electronic state there are many fluorescing transitions, corresponding to various vibrational and rotational quantum numbers of the final state. The wavelengths of the various Stokes and anti-Stokes lines (i.e. the Raman frequencies) characterize the particular molecular species, and so they have provided a valuable diagnostic tool for spectroscopists.
We have calculated the cross section for Raman scattering of light from a hydrogenic atom, for a wide range of photon energies. The calculation assumes the photon encounters the atom in its ground state and excites it to the
2s state. Since various contributions to the matrix element may be isolated in the computation, the calculation allows one to obtain a notion of the relative importance of various classes of intermediate states in a given frequency range. We also point out that the Raman efficiency
S may be expressed in terms of the derivative of the electronic polarizability tensor with respect to a parameter that measures the degree of excitation of the atom. Thus, the formal expression for
S assumes an appearance identical to the expression encountered in the phenomenological theory of the first-order Raman effect in solids.