21 research outputs found

    Synthesis and properties of novel star-shaped oligofluorene conjugated systems with BODIPY cores

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    Star-shaped conjugated systems with varying oligofluorene arm length and substitution patterns of the central BODIPY core have been synthesised, leading to two families of compounds, T-B1–T-B4 and Y-B1–Y-B4, with T- and Y-shaped motifs, respectively. Thermal stability, cyclic voltammetry, absorption and photoluminescence spectroscopy of each member of these two families were studied in order to determine their suitability as emissive materials in photonic applications

    Synthesis and properties of novel star-shaped oligofluorene conjugated systems with BODIPY cores

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    Star-shaped conjugated systems with varying oligofluorene arm length and substitution patterns of the central BODIPY core have been synthesised, leading to two families of compounds, T-B1-T-B4 and Y-B1-Y-B4, with T- and Y-shaped motifs, respectively. Thermal stability, cyclic voltammetry, absorption and photoluminescence spectroscopy of each member of these two families were studied in order to determine their suitability as emissive materials in photonic applications

    Solid state optical conjugated polymer amplifier; with ultrafast gain switching

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    Conjugated polymers are organic materials which are attractive as optoelectronic devices because they have a combination of broad band emission, high gain, versatility in processing, are ductile and can be electrically pumped. This thesis describes work conducted on such conjugated polymers as amplifier devices. The conjugated polymers used in this thesis were MEH-PPV, F8BT, GP1302 and ADS233YE. The amplifier devices used were grating coupled and end coupling waveguides. Amplification of light was demonstrated and characterised on single and multiple pulses using the grating coupled structure. Single pulse measurements obtained gains of 21 and 17 dB in a 1 mm long waveguide using the conjugated polymers MEHPPV and F8BT. Annihilation rate was also analysed in the single pulse method with MEH-PPV, giving a value of γ ≈ (3 ± 0.1) x 10⁻⁹ cm³/s. Amplification of a single pulse led to demonstrate amplification and the capability of the amplifier to function with multiple pulses, which resulted in F8BT being used as the gain medium. An average gain of 18 dB was obtained with F8BT in a 1 mm waveguide channel. Amplification was also investigated with end coupled waveguides. This led into investigating a suitable material or suitable combination of material for amplification with the waveguides. Switching of an amplified pulse was attempted on F8BT and GP1302 in the amplifier device at 5 kHz. Switching of F8BT was problematic which lead to attempt switching in GP1302 which was a co-polymer of PFO and F8BT. A 70 % switching effect was obtained with GP1302. Gain recovery dynamics of F8BT, GP1302 and ADS233YE was also investigated. These measurements established a switching rate of 500 GHz for GP1302 and ADS233YE, and F8BT showed partial gain recovery indicating the presence of long lived species. Switching was also attempted on a polymer laser. This resulted in a 100 % switched pulse with a combination of weak pump and strong switch pulse of 40 nJ and 2 μJ respectively. And a strong pump and weak switch pulse of 200 and 50 nJ respectively. Temporal delay of the switch pulse relative to the pump pulse resulted in re-timing of the laser output. Amplification and switching of light pulses were also attempted at a higher repetition rate of 50 kHz with F8BT, GP1302, ADS233YE and MEH-PPV. This resulted in strong amplification of light in MEH-PPV and F8BT with gains of 21 and 13 dB respectively in a waveguide length of 422 μm. Weak amplification of light in ADS233YE and GP1302 was also obtained with a maximum gain of 8 and 3 dB respectively. Switching was attempted on MEH-PPV and ADS233YE

    Synthesis and properties of novel star-shaped oligofluorene conjugated systems with BODIPY cores

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    The authors wish to thank the EPSRC for funding. PJS thanks the Royal Society for a Wolfson Research Merit Award.Star-shaped conjugated systems with varying oligofluorene arm length and substitution patterns of the central BODIPY core have been synthesised, leading to two families of compounds, T-B1-T-B4 and Y-B1-Y-B4, with T- and Y-shaped motifs, respectively. Thermal stability, cyclic voltammetry, absorption and photoluminescence spectroscopy of each member of these two families were studied in order to determine their suitability as emissive materials in photonic applications.Publisher PDFPeer reviewe

    Organic Semiconductor Optical Amplifiers

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    Organic semiconducting materials have been researched for novel optoelectronic devices due to their efficient light emission and high gain properties. Such devices range from organic light-emitting diodes and solar cells to lasers and amplifiers. This paper explores the research carried out on one of these devices: organic semiconductor amplifiers that have shown to give high gains of 20-40 dB in solution and solid state.</p

    High-Gain Broadband Solid-State Optical Amplifier using a Semiconducting Copolymer

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    A dilute fluorene copolymer produces enhanced optical amplification. High gain with 1000 times optical amplification and a long lifetime is achieve in only 1mm of the material, and exciton-exciton annihilation is suppressed.</p

    Wavelength conversion from silica to polymer optical fibre communication wavelengths via ultrafast optical gain switching in a distributed feedback polymer laser

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    The output of red (similar to 650 nm) light emitting polymer DFB lasers can be modulated by exposure to infrared (similar to 1.3 mu m) control pulses that depopulate the S, level (see figure). This offers the prospect of an effective wavelength conversion between silica and polymer optical fibre communication wavelengths.</p

    Carrier motion in as-spun and annealed P3HT:PCBM blends revealed by ultrafast optical electric field probing and Monte Carlo simulations

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    Charge transport dynamics in solar cell devices based on as-spun and annealed P3HT:PCBM films are compared using ultrafast time-resolved optical probing of the electric field by means of field-induced second harmonic generation. The results show that charge carriers drift about twice as far during the first 3 ns after photogeneration in a device where the active layer has been thermally annealed. The carrier dynamics were modelled using Monte-Carlo simulations and good agreement between experimental and simulated drift dynamics was obtained using identical model parameters for both cells, but with different average PCBM and polymer domain sizes. The calculations suggest that small domain sizes in as-spun samples limit the carrier separation distance disabling their escape from geminate recombination
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