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Sökning: L773:0935 9648 OR L773:1521 4095

  • Resultat 11-20 av 385
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11.
  • Aparicio, Francisco J., et al. (författare)
  • Transparent Nanometric Organic Luminescent Films as UV-Active Components in Photonic Structures
  • 2011
  • Ingår i: Advanced Materials. - : Wiley. - 0935-9648 .- 1521-4095. ; 23:6, s. 761-765
  • Tidskriftsartikel (refereegranskat)abstract
    • A new kind of visible-blind organic thin-film material, consisting of a polymeric matrix with a high concentration of embedded 3-hydroxyflavone (3HF) dye molecules, that absorbs UV light and emits green light is presented. The thin films can be grown on sensitive substrates, including flexible polymers and paper. Their suitability as photonic active components in photonic devices is demonstrated.
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12.
  • Apostolopoulou-Kalkavoura, Varvara, 1988-, et al. (författare)
  • Thermally Insulating Nanocellulose-Based Materials
  • 2021
  • Ingår i: Advanced Materials. - : Wiley. - 0935-9648 .- 1521-4095. ; 33:28
  • Forskningsöversikt (refereegranskat)abstract
    • Thermally insulating materials based on renewable nanomaterials such as nanocellulose could reduce the energy consumption and the environmental impact of the building sector. Recent reports of superinsulating cellulose nanomaterial (CNM)-based aerogels and foams with significantly better heat transport properties than the commercially dominating materials, such as expanded polystyrene, polyurethane foams, and glass wool, have resulted in a rapidly increasing research activity. Herein, the fundamental basis of thermal conductivity of porous materials is described, and the anisotropic heat transfer properties of CNMs and films with aligned CNMs and the processing and structure of novel CNM-based aerogels and foams with low thermal conductivities are presented and discussed. The extraordinarily low thermal conductivity of anisotropic porous architectures and multicomponent approaches are highlighted and related to the contributions of the Knudsen effect and phonon scattering.
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13.
  • Arjmandi-Tash, Hadi, et al. (författare)
  • Zero-Depth Interfacial Nanopore Capillaries
  • 2018
  • Ingår i: Advanced Materials. - : WILEY-V C H VERLAG GMBH. - 0935-9648 .- 1521-4095. ; 30:9
  • Tidskriftsartikel (refereegranskat)abstract
    • High-fidelity analysis of translocating biomolecules through nanopores demands shortening the nanocapillary length to a minimal value. Existing nanopores and capillaries, however, inherit a finite length from the parent membranes. Here, nanocapillaries of zero depth are formed by dissolving two superimposed and crossing metallic nanorods, molded in polymeric slabs. In an electrolyte, the interface shared by the crossing fluidic channels is mathematically of zero thickness and defines the narrowest constriction in the stream of ions through the nanopore device. This novel architecture provides the possibility to design nanopore fluidic channels, particularly with a robust 3D architecture maintaining the ultimate zero thickness geometry independently of the thickness of the fluidic channels. With orders of magnitude reduced biomolecule translocation speed, and lowered electronic and ionic noise compared to nanopores in 2D materials, the findings establish interfacial nanopores as a scalable platform for realizing nanofluidic systems, capable of single-molecule detection.
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14.
  • Arseneault, Mathieu, et al. (författare)
  • The Dawn of Thiol-Yne Triazine Triones Thermosets as a New Material Platform Suited for Hard Tissue Repair
  • 2018
  • Ingår i: Advanced Materials. - : Wiley. - 0935-9648 .- 1521-4095. ; 30:52
  • Tidskriftsartikel (refereegranskat)abstract
    • The identification of a unique set of advanced materials that can bear extraordinary loads for use in bone and tooth repair will inevitably unlock unlimited opportunities for clinical use. Herein, the design of high-performance thermosets is reported based on triazine-trione (TATO) monomers using light-initiated thiol-yne coupling (TYC) chemistry as a polymerization strategy. In comparison to traditional thiol-ene coupling (TEC) systems, TYC chemistry has yielded highly dense networks with unprecedented mechanical properties. The most promising system notes 4.6 GPa in flexural modulus and 160 MPa in flexural strength, an increase of 84% in modulus and 191% in strength when compared to the corresponding TATO system based on TEC chemistry. Remarkably, the mechanical properties exceed those of polylactide (PLA) and challenge poly(ether ether ketone) PEEK and today's methacrylate-based dental resin composites. All the materials display excellent biocompatibility, in vitro, and are successfully: i) molded into medical devices for fracture repair, and ii) used as bone adhesive for fracture fixation and as tooth fillers with the outstanding bond strength that outperform methacrylate systems used today in dental restoration application. Collectively, a new era of advanced TYC materials is unfolded that can fulfill the preconditions as bone fixating implants and for tooth restorations.
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15.
  • Atxabal, Ainhoa, et al. (författare)
  • Energy Level Alignment at Metal/Solution-Processed Organic Semiconductor Interfaces
  • 2017
  • Ingår i: Advanced Materials. - : WILEY-V C H VERLAG GMBH. - 0935-9648 .- 1521-4095. ; 29:19
  • Tidskriftsartikel (refereegranskat)abstract
    • Energy barriers between the metal Fermi energy and the molecular levels of organic semiconductor devoted to charge transport play a fundamental role in the performance of organic electronic devices. Typically, techniques such as electron photoemission spectroscopy, Kelvin probe measurements, and in-device hot-electron spectroscopy have been applied to study these interfacial energy barriers. However, so far there has not been any direct method available for the determination of energy barriers at metal interfaces with n-type polymeric semiconductors. This study measures and compares metal/solution-processed electron-transporting polymer interface energy barriers by in-device hot-electron spectroscopy and ultraviolet photoemission spectroscopy. It not only demonstrates in-device hot-electron spectroscopy as a direct and reliable technique for these studies but also brings it closer to technological applications by working ex situ under ambient conditions. Moreover, this study determines that the contamination layer coming from air exposure does not play any significant role on the energy barrier alignment for charge transport. The theoretical model developed for this work confirms all the experimental observations.
