Publications by authors named "Deirdre O'Carroll"

Several recent studies of carbon dots (CDs) synthesized by bottom-up methods under mild conditions have reported the presence of organic molecular fluorophores in CD dispersions. These fluorophores have a tendency to aggregate, and their properties strongly depend on whether they are present in the form of discrete molecules or aggregates. The aggregation becomes more prominent in the solid state, which motivates the study of the properties of the fluorophores associated with CDs in the solid state.

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Organometallic phosphors are an important class of emissive materials used in high-efficiency organic light-emitting devices. However, problems of low photostability arise for blue-emitting phosphors due to chemical and environmental degradation and triplet quenching processes. Various approaches have been developed to improve the photostability of such phosphors, including the design of new organometallic molecules and control of host-dopant composition in thin films.

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Self-assembled monolayers (SAMs) formed from thiol compounds bound to Ag and Au electrodes have been used as an important strategy in improving the stability and efficiency of optoelectronic devices. Thiol compounds provide only one binding site with the metal electrode which limits their influence. Dithiolane/dithiol compounds can provide multiple binding sites and could be useful in enhancing the performance of the device.

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The abilities of scanning electron microscopy (SEM) and focused ion beam (FIB) milling for obtaining high-resolution images from top surfaces, cross-sectional surfaces, and even in three dimensions, are becoming increasingly important for imaging and analyzing tooth structures such as enamel and dentin. FIB was originally developed for material research in the semiconductor industry. However, use of SEM/FIB has been growing recently in dental research due to the versatility of dual platform instruments that can be used as a milling device to obtain low-artifact cross-sections of samples combined with high-resolution images.

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Magnesium silicate is an inorganic compound used as an ingredient in product formulations for many different purposes. Since its compatibility with other components is critical for product quality and stability, it is essential to characterize the integrity of magnesium silicate in different solutions used for formulations. In this paper, we have determined the magnitude of dissociation of synthetic magnesium silicate in solution with positively charged, neutral, and negatively charged compounds using Scanning Electron Microscopy (SEM), Energy Dispersive X-ray Spectroscopy (EDS), and Liquid Chromatography-High Resolution Mass Spectrometry (LC-HRMS).

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Photon recycling (PR) plays an important role in the study of semiconductor materials and impacts the properties of their optoelectronic applications. However, PR has not been investigated comprehensively and it has not been demonstrated experimentally in many different kinds of semiconductor materials and devices. In this review paper, first, the authors introduce the background of PR and describe how this phenomenon was originally identified in semiconductors.

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The recent pandemic of the novel coronavirus disease 2019 (COVID-19) has caused huge worldwide disruption due to the lack of available testing locations and equipment. The use of optical techniques for viral detection has flourished in the past 15 years, providing more reliable, inexpensive, and accurate detection methods. In the current minireview, optical phenomena including fluorescence, surface plasmons, surface-enhanced Raman scattering (SERS), and colorimetry are discussed in the context of detecting virus pathogens.

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Carbon dots (CDs) are fluorescent nanoparticles that exhibit strong photoluminescence (PL) emission throughout the visible range of the electromagnetic spectrum. Recent studies highlight the presence of fluorescent impurities in CD dispersions. Here, the long-term impact of these impurities on the stability of the physical and optical properties of CDs synthesized by the solvothermal method is studied.

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Strong plasmon-exciton coupling between tightly-bound excitons in organic molecular semiconductors and surface plasmons in metal nanostructures has been studied extensively for a number of technical applications, including low-threshold lasing and room-temperature Bose-Einstein condensates. Typically, excitons with narrow resonances, such as -aggregates, are employed to achieve strong plasmon-exciton coupling. However, -aggregates have limited applications for optoelectronic devices compared with organic conjugated polymers.

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Metal electrodes are playing an increasingly important role in controlling photon absorption and in promoting optimal light management in thin-film semiconductor devices. For organic optoelectronic devices, the conventional fabrication approach is to build the device on top of a transparent electrode, with metal electrode deposition as the last step. This makes it challenging to control the surface of the metal electrode to promote good light management properties.

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Doped polymer thin films have several applications in electronic, optoelectronic and thermoelectric devices. Often the electrical properties of doped conjugated polymer thin films are affected by their local physical and mechanical characteristics. However, investigations into the effects of doping on local domain properties have not been carried out.

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Inorganic semiconductor materials are best known for their superior physical properties, as well as their structural rigidity and stability. However, the poor solubility and solution-processability of these covalently bonded network structures has long been a serious drawback that limits their use in many important applications. Here, we present a unique and general approach to synthesize robust, solution-processable, and highly luminescent hybrid materials built on periodic and infinite inorganic modules.

