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Träfflista för sökning "L773:2051 6347 OR L773:2051 6355 srt2:(2020)"

Sökning: L773:2051 6347 OR L773:2051 6355 > (2020)

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1.
  • Almquist, Ben, et al. (författare)
  • Outstanding Reviewers for Materials Horizons in 2019
  • 2020
  • Ingår i: Materials Horizons. - : ROYAL SOC CHEMISTRY. - 2051-6347 .- 2051-6355. ; 7:5, s. 1207-1207
  • Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
    • We would like to take this opportunity to highlight the Outstanding Reviewers for Materials Horizons in 2019, as selected by the editorial team for their significant contribution to the journal.
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2.
  • Dong, Zhiyue, et al. (författare)
  • A cationitrile sequence encodes mild poly(ionic liquid) crosslinking for advanced composite membranes
  • 2020
  • Ingår i: Materials Horizons. - : Royal Society of Chemistry (RSC). - 2051-6347 .- 2051-6355. ; 7:10, s. 2683-2689
  • Tidskriftsartikel (refereegranskat)abstract
    • Polymer crosslinking is crucial for the preparation and consolidation of hierarchical nano- and micro-structures, hybrid interfaces, and collective assemblies. Here, for the first time, we showed that a cation-methylene-nitrile (CMN) functionality sequence encoded within repeating units of poly(ionic liquid)s (PILs) allowed for mild cyclizations of nitriles, processes otherwise requiring high temperatures and harsh catalysts. These new reactions facilitated by the CMN sequence were readily translated into freestanding nanomembranes (similar to 19 nm in thickness) and nanocomposite membranes by treating the PILs with mild ammonia vapor (0.2 bar, 20 degrees C). These materials were observed to be stable in various solvents, at different pH levels, and even in boiling water, exhibiting exceptional mechanical strength and solar-thermal desalination performance. The sequence was easy to synthesize, transferable in copolymers, and applicable to various cations, such as imidazolium, pyridinium, and triazolium. We expect it to provide a molecular code promoting programmable polymer crosslinking and the formation of hybrid structures for sustainable energy and water applications.
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3.
  • Hermerschmidt, Felix, et al. (författare)
  • Finally, inkjet-printed metal halide perovskite LEDs-utilizing seed crystal templating of salty PEDOT:PSS
  • 2020
  • Ingår i: Materials Horizons. - : Royal Society of Chemistry (RSC). - 2051-6347 .- 2051-6355. ; 7:7, s. 1773-1781
  • Tidskriftsartikel (refereegranskat)abstract
    • Solution-processable metal halide perovskites are increasingly implemented in perovskite-based light-emitting diodes (PeLEDs). Especially green PeLEDs based on methylammonium lead bromide (MAPbBr3) composites exhibit impressive optoelectronic properties, while allowing processing by low-cost and upscalable printing methods. In this study, we have investigated the influence of potassium chloride (KCl) blended into the common hole injection material poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS) to boost PeLED device performance. The inclusion of KCl firstly results in a change in morphology of the PEDOT:PSS layer, which then acts as a template during deposition of the perovskite layer. A MAPbBr3:polyethylene glycol (PEG) composite was used, which does not require the deposition of an anti-solvent droplet to induce preferential perovskite crystallization and is therefore suitable for spin coating and scalable inkjet printing processes. PeLEDs utilizing the KCl induced templating effect on a planar PEDOT:PSS/MAPbBr3:PEG architecture show improved performance, predominantly due to improved crystallization. PeLEDs incorporating spin-coated perovskite layers yield a 40-fold increase in luminance (8000 cd m-2) while the turn-on voltage decreases to 2.5 V. KCl-modified PEDOT:PSS contact layers enabled the realization of inkjet-printed PeLEDs with luminance increased by a factor of 20 at a maximum of 4000 cd m-2 and a turn-on voltage of 2.5 V. This work paves the way for inkjet-printed perovskite light-emitting devices for a wide variety of low-cost and customizable applications. This journal is
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4.
  • Jin, Handong, et al. (författare)
  • It's a trap! on the nature of localised states and charge trapping in lead halide perovskites
  • 2020
  • Ingår i: Materials Horizons. - : Royal Society of Chemistry (RSC). - 2051-6347 .- 2051-6355. ; 7:2, s. 397-410
  • Forskningsöversikt (refereegranskat)abstract
    • The recent surge of scientific interest for lead halide perovskite semiconductors and optoelectronic devices has seen a mix of materials science sub-fields converge on the same "magical" crystal structure. However, this has ultimately shaped some ambiguity in the definitions shared between researchers across different research areas. For example, scientists aiming to decipher the nature of localized states within metal halide perovskites sometimes over simplify the problem, using identifers such as "defects" or "states". Herein, we review the topic of charge carrier trapping within lead halide perovskites, overviewing their causes and influences, as well as specifying their potential resolutions. We assess the popular lead triiodide perovskites for case study and examine the origins of both intrinsic and extrinsic defects leading to charge carrier trapping in performant perovskite-based solar cells, and review the state-of-the-art actions being taken to limit their effects and achieve world-record conversion efficiencies. Finally, we also draw brief comparisons to other emerging lead-free systems and highlight promising optical tools and design principles moving forward.
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5.
  • Moreno, Adrian, et al. (författare)
  • Lignin-based smart materials : a roadmap to processing and synthesis for current and future applications
  • 2020
  • Ingår i: Materials Horizons. - : Royal Society of Chemistry (RSC). - 2051-6347 .- 2051-6355. ; 7:9, s. 2237-2257
  • Forskningsöversikt (refereegranskat)abstract
    • Biomass-derived materials are green alternatives to synthetic plastics and other fossil-based materials. Lignin, an aromatic plant polymer, is one of the most appealing renewable material precursors for smart materials capable of responding to different stimuli. Here we review lignin-based smart materials, a research field that has seen a rapid growth during the last five years. We describe the main processing and chemical synthesis routes available for the fabrication of lignin-based smart materials, and focus on their use as sensors, biomedical systems, and shape-programmable materials. In addition to benchmarking their performance to the state of the art fossil counterparts, we identify challenges and future opportunities for the development of lignin-based smart materials towards new high-performance applications.
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