The effect of velocity-changing collisions in an extended-pulse photon echo is studied. In an extended-pulse photon echo, the second excitation pulse has a duration comparable with the relaxation time of an atomic system. We present an analytic solution of the quantum-mechanical transport equation in the perturbation-theory limit and apply it to the extended-pulse photon echo. It is found that the decay rate of the echo signal due to velocity-changing collisions is significantly modified by the variation of the second pulse's duration. The results are compared with those of conventional theories of two- and three-pulse echoes using temporally narrow excitation pulses. A physical interpretation of the results is given using both time- and frequency-domain arguments.
We have developed a general technique for obtaining analytical expressions for coherent transient signals arising from atoms interacting with two or more laser pulses having Gaussian spatial profiles. After deriving the Maxwell-Bloch equations for short laser pulses incident on an ensemble of three-level atoms, we specialize to photon echo spectroscopy. As an example, the stimulated photon echo signal is calculated as a function of the time delay between pulses. Our exact results are compared with both the lowest-order perturbative limit and a calculation in which transit time is treated phenomenologically. We conclude by commenting on the extension of our technique to atoms undergoing velocity-changing collisions. \textcopyright{} 1996 The American Physical Society.
It has been shown recently that molecular gas samples excited with coherent light can display a variety of transient phenomena, similar to those found in nuclear magnetic resonance. This article elucidates how these coherence effects can be used to isolate or unfold molecular collision mechanisms that normally remain hidden within the optical line shape. Elastic collisions, for example, are easily detected here in two-pulse photon echo experiments for a
13CH3F vibration-rotation transition. The echo-decay function which provides a signature for the velocity-changing collision diffusion mechanism, is not just a simple exponential in time but exhibits an $\mathrm{exp}(\ensuremath{-}K{t}^{3})$ contribution for short times and an $\mathrm{exp}(\ensuremath{-}\ensuremath{\Gamma}t)$ decay for long times. This behavior, which is unknown heretofore, contrasts with spin echoes in molecular liquids where Brownian motion leads only to the cubic decay law. An $\mathrm{exp}(\ensuremath{-}K{t}^{3})$ behavior can be understood in terms of a solution of the Fokker-Planck equation which describes the effect of Brownian motion on echo decay. Such a treatment is valid for small phase excursions; in the case of a gas, this implies the Doppler phase factor $k\ensuremath{\Delta}u\ensuremath{\tau}\ensuremath{\ll}1$, where $\stackrel{\ensuremath{\rightarrow}}{\mathrm{k}}$ is the propagation vector of light, $\ensuremath{\Delta}u$ is a characteristic velocity jump for a binary collision, and $\ensuremath{\tau}$ is the echo-pulse delay time. When $k\ensuremath{\Delta}u\ensuremath{\tau}\ensuremath{\gg}1$ as in the long-time regime, the Fokker-Planck solution fails. We, therefore, present a new solution to the Boltzmann transport equation using a weak collision model and find agreement with the entire echo time dependence observed. The echo measurements indicate very small changes in longitudinal velocity per
13CH3F-
13CH3F collision, i.e., $\ensuremath{\Delta}u=85$ cm/sec, thereby justifying the weak-collision model. The total elastic collision cross section is 430
A˚2. It follows that elastic collisions lead to velocity thermalization in a time of \ensuremath{\sim}5 sec when the
13CH3F pressure is 1 mTorr. A comparison is also made of the
13CH3F dephasing time ${\ensuremath{\tau}}_{2}$ in a coherent Raman beat decay, which is independent of velocity-changing collisions, with the longitudinal decay time
T1. Here,
T1 represents the molecule-optical interaction time, due largely to jumps in molecular rotation (
J) and orientation (
M) state, and is obtained from a delayed nutation measurement. The fact that the pressure dependent part of ${\ensuremath{\tau}}_{2}={T}_{1}$ shows that
T1 is also independent of velocity diffusion. Futhermore, when a hole is burned in the Doppler distribution, population recovery must be due to inelastic rather than elastic collisions. Optical Carr-Purcell echoes, multiple pulse echoes, provide a direct measure of the
13CH3F transverse dephasing time
T2 without the effect of elastic collisions while being sensitive to "phase interrupting collisions." Again, we find that
T2=T1 so that phase interruptions are negligible. Had such a process dominated the two-pulse echo, an $\mathrm{exp}(\ensuremath{-}\frac{t}{{T}_{2}})$ damping would have been noticed with no $\mathrm{exp}(\ensuremath{-}K{t}^{3})$ contribution. Thus, the present study covers several new aspects of molecular collisions. It represents the first detailed examination of velocity-changing collisions by coherence methods and without the complication of Doppler broadening.
One of the long-standing difficulties in working with intense incoherent light has been the lack of a theory for predicting and explaining experimental results. The diagrammatic theory of Friedberg and Hartmann provides a solution to this problem by allowing one to study the interaction of intense incoherent light and matter with no restrictions on the intensity of the pulses. In the present investigation, two-pulse photon-echo experiments were performed with intense incoherent light in atomic sodium vapor and the results were compared with predictions calculated from the Friedberg-Hartmann diagrammatic theory. The dependence of the echo signal on the intensity of the constituent excitation pulses was studied. The results of this investigation indicate that the two-pulse incoherent photon-echo experimental data are consistent with the calculations obtained from the theory presented in the diagrammatic paper of Friedberg and Hartmann when the atomic relaxation times are included. The two-pulse-echo data show good agreement with the theoretical predictions for the case in which 4T2 = T1 (the atomic and transverse lifetimes, respectively), which represents more of a decay than has been theoretically predicted for the experimental parameters used.
The effect of translational velocity of active atoms and molecules on the properties of photon echo is investigated using the technique of coherent transient processes. A variation in the photon-echo decay with a frequency detuning of the excitation radiation relative to the center of the vibrational-rotational transition 0 ↔ 1 ν3 R(4, 3) is observed in a mixture of 13CH3F with atomic buffers. The results are interpreted using the dependence of the echo decay rate on the magnitude of the translational velocity of active particles. The dependence of the relaxation matrix on the direction of the velocity of active atoms results in a new phenomenon of the collision-induced echo, which is investigated at the transition 0 ↔ 1 174Yb in mixtures with atomic buffers.
Abstract : Work is summarized in areas of: Laser Assisted Collisions; Velocity Changing collisions in Atomic Vapors; Coherent Transients; Collision Induced Extra Resonances; Breakdown of the Optical Bloch Equations; Saturation Spectroscopy; Dynamics of Two-and Three-level Atoms Interacting with Radiation Fields; Pulse Propagation. Keywords: Laser spectroscopy, Optical collisions, Radiative collisions, Two-level atom, Atomic coherence, Degenerate four-wave mixing, Saturation spectroscopy, Laser propagation,, Dressed atom, Photon echo, Bloch equations, Collision kernal, Collisions, Optical noise.