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Developing rare-earth element (REE) free yellow phosphors that can be excited by 455 nm blue light will help to decrease the environmental impact of manufacturing energy efficient white light-emitting diodes (WLEDs), decrease their cost of production, and accelerate their adoption across the globe. Luminescent metal-organic frameworks (LMOFs) demonstrate strong potential for use as phosphor materials and have been investigated intensively in recent years. However, the majority are not suitable for the current WLED technology due to their lack of blue excitability.

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Tunable plasmonic structure at the nanometer scale presents enormous opportunities for various photonic devices. In this work, we present a hybrid plasmonic thin film platform: , a vertically aligned Au nanopillar array grown inside a TiN matrix with controllable Au pillar density. Compared to single phase plasmonic materials, the presented tunable hybrid nanostructures attain optical flexibility including gradual tuning and anisotropic behavior of the complex dielectric function, resonant peak shifting and change of surface plasmon resonances (SPRs) in the UV-visible range, all confirmed by numerical simulations.

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The optical properties of metal-film-coupled nanoparticles (NPs) are highly sensitive to physical and optical interactions between the NPs and the spacer medium in the gap between the NP and metal film. Here, we investigate the physical and optical interactions between gold NPs (AuNPs) and semiconducting conjugated polymer thin-film spacers in a "sphere-on-plane" type metal-film-coupled NP system, and their influence on the plasmonic scattering of individual AuNPs. We choose two different conjugated polymers: one with an absorption spectrum that is resonant with the plasmonic modes of the AuNPs and another that is non-resonant.

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Extensive research has been pursued to develop low-cost and high-performance functional inorganic-organic hybrid materials for clean/renewable energy related applications. While great progress has been made in the recent years, some key challenges remain to be tackled. One major issue is the generally poor stability of these materials, which originates from relatively fragile/weak bonds between inorganic and organic constituents.

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Hybrid organic-inorganic heterostructures are attracting tremendous attention for optoelectronic applications due to their low-cost processing and high performance in devices. In particular, van der Waals p-n heterojunctions formed between inorganic two-dimensional (2D) materials and organic semiconductors are of interest due to the quantum confinement effects of 2D materials and the synthetic control of the physical properties of organic semiconductors, enabling a high degree of tunable optoelectronic properties for the heterostructure. However, for photovoltaic applications, hybrid 2D-organic heterojunctions have demonstrated low power conversion efficiencies due to the limited absorption from constraints on the physical thickness of each layer.

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Integration of organic/inorganic hybrid perovskites with metallic or semiconducting phases of 2D MoS nanosheets via solution processing is demonstrated. The results show that the collection of charge carriers is strongly dependent on the electronic properties of the 2D MoS with metallic MoS showing high responsivity and the semiconducting phase exhibiting high on/off ratios.

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Interactions between absorbers and plasmonic metasurfaces can give rise to unique optical properties not present for either of the individual materials and can influence the performance of a host of optical sensing and thin-film optoelectronic applications. Here we identify three distinct mode types of absorber-coated plasmonic metasurfaces: localized and propagating surface plasmons and a previously unidentified optical mode type called absorption-induced scattering. The extinction of the latter mode type can be tuned by controlling the morphology of the absorber coating and the spectral overlap of the absorber with the plasmonic modes.

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We present an experimental and theoretical study of the electromagnetic interaction between a single gold nanoparticle and a thin gold substrate separated by a sub-50 nm-thick optically absorptive polythiophene spacer layer. Single-particle dark-field scattering spectra show distinct resonance features assigned to four different modes: a horizontal image dipole coupling mode, a vertical image dipole coupling mode and horizontal and vertical coupling modes between localized surface plasmon resonances (LSPRs) and surface plasmon polaritons (SPPs). Relatively broadband spectral tuning of the modes can be achieved by modification of the thickness of either the absorptive spacer or the underlying metal film.

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Optical detection of volatile electron deficient analytes via fluorescence quenching is demonstrated using ca. 200 nm diameter template-synthesized polyfluorene nanofibers as nanoscale detection elements. Observed trends in analyte quenching effectiveness suggest that, in addition to energetic factors, analyte vapor pressure and polymer/analyte solubility play an important role in the emission quenching process.

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The light outcoupling efficiency of organic light-emitting optoelectronic devices is severely limited by excitation of tightly bound surface plasmon polaritons at the metal electrodes. We present a theoretical study of an organic semiconductor-silver-SiO(2) waveguide and demonstrate that by simple tuning of metal film thickness and the emission regime of the organic semiconductor, a significant fraction of surface plasmon polariton mode amplitude is leaked into the active semiconductor layer, thereby decreasing the amount of optical energy trapped by the metal. At visible wavelengths, mode leakage increases by factors of up to 3.

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