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Relevant bibliographies by topics / Polymer luminescence

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Academic literature on the topic 'Polymer luminescence'

Author: Grafiati

Published: 4 June 2021

Last updated: 5 February 2022

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Journal articles on the topic "Polymer luminescence"

1

Zhao, Zhihuan, Yao Wang, Haoyang Jiang, et al. "Optical Features of Lanthanide Luminescent Hydrogel Based on Polyethylene Glycol with Silica Nanoparticles." Science of Advanced Materials 13, no. 1 (2021): 123–30. http://dx.doi.org/10.1166/sam.2021.3850.

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Inorganic/polymer hybrid hydrogels generally exhibit excellent mechanical properties, while extra function include luminescence are extremely explored due to the further application in sensors and optoelectronic devices. Herein, we report the rare-earth (RE) complex/silica nanoparticles (SNs) luminescent hybrid polyethylene glycol (PEG) hydrogels showing stable luminescence. The hybrid hydrogels coordinated with RE (Eu3+) complex are fabricated via a convenient in situ photocrosslinked procedure. The coordination polymers showed red luminescent color under the 365 nm UV irradiation. Furthermore, the hybrid hydrogel exhibited long luminescence lifetime. These properties of hybrid luminescent hydrogel gave rise to a great improvement in the potential applications as a soft material.

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Abdullah, M. "Effect Of Polymer Molecular Weight On The Luminescence Properties Of Nanocomposite Zinc Oxide/Polyethylene Glycol." REAKTOR 7, no. 1 (2017): 47. http://dx.doi.org/10.14710/reaktor.7.1.47-51.

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Luminescence Properties Of Nanocomposite (Zinc Oxide/Polyethylene Glycol: Lithium ions) have been synthesized using different molecular weight of polymer. Changing the molecular weight produced no effect of the crystallinity of ZnO nanoparticles if similar molarity of ethylene glycol unit were used. However, the use of high molecular weight of polymers tended to reduce the size of nanoparticles, which implied to the enhancement in the luminescence spectra due to increasing in the particle number concentration. TEM picture of sample prepared using PEG of molecular weight 0f 500,000 exhibitef a particle size of 5 nm, which was close to the value predicted y Waaent-Schere formula or size dependent band gap.Keywords : nanocomposite, luminescent polymer electrolytes, zinc oxide, polyethylene glycol

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Cui, Fang, Tong Jie Yao, Jing Yu, and Ke Ning Sun. "Synthesis and Characterization of Luminescent TiO₂/Polymer Nanocomposites." Advanced Materials Research 873 (December 2013): 492–95. http://dx.doi.org/10.4028/www.scientific.net/amr.873.492.

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Transparent luminescent TiO2/polymer nanocomposites were obtained through the combined use of copolymerization of a novel titanium ion containing monomer with a liquidsolid reaction. The titanium ions are covalently introduced into polymer chains and transformed into TiO2 nanocrystals directly in the solid-state polymer matrices. That allows the generation of high-quality anatase TiO2 nanocrystals with a narrow size distribution in the polymer matrices. The luminescence of the TiO2 nanocrystals is dominated by band-edge luminescence at room temperature.

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Kondo, Mizuho, Yuya Morita, and Nobuhiro Kawatsuki. "Blue-Shifting Mechanofluorochromic Luminescent Behavior of Polymer Composite Films Using Gelable Mechanoresponsive Compound." Crystals 11, no. 8 (2021): 950. http://dx.doi.org/10.3390/cryst11080950.

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Mechanochromic luminescent dyes change their luminescence color upon exposure to external mechanical stimuli. In this study, we synthesized a liquid crystalline mechanochromic luminescent dye containing a terminal cholesterol molecule. The dissolution of the dye in 1,4-dioxane resulted in the formation of a gel. The luminescence of the xerogel obtained from the dioxane solution changed from green to blue upon grinding, indicating mechanochromic luminescence behavior. The anisotropic patterning of short-wavelength-shifted luminescence color change by directional handwriting on surface layer of liquid crystal was successfully demonstrated. Furthermore, blue-shifting mechanoresponsive polymer composite surface was fabricated by using the luminophore.

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Carotenuto, G., M. L. Nadal, P. Repetto, P. Perlo, L. Ambrosio, and L. Nicolais. "New Polymeric Additives for Allowing Photoelectric Sensing of Plastics during Manufacturing." Advanced Composites Letters 16, no. 3 (2007): 096369350701600. http://dx.doi.org/10.1177/096369350701600303.

