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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 6927-6939 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We studied the optical transient bleaching of ∼40 A(ring), ammonia-passivated CdS clusters in a polymer with nanosecond and picosecond pump-probe techniques. The transient bleaching spectra behave differently in different time regimes. Within the 30-ps pump laser pulse width, we tentatively attribute the bleaching to the exciton-exciton interaction, and the magnitude can be enhanced by surface passivation. On time scales of tens of picoseconds and longer following the pump pulse, when only trapped electron-hole pairs remain from the pump excitation, the bleaching is due to the interaction between such a trapped electron-hole pair and a bound exciton produced by the probe light. Experimentally we determined that roughly one trapped electron-hole pair can bleach the excitonic absorption of the whole CdS cluster. We developed a theoretical model which considers the effects of the trapped electron-hole pair on the energy of the exciton transition and its oscillator strength. We found that, when a trapped electron and hole are present, the lowest exciton absorption is red-shifted from the original exciton absorption, and this transition has a weak oscillator strength, which explains the observed efficient bleaching. The model also predicts that a trapped electron is more efficient than a trapped hole for bleaching the excitonic absorption of CdS clusters in the size regime considered here. This is confirmed by pulse radiolysis results. Finally, we discuss the possible effects of charged surface defects on the linear absorption spectra of semiconductor clusters.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 3435-3441 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We report a picosecond pump–probe study of 55 A(ring) cadmium sulfide microcrystallites embedded in polymer films. Large negative absorbance changes at wavelengths corresponding to energies near the band gap are observed. This absorption bleaching and the associated changes in refractive index are mainly responsible for the large nonlinearity observed in degenerate four-wave mixing experiments. Based on photoluminescence data, the known electron-trapping cross section of defects, and these pump–probe experiments, we show that the conventional carrier density-dependent band-filling mechanism cannot account for the data, and the absorption bleaching is due to the saturation of the excitonic transition. We further show that the phase-space filling and exchange effects from exciton–exciton and exciton-free carrier interactions fail to account for the observed data. Instead, we propose that the exciton-trapped carrier interaction is mainly responsible for the observed bleaching of the excitonic absorption. This interaction is unique for small semiconductor clusters since the presence of a high density of defects (most likely on the surfaces) causes the extremely rapid trapping of free carriers. According to this model, the recovery time of the absorption bleaching is determined by the trapped-carrier relaxation time, which is sensitive to the fabrication methods and can be controlled by surface chemistry. Our study also demonstrates that one needs to understand the effects of surfaces and control the surface chemistry before the important question of size effects on the nonlinear optical properties can be addressed.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 66 (1989), S. 3417-3419 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: We report the first study, to the best of our knowledge, of the nonresonant third-order optical nonlinearity of quantum-confined CdS clusters using third harmonic generation from 1.91 to 0.64 μm. We observe that the nonlinearity increases with the increase in the cluster size. The intrinsic, nonresonant χ(3)CdS for ∼30, ∼15 A(ring) thiophenolate-capped CdS clusters and [Cd10S4(SPh)16]−4 molecular clusters are 3.3×10−10, 2.5×10−11, 4.7×10−12 esu, respectively. To utilize this large nonresonant nonlinearity it is necessary to incorporate these clusters into a sample in high concentrations.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 61 (1992), S. 124-126 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Using variable-angle ellipsometry and normal incidence reflection/transmission optical techniques we have measured the dielectric function ε(ω) at room temperature for solid C70 films over the photon energy range 0.5≤E≤5.3 eV. The onset of absorption across the highest-occupied-molecular-orbit (HOMO)–lowest-unoccupied-molecular-orbit (LUMO) gap is measured to be 1.25 eV. Furthermore, structure in the interband absorption at 2.41, 3.10, 3.50, and 4.45 eV is observed. The refractive index at zero frequency is estimated to be n(0)=1.94 as compared to the value n(0)=1.90, which we obtained for solid C60 from our previous study.
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  • 5
    Publication Date: 2015-06-06
    Description: The Cu-doping effect on the lattice and magnetic properties in Mn 3 Ni 1−x Cu x N (x = 0, 0.3, 0.5, 0.7, 1.0) was extensively investigated. We observed that the Cu-doping at the Ni site complicated the magnetic ground states, which induced the competition of antiferromagnetic and ferromagnetic interactions. Spin-glass-like behavior, arising from possible site-randomness and competing interactions of magnetism, was observed in compounds with x = 0.3, 0.5, and 0.7, and typically discussed by means of the measurement of ac magnetic susceptibility for x = 0.7. The negative thermal expansion (NTE) behavior, due to the magnetic ordering transition, was observed in Mn 3 Ni 1−x Cu x N compounds using variable temperature x-ray diffraction. It reveals that the introduction of Cu effectively broadens the temperature range displaying negative thermal expansion. The relationship between the local lattice distortion and the competing magnetic ground states might play an important role in broadening the NTE temperature range in this antiperovskite compound.
