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  • 1
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 69 (1991), S. 2568-2576 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: We have studied second-order nonlinear optical properties and dielectric relaxation characteristics for two amorphous epoxy polymers based on bisphenol-A with nitroaniline-type nonlinear optical moieties covalently attached as part of the main chain. The nonlinearities, rather large immediately after corona poling, undergo a slow decay at ambient temperature (e.g., ∼29% reduction in the nonlinear coefficient d33 in 28 days), even though the nominal glass transition temperature Tg is ∼80 °C. In dielectric relaxation measurements, both the unpoled and poled samples exhibit two relaxation modes: an α relaxation attributed to glass transition and a β relaxation due to local segmental motions of the main chain. Surprisingly, the critical temperature T∞ associated with the glass transition, obtained by a WLF [M. L. Williams, R. F. Landel, and J. P. Ferry, J. Am. Chem. Soc. 77, 3701 (1955)] fit of the α relaxation characteristics, shows a significant decrease (as much as 40 °C) with increasing poling field. Moreover, the relaxation times of temporal decay of field-induced alignment at ambient temperature, as determined from the stretched exponential function fit of birefringence changes, are found to be consistent with extrapolations from the the dielectric α relaxation characteristics of poled samples.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: A new linear epoxy polymer containing 4-amino-4'-nitrotolane chromophores attached to the chain backbone was synthesized in an attempt to enhance both the poling-induced nonlinear optical susceptibility and its long-term stability. The polymer films poled by corona discharge showed very large nonlinear optical doubling coefficients of d33 (approximately-equal-to) 89 pm/V and d31(approximately-equal-to)25 pm/V for incident light of 1.06 μm wavelength, and a linear electro-optic coefficient r13(approximately-equal-to)8 pm/V at 633 nm wavelength. Poling-induced alignment of the nonlinear optical moieties showed no detectable decay in two weeks at ambient temperature, as studied by the birefringence. Even at 100 °C the relaxation time estimated from the birefringence decay was ca. 450 h, consistent with roughly 16% decrease in dij coefficients in 20 h at this temperature and also the extrapolation from the dielectric α relaxation characteristics. The dielectric α relaxation temperatures of the poled polymer samples exhibited higher values than that of the unpoled counterpart. This unusual behavior may be due to a significant contribution of Maier–Saupe thermotropic interactions among the tolane moieties that favor parallel alignment.
    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 95 (1991), S. 4709-4714 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Stochastic dynamics simulations of n-alkane melts (C13H28 and C28H58 ) have been performed in order to calculate their static properties. The system consists of linear chains of mass points, which are connected by fixed bond lengths. Each point of a chain is subjected to valence bond and torsional forces. Additionally, nonbonded interactions are taken into account by a truncated, Lennard-Jones potential. The mean-square end-to-end distance and the radius of gyration of the chains as well as the average fraction of trans conformations were calculated and compared with the results obtained by Monte Carlo simulations and by unperturbed rotational isomeric states model calculations. The comparison exhibits very good agreement between the results of the different approaches, and demonstrates the potential advantages of stochastic dynamics simulations for polymeric systems. An investigation of different torsional potentials exhibited the subtle effect of the curvature of the torsional potential on bulk structures.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 56 (1990), S. 2610-2612 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Extending the novel method of Eich et al. [J. Appl. Phys. 66, 3241 (1989)] to prepare highly stable second-order nonlinear optical (NLO) polymers via chemical cross-linking under electric field, we have obtained a new polymer exhibiting large and stable second-order optical nonlinearities after relaxation at 80 °C. This was achieved by forming a network polymer from two NLO-active monomers, bifunctional N,N-(diglycidyl)-4-nitroaniline and trifunctional N-(2-aminophenyl)-4-nitroaniline. Here, every NLO moiety is connected to the network by a single covalent bond. After full cure under corona poling at 120 °C, the sample exhibited at ambient conditions d33(approximately-equal-to)50 pm/V and d31(approximately-equal-to)16 pm/V at 1064 nm fundamental wavelength, as estimated from the Maker fringe data. Upon heating to 80 °C, the nonlinearities decreased somewhat initially, but leveled off and remained stable at 80 °C. This stable sample gave d33(approximately-equal-to)42 pm/V and d31(approximately-equal-to)14 pm/V at ambient conditions. Furthermore, the linear electro-optical coefficient of this sample, measured with a Mach–Zehnder interferometer, was r13(approximately-equal-to)6.5 pm/V at 530.9 nm. From this r13 coefficient one estimates d31(approximately-equal-to)11 pm/V at 1064 nm, in good agreement with the Maker fringe value.