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J Zyss

Publications and source records attributed to J Zyss.

11 recordsLinked to original sources

Air-stable PbSe/PbS and PbSe/PbSexS1-x core-shell nanocrystal quantum dots and their applications.

The optical properties and functionality of air-stable PbSe/PbS core-shell and PbSe/PbSexS1-x core-alloyed shell nanocrystal quantum dots (NQDs) are presented. These NQDs showed chemical robustness over months and years and band-gap tunability in the near infrared spectral regime, with a reliance on the NQD size and composition. Furthermore, these NQDs exhibit high emission quantum efficiencies of up to 65% and an exciton emission band that is narrower than that of the corresponding PbSe NQDs. In addition, the emission bands showed a peculiar energy shift with respect to the relevant absorption band, changing from a Stokes shift to an anti-Stokes shift, with an increase of the NQD diameter. The described core-shell structures and the corresponding PbSe core NQDs were used as passive Q-switches in eye-safe lasers of Er:glass, where they act as saturable absorbers. The absorber saturation investigations revealed a relatively large ground-state cross-section of absorption (sigma gs = 10(-16) - 10(-15) cm2) and a behavior of a "fast" absorber with an effective lifetime of tau eff approximately 4.0 ps is proposed. This lifetime is associated with the formation of multiple excitons at the measured pumping power. The product of sigma gs and tau eff enables sufficient Q-switching performance and tunability in the near infrared spectral regime. The amplified spontaneous emission properties of PbSe NQDs were examined under continuous illumination by a diode laser at room temperature, suitable for standard device conditions. The results revealed a relatively large gain parameter (g = 2.63 - 6.67 cm-1). The conductivity properties of PbSe NQD self-assembled solids, annealed at 200 degrees C, showed an Ohmic behavior at the measured voltages (up to 30 V), which is governed by a variable-range-hopping charge transport mechanism.

Air↗

Deciphering output coupling mechanisms in spiral microcavities with femtosecond light bullets.

A pump-probe two-photon-excited fluorescence technique deciphers in space and time the propagation of ballistic wave packets sustained by whispering-gallery modes (WGMs) in a spiral-shaped microcavity. Diffraction on the spiral discontinuity does not prevent the WGMs from closing. The resultant average Q of the resonator is 3 x 10(4) +/- 50%. Experimental results are compared with numerical simulations, providing evidence of a new contribution to output coupling: Part of the WGM evanescent wave is reflected at the spiral notch and leads to a propagating wave at an angle that matches the previously observed laser emission direction in 4-dicyanomethylene-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran-doped poly(methyl methacrylate) and InGaN spiral lasers.

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Direct evidence of open ray orbits in a square two-dimensional resonator of dye-doped polymers.

Lasing has been observed in optically pumped 4-dicyanomethylene-2-methyl-6-( p-dimethylaminostyrl)-4H-pyran-doped poly(methyl methacrylate) square-shaped micropillars that allow four-bounce closed and open ray orbits with internal incident angle theta(inc) > theta(c) (the critical angle for total internal reflection) and with the associated surface waves that emit at the four corners. We also detect strongly TE-polarized and spatially varying emission from the square sidewalls that is due to leaky open ray orbits with theta(inc) near but less than theta(c) for two of the four bounces. By selectively pumping the square microcavity with a stripe-shaped beam, we excite different four-bounce ray orbits.

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Spectral encoding of the polarization state of light in multiplexed polarization-sensitive lasing structures.

We report the experimental demonstration of spectral encoding of the polarization state of light by use of multiplexed distributed-feedback lasers in a dye-doped organic thin film by exploiting the pump polarization selectivity of the superimposed resonators. Measurement of the Stokes parameters of the pump light without a priori knowledge of the lasing properties of the structure is discussed.

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Local second-harmonic generation enhancement on gold nanostructures probed by two-photon microscopy.

The localization of surface second-harmonic generation (S-SHG) enhancements from granular gold structures that exhibit local plasmon resonance was investigated. A two-photon microscopy technique was used to perform high spatial resolution S-SHG imaging. The magnitude and the spatial density of S-SHG enhancement confined in submicroscopic regions are strongly dependent on the morphology of the gold's surface. Polarization measurements of local S-SHG responses reveal the local field anisotropy in enhancement regions and furthermore prove the incoherent and strongly depolarized nature of the emission, which is attributed to ultrafast fluctuations of the enhancement location in the focal volume.

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A hyperpolar, multichromophoric cyclodextrin derivative: synthesis, and linear and nonlinear optical properties.

A chiral, highly polar, multichromophoric supermolecule has been designed by gathering seven push-pull chromophores onto a beta-cyclodextrin assembling unit through covalent flexible linkers. The photophysical and nonlinear optical properties of this mutichromophoric conical bundle were investigated and compared with those of the monomeric chromophore. The strongly absorbing multichromophoric system combines interesting features: it has a high molecular first-order hyperpolarisability and a very large dipolar moment (u = 38 D) which reveal a self-arrangement of the dipolar chromophores within the supermolecule. The confinement of the push-pull chromophores within the nanoscopic bundle affects their optical properties and promotes interactions: the multichromophoric supermolecule is hypochromically and hypsochromically shifted with respect to its monomeric analogue. In addition, the close proximity promotes excitonic coupling, as well as excimer formation phenomena.

Circular Dichroism↗

Dipolar donor-acceptor-substituted schiff base complexes with large off-diagonal second-order nonlinear optical tensor components.

The synthesis, characterization, and two-dimensional second-order nonlinear optical (NLO) response of a dipolar NiII donor- acceptor Schiff base complex and the related ligand are reported. Electric-field-induced second-harmonic generation and harmonic light (hyper-Rayleigh) scattering techniques, in combination with INDO/SCI-SOS theoretical calculations, were used to investigate the vector part of the hyperpolarizability tensor and the two-dimensional character of the molecular nonlinearity, respectively. Off-diagonal hyperpolarizability tensors can be related to charge-transfer transitions that are polarized perpendicular to the molecular dipolar axis, while parallel transitions account for the diagonal hyperpolarizability tensor. The role of the metal center in enhancing the two-dimensional NLO response of such molecules is twofold since it acts both as the donor and the bridging moiety of the planar donor-(pi-conjugate-bridge)-acceptor system. These dipolar two-dimensional molecules are interesting candidates from the perspective of polarization-independent NLO materials.

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