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Sökning: L773:0935 9648 OR L773:1521 4095

  • Resultat 51-60 av 377
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51.
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52.
  • Chen, Shangshang, et al. (författare)
  • Efficient Nonfullerene Organic Solar Cells with Small Driving Forces for Both Hole and Electron Transfer
  • 2018
  • Ingår i: Advanced Materials. - : WILEY-V C H VERLAG GMBH. - 0935-9648 .- 1521-4095. ; 30:45
  • Tidskriftsartikel (refereegranskat)abstract
    • State-of-the-art organic solar cells (OSCs) typically suffer from large voltage loss (V-loss) compared to their inorganic and perovskite counterparts. There are some successful attempts to reduce the V-loss by decreasing the energy offsets between the donor and acceptor materials, and the OSC community has demonstrated efficient systems with either small highest occupied molecular orbital (HOMO) offset or negligible lowest unoccupied molecular orbital (LUMO) offset between donors and acceptors. However, efficient OSCs based on a donor/acceptor system with both small HOMO and LUMO offsets have not been demonstrated simultaneously. In this work, an efficient nonfullerene OSC is reported based on a donor polymer named PffBT2T-TT and a small-molecular acceptor (O-IDTBR), which have identical bandgaps and close energy levels. The Fourier-transform photocurrent spectroscopy external quantum efficiency (FTPS-EQE) spectrum of the blend overlaps with those of neat PffBT2T-TT and O-IDTBR, indicating the small driving forces for both hole and electron transfer. Meanwhile, the OSCs exhibit a high electroluminescence quantum efficiency (EQE(EL)) of approximate to 1 x 10(-4), which leads to a significantly minimized nonradiative V-loss of 0.24 V. Despite the small driving forces and a low V-loss, a maximum EQE of 67% and a high power conversion efficiency of 10.4% can still be achieved.
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53.
  • Chen, Song, et al. (författare)
  • Formation of Amorphous Iron-Calcium Phosphate with High Stability
  • 2023
  • Ingår i: Advanced Materials. - : John Wiley & Sons. - 0935-9648 .- 1521-4095. ; 35:33
  • Tidskriftsartikel (refereegranskat)abstract
    • Amorphous iron-calcium phosphate (Fe-ACP) plays a vital role in the mechanical properties of teeth of some rodents, which are very hard, but its formation process and synthetic route remain unknown. Here, the synthesis and characterization of an iron-bearing amorphous calcium phosphate in the presence of ammonium iron citrate (AIC) are reported. The iron is distributed homogeneously on the nanometer scale in the resulting particles. The prepared Fe-ACP particles can be highly stable in aqueous media, including water, simulated body fluid, and acetate buffer solution (pH 4). In vitro study demonstrates that these particles have good biocompatibility and osteogenic properties. Subsequently, Spark Plasma Sintering (SPS) is utilized to consolidate the initial Fe-ACP powders. The results show that the hardness of the ceramics increases with the increase of iron content, but an excess of iron leads to a rapid decline in hardness. Calcium iron phosphate ceramics with a hardness of 4 GPa can be achieved, which is higher than that of human enamel. Furthermore, the ceramics composed of iron-calcium phosphates show enhanced acid resistance. This study provides a novel route to prepare Fe-ACP, and presents the potential role of Fe-ACP in biomineralization and as starting material to fabricate acid-resistant high-performance bioceramics.
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54.
  • Chen, Shangzhi, et al. (författare)
  • Tunable Structural Color Images by UV-Patterned Conducting Polymer Nanofilms on Metal Surfaces.
  • 2021
  • Ingår i: Advanced Materials. - : Wiley. - 0935-9648 .- 1521-4095. ; 33:33
  • Tidskriftsartikel (refereegranskat)abstract
    • Precise manipulation of light-matter interactions has enabled a wide variety of approaches to create bright and vivid structural colors. Techniques utilizing photonic crystals, Fabry-Pérot cavities, plasmonics, or high-refractive-index dielectric metasurfaces have been studied for applications ranging from optical coatings to reflective displays. However, complicated fabrication procedures for sub-wavelength nanostructures, limited active areas, and inherent absence of tunability of these approaches impede their further development toward flexible, large-scale, and switchable devices compatible with facile and cost-effective production. Here, a novel method is presented to generate structural color images based on monochromic conducting polymer films prepared on metallic surfaces via vapor phase polymerization and ultraviolet (UV) light patterning. Varying the UV dose enables synergistic control of both nanoscale film thickness and polymer permittivity, which generates controllable structural colors from violet to red. Together with grayscale photomasks this enables facile fabrication of high-resolution structural color images. Dynamic tuning of colored surfaces and images via electrochemical modulation of the polymer redox state is further demonstrated. The simple structure, facile fabrication, wide color gamut, and dynamic color tuning make this concept competitive for applications like multifunctional displays.
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55.
  • Christian Roelofs, W. S., et al. (författare)
  • Fundamental Limitations for Electroluminescence in Organic Dual-Gate Field-Effect Transistors
  • 2014
  • Ingår i: Advanced Materials. - : Wiley-VCH Verlag. - 0935-9648 .- 1521-4095. ; 26:26, s. 4450-
  • Tidskriftsartikel (refereegranskat)abstract
    • A dual-gate organic field-effect transistor is investigated for electrically pumped lasing. The two gates can independently accumulate electrons and holes, yielding current densities exceeding the lasing threshold. Here, the aim is to force the electrons and holes to recombine by confining the charges in a single semiconducting film. It is found that independent hole and electron accumulation is mutually exclusive with vertical recombination and light emission.
