Linear and nonlinear optical studies of CdS1−x Se x quantum dots

In this contribution we present and discuss our measurements on CdS_1?x Se _x quantum dots in a glass matrix. In linear absorption measurements we find the typical blue shift of the transitions with decreasing crystallite radius due to quantization. The luminescence shows a significant Stokes shift with respect to absorption, which is interpreted in terms of strong exciton-phonon coupling and allows to deduce the Huang-Rhys factor S. Under high excitation we find an additional emission band on the high energy side, which can be attributed to the recombination of an excited two electron-hole pair state to a one electron-hole pair state in agreement with theory. Pump and probe beam experiments give a bleaching but no hole burning. Finally we discuss some open questions especially concerning the high energy structures in the absorption spectrum.     

Polar,non-coordinating ionic liquids as solvents for the alternating copolymerization of styrene and CO catalyzed by cationic palladium catalysts

The palladium-catalyzed copolymerization of styrene and CO in an ionic liquid solvent, 1-hexylpyridinium bis(trifluoromethanesulfonyl)imide, gave improved yields and increased molecular weights compared to polymerizations run in methanol.     

Plasma induced optical nonlinearities and optical bistability in CdS

The transition from a low density gas of excitons to an electron-hole plasma is connected with strong variations of the optical properties. In this contribution we investigate both the optical nonlinearities produced in CdS by an intense laser beam in the spectral region close to the absorption edge and at the position of the laser itself. In a second part it is shown that the nonlinearities at the photon energy of the incident laser may lead to absorptive and dispersive optical bistability.     

Two-Photon Raman scattering and high excitation luminescence in ZnTe

Two-Photon-Raman Scattering (TPRS) and the luminescence of ZnTe are investigated when the samples are highly excited with a tunable narrow-band dye-laser. In luminescence, one observes emission bands due to the well-known inelastic exciton-exciton scattering at intermediate excitation intensities, and the recombination radiation of an electronhole plasma (EHP) at the highest excitation levels. For the first time, TPRS is reported in ZnTe. From the change in the TPRS lines in magnetic fields up to 10T we deduce a diamagnetic shift of 1.2°10^?2 meV/T² of the free longitudinal exciton. This value is in good agreement with results obtained by other authors from reflection spectroscopy.     

Excitation spectroscopy on the M-band of red HgI2

The luminescence of red HgI₂ is investigated as a function of excitation intensity and -wavelength. At low excitation, emission is due to free and bound exciton recombination, at high levels a “M-band” is dominating. This M-band is partially ascribed to biexciton decay, this assumption being supported by resonances found in the excitation spectra. The biexciton binding energy is determined to be 6±1 meV.     

The effect of external modulation of the incident intensity on the self-oscillations of an induced absorber (CdS) in a (hybrid-)ring-cavity

In contrast to a dispersive nonlinearity, induced absorption may without a cavity lead to intrinsic optical bistability. If however such an absorber is placed in a ring-cavity with a round trip time larger than the relaxation time constant of the medium, oscillatory instabilities have been (theoretically) predicted. We investigate CdS at room temperature (photo-thermal effects) in a hybrid ring-cavity. A Farey-tree structure of the oscillation period as a function of the incident intensity is observed. In the present paper we discuss the influence an external modulation of the incident intensity has on the oscillation modes both, experimentally and with simple model calculations. Again a Farey-tree structure of the average period of the oscillation modes in multiples of the modulation period is obtained both as a function of the modulation frequency and the modulation amplitude.     

Palladium-catalyzed hydroesterification of styrene derivatives in the presence of ionic liquids

The palladium-catalyzed hydroesterification of olefins occurs efficiently in a range of ionic liquid media. Selectivities ranging from 5-7:1 for the linear ester were obtained with styrene in a range of IL solvents. The use of ILs allowed the catalyst to be easily separated from the organic product by either extraction or distillation. The (Ph₃P)₂PdCl₂ precatalyst could be recovered unchanged from the ionic liquid phase. The IL/catalyst phase could be recycled five times with an average yield of 68%.     

Long-time luminescence kinetics of localized excitons and conduction band edge smearing in ZnSe(1−c)Tec solid solutions

It is shown that the integrated luminescence intensity of localized excitons in solid solutions ZnSe_(1?c)Te_c has a component slowly decaying with time. After the excitation above the mobility threshold, the long-time intensity decreases exponentially, with a fractional exponent changing from a value corresponding to the critical index of anomalous diffusion to the index of normal diffusion as the temperature increases from 5 to 80 K. This change allows estimation of the energy scale for the fluctuation tail of the conduction band.     

Optical and thermal orientation of localized excitons in solid solutions under resonant excitation in a longitudinal magnetic field

A theoretical and experimental study of the effect of a longitudinal magnetic field on optical orientation and magneto-circular polarization of the luminescence of localized excitons in semiconducting solid solutions is reported. It is shown that recombination takes place through two types of emitting states differing substantially in the degree of anisotropy, g factor, and spin relaxation time. Estimates are made of the g factors, anisotropic and exchange splittings, lifetime, and spin relaxation time of localized states in a CdS_0.96Se_0.04/GaAs solidsolution epitaxial layer. Fiz. Tverd. Tela (St. Petersburg) 40, 900–902 (May 1998)