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 65 (1989), S. 2766-2771 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The electrical and interfacial properties of gold-polyimide-silicon structures were studied experimentally by measuring the capacitance-voltage (C-V) characteristics. Two different polyimides of PMDA-ODA (synthesized from pyromellitic dianhydride and oxydianiline) and BTDA-ODA (from benzophenone tetracarboxylic dianhydride and oxydianiline), respectively, were employed. Polyimide coatings on n-type silicon (with a doping level N=5×1014 cm−3) were prepared by spin coating followed by thermal cure to range from 0.4 to 2.1 μm in thickness. The resulting high frequency C-V plots of these structures were well defined and could be described by the basic theory on metal-insulator-semiconductor (MIS) devices. Distinct differences in the C-V characteristics were observed, depending upon the polyimides. PMDA-ODA dielectrics resulted in C-V hysteresis, believed to be caused by charge injection. On the other hand, BTDA-ODA showed much smaller hysteresis, but some stretch-out in the C-V curve. These differences are attributed to the different interfacial properties of these polyimides in contact with silicon substrates.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 60 (1986), S. 318-326 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Electrical conduction phenomena in polyimide (Kapton) films were studied with particular attention devoted to the separation of interface and bulk phenomena. The measurements were carried out with a variety of methods in the temperature range of 50 to 270 °C at electrical fields of 104 to 6×105 V/cm and at time intervals of up to 2×104 s after voltage application. Biased, two-side metallized samples yield, after sufficiently long voltage application, interface-controlled steady-state currents described by Schottky injection, modified by space-charge layers in the vicinity of the electrodes. The effective work function for aluminum-polyimide is estimated to be 1.7 eV in the temperature range between 100 and 270 °C. A distinct dependence of these currents on electrode material is observed. Bulk phenomena were studied on one-side metallized samples subject to positive-corona charge injection. At temperatures below 200 °C, significantly larger currents than those for biased, two-side metallized samples were observed. The current-voltage characteristics are ohmic at low fields and space-charge limited at high fields. From these data, trap modulated mobilities for positive carriers of 4×10−12 cm2/V s at 50 °C and 10−9 cm2/V s at 200 °C, ohmic bulk conductivities of 10−16 (Ω cm)−1 at 100 °C and 10−14 (Ω cm)−1 at 200 °C and an intrinsic carrier density of 5×1013 cm−3 independent of temperature are obtained. Activation energies for the mobility are between 0.2 and 0.8 eV for the temperature range between 50 and 200 °C.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 59 (1991), S. 1043-1045 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Thin films ranging from 400 nm to 4 μm thickness of poly( p-phenylene biphenyltetracarboximide) (BPDA-PDA), prepared by thermal imidization of the precursor poly(amic acid) on substrates, have been investigated by the optical waveguide spectroscopy. These polyimide films, most prominent for potential applications as the interlevel dielectrics in multilevel interconnect technologies owing to their low coefficients of thermal expansion and excellent thermal/mechanical properties, are found to exhibit an extraordinarily large anisotropy in the refractive index, with the measured in-plane refractive index n(parallel)(approximately-equal-to)1.852 and the out-of-plane value n⊥(approximately-equal-to)1.612 at 632.8 nm wavelength, nearly independent of the film thickness. This large optical anisotropy indicates a very strong preference of polymer chains to orient along the film surface, and suggests a considerably larger (by ca. 27%) dielectric constant in the film plane than that along the film thickness. Moreover, there is some evidence for the existence of a very thin polyimide layer of slightly lower density and higher anisotropy adjacent to the substrate.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 68 (1996), S. 1930-1932 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Thin polyimide films with dispersed nano-foam morphology have been prepared for the purpose of obtaining low dielectric polymer insulators for microelectronic applications. They were obtained by utilizing micro phase-separated triblock copolymers where the thermally stable polyimide matrix component was derived from pyromellitic dianhydride (PMDA) with 1,1-bis(4-aminophenyl)-1-phenyl-2,2,2-trifluoroethane (3F) and a thermally labile poly(propylene oxide)(PO) component comprised the outside block of the ABA triblock architecture. TEM studies show that the initial irregular nanoscale phase-separated morphology of polyimide triblock copolymers are mostly maintained in the final nano-foam films upon thermal decomposition of the dispersed PO component. The nano-foam polyimide films exhibit significantly lower dielectric constants ε′ (e.g., 2.3 at 19% porosity) as compared with ε′≈2.9 for the homopolymer, as predicted by Maxwell–Garnett theory, with the nano-pore structures remaining stable at 350 °C. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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