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Efrat Lifshitz

Publications and source records attributed to Efrat Lifshitz.

8 recordsLinked to original sources

Spray-produced coral-shaped assemblies of MnS nanocrystal clusters.

A novel spray-based technique enables the production of high-quality, free, uncoated semiconductor nanocrystals. Their collection, following spray droplet desolvation during flight, could result in unusual structures. We report on spray-produced ordered clusters (approximately 50 nm diameter) of MnS nanocrystals with grain size range of 1-2 nm and their assembly into micron-sized coral-shaped fractal aggregates. Ballistic cluster-particle aggregation, with the introduction of physical interaction between particles, is suggested as a model for the assemblies' growth.

Journal Article↗

Nanocrystals of PbSe core, PbSe/PbS, and PbSe/PbSxS(1-x) core/shell as saturable absorbers in passively Q-switched near-infrared lasers.

The saturable optical absorption properties of PbSe core nanocrystals (NCs), and their corresponding PbSe/PbScore/shell and PbSe/PbSexS(1-x) core/alloyed-shell NCs, were examined at lambda = 1.54 microm. Saturation intensities of approximately 100 MW/cm2 were obtained. The NCs act as passive Q switches in near-infrared pulsed lasers. Q-switched output pulse energies up to 3 mJ, with a pulse duration of 40-55 ns were demonstrated. Analysis of the optical transmission versus pulse light intensity was carried out according to a model that includes ground-state as well as excited-state absorption. For pulses approximately 10 ns long, the NCs act as fast saturable absorbers. The theoretical fits yield a ground-state absorption cross section of 10-16-10-15 cm2, an excited-state absorption cross section of sigma(es) is congruent to 10(-16) cm2, and an effective lifetime of tau(eff) is congruent to 5 x 10(-12) s.

Journal Article↗

Electrostatic and covalent interactions in CdTe nanocrystalline assemblies.

This paper focuses on the interactions between cysteamine-stabilized CdTe nanocrystals [CdTe(CA) NCs] and thioglycolic-acid-stabilized CdTe nanocrystals [CdTe(TGA) NCs]. These interactions were examined by the absorption, continuous, and time-resolved photoluminescence (PL) spectra of the electrostatically mixed and the covalently linked NCs assemblies comprised of the oppositely surface charged CdTe(CA) and CdTe(TGA) NCs and by a comparison with those of the corresponding pristine NCs. The CdTe(CA)-CdTe(TGA) coupling is dictated by the surfactant spacer, ranging between 0.93 and 1.14 nm and by electrostatic and covalent interactions, enabling a Förster resonance energy transfer (FRET) process among the NCs. The results revealed an excellent spectral overlap between the emission of the CdTe(TGA) NCs and the absorption of the CdTe(CA) NCs as well as a PL spectral red shift on the formation of electrostatic and covalent interactions. Furthermore, the measurements showed a lifetime ranging between 1.2 and 3 ns for the electrostatically mixed and the covalently linked assemblies, shorter than those of the pristine CdTe(CA) NCs and CdTe(TGA) NCs, both of which measured as approximately 5.5 ns. When CdTe(TGA) NCs performed as the most efficient donors, FRET rates of 10(10)-10(11) s(-1) were calculated for the electrostatically mixed NCs or covalently linked NCs.

Cadmium↗

Spectroscopy and photophysics of self-organized zinc porphyrin nanolayers. 3. Fluorescence detected magnetic resonance of triplet States.

Fluorescence detected magnetic resonance (FDMR) has been applied to approximately 25-nm-thick porphyrin films, containing ordered domains of zinc tetra-(p-octylphenyl)-porphyrin (ZnTOPP) spin-coated onto quartz slides. Illuminating the films at 1.4 K with 457.9-nm light from a continuous wave Ar(+) laser produces at least two different, Jahn-Teller-distorted, ZnTOPP triplet species, labeled i and ii. Microwave-induced magnetic resonance of i and ii in the absence or presence of an externally applied magnetic field affects the fluorescence intensity of ZnTOPP, thus allowing FDMR. For triplet species i, formed in films spin-coated from toluene solution, the zero-field splitting (ZFS) parameters were determined as |D| = (316.9 +/- 0.1) x 10(-4) cm(-1) and |E| = (32.0 +/- 0.5) x 10(-4) cm(-1). By exposure of the spin-coated films to chloroform vapor at room temperature, triplet i is converted into species ii, with |D| = (295 +/- 3) x 10(-4) cm(-1) and |E| = (121 +/- 3) x 10(-4) cm(-1). For the excited triplet state of ZnTOPP in a toluene glass, ZFS parameters with values of |D| = (295 +/- 1) x 10(-4) cm(-1) and |E| = (91 +/- 1) x 10(-4) cm(-1) are found. From a combined study of the FDMR- and microwave-induced fluorescence spectra, i and ii are identified as unligated and ligated ZnTOPP triplet species, respectively. From the asymmetrically shaped zero-field FDMR signals of i, we conclude that the local crystal field perturbations of the stacked molecules are anisotropic. The FDMR results of the ZnTOPP films are compared with those for a film of zinc tetraphenylporphyrin (ZnTPP), which lacks the octyl substituents, and therefore is nonordered. Upon illumination, the ZnTPP films contain only a single, ligated, triplet species with ZFS parameters very similar to those of ligated ZnTOPP. At approximately 5 K, the lifetime of triplet i is considerably shortened compared to that of ZnTOPP in a glass at the same temperature.

