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  • 1
    Digitale Medien
    Digitale Medien
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 91 (2002), S. 3955-3980 
    ISSN: 1089-7550
    Quelle: AIP Digital Archive
    Thema: Physik
    Notizen: Optical waveguide amplifiers based on polymer materials offer a low-cost alternative for inorganic waveguide amplifiers. Due to the fact that their refractive index is similar to that of standard optical fibers, they can be easily coupled to existing fibers with low coupling losses. Doping the polymer with rare-earth ions that yield optical gain is not straightforward, as the rare-earth salts are poorly soluble in the polymer matrix. This review article focuses on two different approaches to dope a polymer waveguide with rare-earth ions. The first approach is based on organic cage-like complexes that encapsulate the rare-earth ion and are designed to provide coordination sites to bind the rare-earth ion and to shield it from the surrounding matrix. These complexes also offer the possibility of attaching a highly absorbing antenna group, which increases the pump efficiency significantly. The second approach to fabricate rare-earth doped polymer waveguides is obtained by combining the excellent properties of SiO2 as a host for rare-earth ions with the easy processing of polymers. This is done by doping polymers with Er-doped silica colloidal spheres. © 2002 American Institute of Physics.
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 83 (1998), S. 497-503 
    ISSN: 1089-7550
    Quelle: AIP Digital Archive
    Thema: Physik
    Notizen: The optical properties of different erbium (Er)-doped polydentate hemispherand organic cage complexes are studied, for use in polymer-based planar optical amplifiers. Room temperature photoluminescence at 1.54 μm is observed, due to an intra-4f transition in Er3+. The Er is directly excited into one of the 4f manifolds (at 488 nm), or indirectly (at 287 nm) via the aromatic part of the cage. The luminescence spectrum is 70 nm wide (full width at half maximum), the highest known for any Er-doped material, enabling high gain bandwidth for optical amplification. The absorption cross section at 1.54 μm is 1.1×10−20 cm2, higher than in most other Er-doped materials, which allows the attainment of high gain. Measurements were performed on complexes in KBr tablets, in which the complex is present in the form of small crystallites, or dissolved in the organic solvents dimethylformamide and butanol-OD. In KBr the luminescence lifetime at 1.54 μm is 〈0.5 μs, possibly due to concentration quenching effects. In butanol-OD solution, the lifetime is 0.8 μs, still well below the radiative lifetime of 4 ms estimated from the measured absorption cross sections. Experiments on the selective deuteration of the near-neighbor C–H bonds around the Er3+-ion indicate that these are not the major quenching sites of the Er3+ luminescence. Temperature dependent luminescence measurements indicate that temperature quenching is very small. It is therefore concluded that an alternative luminescence quenching mechanism takes place, presumably due to the presence of O–H groups on the Er-doped complex (originating either from the synthesis or from the solution). Finally a calculation is made of the gain performance of a planar polymer waveguide amplifier based on these Er complexes, resulting in a threshold pump power of 1.4 mW and a typical gain of 1.7 dB /cm. © 1998 American Institute of Physics.
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 76 (2000), S. 3682-3684 
    ISSN: 1077-3118
    Quelle: AIP Digital Archive
    Thema: Physik
    Notizen: Silica colloids with a diameter of 240–360 nm, grown by wet chemical synthesis using ethanol, ammonia, water, and tetraethoxysilane, were implanted with 350 keV Er ions, to peak concentrations of 0.2–1.1 at. % and put onto a silicon or glass substrate. After annealing at 700–900 °C the colloids show clear room-temperature photoluminescence at 1.53 μm, with lifetimes as high as 17 ms. By comparing data of different Er concentrations, the purely radiative lifetime is estimated to be 20–22 ms, indicating a high quantum efficiency of about 80%. This high quantum efficiency indicates that, after annealing, the silica colloids are almost free of OH impurities. Spinning a layer of polymethylmethacrylate over the silica spheres results in an optically transparent nanocomposite layer, that can be used as a planar optical waveguide amplifier at 1.5 μm that is fully compatible with polymer technology. © 2000 American Institute of Physics.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 79 (2001), S. 3585-3587 
    ISSN: 1077-3118
    Quelle: AIP Digital Archive
    Thema: Physik
    Notizen: Spherical SiO2 colloids with two different diameters (175 nm, 340 nm) were doped with erbium at different concentrations. The spheres show sharply peaked photoluminescence centered at 1.535 μm, due to intra-4f transitions in Er3+. From measurements of the Er decay rate for different Er concentrations the decay rate of isolated Er ions (i.e., in absence of concentration quenching) was determined for the two colloid diameters. The data were compared to spontaneous emission rates derived from calculations of the local optical density of states in the colloids. The calculation predicts a large difference in the spontaneous emission rate for both colloid sizes (61 vs 40 s−1), in perfect agreement with the measured data. © 2001 American Institute of Physics.
    Materialart: Digitale Medien
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  • 5
    Digitale Medien
    Digitale Medien
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 78 (2001), S. 2122-2124 
    ISSN: 1077-3118
    Quelle: AIP Digital Archive
    Thema: Physik
    Notizen: We report 890 nm luminescence from a neodymium-doped polymer light-emitting diode. The active layer is a blend of poly(dioctylfluorene-co-benzothiadiazole), F8BT, and a lissamine-functionalized terphenyl-based neodymium complex. We detect electroluminescence from both the lissamine (580 nm) and the Nd3+ complex (890 nm). By comparison with lissamine-free devices we show that the lissamine is crucial to infrared emission. The neodymium/lissamine luminescence intensity ratio is higher under electrical excitation than under optical excitation, showing that more triplets reach Nd3+ under electrical excitation. High turn-on voltages provide a clear indication for charge trapping onto the lissamine, and we consider direct triplet formation on the lissamine to be competing efficiently with respect to slower Dexter-type triplet transfer from the F8BT to the lissamine. © 2001 American Institute of Physics.
    Materialart: Digitale Medien
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