Spectral hole-burning studies of nile red and cresyl violet in polyvinylbutyral and polyvinylformal films have been performed. From the shape of spectral holes under the influence of an electric field, the dipole moment difference between the ground and excited state of both dyes has been determined. The Stark effect was investigated at different positions in the inhomogeneously broadened absorption band of the guest molecules. The observed dipole moment difference decreases with increasing wavelength. This variation is caused by the matrix induced dipole moment. For nile red, which is a neutral and polar molecule, the distribution of induced dipole moments is strongly correlated with the orientation of its ground state dipole moment. In the case of cresyl violet perchlorate, which is a salt, this distribution is anisotropic for guests absorbing in the blue part of the inhomogeneous band but becomes more isotropic as the absorption wavelength increases. The wavelength dependence of the observed dipole moment is much stronger and is ascribed to the existence of the cresyl violet perchlorate salt in different states of solvation.

Holographic detection of spectral holes is demonstrated in a crystalline host material with signal-to-noise ratios of up to 104. Hole burning occurs in two Pr3+ sites in the Y2SiO5 lattice, in both cases due to population redistribution between the ground-state quadrupole levels. The signal contains contributions due to a resonant hole and several side holes and antiholes, a phenomenon not previously observed using the holographic technique. The diffracted spectrum is modeled in two ways. In the first case the transmission spectrum is used to determine the population gratings and thus the diffraction efficiency. In the second case the transition probabilities between ground- and excited-state Kramer's doublets are used to model the population gratings. The technique is applied to pseudo-Stark-effect measurements from which the crystallographic sites as determined by x-ray analysis are matched to the spectroscopic data presented here. The time decay of the diffracted signal is used to study nuclear spin-lattice relaxation. It is shown that at 1.6 K temperature-dependent phonon-induced processes make no contribution to this decay. The nonexponential time decay of the population upon radio-frequency irradiation resonant with a ground-state quadrupole splitting is attributed to Pr-Pr cross relaxation

The constructive interference between two Stark-effect-broadened holograms produced by spectral hole burning is discussed. The holograms are burned at the same frequency but at different external electric-field values. The phase difference is selected to be zero so that constructive interference between the waves diffracted by each grating occurs. Experimentally it is found that a dip in the hologram efficiency that is not predicted by previous theory occurs for all reconstruction external electric-field values in the region between the original burn values. This dip is interpreted as being due to the time nonlinearity of the hologram burn process. The dip corresponds to those molecules, oriented in a specific direction with respect to the electric field, for which no Stark shift occurs and that are therefore resonant with the laser during the production of both holograms. The width of the anomalous feature is close to that of the hologram when the hologram is reconstructed at the original burn external electric-field strength. Other molecular orientations may be selected by burning pairs of holographic gratings at other combinations of the frequency and the electric field.