In homogenous broadened dielectric a transient polarization of induction(TPI)is created by ultra-short laser pulse.The frequency of the TPI is the same as that of the pump field and the delay of phase is π/2 at maximum the magnitude of amplitude of the TPI is in circumstance associate with the original state of the dielectric and the decay is exponential with time and associated with dephasing of the quantum coherent carrier.
In homogenous broadened dielectric a transient polarization of induction(TPI)is created by ultra-short laser pulse.The frequency of the TPI is the same as that of the pump field and the delay of phase is π/2 at maximum the magnitude of amplitude of the TPI is in circumstance associate with the original state of the dielectric and the decay is exponential with time and associated with dephasing of the quantum coherent carrier.
A method of making the dephasing time T2u measurement in an ensemble of inhomogeneously broadened two-level systems is proposed. This method has its origin in the spin-locking technique developed in NMR. It is shown that in spite of inhomogeneous broadening it is possible to lock the induced polarization in phase with the driving field. The amplitude of the locked polarization can be as large as half of the first maximum of the nutation signal, i.e., of the polarization bump just after the pulse switch on. Decay of the locked polarization is caused by the T2u dephasing or by the dephasing of the in-phase component of polarization.
When an intense and short laser pulse or a fast-switching-on/off laser field interacts with a resonant absorbing medium, several optical coherent transient effects can be observed, including the self-induced transparency effect, photon echo effect, optical nutation effect, and the optical free induction decay effect. The study of these effects enables us to gain a deeper understanding of the coherent transient interaction of an intense pulsed or rapidly switched optical field with the resonant medium, and to measure the magnitude of the dipole-moment matrix elements, relaxation parameters, and spectral broadening mechanisms of the investigated materials. On the other hand, these optical coherent transient effects can also be applied for developing special techniques of optical pulse delay, pulse reshaping, and optical pulse manipulation.
The effect that may be exerted by an interatomic near dipole-dipole interaction upon optical transient processes in dense resonance media is analyzed. The behavior of the macroscopic polarization after a one-pulse excitation of a dense ensemble of two-level atoms is considered. It is shown that the free polarization signal is of oscillatory nature, with the oscillation frequency varying in time and being dependent on the dipole-dipole interaction constant, the intensity and duration of the exciting pulse, and the detuning of its carrier frequency from the resonance. The free polarization signal decay, which depends on the magnitude and sign of the sum of the detuning of the exciting pulse carrier frequency from the resonance and the Lorentz frequency, may obey either a power or an exponential law. The signal decay rate is determined not only by the inhomogeneous broadening, but also by the ratio of the above parameters. The peculiarities of echo-responses under one- or two-pulse excitation conditions are studied.
Within the framework of light-semiconductor interaction and the Lutting-Kohn model for the semiconductor band structure, we theoretically studied the mechanism of the polarization switch with coherent transient features. The result shows, in the coherent limitation, when the pump pulse Ep and signal pulse Es are orthogonal polarized, the third order polarization P(3), with first order of Es and second order of |Ep|, approach to zero, due to the destructive quantum interference, which results in an ultrafast pump-signal relative polarization dependent P(3), therewith a polarization switch. The study also shows that, when the light interacts with semiconductors coherently, the polarization state of the light is transferred to the relative phase of the electron spin, rather than the electron spin itself. The population of the polarization eigenstate excited by the pump pulse, do not origin from the Coulomb force of electrons, and should not thought phenomenologically as the exciton characterized by light polarization. This population will dephase to real carriers population, i.e. electron with exact spin |↑> or |↓>, by losing phase coefficients of the polarization eigenstates, in an ultrashort quantum dephase time.
A novel form of laser frequency switching is devised which extends coherent optical transient studies to a 100-psec time scale. The technique incorporates a traveling-wave electro-optic element which imposes with unit efficiency a uniform time-varying phase and thus a frequency shift on a cw laser beam. In contrast to earlier optical traveling-wave modulators which are driven by a microwave oscillator, here the optical phase change is induced rapidly and easily by a dc electric field pulse that propagates in a microwave guide either parallel or antiparallel to the light wave. This advance enables optical free-induction decay (FID) studies on a subnanosecond time scale and reveals such new features as a rapid first-order FID that dephases with the inhomogeneous dephasing time T2∗. The well-known nonlinear FID can interfere with the first-order component at short times and decays over the much longer period $\frac{{T}_{2}}{[1+{(1+{\ensuremath{\chi}}^{2}{T}_{1}{T}_{2})}^{\frac{1}{2}}]}$, where $\ensuremath{\chi}$ is the Rabi frequency. A complete analytical expression is derived for optical FID of a transition subject to homogeneous and inhomogeneous broadening and supports detailed observations of the sodium D1 line.
The effect that may be exerted by an interatomic dipole-dipole interaction upon optical transient processes in dense resonance media, in particular, free polarization decay, is analyzed. The behavior of the macroscopic polarization after a single-pulse excitation of a dense ensemble of two-level atoms is considered. It is shown that the free polarization signal is of oscillatory nature, with the oscillation frequency varying in time and being dependent on the dipole-dipole interaction constant, the intensity and duration of the exciting pulse, and the detuning of its carrier frequency from the resonance. The free polarization signal decay, which depends on the magnitude and sign of the sum of the detuning of the exciting pulse carrier frequency from the resonance and the Lorentz frequency, may obey either a power or an exponential law. The signal decay rate is determined not only by the inhomogeneous broadening, but also by the ratio of the above parameters.