Magnetics↗

A spray-based method for the production of semiconductor nanocrystals.

We present a spray based-method for the formation and production of semiconductor nanocrystals that provides an attractive alternative to the commonly used epitaxial and colloidal procedures. According to this spray-based method, mainly thermospray, solutions of semiconductor salts are first sprayed into monodispersed droplets, which subsequently become solid nanocrystals by solvent evaporation. A semiconductor nanocrystal is produced from a single spray droplet upon the full vaporization of the solvent. The average diameter and size distribution of the final nanocrystals are controlled and determined by the solute concentration of the sprayed solution and by the droplet size, hence by the spray production parameters. The spray-produced nanocrystals are collected on any selected solid support. Representative results, shown in this letter, reveal the formation of CdS nanocrystals in the size range of 3 to 6 nanometers and with a size distribution of as low as five percent. A further structural analysis of these nanocrystals showed that they were formed in the zinc blend phase with a high degree of crystallinity.

Letter↗

Magneto-optical studies of HgTe/HgxCd1-xTe(S) core-shell nanocrystals.

The synthesis and magneto-optical properties of HgTe nanocrystals capped with HgxCd1-xTe(S) alloyed shells have been investigated. The magneto-optical measurements included the use of optically detected magnetic resonance (ODMR) and circular polarized photoluminescence (CP-PL) spectroscopy. The PL spectra suggest the existence of luminescence events from both the core HgTe and the HgxCd1-xTe(S) shells. The continuous-wave (cw) and time-resolved ODMR measurements revealed that the luminescence at the shell regime is associated with a trap-to-band recombination emission. The electron trap is comprised of a Cd-Hg mixed site, confirming the existence of an alloyed HgxCd1-xTe(S) composition. The ODMR data and the CP-PL measurements together revealed the g-values of the trapped electron and the valence band hole.

Journal Article↗

Magneto-optical measurements of chromophore/semiconductor nanocrystalline superstructures.

The magneto-optical properties of chromophore/semiconductor nanocrystalline superstructures were examined using optically detected magnetic resonance (ODMR) and time-resolved photo-luminescence (PL) spectroscopy. The samples consisted of CdS or PbS nanocrystals separated by conjugated organic chains, forming three-dimensional superstructures. The ODMR measurements revealed that the magnetooptical properties of the superstructures are mainly controlled by the individual characteristic of the nanocrystals. The ODMR spectra were compared with simulated curves generated by the diagonalization of a spin Hamiltonian, indicating the existence of the following luminescence events. a) Recombination between electron-hole pairs trapped at a stoichiometric defect (metal or sulfur vacancies) or oxygen adatom sites at the surface of the nanocrystals. These electron-hole pairs showed anistropic g-factors and weak exchange interactions. b) Bound exciton emission, from strongly coupled electron-hole pairs trapped at intrinsic stoichiometric or structural defects at the core of the nanocrystals. The existence of the two overlapping luminescence events is further confirmed by the acceptance of biexponential PL decay processes.

Journal Article↗

Hybrid composites of monodisperse pi-conjugated rodlike organic compounds and semiconductor quantum particles.

Composite materials of quantum particles (Q-particles) arranged in layers within crystalline powders of pi-conjugated, rodlike dicarboxylic acids are reported. The synthesis of the composites, either as three-dimensional crystals or as thin films at the air-water interface, comprises a two-step process: 1) The preparation of the Cd salts 6 (Cd), 8 (Cd) or Pb salts 6 (Pb), 8 (Pb) of the oligo(p-phenyleneethynylene)dicarboxylic acids 6 (H), 8 (H), in which the metal ions are arranged in ribbons and are separated by the long axis of the organic molecules, as demonstrated by X-ray powder diffraction analysis of the solids and grazing incidence X-ray diffraction analysis of the films on water. 2) Topotactic solid/gas reaction of these salts with H(2)S to convert the metal ions into Q-particles of CdS or PbS embedded in the organic matrix that consists of the acids 6 (H) and 8 (H). These hybrid materials have been characterized by X-ray photoelectron spectroscopy and transmission electron microscopy.

Journal Article↗