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Physical Review A

Molecules probed with a slow chirped-pulse excitation: Analytical model of the free-induction-decay signal

Daniele Fontanari, C. Bray, Guillaume S. F. Dhont, Gaël Mouret, Arnaud Cuisset, Francis P. Hindle, Robin Bocquet, Kevin M. Hickson

Published Oct 14, 2019• 4 citations
Publisher

Abstract

Most chirped-pulse experiments refer to a theoretical study from McGurk, Schmalz, and Flygare [J. Chem. Phys. 60, 4181 (1974)] which is well tailored to interpret the signals obtained with very fast chirped pulses, but is not sufficient to account for the signals in the case of slower chirped pulses used in spectroscopy to increase the signal-to-noise ratio. A theoretical study of the polarization of molecules subjected to a chirped pulse in a cell, uniform supersonic flow, or molecular beam is presented. Three degrees of approximation for the polarization are introduced and are compared with the numerical solution of the optical Bloch equations. These expressions enter the analytic expression of the free-induction-decay signal which is validated against experimental data on the rotational emission spectra of OCS molecules. A relation among the pulse duration, the line position in the chirped pulse, and the signal amplitude is proposed in the thermalized case. It assists in the optimization of the chirped-pulse parameters and in the estimation of the error associated with the line intensity.

