Mostrando 681 - 700 Resultados de 1,845 Para Buscar 'fulereno~', tiempo de consulta: 3.66s Limitar resultados
  1. 681
    “…It is expected that the same procedure can be applied to other non-fullerene acceptor-based organic solar cells, leading to an even higher efficiency with minimal effect on the environment.…”
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  2. 682
    “…Herein, we fabricated a ROS-scavenging hybrid hydrogel by incorporating mussel-inspired fullerene nanocomposites (C60@PDA) into gelatin methacryloyl (GelMA) hydrogel. …”
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  3. 683
    “…A panchromatic light-absorbing [70]fullerene-perylene-BODIPY triad (C(70)-P-B) was synthesized and applied as a heavy atom-free organic triplet photosensitizer for photooxidation. …”
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  4. 684
    “…As of today, influenza viruses remain a relevant target for the development of antiviral compounds due to their rapid evolution and acquisition of the resistance to existing drugs. Fullerene derivatives have already shown the ability to successfully interact with viruses, and polyhydrated fullerenes (or fullerenols) are particularly attractive due to their compatibility with biological fluids and low toxicity. …”
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  5. 685
  6. 686
  7. 687
    “…Herein, fullerenol (Ful), a highly water-soluble derivative of C(60) fullerene with demonstrated antioxidant activity, is incorporated into calcium phosphate cements (CPCs) to enhance their osteogenic ability. …”
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  8. 688
    “…The theoretical study of the interaction between CH(2) and fullerene (C(60)) suggests the existence of an addition reaction mechanism; this feature is studied by applying an analysis of electronic properties. …”
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  9. 689
    “…As the use of carbon fullerene increases in the chemical industry, the concern over its biological and toxicological effects is also increasing. …”
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  10. 690
    por Pires, Nuno Miguel Matos, Dong, Tao
    Publicado 2013
    “…Waterborne Escherichia coli O157:H7, Campylobacter jejuni and adenovirus were targeted in the PMMA chip, and detection of captured pathogens was conducted by poly(2,7-carbazole)/fullerene OPDs which showed a responsivity over 0.20 A/W at 425 nm. …”
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  11. 691
  12. 692
    “…Fullerenes have attracted considerable attention due to their unique chemical structure and potential applications which has opened wide venues for possible human exposure to various fullerene types. …”
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  13. 693
    “…In this work, by employing a novel bi-level surface modification approach using FCVA, the formation of a high sp(3) bonded ultrathin (~1.7 nm) amorphous carbon overcoat with interspersed graphene/fullerene-like nanostructures, grown on magnetic hard disk media, is reported. …”
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  14. 694
  15. 695
    “…The polymer solar cells obtained by pairing this polymer with a non-fullerene acceptor demonstrated a high power conversion efficiency of 11.41% with both high open circuit voltage of 0.94 V and high short circuit current density of 17.32 mA cm(−2) benefitted from the complementary absorption of the donor and acceptor, and the high hole transfer efficiency from acceptor to donor although the highest occupied molecular orbital level difference between the donor and acceptor is only 0.11 eV. …”
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  16. 696
  17. 697
    “…This data contains additional data related to the article “Influence of Substrate Temperature on the Film Morphology and Photovoltaic Performance of Non-fullerene Organic Solar Cells” (Jicheng Zhang et al., In press) [1]. …”
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  18. 698
    “…In this work, we report the application of periodic density functional theory together with the coupled perturbed Kohn–Sham method to calculate the electronic contribution to the dielectric constant for fullerene C(60) derivatives, a ubiquitous class of molecules in the field of OPVs. …”
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  19. 699
    “…Helical perylene diimide-based (hPDI) acceptors have been established as one of the most promising candidates for non-fullerene organic solar cells (OSCs). In this work, we report a novel hPDI-based molecule, hPDI(2)-CN(2), as an electron acceptor for OSCs. …”
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  20. 700
    “…Co-crystallization of P2 and the fullerene guests C(60) and C(70) afforded the 2 : 1 host–guest complexes (P2)(2) ⊃ C(60) and (P2)(2) ⊃ C(70), in which the two concave surfaces of P2 encapsulate the convex surface of the fullerenes in a sandwich fashion. …”
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