It is shown that optical free-induction decay (OFID) in fractals is governed by a power-law time dependence. The scale invariance of the OFID in the time domain results from the self-similar distribution of the dipolar eigenmodes in fractals.
A novel form of laser frequency switching is devised that extends coherent optical transient studies to a 100-picosecond time scale, the measurements being performed in real time. Free-induction decay (FID) on a subnanosecond time scale reveals new features, such as a first-order FID that dephases with the inhomogeneous dephasing time T2* and interferes with the well-known nonlinear FID. A complete analytical expression for optical FID is derived and supports our FID observations for the sodium D1transition.
In this paper we examine the effect of radiative and radiationless processes on optical free induction decay (OFID) in singlet–singlet transitions of molecules in the condensed phase. The main conclusion is that the applicability of OFID to molecular singlet–singlet transitions is severely limited by the presence of an intermediate triplet state, which quite often forms a bottleneck in the optical pumping cycle. Using the theoretically derived formulas for the OFID signal, we examine the feasibility of OFID experiments on the mixed crystals of porphin in n-octane and naphthalene in durene and conclude that such experiments, if at all fruitful, would be difficult to execute. We re-evaluate the reported OFID results of pentacene in p-terphenyl and obtain for the lowest 1B2u←1A1g transition a dipole moment of 0.9±0.3 D.
The free-induction decay (FID) signals emitted by a two-level spin system (E1′ centers in glassy silica), coherently prepared by a short pulse of resonant radiation, have been experimentally investigated in the frequency domain. Our results show that, under the same conditions in which FID signals are oscillatory in the time domain, the spectra are characterized by a regular series of emission zeros. A vectorial model accounts for the occurrence of the zeros and for their spectral positions.
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.