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Metallic mercaptides are inert organic compounds (i.e., Mex( SR) y) that can be used to make thermoplastic polymers high luminescent to UV-light. Luminescence is strictly required in polymer manufacturing since this characteristic allows detection of polymer pieces by photoelectric sensors. Luminescent Au, CdS, and ZnS nanoparticles can be generated into thermoplastics like: polystyrene, polycarbonate, poly(vinyl acetate), etc. by thermolysis of the corresponding mercaptides. PL spectra of polymeric films embedding these nanoparticles show intensive visible light emission in different spectral regions. The formation of nanoparticles was probably related to the viscous nature of reaction medium which significantly limit the growth stage.

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Kuřitka, Ivo, Vladimír Sedlařík, Diana Harea, et al. "Polymer Labelling with a Conjugated Polymer-Based Luminescence Probe for Recycling in the Circular Economy." Polymers 12, no. 6 (2020): 1226. http://dx.doi.org/10.3390/polym12061226.

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In this paper, we present the use of a disubstituted polyacetylene with high thermal stability and quantum yield as a fluorescence label for the identification, tracing, recycling, and eventually anti-counterfeiting applications of thermoplastics. A new method was developed for the dispersion of poly[1-phenyl-2-[p-(trimethylsilyl)phenyl]acetylene] (PTMSDPA) into polymer blends. For such purposes, four representative commodity plastics were selected, i.e., polypropylene, low-density polyethylene, poly(methyl methacrylate), and polylactide. Polymer recycling was mimicked by two reprocessing cycles of the material, which imparted intensive luminescence to the labelled polymer blends when excited by proper illumination. The concentration of the labelling polymer in the matrices was approximately a few tens ppm by weight. Luminescence was visible to the naked eye and survived the simulated recycling successfully. In addition, luminescence emission maxima were correlated with polymer polarity and glass transition temperature, showing a marked blueshift in luminescence emission maxima with the increase in processing temperature and time. This blueshift results from the dispersion of the labelling polymer into the labelled polymer matrix. During processing, the polyacetylene chains disentangled, thereby suppressing their intermolecular interactions. Moreover, shear forces imposed during viscous polymer melt mixing enforced conformational changes, which shortened the average conjugation length of PTMSDPA chain segments. Combined, these two mechanisms shift the luminescence of the probe from a solid- to a more solution-like state. Thus, PTMSDPA can be used as a luminescent probe for dispersion quality, polymer blend homogeneity, and processing history, in addition to the identification, tracing, and recycling of thermoplastics.

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Li, Cheng Zhou, Yoshio Adachi, Yusuke Imai, Keiko Nishikubo, and Chao Nan Xu. "Elastico-Luminescent Nanoparticles Prepared via Polymer-Coated Precursor Formed in Reverse Micelles." Key Engineering Materials 368-372 (February 2008): 355–58. http://dx.doi.org/10.4028/www.scientific.net/kem.368-372.355.

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Europium-doped strontium aluminate is a famous green phosphor that can give luminescence under a mechanical stress that is named elastico-luminescence. This paper reports a modified reverse micelles process for preparing the europium-doped strontium aluminate nanoparticles. A polymeric matrix was coated on the surface of the precursor formed in the reverse micelles. The polymeric matrix is considered to prevent the particle agglomeration by forming a carbon layer while the precursor was heat-treated. Consequently, the luminescent nanoparticles were achieved after removing the carbon layer and forming the luminescent center under a reducing atmosphere. The processing and properties of the luminescent nanoparticles were discussed in this paper.

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Bachman, Robert E., and Sheri A. . Bodolosky-Bettis. "Construction of Luminescent Gold(I) Aryl Thiolates via Isonitrilegold(I) Complexes: Influence of Synthetic Methodology and the Thiolate Ligand on Structure and Properties." Zeitschrift für Naturforschung B 64, no. 11-12 (2009): 1491–99. http://dx.doi.org/10.1515/znb-2009-11-1233.

