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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 96 (1992), S. 10688-10693 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 80 (1996), S. 3162-3166 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: We investigated both time and temperature dependence of chromophore movements by means of in situ second-harmonic generation (SHG) measurements. Using real-time detection of the SHG intensities during and after poling of various nonlinear-optical polymer films we observed differences between main-chain and side-chain polymers regarding the nonlinear coefficients d33 and the glass transition dynamics. We present experimental data on new main-chain polymers with polar stilbene chromophores attached in the most common transverse position to the backbones (MC-T) or incorporated in a linear fashion where they are a part of the main-chain (MC-L). The side-chain polymer (SC) presented here has been developed for photorefractive applications and is a copolymer containing Disperse Red 1 and a photoconducting carbazole unit in the side chain. The influence of the macromolecular structure on the chromophore dynamics is striking. This is verified by means of in situ corona poling experiments and thermal experiments based on temperature ramps on poled polymers. MC-T and especially MC-L polymers show a better thermal stability of the chromophore orientation relative to the glass transition temperature than SC polymers; however, chromophores of main-chain polymers are, as can be expected, less mobile during the poling process. We obtained resonance enhanced nonlinear optical coefficients d33 of 100 pm/V in a SC polymer, 90 pm/V in a MC-T polymer, and 30 pm/V in a MC-L polymer. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 112 (2000), S. 7190-7194 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We report on a novel binary glass consisting of an electron donor and an electron acceptor molecule. It contains up to 25% of charge-transfer complexes and displays excellent hole as well as electron transport properties. Charge carrier mobilities have been measured by time-of-flight for various donor–acceptor ratios and are discussed within the framework of the disorder model of Bässler and co-workers. The results demonstrate that the presence of the donor molecules has no influence on the electron transport properties. In contrast to this, the hole transport is apparently affected by dipolar interactions between donor and acceptor molecules. Surprisingly the highest nondiagonal disorder for hole transport of about Σ=5 is found in samples with similar amounts of donor and acceptor indicating that the formation of charge-transfer complexes causes additional positional disorder. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 111 (1999), S. 10633-10639 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The holographic properties of the photorefractive polymer composite PSX:DMNPAA:TNF are determined as a function of the grating spacing by use of two-beam coupling and degenerate four-wave mixing measurements. The phase shift was quantified with the grating translation technique. In particular, an almost constant mean drift length of the charge carriers of about 0.5 μm was obtained. The resulting discrepancies between the standard theory of crystals, which is generally used as an approximation for amorphous organic materials, and the experimental data are discussed and attributed to the different mechanisms of charge transport in amorphous organic materials. To verify our conclusions we performed time-of-flight and degenerate four-wave mixing measurements on the two photorefractive organic glasses DRDCTA:DOP:C60 and DRDCTA:EHMPA:C60, which differ in the degree of dispersivity of charge carrier transport and, hence, the involved trap energy distributions. Comparing the behavior of the two materials under investigation, we obtained a qualitative relationship between dispersivity and a theoretically unexpected drop in the diffraction efficiency: The larger the dispersivity the earlier the drop in the efficiency. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 110 (1999), S. 4944-4951 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The maximum achievable diffraction efficiency of organic photorefractive materials is strongly influenced by the properties of the nonlinear optical chromophores. Here we report on a novel evaluation method of frequency dependent ellipsometric measurements. We fit our theory to the phase shift between the alternating electric field and the detected signal as a function of the applied frequency. The presented method is based on an improved theoretical description of electro-optic relaxation spectroscopy when compared to earlier publications. It allows for the determination of the birefringence contribution CBR to the refractive index change in materials with low glass transition temperature Tg. We apply our method to data obtained on highly efficient photorefractive guest–host systems based on polysiloxane. The nonlinear contributions were also determined and the results are briefly discussed. An error estimate for the value of CBR yields an accuracy of about ±10%. A comparison of electro-optic relaxation spectroscopy with photorefractive methods for determining the ratio CBR/CEO is presented. We conclude that this method allows for an estimate of the orientational enhancement with a relatively simple setup which is independent of the photorefractive experiment. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 105 (1996), S. 10648-10650 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The first photon echo experiments on polymethylmethacrylate (PMMA) down to temperatures below 1 K are reported. A linear temperature dependence of the linewidth of the chromophore zinc-meso-tetraphenylporphine (ZnTPP) is obtained below 1 K. Based on this result a flat distribution of two-level system energies E on the time scale of our experiment is deduced. Above 1 K an activated process with an energy of 5 cm−1 is found, which explains the power law dependence usually measured by photon echo experiments in the temperature region 1.2–2.1 K. The fit parameters of the proposed process are shown to be in agreement with hole burning measurements and with specific heat data on PMMA. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 87 (2000), S. 3872-3877 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The photocarrier generation and recombination mechanism in double layer cells of dye sensitized liquid crystalline hexahexylthiotriphenylene (HHTT) have been studied by steady-state photoconduction measurements. From the dependence of the photocurrent on light intensity we could determine the charge carrier generation mechanism in an azo pigment 4,4'-[(2,5-diphenyl1,3,4-oxadiazol)-bis(azo)]-bis[3-hydroxy-(2H-benzimidazo[2,1-a]benz[d,e]isoquinolin-7-one)] as surface enhanced whereas in titanylphthalocyanine charge generation takes place in the bulk of the dye. We investigated the actionspectra of a single HHTT cell and an azo sensitized cell in the different phases of HHTT to show the influence of azo on the spectral response of the photocurrent. The quantum efficiency in a single HHTT cell as well as in a double layer cell with azo as charge generation layer was determined. By solving the diffusion equation for excitons we carried out an estimation of the exciton diffusion length in azo. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 62 (1987), S. 4226-4230 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Persistent spectral holes in a thin film of poly(vinyl butyral) doped with a substituted Zn-tetrabenzoporphin show irreversible broadening effects when high electric field strengths (some hundred kV/cm) are applied. A small field (a few kV/cm) with opposite sign, however, cancels the broadening almost completely and restores the original hole width. Therefore, the broadening is not due to field-induced spectral diffusion, but to permanent electric fields generated in the sample. Our interpretation in terms of electret theory shows that the source of these fields is charges near the surface of the sample, which are injected from the electrodes.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 88 (1988), S. 679-686 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: In this paper we report an analysis of hole burning line shapes yielding both reversible and irreversible contributions to the linewidth which are due to spectral diffusion. These terms show a linear T dependence and can, through cycling experiments, be investigated in the temperature range of 0.5〈T〈25 K. The range 1〈T〈25 K is particularly interesting because, under normal conditions, Debye contributions and local mode contributions overwhelm the small spectral diffusion terms at these temperatures. Comparison between optical data and specific heat data supports our model of spectral diffusion.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 86 (1987), S. 5300-5307 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A simple analytical model is presented describing the shape of a persistent spectral hole in a homogeneous electric field for random orientation of the dye molecules in the host matrix. We consider the two cases that the absorbers have either one fixed value or a distribution of values of the electric dipole moment difference Δμ between the ground and excited electronic states. Comparison with experiment yields the Δμ values for chlorin (Δμ=0.214 D) and a substituted Zn-tetrabenzoporphin (∼(Δμ) =0.174 D) in poly(vinylbutyral). In the latter case the isolated dye molecule has inversion symmetry, yet there is nevertheless a dipole moment through the interaction with the polar matrix of low local symmetry.
    Type of Medium: Electronic Resource
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