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16.
  • Aziz, Shazed, et al. (författare)
  • Plant-Like Tropisms in Artificial Muscles
  • 2023
  • Ingår i: Advanced Materials. - : WILEY-V C H VERLAG GMBH. - 0935-9648 .- 1521-4095.
  • Tidskriftsartikel (refereegranskat)abstract
    • Helical plants have the ability of tropisms to respond to natural stimuli, and biomimicry of such helical shapes into artificial muscles has been vastly popular. However, the shape-mimicked actuators only respond to artificially provided stimulus, they are not adaptive to variable natural conditions, thus being unsuitable for real-life applications where on-demand, autonomous operations are required. Novel artificial muscles made of hierarchically patterned helically wound yarns that are self-adaptive to environmental humidity and temperature changes are demonstrated here. Unlike shape-mimicked artificial muscles, a unique microstructural biomimicking approach is adopted, where the muscle yarns can effectively replicate the hydrotropism and thermotropism of helical plants to their microfibril level using plant-like microstructural memories. Large strokes, with rapid movement, are obtained when the individual microfilament of yarn is inlaid with hydrogel and further twisted into a coil-shaped hierarchical structure. The developed artificial muscle provides an average actuation speed of approximate to 5.2% s(-1) at expansion and approximate to 3.1% s(-1) at contraction cycles, being the fastest amongst previously demonstrated actuators of similar type. It is demonstrated that these muscle yarns can autonomously close a window in wet climates. The building block yarns are washable without any material degradation, making them suitable for smart, reusable textile and soft robotic devices.
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17.
  • Bao, Chunxiong, et al. (författare)
  • High Performance and Stable All-Inorganic Metal Halide Perovskite-Based Photodetectors for Optical Communication Applications
  • 2018
  • Ingår i: Advanced Materials. - : WILEY-V C H VERLAG GMBH. - 0935-9648 .- 1521-4095. ; 30:38
  • Tidskriftsartikel (refereegranskat)abstract
    • Photodetectors are critical parts of an optical communication system for achieving efficient photoelectronic conversion of signals, and the response speed directly determines the bandwidth of the whole system. Metal halide perovskites, an emerging class of low-cost solution-processed semiconductors, exhibiting strong optical absorption, low trap states, and high carrier mobility, are widely investigated in photodetection applications. Herein, through optimizing the device engineering and film quality, high-performance photodetectors based on all-inorganic cesium lead halide perovskite (CsPbIxBr3-x), which simultaneously possess high sensitivity and fast response, are demonstrated. The optimized devices processed from CsPbIBr2 perovskite show a practically measured detectable limit of about 21.5 pW cm(-2) and a fast response time of 20 ns, which are both among the highest reported device performance of perovskite-based photodetectors. Moreover, the photodetectors exhibit outstanding long-term environmental stability, with negligible degradation of the photoresponse property after 2000 h under ambient conditions. In addition, the resulting perovskite photodetector is successfully integrated into an optical communication system and its applications as an optical signal receiver on transmitting text and audio signals is demonstrated. The results suggest that all-inorganic metal halide perovskite-based photodetectors have great application potential for optical communication.
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18.
  • Bao, Jiming, et al. (författare)
  • Nanowire-induced Wurtzite InAs Thin Film on Zinc-Blende InAs Substrate
  • 2009
  • Ingår i: Advanced Materials. - : Wiley. - 1521-4095 .- 0935-9648. ; 21:36, s. 3654-3654
  • Tidskriftsartikel (refereegranskat)abstract
    • InAs pyramids and platelets on a zinc-blende InAs substrate are found to exhibit a wurtzite crystal structure. induced by wurtzite InAs nanowires, wurtzite InAs thin film and its associated zinc-blende/wurtzite heterocrystalline heterostructures may open up new opportunities in band-gap engineering and related device applications.
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19.
  • Barbero, David, et al. (författare)
  • Carbon nanotube networks : nano-engineering of SWNT networks for enhanced charge transport at ultralow nanotube loading
  • 2014
  • Ingår i: Advanced Materials. - : Wiley-VCH Verlagsgesellschaft. - 0935-9648 .- 1521-4095. ; 26:19, s. 3164-
  • Tidskriftsartikel (refereegranskat)abstract
    • Arrays of nano-engineered carbon nanotube networks embedded in nanoscale polymer structures enable highly efficient charge transport as demonstrated by D. R. Barbero and co-workers on page 3111. An increase in charge transport by several orders of magnitude is recorded at low nanotube loading compared to traditional random networks in either insulating (polystyrene) or semiconducting (polythiophene) polymers. These novel networks are expected to enhance the performance of next generation hybrid and carbon based photovoltaic devices.
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20.
  • Barbero, David, et al. (författare)
  • Nano-engineering of SWNT networks for enhanced charge transport at ultralow nanotube loading
  • 2014
  • Ingår i: Advanced Materials. - : John Wiley & Sons. - 0935-9648 .- 1521-4095. ; 26:19, s. 3111-3117
  • Tidskriftsartikel (refereegranskat)abstract
    • We demonstrate a simple and controllable method to form periodic arrays of highly conductive nano-engineered single wall carbon nanotube networks from solution. These networks increase the conductivity of a polymer composite by as much as eight orders of magnitude compared to a traditional random network. These nano-engineered networks are demonstrated in both polystyrene and polythiophene polymers.
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