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Gold thiolate polymers ([ArSAu]n) were prepared via two synthetic routes - the direct reaction of an aromatic thiolate (ArSH) with HAuCl4, or the reaction of an isonitrilegold(I) chloride complex with a thiolate anion. The former route, which is general to almost all thiols, yields an amorphous and non-luminescent material. The latter route, which is more limited in scope, proceeds via an isonitrilegold( I) thiolate complex and typically yields a crystalline and luminescent material. Addition of electron-donating groups to the thiol aromatic ring leads to more rapid polymer formation and loss of luminescence while addition of electron-withdrawing groups slows or stops polymer formation and leads to a red-shift of the luminescence of the final polymeric materials. Two isonitrilegold(I) thiolate complexes with varying numbers of fluorine substituents on the thiolate aromatic ring were characterized crystallographically - C8H17NCAu(p-FC6H4S) and C12H25NCAu(2,4-F2C6H3S). As the fluorination of the aromatic ring increases, no significant changes were observed in the bond lengths of the complexes; however, the intermolecular Au-S distances lengthen while the aurophilic interaction distances decrease. These results suggest clear relationships between the molecular structure and both the supramolecular structure and photophysical properties in these materials

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Liu, Jian-Jun, Shu-Biao Xia, Qi-Tao Que, et al. "Naphthalimide-containing coordination polymer with mechanoresponsive luminescence and excellent metal ion sensing properties." Dalton Transactions 49, no. 10 (2020): 3174–80. http://dx.doi.org/10.1039/c9dt04928b.

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A new multifunctional luminescent Cd(ii) coordination polymer based on a 1,8-naphthalimide has been synthesized. It exhibits interesting mechanoresponsive luminescence properties and sensing ability for the detection of the toxic Cr<sup>3+</sup> ion.

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Sorokin, A. V. "Plasmon enhancement of thiacyanine J-aggregates luminescence in polymer films." Functional materials 22, no. 3 (2015): 316–21. http://dx.doi.org/10.15407/fm22.03.316.

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Dissertations / Theses on the topic "Polymer luminescence"

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Katta, Kartheek [Verfasser]. "Luminescence properties in polymer and polymer/inorganic nanocapsule / Kartheek Katta." Mainz : Universitätsbibliothek Mainz, 2016. http://d-nb.info/1116979160/34.

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Fang, Yu Lianshe. "Luminescence studies of polymer interactions in aqueous media." Thesis, Lancaster University, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.246121.

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Carey, Michelle Jocelyn. "The photophysics of naphthalene containing synthetic polymers." Thesis, Imperial College London, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.320273.

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Annable, Tom. "A luminescence investigation of the physical and photophysical behaviour of macromolecules." Thesis, Lancaster University, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.235595.

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Lucas, David M. "Luminescence studies of polymer behaviour in the solution and solid states." Thesis, Lancaster University, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.334750.

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Gonzalez-Rabade, A. "Correlation of heterojunction luminescence and photocurrent in polymer blend photovoltaic diodes." Thesis, University of Cambridge, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.599488.

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This thesis focuses on the electronic and photophysical phenomena that occur at the heterojunction between two distinct organic semiconductor materials. The hetero junction luminescence is correlated to the photovoltaic performance in a polymer blend diode. Polymer semiconductor blends allow efficient operation of photovoltaic diodes when there is a large interfacial area of hetero junction between electron donor and acceptor polymers. In this thesis, we use electromodulation spectroscopy to investigate the luminescent and photovoltaic behaviour of electron- and hole-transporting polyfluorenes blends at a broad range of blend ratios, temperatures and electric fields. In the systems investigated, an exciton at the hetero junction produces either free charges or an exciplex (or a similar interfacially-bound charge-transfer pair). We find that an externally-applied electric field increases the number of free charges and quenches the exciplex luminescence with a one-to-one correspondence: the increase of the photocurrent internal quantum efficiency is equal to the reduction in the exciplex emission. We conclude that, independent of temperature and morphology, the photovoltaic quantum yield is predominantly limited by the dissociation of the geminate electron-hole pair intermediate at the hetero junction. Once the charges are fully separated they are transported across the material and collected at the external circuit with nearly unit efficiency.

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Dailey, Stuart. "A study of conjugated polymers and their applications in light-emitting diodes." Thesis, Durham University, 1998. http://etheses.dur.ac.uk/4744/.

