Differential Raman scattering from impurity soft modes in mixed crystals of K1−xNaxTaO3 and K1−xLixTaO3

Impurity modes are observed in crystals of KTaO₃ doped with Na and Li, using differential Raman spectroscopy. One of the modes is shown to soften as the temperature approaches the ferroelectric transition temperature. Analysis of the results shows that the Na and Li ions do not occupy center of inversion positions. The roll of this observation in the inducement of ferroelectricity in these crystals is briefly discussed.     

Conditions for the existence of double resonance effects in Raman scattering

The condition for the existence of Double Resonance effects in Raman scattering are analyzed. It is shown that the existence of points in the electronic momentum space for which both denominators in the expression for Raman scattering vanish is not sufficient. Based on this analysis, it is shown that double resonance effects cannot show up in Resonant Raman scattering in the vicinity of the E₁ point in InSb.     

Preferential Solvation in Mixed Solvents X. Completely Miscible Aqueous Co-Solvent Binary Mixtures at 298.15 K

Summary.  The Kirkwood-Buff integrals for 18 completely miscible aqueous co-solvent binary mixtures have been recalculated from thermodynamic data, and the volume-corrected preferential solvation parameters derived from them are presented. Also presented are these latter quantities for 15 additional such mixtures, for which the volume correction has not been applied previously. The self-interaction of the water, the mutual interaction of the water and the co-solvent, and the self-interaction of the co-solvent at infinite dilution derived from these integrals and parameters are then discussed. The systems studied include aqueous hydrogen peroxide, methanol, ethanol, 1- and 2-propanol, 2-methyl-2-propanol, 2,2,2-trifluoroethanol, 1,1,1,3,3,3-hexafluoro-2-propanol, ethane-1,2-diol, glycerol, 2-methoxyethanol (at 313 and 343 K), 2-ethoxyethanol, 2-butoxyethanol, 2-aminoethanol, N-methyl- and N,N-dimethyl-2-aminoethanol, tetrahydrofuran, 1,4-dioxane, acetone, formic, acetic, and propanoic acids, piperidine, pyridine, acetonitrile, formamide, N-methyl- and N,N-dimethylformamide, N-methylacetamide, N-methylpyrrolidin-2-one (at 303 K), hexamethyl phosphoric triamide, dimethylsulfoxide, and tetramethylenesulfone (at 303 K). Received January 10, 2001. Accepted (revised) February 20, 2001     

Use of differential impurity induced spectra for the investigation of phonon dispersion relations

The use of differential impurity induced spectra for the investigation of elementary excitations in solids is discussed. It is shown theoretically that the differential spectra are expected to have peaks at energies corresponding to energies of the excitation at critical points of the pure crystal independent of the nature of the impurity used. As an example we present experimental results of the derivative of the intensity of Raman scattered light with respect to wavelength from Tl doped KBr crystals.     

Preparing, manipulating, and measuring quantum states on a chip

We use gate voltage control of the exchange interaction to prepare, manipulate, and measure two-electron spin states in a GaAs double quantum dot. By placing two electrons in a single dot at low temperatures we prepare the system in a spin singlet state. The spin singlet is spatially separated by transferring an electron to an adjacent dot. The spatially separated spin singlet state dephases in due to the contact hyperfine interaction with the GaAs host nuclei. To combat the hyperfine dephasing, we develop quantum control techniques based on fast electrical control of the exchange interaction. We demonstrate coherent spin-state rotations in a singlet–triplet qubit and harness the coherent rotations to implement a singlet–triplet spin echo refocusing pulse sequence. The singlet–triplet spin echo extends the spin coherence time to .     

On the preferential solvation of drugs and PAHs in binary solvent mixtures

The preferential solvation parameters, i.e., the differences between the local and bulk mole fractions of the solvents in solutions of certain drugs and polycyclic aromatic hydrocarbons (PAHs) are derived from their solubilities in binary solvent mixtures by means of the inverse Kirkwood-Buff integral (IKBI) and the quasi-lattice quasi-chemical (QLQC) methods. The solutes include caffeine, niflumic acid, diazepam, benzocaine, phenacetin, paracetamol, nalidixic acid, anthracene, and tr-stilbene and both aqueous and non-aqueous mixtures are considered. The findings are rationalized in terms of the interactions between the solute and solvents and the solvent components among themselves.