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56.
  • Cohen, Adi, et al. (författare)
  • Diverging Expressions of Anharmonicity in Halide Perovskites
  • 2022
  • Ingår i: Advanced Materials. - : Wiley-V C H Verlag GMBH. - 0935-9648 .- 1521-4095. ; 34:14
  • Tidskriftsartikel (refereegranskat)abstract
    • Lead-based halide perovskite crystals are shown to have strongly anharmonic structural dynamics. This behavior is important because it may be the origin of their exceptional photovoltaic properties. The double perovskite, Cs2AgBiBr6, has been recently studied as a lead-free alternative for optoelectronic applications. However, it does not exhibit the excellent photovoltaic activity of the lead-based halide perovskites. Therefore, to explore the correlation between the anharmonic structural dynamics and optoelectronic properties in lead-based halide perovskites, the structural dynamics of Cs2AgBiBr6 are investigated and are compared to its lead-based analog, CsPbBr3. Using temperature-dependent Raman measurements, it is found that both materials are indeed strongly anharmonic. Nonetheless, the expression of their anharmonic behavior is markedly different. Cs2AgBiBr6 has well-defined normal modes throughout the measured temperature range, while CsPbBr3 exhibits a complete breakdown of the normal-mode picture above 200 K. It is suggested that the breakdown of the normal-mode picture implies that the average crystal structure may not be a proper starting point to understand the electronic properties of the crystal. In addition to our main findings, an unreported phase of Cs2AgBiBr6 is also discovered below approximate to 37 K.
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57.
  • Colodrero, Silvia, et al. (författare)
  • Porous One-Dimensional Photonic Crystals Improve the Power-Conversion Efficiency of Dye-Sensitized Solar Cells
  • 2009
  • Ingår i: Advanced Materials. - : Wiley. - 0935-9648 .- 1521-4095. ; 21:7, s. 764-
  • Tidskriftsartikel (refereegranskat)abstract
    • The solar-to-electric power-conversion efficiency (71) of dye-sensitized solar cells can be greatly enhanced by integrating a mesoporous, nanoparticle-based, 1D photonic crystal as a coherent scattering layer in the device. The photogenerated current is greatly improved without altering the open-circuit voltage of the cell, while keeping the transparency of the cell intact. Improved average 77 values between 15% and 30% are attained.
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58.
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59.
  • Cucchi, Matteo, et al. (författare)
  • In Liquido Computation with Electrochemical Transistors and Mixed Conductors for Intelligent Bioelectronics
  • 2023
  • Ingår i: Advanced Materials. - : WILEY-V C H VERLAG GMBH. - 0935-9648 .- 1521-4095. ; 35:15
  • Tidskriftsartikel (refereegranskat)abstract
    • Next-generation implantable computational devices require long-term-stable electronic components capable of operating in, and interacting with, electrolytic surroundings without being damaged. Organic electrochemical transistors (OECTs) emerged as fitting candidates. However, while single devices feature impressive figures of merit, integrated circuits (ICs) immersed in common electrolytes are hard to realize using electrochemical transistors, and there is no clear path forward for optimal top-down circuit design and high-density integration. The simple observation that two OECTs immersed in the same electrolytic medium will inevitably interact hampers their implementation in complex circuitry. The electrolytes ionic conductivity connects all the devices in the liquid, producing unwanted and often unforeseeable dynamics. Minimizing or harnessing this crosstalk has been the focus of very recent studies. Herein, the main challenges, trends, and opportunities for realizing OECT-based circuitry in a liquid environment that could circumnavigate the hard limits of engineering and human physiology, are discussed. The most successful approaches in autonomous bioelectronics and information processing are analyzed. Elaborating on the strategies to circumvent and harness device crosstalk proves that platforms capable of complex computation and even machine learning (ML) can be realized in liquido using mixed ionic-electronic conductors (OMIECs).
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60.
  • Cui, Yong, et al. (författare)
  • Efficient Semitransparent Organic Solar Cells with Tunable Color enabled by an Ultralow-Bandgap Nonfullerene Acceptor
  • 2017
  • Ingår i: Advanced Materials. - : WILEY-V C H VERLAG GMBH. - 0935-9648 .- 1521-4095. ; 29:43
  • Tidskriftsartikel (refereegranskat)abstract
    • Semitransparent organic solar cells (OSCs) show attractive potential in power-generating windows. However, the development of semitransparent OSCs is lagging behind opaque OSCs. Here, an ultralow-bandgap non-fullerene acceptor, "IEICO-4Cl", is designed and synthesized, whose absorption spectrum is mainly located in the near-infrared region. When IEICO-4Cl is blended with different polymer donors (J52, PBDB-T, and PTB7-Th), the colors of the blend films can be tuned from purple to blue to cyan, respectively. Traditional OSCs with a nontransparent Al electrode fabricated by J52: IEICO-4Cl, PBDB-T: IEICO-4Cl, and PTB7-Th: IEICO-4Cl yield power conversion efficiencies (PCE) of 9.65 +/- 0.33%, 9.43 +/- 0.13%, and 10.0 +/- 0.2%, respectively. By using 15 nm Au as the electrode, semitransparent OSCs based on these three blends also show PCEs of 6.37%, 6.24%, and 6.97% with high average visible transmittance (AVT) of 35.1%, 35.7%, and 33.5%, respectively. Furthermore, via changing the thickness of Au in the OSCs, the relationship between the transmittance and efficiency is studied in detail, and an impressive PCE of 8.38% with an AVT of 25.7% is obtained, which is an outstanding value in the semitransparent OSCs.
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