Metallicity Calibration and Photometric Parallax Estimation: I. UBV photometry

We present metallicity and photometric parallax calibrations for the F and G type dwarfs with photometric, astrometric and spectroscopic data. The sample consists of 168 dwarf stars covering the colour, iron abundance and absolute magnitude intervals $0.30<(B-V)_0<0.68$ mag, $-2.0<[Fe/H]<0.4$ dex and $3.4<M_V<6.0$ mag, respectively. The means and standard deviations of the metallicity and absolute magnitude residuals are small, i.e. $\langle\Delta[Fe/H]_{res}\rangle=0$ and $\sigma=0.134$ dex, and $\langle\Delta (M_V)_{res}\rangle=0$ and $\sigma=0.174$ mag, respectively, which indicate accurate metallicity and photometric parallax estimations.Comment: 13 pages, 11 figures and 2 tables, accepted for publication in Astrophysics and Space Scienc

Quantum efficiency enhancement in film by making nanoparticles of polyfluorene

Cataloged from PDF version of article.We report on conjugated polymer nanoparticles of polyfluorene that were formed to exhibit higher fluorescence quantum efficiency in film (68%) and reduce undesired emission peak wavelength shifts in film (by 20 nm), compared to the solid-state polymer thin film made directly out of the same polymer solution without forming nanoparticles. Using the facile reprecipitation method, solutions of poly[9,9-dihexyl-9H-fluorene] in THF were added at different volume ratios to obtain different size distributions of nanoparticle dispersions in water. This allowed us to control the sizedependent optical emission of our polyfluorene nanoparticles. Such organic nanoparticles hold great promise for use as efficient emitters in optoelectronic device applications. (C) 2008 Optical Society of America

Non-radiative resonance energy transfer in bi-polymer nanoparticles of fluorescent conjugated polymers

Cataloged from PDF version of article.his work demonstrates the comparative studies of non-radiative resonance energy transfer in bi-polymer nanoparticles based on fluorescent conjugated polymers. For this purpose, poly[(9,9-dihexylfluorene) (PF) as a donor (D) and poly[2-methoxy-5-(2'-ethyl-hexyloxy)-1,4-phenylene vinylene] (MEH-PPV) as an acceptor (A) have been utilized, from which four different bi-polymer nanoparticle systems are designed and synthesized. Both, steady-state fluorescence spectra and time-resolved fluorescence measurements indicate varying energy transfer efficiencies from the host polymer PF to the acceptor polymer MEH-PPV depending on the D-A distances and structural properties of the nanoparticles. The first approach involves the preparation of PF and MEH-PPV nanoparticles separately and mixing them at a certain ratio. In the second approach, first PF and MEH-PPV solutions are mixed prior to nanoparticle formation and then nanoparticles are prepared from the mixture. Third and fourth approaches involve the sequential nanoparticle preparation. In the former, nanoparticles are prepared to have PF as a core and MEH-PPV as a shell. The latter is the reverse of the third in which the core is MEH-PPV and the shell is PF. The highest energy transfer efficiency recorded to be 35% is obtained from the last system, in which a PF layer is sequentially formed on MEH-PPV NPs. © 2010 Optical Society of America

On the origin of high quality white light emission from a hybrid organic/inorganic light emitting diode using azide functionalized polyfluorene