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The initiation of research into conjugated polymer electroluminescent devices in Durham is reported. The apparatus required for the fabrication and characterisation of polymer light-emitting diodes (LEDs) is outlined, and the essential assumptions and calculations required to determine their efficiency, brightness and colour are summarised. Optical and electrical characterisation of a range of polymers is reported, including polypyridine (PPY) and a range derivatives, poly(p-phenylene vinylene) (PPV) and poly(2-methoxy, 5-(2'ethyl-hexyloxy)-p-phenylene vinylene) (MEH-PPV). The optical properties of PPY in solution, film and dilute solid state are characterised. The conjugation length of PPY is investigated by deliberate disruption of the conjugation by the inclusion meta-links in the otherwise para-linked polymer. The effect of altering the chemical structure of PPY is investigated by the study of some PPY derivatives including random and regular copolymers. The consequences of using precursor polymers, especially the effects of conversion on indium tin oxide coated substrates are investigated using absorption and luminescence spectroscopy and capacitance-voltage analysis. Electroluminescence from a number of conjugated polymers is reported and the efficiency, spectral output and device characteristics are presented. The formation of Schottky barriers in some polymer devices is investigated using quasi-static capacitance-voltage measurements. Improvements in the quantum and power efficiency of polymer LEDs have been achieved using two hole-transporting polymers, poly(vinyl carbazole) and the doped, conducting form of polyaniline. A substantial improvement in quantum efficiency has also been demonstrated when PPY is used as an electron-transporting layer in PPV and MEH-PPV based light-emitting diodes. The variation in quantum efficiency and emission spectrum with the ratio of the thickness of the two polymer layers is reported and analysed.

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Thomas, Janet Lyn. "The effect of dyeing parameters on the lightfastness properties of acid dyes in nylon 6,6 fibres." Thesis, Manchester Metropolitan University, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296491.

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Kage, Daniel. "Studies on fluorophore-loaded polymer microbeads and luminescence lifetime encoding in flow cytometry." Doctoral thesis, Humboldt-Universität zu Berlin, 2019. http://dx.doi.org/10.18452/20608.

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Die Dissertation umfasst zwei Themenblöcke: Zum einen wurden die optisch-spektroskopischen Eigenschaften von fluoreszenten, farbstoffbeladenen Polymer-Mikropartikeln untersucht. Zum anderen wurde die Anwendbarkeit solcher Partikel für die Lumineszenzlebensdauer-Kodierung in der Durchflusszytometrie evaluiert. Die Charakterisierung der farbstoffbeladenen Mikropartikel erfolgte mittels optischer Spektroskopie. Am Beispiel mit Rhodamin 6G beladener Polymethylmethacrylat-Partikel konnte ein besseres Verständnis des Einbaus der Farbstoffmoleküle und der resultierenden Fluoreszenz-Charakteristika gewonnen werden. Es stellte sich heraus, dass die Beladungseffizienz stark vom mittleren Partikeldurchmesser und den Synthesebedingungen abhängt. In Verbindung mit den beobachteten optisch-spektroskopischen Eigenschaften wurde geschlussfolgert, dass sich eine farbstoffreiche Schicht an der Oberfläche der Partikel bildet, die sich wesentlich von den sterisch eingebauten Farbstoffmoleküle im Partikelvolumen unterscheidet. Hohe Farbstoffkonzentrationen in dieser Oberflächenschicht führen vermutlich zu Aggregation. Des Weiteren deuten Veränderungen der Fluoreszenzeigenschaften auf intrapartikuläre Energiewanderung bei zunehmender Farbstoffkonzentration hin. Diese Interpretation der experimentellen Ergebnisse konnte qualitativ durch einen Algorithmus zur Simulation der Energiewanderung bestätigt werden. Die Anwendbarkeit der Lumineszenzlebensdauer als Kodierungsparameter in der Zeitdomäne konnte unter Verwendung eines Durchflusszytometer-Prototypen analysiert werden. Die wohl größte Herausforderung bei der Lebensdauermessung in der Durchflusszytometrie ist die kurze Interaktionszeit zwischen Objekt und Anregungslicht. Synthetische Daten wurden herangezogen, um den Einfluss einzelner Messparameter und -bedingungen unabhängig voneinander abzuschätzen. Es konnte festgestellt werden, dass die Lumineszenzlebensdauer als Kodierungsparameter in der Zeitdomäne prinzipiell zugänglich ist.<br>This thesis comprises two main topics. First, the optical-spectroscopic properties of fluorescent microbeads loaded with organic dyes were studied. In the second part, the feasibility of time-domain luminescence lifetime encoding in flow cytometry based on such microbeads was assessed. The study of the dye-loaded polymer microbeads was based on optical spectroscopy. Poly(methyl methacrylate) beads loaded with rhodamine 6G were used as an example system to achieve a better understanding of the dye incorporation procedure. The dye loading efficiency turned out to be strongly dependent on the mean diameter of the beads and on the amounts of certain compounds used for the bead synthesis. In correlation with the observed fluorescence characteristics, it was deduced that a layer with high local dye concentration forms around each bead. The properties of this layer substantially differ from those of the sterically incorporated dye molecules in the bead core. The high dye concentration in this layer results in aggregation accompanied by the respective changes of the fluorescence characteristics of the beads. Moreover, the observed changes in fluorescence properties indicated the existence of an intra-particulate energy migration process at increased dye loading concentrations. A simulation of the energy migration process based on a random walk algorithm confirmed the interpretation of the experimental results. For the assessment of luminescence lifetime encoding in time-domain flow cytometry, a prototype setup was used. The main issue of lifetime determination in flow cytometry is represented by the short interaction time of only tens of microseconds of the objects with the excitation light spot. Synthetic data were used to study certain measurement parameters and conditions as well as the data analysis procedure independently of other influences. As a result, luminescence lifetime is generally applicable as an encoding parameter in time-domain flow cytometry.