    Print ISSN: 0021-8979
    Electronic ISSN: 1089-7550
    Topics: Physics
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  • 6
    Publication Date: 2015-06-27
    Description: Oxyfluogermanate glasses with good thermal stability were prepared by melt-quenching method. The investigation of 2.7  μ m fluorescence spectra and energy transfer mechanism was performed pumped by an 808 nm laser diode. The 2.7  μ m radiative transition probability and emission cross section are 32.62 s −1 and 12.88 × 10 −21 cm 2 , respectively. The energy transfer parameters between 4 I 11/2 and 4 I 13/2 levels were calculated by Inokuti-Hirayama and Yokota-Tanimoto's model to further elucidate 2.7  μ m fluorescent behaviors. It is found that the energy transfer mechanism among Er 3+ is mainly dominated by dipole-dipole interactions. Results indicate that the prepared oxyfluogermanate glass is a promising candidate for mid-infrared laser applications.
    Print ISSN: 0021-8979
    Electronic ISSN: 1089-7550
    Topics: Physics
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  • 7
    Publication Date: 2015-12-19
    Description: The forced translocation of homopolymers through αβα sandwich-like compound channels was investigated by Monte Carlo simulation. The interaction between polymer and part α is strongly attractive, whereas that between polymer and part β is purely repulsive. Simulation results show that the translocation is influenced obviously by the length of part β ( L β ) and the starting position of part β ( L α1 ). For small L β , the translocation is mainly governed by the escaping process, and polymer is trapped near the exit of the channel. However, the translocation time can be tuned by varying L α1 and the fastest translocation can be achieved at relatively large L α1 . Whereas for large L β and small L α1 , the translocation is mainly controlled by the filling process. It is difficult for polymer to enter the channel, and polymer is trapped at the first αβ interface. Finally, the dynamics for the filling process and the escaping process are discussed from the view of free-energy landscape, respectively.
    Electronic ISSN: 1931-9223
    Topics: Chemistry and Pharmacology , Physics
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  • 8
    Publication Date: 2015-04-24
    Description: The effect of Ga ion irradiation intensity on the surface of multilayer graphene was examined. Using Raman spectroscopy, we determined that the irradiation caused defects in the crystal structure of graphene. The density of defects increased with the increase in dwell times. Furthermore, the strain induced by the irradiation changed the crystallite size and the distance between defects. These defects had the effect of doping the multilayer graphene and increasing its work function. The increase in work function was determined using contact potential difference measurements. The surface morphology of the multilayer graphene changed following irradiation as determined by atomic force microscopy. Additionally, the adhesion between the atomic force microscopy tip and sample increased further indicating that the irradiation had caused surface modification, important for devices that incorporate graphene.
    Print ISSN: 0021-8979
    Electronic ISSN: 1089-7550
    Topics: Physics
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  • 9
    Publication Date: 2015-12-19
    Description: The forced translocation of homopolymers through αβα sandwich-like compound channels was investigated by Monte Carlo simulation. The interaction between polymer and part α is strongly attractive, whereas that between polymer and part β is purely repulsive. Simulation results show that the translocation is influenced obviously by the length of part β ( L β ) and the starting position of part β ( L α1 ). For small L β , the translocation is mainly governed by the escaping process, and polymer is trapped near the exit of the channel. However, the translocation time can be tuned by varying L α1 and the fastest translocation can be achieved at relatively large L α1 . Whereas for large L β and small L α1 , the translocation is mainly controlled by the filling process. It is difficult for polymer to enter the channel, and polymer is trapped at the first αβ interface. Finally, the dynamics for the filling process and the escaping process are discussed from the view of free-energy landscape, respectively.
    Print ISSN: 0021-9606
    Electronic ISSN: 1089-7690
    Topics: Chemistry and Pharmacology , Physics
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  • 10
    Publication Date: 2014-10-07
    Description: We report the demonstration of an InGaAs/GaAs quantum well (QW) broadband stimulated emission laser with a structure that integrated a GaAs tunnel junction with two QW active regions. The laser exhibits ultrabroad lasing spectral coverage of ∼51 nm at a center wavelength of 1060 nm with a total emission power of 790 mW, corresponding to a high average spectral power density of 15.5 mW/nm, under pulsed current conditions. Compared to traditional lasers, this laser with an asymmetric separate-confinement heterostructure shows broader lasing bandwidth and higher spectral power density.
    Print ISSN: 0003-6951
    Electronic ISSN: 1077-3118
    Topics: Physics
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