High quality white light generation with high colour rendering index (CRI) was achieved by integrating a cross-linkable azide functionalized polyfluorene derivative, namely poly[(9,9-dihexylfluorene)-co-alt-(9,9-bis(6-azidohexyl) fluorene)] (PFA), as a down-converting fluorescent material on the inorganic n-UV InGaN/GaN LED platform. For comparison, two other polyfluorene based polymers, namely poly[(9,9-dihexylfluorene)-co-alt-(9,9-bis(6-bromohexyl) fluorene)] (PFB) and poly[9,9-dihexyl-9H-fluorene] (PF), were tested for white light generation. While PFA and PF both led to white light generation, PFB fell out of the white region on the chromaticity diagram. Compared to PFA, both of the control groups (PF and PFB) exhibited much lower CRI. To gain a better insight into the mechanisms playing a key role for the generation of such high quality white light in PFA, all of these polymers were further subjected to a series of experiments such as controlled exposure to heat at 220 °C for 2 h under Ar and in air. The polymers PFA and PFB, which include cross-linkable groups, produced broad emission spectra in the region of 430-650 nm upon annealing in the absence of oxygen under Ar atmosphere while almost no change was observed in the emission spectrum of PF without any cross-linkable groups. PFA undergoes cross-linking through the decomposition of azide leading to reactive nitrene species, whereas in PFB cross-linking probably occurs via debromination. This result clearly proved that the broadening can not be attributed only to photo or thermal oxidation, but it is also due to cross-linking. PFA was also exposed to n-UV light from the InGaN/GaN LED to investigate its photostability. In these experiments, the spectral changes in absorbance and emission properties and thermal transitions of these polymers were monitored by FT-IR, UV-Vis and fluorescent spectrometry, and differential scanning calorimetry (DSC). These experiments indicated that PFA provides high quality white light opportunely via cross-linking and remains stable once cross-linking is formed in a solid film. © 2008 The Royal Society of Chemistry

Image sequence analysis for emerging interactive multimedia services - The European COST 211 framework

Cataloged from PDF version of article.Flexibility and efficiency of coding, content extraction, and content-based search are key research topics in the field of interactive multimedia. Ongoing ISO MPEG-4 and MPEG-7 activities are targeting standardization to facilitate such services. European COST Telecommunications activities provide a framework for research collaboration. COST 211bis and COST 211ter activities have been instrumental in the definition and development of the ITU-T H.261 and H.263 standards for videoconferencing over ISDN and videophony over regular phone lines, respectively. The group has also contributed significantly to the ISO MPEG-4 activities. At present a significant effort of the COST 211ter group activities is dedicated toward image and video sequence analysis and segmentation—an important technological aspect for the success of emerging object-based MPEG-4 and MPEG-7 multimedia applications. The current work of COST 211 is centered around the test model, called the Analysis Model (AM). The essential feature of the AM is its ability to fuse information from different sources to achieve a high-quality object segmentation. The current information sources are the intermediate results from frame-based (still) color segmentation, motion vector based segmentation, and changedetection-based segmentation. Motion vectors, which form the basis for the motion vector based intermediate segmentation, are estimated from consecutive frames. A recursive shortest spanning tree (RSST) algorithm is used to obtain intermediate color and motion vector based segmentation results. A rule-based region processor fuses the intermediate results; a postprocessor further refines the final segmentation output. The results of the current AM are satisfactory; it is expected that there will be further improvements of the AM within the COST 211 project

White emitting polyfluorene functionalized with azide hybridized on near-UV light emitting diode for high color rendering index

Cataloged from PDF version of article.We develop and demonstrate high-quality white light generation that relies on the use of a single-type simple conjugated polymer of polyfluorene functionalized with azide groups (PFA) integrated on a near-UV LED platform. The high-quality white emission from the polyfluorene is achieved by using the azide functionalization to facilitate cross-linking intentionally when cast into solid-state form. Hybridized on n-UV InGaN/GaN LED at 378 nm, the PFA emitters collectively generate a very broad down-converting photoluminescence at longer wavelengths across the entirety of the visible spectrum, yielding high color rendering indices up to 91. (c) 2008 Optical Society of America

White-emitting Conjugated Polymer Nanoparticles with Cross-Linked Shell for Mechanical Stability and Controllable Photometric Properties in Color-Conversion LED Applications