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Thomas, Tudor Huw. "Enhancing fluorescence and charge transport in disordered organic semiconductors." Thesis, University of Cambridge, 2018. https://www.repository.cam.ac.uk/handle/1810/283199.

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High performance optoelectronic applications require simultaneously high mobility ($\mu$) and high quantum efficiency of fluorescence ($\Phi$). While this has been realised for organic small molecule semiconductors, applications such as high efficiency organic photovoltaics and bright organic light-emitting diodes towards electrically driven lasing are hampered by an apparent trade-off between $\mu$ and $\Phi$ in disordered systems. Recent reports of state-of-the-art device performance often optimise $\mu$ and $\Phi$ in disordered organic materials separately, and employ multi-layer architectures. In this work, we investigate materials in a class of donor-acceptor polymer materials; the indacenodithiophene-$\textit{alt}$-benzothiadiazole family, which demonstrate high $\mu$ in spite of a low long-range structural order, to understand the interplay between these two important device figures-of-merit. In the first section, we evaluate the effect of various tuneable parameters on $\mu$ and device performance in organic field-effect transistors. Using chemical modifications to the solubilising side chains, we observe that the substitution of bulky groups leads to a reduction of the hole mobility $\mu_h$ > 2 cm$^{2}$/Vs to ~ 0.5 cm$^{2}$/Vs in the benchmark polymer of this family, indacenodithiophene-$\textit{alt}$-benzothiadiazole. Crystallographic and exciton-quenching based experiments confirm this observation is closely related to the degree of polymer backbone aggregation, and this leads to a different temperature evolution of the transport behaviour. In order to reliably improve $\mu$ in these systems, an elongation of the donor subunit is required. This increases the $\pi$-electron density on the donor, and can lead to an improvement in $\mu$ where the side chain density is decreasing. This chemical design, leading to a more highly aggregated structural motif is much more potent in determining $\mu$, it seems, than design strategies to further improve the energetic disorder in the joint density of states and the potential barrier to torsion, which may be near optimised in these low-disorder systems. In the second section, we unpick the precise relationship between the degree of aggregation apparently linking high $\mu$ to low $\Phi$. With a prototype system, we compare the photophysics of two indacenodithiophene-$\textit{alt}$-benzothiadiazole polymers differing by side chain bulkiness. Despite the aforementioned suppression of $\mu$, we observe an improvement to $\Phi$ of $< 0.02$ to $\sim 0.18$ upon backbone separation. This derivative has the highest $\Phi$ reported for any polymer with $\mu$ exceeding that of amorphous-Si. However, the $\Phi$ in the more aggregated derivative is not limited by the formation of non-emissive excitons, but rather by an additional internal conversion pathway which is strongly temperature dependent, and mediated by Raman-active vibrations and close chain coupling. Extending this study, we analyse additional materials in this family with the highest $\Phi \cdot \mu$ values reported for conjugated polymers. We find that increasing the energy gap leads to an increase in $\Phi$, and secondary emission pathways via weakly luminescent inter-chain charge transfer species. By solving the rate equations for exciton recombination, we use the radiative rate of inter-chain luminescence as a probe to show strong wavefunction mixing at close-contact points for some polymers, and suggest this as the origin for a superior $\mu$ in dithiopheneindenofluorene-$\textit{alt}$-benzothiadiazole compared to indacenodithiophene-$\textit{alt}$-benzothiadiazole. We demonstrate how low $\mu$ can be decoupled from the energy gap ($E_g$), and propose backbone elongation leading to increased inter-chain wavefunction overlap and a higher $E_g$ as a design rule to increase $\Phi$ and $\mu$ together. Finally, we assess the role of low-frequency vibrations in organic semiconductors displaying thermally activated delayed fluorescence (TADF). In the low-aggregation limit where $\Phi$ is maximised, we show that non-radiative triplet recombination is strongly related to low frequency torsional motion, and both are reduced in the presence of a rigid polymer host matrix for various TADF materials across different classes. However, we also explore the importance of rotational freedom in determining the oscillator strength, exchange energy, and spin-orbit coupling matrix elements which mediate luminescence in the absence of a rigid host. We demonstrate that suppressing dynamic motion is a powerful tool to modulate the photophysical properties of these emitters, and can lead to improved $\Phi$ particularly for low $E_g$ emitters.