DOI
10.1103/physreva.100.043407

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Most chirped-pulse experiments refer to a theoretical study from McGurk, Schmalz, and Flygare [J. Chem. Phys. 60, 4181 (1974)] which is well tailored to interpret the signals obtained with very fast chirped pulses, but is not sufficient to account for the signals in the case of slower chirped pulses used in spectroscopy to increase the signal-to-noise ratio. A theoretical study of the polarization of molecules subjected to a chirped pulse in a cell, uniform supersonic flow, or molecular beam is presented. Three degrees of approximation for the polarization are introduced and are compared with the numerical solution of the optical Bloch equations. These expressions enter the analytic expression of the free-induction-decay signal which is validated against experimental data on the rotational emission spectra of OCS molecules. A relation among the pulse duration, the line position in the chirped pulse, and the signal amplitude is proposed in the thermalized case. It assists in the optimization of the chirped-pulse parameters and in the estimation of the error associated with the line intensity.
We present a time-domain treatment of pump–probe experiments with chirped pulses derived from the same laser source. In this theory we treat the nonlinearities as decaying either instantaneously or exponentially. Therefore the results from it cover different mechanisms originating from electronic orbitals, molecular vibrations, molecular orientations, excited-state populations, etc., as long as their decay falls into one of the two classes. We derive expressions for the transmission of the probe in each case. We divide the transmission expression from nonlinearities with exponential decay into a number of terms, each of which describes a unique situation. These include two-beam coupling in the coherent region that is not present with chirp-free pulses, two-photon absorption, and excited-state absorption. We give analytical expressions for the transmission where possible, and we give the first-order approximation and the estimated error when expression in closed form is unattainable. We discuss various aspects of these terms.
We model the response of a molecular medium to an intense pulse of light. We begin by reducing the Maxwell-Bloch equations for a multilevel molecular model system to a set of simplified propagation equations. We thereby obtain expressions for the frequency, temperature, and field intensity dependence of the ground and excited electronic state absorption cross sections, and the emission cross section, as well as the temperature dependence of the decay rate of the excited state. The phenomena of saturation, excited-state absorption, optically induced dichroism and birefringence, vibronic energy transfer, induced molecular alignment, decay of the matter-field interaction energy, and rotational diffusion are considered within the general formalism for describing the propagation of an intense pulse of light in the molecular medium. We find that the cross section for absorption (emission) of a photon is not identical to the cross section for molecular excitation (deexcitation) via the matter-field interaction. This is explained in terms of an energy balance between the matter, radiation, the matter-radiation interaction, and the bath responsible for the broadening of the molecular transitions. The inequality of these cross sections determines whether the system supplies or draws energy from the thermal bath. The rise in the vibrational temperature of molecules subjected to an intense short pulse is shown to significantly affect propagation of the pulse. The alignment of the molecular system resulting from saturation of the ground-state transition by a polarized laser pulse and the effects of the orientational dependence of the matter-field interaction including effects of rotational diffusion are determined. As an example of the formalism we consider pulse propagation in a Rhodamine 6G solution. We fit the parameters of the model to determine the frequency dependence of the ground- and excited-state absorption cross sections and the emission cross section and compare with experimentally determined cross sections. We describe the propagation of a pulse whose temporal width is comparable to the rotational diffusion time of the molecules in the dye solution and calculate polarization pulse probe signals.
Large-amplitude oscillations are predicted in the free-induction decay (FID) of atomic or spin two-level quantum systems that are coherently prepared by a resonant electromagnetic field in the form of a square amplitude pulse of duration TTT. The effect should be detectable in nuclear magnetic resonance (NMR) or in optical resonance experiments when the transition line shape is inhomogeneously broadened (${T}_{2}^{*}\ensuremath{\ll}{T}_{2}$) and the applied field is intense enough that the pulse area $\ensuremath{\chi}T\ensuremath{\ge}2\ensuremath{\pi}$, where $\ensuremath{\chi}$ is the Rabi frequency. Physically, the effect is due to Rabi oscillations which are generated in the preparative stage and are then reproduced because of atomic memory in the radiative period which follows. The atomic polarization derived from the Bloch equations assumes the form of an integral over the inhomogeneous line shape, and can be evaluated numerically for arbitrary linewidth $\ensuremath{\sigma}$ or analytically when $\ensuremath{\sigma}\ensuremath{\rightarrow}\ensuremath{\infty}$. The characteristics of the oscillation are unusual since the oscillation frequency, which is of order $\ensuremath{\chi}$, increases with time while the oscillation envelope vanishes identically for times $t\ensuremath{\ge}2T$. Coherent emission is therefore confined to one pulse width TTT immediately following the pulse. Previous NMR and infrared FID experiments with small-area pulses ($\ensuremath{\chi}T\ensuremath{\le}4\ensuremath{\pi}$), interpreted erroneously in terms of an edge echo effect, support the oscillatory FID behavior described here. For the case $\ensuremath{\chi}T>4\ensuremath{\pi}$, an experimental test would be even more decisive, as the oscillations are more pronounced.
A simple application of the Stark-pulse technique, developed by Brewer and Shoemaker, demonstrates optical free induction decay-the optical analog of free induction decay in NMR. A molecular sample which is coherently prepared by a cw laser beam exhibits such a decay when it is suddenly switched out of resonance by a Stark field. Observations are presented for a nondegenerate Doppler-broadened infrared transition of NH2{\mathrm{H}}_{2}H2​D, where the sample is optically thin, and the decay behavior can be compared quantitatively with a solution of the Bloch equations. When the molecular sample is prepared under steady-state conditions, the solutions are analytic; for pulse excitation, a numerical solution is required. The treatment invokes a hard-collision relaxation model. Such characteristics as the abrupt termination of the decay and the related edge echo, which result from Doppler dephasing, can be examined for Stark pulses of finite extent.
The excitation of a two-level system by a chirped laser pulse is analyzed using an analytical approach (in the perturbation-theory limit) that involves the modified rotating-wave approximation and the numerical solution to the Bloch equation. The dependence of the population of the upper energy level on the chirp is studied for various radiation intensities and pulse durations. An exact solution is compared with the result obtained using the modified rotating-wave approximation and the perturbation theory. It is demonstrated that, for a certain range of parameters, the excitation probability of a two-level system can be effectively controlled via a variation in the chirp.
The delayed or time-domain four-wave-mixing experiment is treated in the regime of intense near-resonant pulses. The interaction with the radiation during both pump and probe pulses is considered to all powers of the electric field amplitude. Analytical results are obtained for an effective four-level system. These include the dependence of the coherence amplitudes on the ratio of the pump-field intensities when there is a large vibrational discrepancy between ground and excited electronic states and a general solution for the unitary time development during the probe pulse. For the first time, delayed coherent anti-Stokes Raman scattering is detected from highly dilute (10-ppm) guest molecules. Illustrative examples are presented for the system of pentacene in benzoic acid at low temperature. Vibronic-free induction decay and the effect of field inhomogeneity across the beam profile are found to be essential for understanding the observed intensity and spectral distribution of the signal beam in the region of optimum pulse intensity.