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Subject: Hybrid materials × WGL Institute: IPHT ×

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Now showing 1 - 5 of 5
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    Hybrid Optical Fibers – An Innovative Platform for In‐Fiber Photonic Devices
    (Weinheim : Wiley-VCH, 2015) Alexander Schmidt, Markus; Argyros, Alexander; Sorin, Fabien
    The field of hybrid optical fibers is one of the most active research areas in current fiber optics and has the vision of integrating sophisticated materials inside fibers, which are not traditionally used in fiber optics. Novel in-fiber devices with unique properties have been developed, opening up new directions for fiber optics in fields of critical interest in modern research, such as biophotonics, environmental science, optoelectronics, metamaterials, remote sensing, medicine, or quantum optics. Here the recent progress in the field of hybrid optical fibers is reviewed from an application perspective, focusing on fiber-integrated devices enabled by including novel materials inside polymer and glass fibers. The topics discussed range from nanowire-based plasmonics and hyperlenses, to integrated semiconductor devices such as optoelectronic detectors, and intense light generation unlocked by highly nonlinear hybrid waveguides.
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    Characterizing photocatalysts for water splitting: from atoms to bulk and from slow to ultrafast processes
    (London : Royal Society of Chemistry (RSC), 2021) Kranz, Christine; Wächtler, Maria
    Research on light-driven catalysis has gained tremendous importance due to the ever-increasing power consumption and the threatening situation of global warming related to burning fossil fuels. Significant efforts have been dedicated to artificial photosynthesis mimicking nature to split H2O into H2 and O2 by solar energy. Novel semiconductor und molecular photocatalysts focusing on one-step excitation processes via single component photocatalysts or via two-step excitation processes mimicking the Z-scheme of natural photosynthesis are currently developed. Analytical and physicochemical methods, which provide information at different time and length scales, are used to gain fundamental understanding of all processes leading to catalytic activity, i.e., light absorption, charge separation, transfer of charges to the reaction centres and catalytic turnover, but also understanding degradation processes of the photocatalytic active material. Especially, molecular photocatalysts still suffer from limited long-Term stability due to the formation of reactive intermediates, which may lead to degradation. Although there is an overwhelming number of research articles and reviews focussing on various materials for photocatalytic water splitting, to date only few reviews have been published providing a comprehensive overview on methods for characterizing such materials. This review will highlight spectroscopic, spectroelectrochemical, and electrochemical approaches in respect to their potential in studying processes in semiconductor and (supra)molecular photocatalysts. Special emphasis will be on spectroscopic methods to investigate light-induced processes in intermediates of sequential electron transfer chains. Further, microscopic characterization methods, which are predominantly used for semiconducting and hybrid photocatalytic materials will be reviewed as surface area, structure, facets, defects, and bulk properties such as crystallinity and crystal size are key parameters for charge separation, transfer processes and suppression of charge recombination. Recent developments in scanning probe microscopy will also be highlighted as such techniques are highly suited for studying photocatalytic active material. © The Royal Society of Chemistry.
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    Preparation of Core-Shell Hybrid Materials by Producing a Protein Corona Around Magnetic Nanoparticles
    (New York, NY [u.a.] : Springer, 2015) Weidner, A.; Gräfe, C.; von der Lühe, M.; Remmer, H.; Clement, J.H.; Eberbeck, D.; Ludwig, F.; Müller, R.; Schacher, F.H.; Dutz, S.
    Nanoparticles experience increasing interest for a variety of medical and pharmaceutical applications. When exposing nanomaterials, e.g., magnetic iron oxide nanoparticles (MNP), to human blood, a protein corona consisting of various components is formed immediately. The composition of the corona as well as its amount bound to the particle surface is dependent on different factors, e.g., particle size and surface charge. The actual composition of the formed protein corona might be of major importance for cellular uptake of magnetic nanoparticles. The aim of the present study was to analyze the formation of the protein corona during in vitro serum incubation in dependency of incubation time and temperature. For this, MNP with different shells were incubated in fetal calf serum (FCS, serving as protein source) within a water bath for a defined time and at a defined temperature. Before and after incubation the particles were characterized by a variety of methods. It was found that immediately (seconds) after contact of MNP and FCS, a protein corona is formed on the surface of MNP. This formation led to an increase of particle size and a slight agglomeration of the particles, which was relatively constant during the first minutes of incubation. A longer incubation (from hours to days) resulted in a stronger agglomeration of the FCS incubated MNP. Quantitative analysis (gel electrophoresis) of serum-incubated particles revealed a relatively constant amount of bound proteins during the first minutes of serum incubation. After a longer incubation (>20 min), a considerably higher amount of surface proteins was determined for incubation temperatures below 40 °C. For incubation temperatures above 50 °C, the influence of time was less significant which might be attributed to denaturation of proteins during incubation. Overall, analysis of the molecular weight distribution of proteins found in the corona revealed a clear influence of incubation time and temperature on corona composition.
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    Controlling optical trapping of metal–dielectric hybrid nanoparticles under ultrafast pulsed excitation: a theoretical investigation
    (Cambridge : Royal Society of Chemistry, 2021) Devi, Anita; Nair, Shruthi S.; Yadav, Sumit; De, Arijit K.
    Crucial to effective optical trapping is the ability to precisely control the nature of force/potential to be attractive or repulsive. The nature of particles being trapped is as important as the role of laser parameters in determining the stability of the optical trap. In this context, hybrid particles comprising of both dielectric and metallic materials offer a wide range of new possibilities due to their tunable optical properties. On the other hand, femtosecond pulsed excitation is shown to provide additional advantages in tuning of trap stiffness through harnessing optical and thermal nonlinearity. Here we demonstrate that (metal/dielectric hybrid) core/shell type and hollow-core type nanoparticles experience more force than conventional core-type nanoparticles under both continuous-wave and, in particular, ultrafast pulsed excitation. Thus, for the first time, we show how tuning both materials properties as well as the nature of excitation can impart unprecedented control over nanoscale optical trapping and manipulation leading to a wide range of applications.
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    Direct observation of modal hybridization in nanofluidic fiber [Invited]
    (Washington, DC : OSA, 2021) Gomes, André D.; Zhao, Jiangbo Tim; Tuniz, Alessandro; Schmidt, Markus A.
    Hybrid-material optical fibers enhance the capabilities of fiber-optics technologies, extending current functionalities to several emerging application areas. Such platforms rely on the integration of novel materials into the fiber core or cladding, thereby supporting hybrid modes with new characteristics. Here we present experiments that reveal hybrid mode interactions within a doped-core silica fiber containing a central high-index nanofluidic channel. Compared with a standard liquid-filled capillary, calculations predict modes with unique properties emerging as a result of the doped core/cladding interface, possessing a high power fraction inside and outside the nanofluidic channel. Our experiments directly reveal the beating pattern in the fluorescent liquid resulting from the excitation of the first two linearly polarized hybrid modes in this system, being in excellent agreement with theoretical predictions. The efficient excitation and beat of such modes in such an off-resonance situation distinguishes our device from regular directional mode couplers and can benefit applications that demand strong coupling between fundamental- and higher-order- modes, e.g. intermodal third-harmonic generation, bidirectional coupling, and nanofluidic sensing.