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Books on the topic "Polymer luminescence"

1

A, Winnik Mitchell, and North Atlantic Treaty Organization. Scientific Affairs Division., eds. Photophysical and photochemical tools in polymer science: Conformation, dynamics, morphology. D. Reidel Pub. Co., 1986.

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Barashkov, N. N. Fluorescent polymers. Ellis Horwood, 1994.

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A, Gunder O., ed. Fluorescent polymers. Ellis Horwood, 1993.

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D, Phillips, ed. Polymer photophysics: Luminescence, energy migration, and molecular motion in synthetic polymers. Chapman and Hall, 1985.

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L, Zlatkevich, ed. Luminescence techniques in solid-state polymer research. M. Dekker, 1989.

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Egan, Luke Solis. Luminescence studies of fluorescently labelled polymer colloid particles. 1987.

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Fleming, Robert John. Studies of the electrical luminescent and configurational properties of some common polymers. 1985.

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Musfeldt, Janice Lynn. Infrared, optical, and luminescent properties of quasi-one-dimensional organic charge transfer salts and polymers. 1992.

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Book chapters on the topic "Polymer luminescence"

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Soutar, Ian. "Applications of Luminescence Spectroscopy in Polymer Science." In Multidimensional Spectroscopy of Polymers. American Chemical Society, 1995. http://dx.doi.org/10.1021/bk-1995-0598.ch020.

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Lu, X., I. Manners, and M. A. Winnik. "Oxygen Diffusion in Polymer Films for Luminescence Barometry Applications." In New Trends in Fluorescence Spectroscopy. Springer Berlin Heidelberg, 2001. http://dx.doi.org/10.1007/978-3-642-56853-4_12.

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Pyshkin, Sergei L., and John Ballato. "Dramatic Expansion of Luminescence Region in GaP/Polymer Nanocomposites." In Supplemental Proceedings. John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118356074.ch46.

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Winnik, Mitchell A. "Luminescence Techniques to Study the Morphology of Prototype Industrial Materials." In Photophysical and Photochemical Tools in Polymer Science. Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4726-9_27.

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Verlan, V. I., M. S. Iovu, I. Culeac, O. Bordian, V. E. Zubareva, and Iu Nistor. "Effective Transfer of UV Energy to Red Luminescence in the Nanocomposites Polymer/Eu Coordination Compounds." In 3rd International Conference on Nanotechnologies and Biomedical Engineering. Springer Singapore, 2016. http://dx.doi.org/10.1007/978-981-287-736-9_4.

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Gooch, Jan W. "Luminescence." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_14146.

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Zlatkevich, Lev. "Luminescence." In Polymers Properties and Applications. Springer New York, 1987. http://dx.doi.org/10.1007/978-1-4613-8695-7_1.

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Montilla, Francisco, and Francisco Huerta. "Electrochemically Monitored Photoluminescence of Conjugated Polymers." In Luminescence in Electrochemistry. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-49137-0_4.

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Seo, Seogjae, and Eunkyoung Kim. "Electrofluorochromic Devices with Organic Dyes and Conjugated Polymers." In Luminescence in Electrochemistry. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-49137-0_5.

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Gooch, Jan W. "Luminescent." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_7064.

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Conference papers on the topic "Polymer luminescence"

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Wesely, E. J., A. P. Marchetti, Y. H. Geng, S. H. Chen, and L. J. Rothberg. "Implications of delayed luminescence for conjugated polymer photophysics." In Laser Science. OSA, 2008. http://dx.doi.org/10.1364/ls.2008.lwf3.