Cataloged from PDF version of article.We report on the synthesis and characterization of water-dispersible, mechanically stable conjugated polymer nanoparticles (CPNs) in shelled architecture with tunable emission and controllable photometric properties via cross-linking. Using a reprecipitation method, white-emitting polymer nanoparticles are prepared in different sizes by varying the concentration of polymer; the emission kinetics are tuned by controlling the shell formation. For this purpose, polyfluorene derivatives containing azide groups are selected that can be decomposed under UV light to generate very reactive species, which opportunely facilitate the inter- and intra-cross-linking of polymer chains to form shells. Nanoparticles before and after UV treatment are characterized by various techniques. Their size and morphologies are determined by using dynamic light scattering (DLS) measurements and imaging techniques including scanning electron microscopy (SEM) and atomic force microscopy (AFM). For optical characterization, UV-vis and steady-state and time-resolved fluorescent spectroscopies are performed. Solid-state behaviors of these CPNs are also Investigated by forming films through drop-casting. Moreover, the photometric calculations are also performed for films and dispersions to determine the color quality. A device has been constructed to show proof-of-principle white light generation from these nanoparticles. Additionally, mechanical stability studies are performed and demonstrated that these nanoparticles are indeed mechanically. stable by removing the solvent after cross-linking using a freeze-dryer and redispersing in water and THF. Optical and imaging data confirm that the redispersed particles preserve their shapes and sizes after cross-linking

Morphology-Dependent Energy Transfer of Polyflorene Nanoparticeles Decorating InGaN/GaN Quantum-Well Nanopillars

Cataloged from PDF version of article.Conjugated polymer nanoparticles (CPNs), prepared in aqueous dispersion from poly[(9,9-bis{3-bromopropyl}fluorenyl-2,7-diyl)-co-(1,4-benzo-{2,1,3}-thiodia- zole)] (PFBT-Br), are incorporated into a nanopillar architecture of InGaN/GaN multiple quantum wells (MQWs) to demonstrate a new organic/inorganic class of nanostructured excitonic model system. This hybrid system enables intimate integration for strong exciton-exciton interactions through nonradiative energy transfer (NRET) between the integrated CPNs and MQW pillars. The NRET of these excitonic systems is systematically investigated at varied temperatures. In these hybrids, InGaN/GaN MQWs serve as the donor of the NRET pair, while immobilized PFBT-Br polymer serves as the acceptor. To understand morphology-dependent NRET, PFBT-Br CPNs coating InGaN/GaN MQWs are made to defold into polymer chains by in situ treatment with a good solvent (THF). The experimental results indicate that NRET is significantly stronger in the case of CPNs compared with their defolded polymer chains. At room temperature, while the NRET efficiency of open polymer chains nanopillar system is only 10%, PFBT-Br CPNs exhibit a substantially higher NRET efficiency of 33% (preserving the total number of polymer molecules). The NRET efficiency of the nanoparticle systems is observed to be 25% at 250 K, 22% at 200 K, 19% at 150 K, and 15% at 100 K. On the other hand, the defolded polymer chains exhibit significantly lower NRET efficiencies of 17% at 250 K, 16% at 200 K, 11% at 150 K, and 5% at 100 K. This work may potentially open up new opportunities for the hybrid organic/inorganic systems where strong excitonic interactions are desired for light generation, light harvesting, and sensing applications

Highly Luminescent CB[7]-Based Conjugated Polyrotaxanes Embedded into Crystalline Matrices

π-Conjugated polymers suffer from low quantum yields (QYs) due to chain–chain interactions. Furthermore, their emission in solid films is significantly quenched due to aggregation leading further decrease in QY. These are the two main issues of these materials hampering their widespread use in optoelectronic devices. To address these issues, here the backbone of poly(9,9′-bis(6″-(N,N,N-trimethylammonium)hexyl)fluorene-alt-co-thiophenelene) is isolated by threading with cucurbit[7]uril (CB7). Subsequently, the conjugated polyrotaxanes are incorporated into organic crystalline matrices to obtain highly efficient color-converting solids suitable for solid-state lighting. Upon threading the polymer backbone with CB7s, although the QY of the resulting polyrotaxane in solution state increases, the quenching problem in their solid state is not completely tackled. To solve this problem, these conjugated polyrotaxanes are embedded into various crystalline matrices and their remarkably high QYs (>50%) in the solution are successfully maintained in the solid state. To demonstrate the suitability of these aforementioned materials for solid-state lighting, a proof-of-concept light-emitting diode is constructed by employing their powders as color converters. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinhei