A semiclassical theory that describes the generation of a coherent anti-Stokes Raman scattering (CARS) signal is presented that maximizes vibrational coherence in a mode predetermined by the pump, the Stokes, and the probe chirped pulse trains and takes into account the field propagation effects in a cloud of molecules. The buildup of the anti-Stokes signal, which may be used as a molecular signature in the backward CARS signal, is demonstrated numerically. The theory is based on the solution of the coupled Maxwell's and Liouville--von Neumann equations and focuses on the quantum effects induced in the target molecules by the control pulse trains. A deep convolutional neural network technique is implemented to evaluate time-dependent phase characteristics of the control fields. The effect of decoherence induced by spontaneous decay and collisional dephasing is examined.
Time-resolved coherent anti-Stokes Raman scattering is applied to prepare and interrogate vibrational coherences on the ground electronic surface of molecular iodine isolated in Ar matrices. The coherence decay time shows a linear dependence on vibrational quantum numbers for v=3–15. The temperature dependence of decoherence rates is negligible for v<7 in the experimental range T=18–32 K. For a v=13, 14 superposition, the temperature dependence indicates dephasing by a 66 cm−1 pseudo-local phonon, just outside the Debye edge of the solid. The accuracy of the data is limited due to two-photon induced dissociation of the molecule, a process which is characterized using polarized fields. The T→0 limit of dephasing is discussed.
Calculations are presented demonstrating controlled intermolecular communication between dopant molecules via lattice phonons in a cryogenic matrix. By simulating a time-resolved coherent anti-Stokes Raman scattering (tr-CARS) experiment on an I2-molecule ‘receiver,’ its reception from a Ca-atom ‘transmitter’ of coherent lattice waves in a compressed linear chain of Ar atoms is monitored. A short pulse resonant with an atomic transition in Ca arrives at the sample before the tr-CARS pulses, and the coherent response of the host medium to the electronic excitation sends a rarefaction wave through the lattice. The arrival of this propagating distortion at the I2 molecule is detected through the tr-CARS difference signal, the difference between tr-CARS signals with and without the Ca pulse. A normal-mode analysis of the equilibrium configuration is used to construct an initial Gaussian wave packet, which is propagated by locally quadratic approximations to the relevant many-body nuclear Hamiltonians. Results are presented for both resonant and sub-resonant excitation of the Ca atom. Calculations show a difference signal that turns on abruptly as the lattice wave generated by resonant Ca excitation reaches the I2 chromophore.
Time-resolved coherent anti-Stokes Raman-scattering (CARS) measurements are carried out for iodine (I2) in solid krypton matrices. The dependence of vibrational dephasing time on temperature and vibrational quantum number v is studied. The v dependence is approximately quadratic, while the temperature dependence of both vibrational dephasing and spectral shift, although weak, fits the exponential form characteristic of dephasing by pseudolocal phonons. The analysis of the data indicates that the frequency of the pseudolocal phonons is approximately 30 cm(-1). The longest dephasing times are observed for v = 2 being approximately 300 ps and limited by inhomogeneous broadening. An increase in the dephasing rate of v = 2 as the temperature is lowered to T = 2.6 K is taken as a clear indication of lattice-strain-induced inhomogeneity of the ensemble coherence.
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.
Spontaneous vibrational Raman scattering is a ubiquitous form of light-matter interaction whose description necessitates quantization of the electromagnetic field. It is usually considered as an incoherent process because the scattered field lacks any predictable phase relationship with the incoming field. When probing an ensemble of molecules, the question therefore arises: What quantum state should be used to describe the molecular ensemble following spontaneous Stokes scattering? We experimentally address this question by measuring time-resolved Stokes-anti-Stokes two-photon coincidences on a molecular liquid consisting of several sub-ensembles with slightly different vibrational frequencies. When spontaneously scattered Stokes photons and subsequent anti-Stokes photons are detected into a single spatiotemporal mode, the observed dynamics is inconsistent with a statistical mixture of individually excited molecules. Instead, we show that the data are reproduced if Stokes-anti-Stokes correlations are mediated by a collective vibrational quantum, i.e. a coherent superposition of all molecules interacting with light. Our results demonstrate that the degree of coherence in the vibrational state of the liquid is not an intrinsic property of the material system, but rather depends on the optical excitation and detection geometry.