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Du, B. X., L. Gu, and Yong Liu. "Luminescence in tracking test of polymer insulating materials." In 2008 International Symposium on Electrical Insulating Materials (ISEIM). IEEE, 2008. http://dx.doi.org/10.1109/iseim.2008.4664600.

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Hsu, Jui-Hung, Wunshain S. Fann, Kuen-Ru Chuang, and Shaw-An Chen. "Aggregated luminescence from light-emitting polymer in dilute solution." In Optical Science, Engineering and Instrumentation '97, edited by Z. Valy Vardeny and Lewis J. Rothberg. SPIE, 1997. http://dx.doi.org/10.1117/12.279293.

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Fanghui, Zhang, Yang Dan, and Wang Xiufeng. "Luminescence mechanism of polymer light-emitting devices with MEH-PPV." In the 2008 International Conference. ACM Press, 2008. http://dx.doi.org/10.1145/1509315.1509336.

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Tu, Li-Wei, K. H. Lee, Chih-Ming Lai, S. J. Bai, and C. C. Wu. "Luminescence of thin films of conjugated rigid-rod polymer PBT." In Symposium on Integrated Optics, edited by H. Walter Yao and E. F. Schubert. SPIE, 2001. http://dx.doi.org/10.1117/12.426849.

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Moses, J. Daniel. "High-quantum-efficiency luminescence from a conducting polymer in solution: a novel polymer laser dye." In OE/LASE'93: Optics, Electro-Optics, & Laser Applications in Science& Engineering, edited by Shahab Etemad. SPIE, 1993. http://dx.doi.org/10.1117/12.148448.

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Panin, G. N., A. N. Baranov, and T. W. Kang. "Electric field-induced color switching of luminescence from ZnO nanoparticle/polymer." In SPIE Proceedings, edited by Igor A. Sukhoivanov, Vasily A. Svich, and Yuriy S. Shmaliy. SPIE, 2008. http://dx.doi.org/10.1117/12.793473.

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Röder, B., E. A. Ermilov, D. Philipp, and M. Köhl. "Observation of polymer degradation processes in photovoltaic modules via luminescence detection." In Solar Energy + Applications, edited by Neelkanth G. Dhere. SPIE, 2008. http://dx.doi.org/10.1117/12.793795.

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Pidenko, S. A., S. D. Bondarenko, A. A. Chibrova, et al. "Quantum dots luminescence in the photonic cristal fibers modified with polymer layers." In 2016 International Conference Laser Optics (LO). IEEE, 2016. http://dx.doi.org/10.1109/lo.2016.7549916.

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Bjorknas, Kristina, Peter Raynes, Sandra Gilmour, Victor Christou, and Kai Look. "Circularly polarized luminescence from an organoterbium emitter embedded in a chiral polymer." In International Symposium on Optical Science and Technology, edited by Akhlesh Lakhtakia, Graeme Dewar, and Martin W. McCall. SPIE, 2002. http://dx.doi.org/10.1117/12.472990.

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Reports on the topic "Polymer luminescence"

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Wei, Kung-Hwa. Surface-Modified Quantum Dots Enhanced Luminescence Polymer Nanocomposites Light Emitting Diode. Defense Technical Information Center, 2006. http://dx.doi.org/10.21236/ada473117.

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Pang, Yi, and Frank E. Karasz. Tailor Pi-Conjugated Polymers for Enhanced Luminescence Efficiency. Defense Technical Information Center, 2003. http://dx.doi.org/10.21236/ada417976.

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Wasielewski, Michael R. SENSORS USING MOLECULAR RECOGNITION IN LUMINESCENT, CONDUCTIVE POLYMERS. Office of Scientific and Technical Information (OSTI), 1999. http://dx.doi.org/10.2172/828084.

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Wasielewski, M. R., K. Raymond, and D. E. Walt. Ion and molecule sensors using molecular recognition in luminescent, conductive polymers. 1998 annual progress report. Office of Scientific and Technical Information (OSTI), 1998. http://dx.doi.org/10.2172/13447.

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Wasielewski, M. R. Ion and molecule sensors using molecular recognition in luminescent, conductive polymers. FY 1997 year-end progress report. Office of Scientific and Technical Information (OSTI), 1997. http://dx.doi.org/10.2172/13446.

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