Mostrando 1,001 - 1,020 Resultados de 1,845 Para Buscar 'fulereno~', tiempo de consulta: 3.81s Limitar resultados
  1. 1001
    “…To investigate this, an extensive approach based on spectroscopic ellipsometry was conducted on ternary blend (D:A(1):A(2)) thin films, involving a donor [D = chlorinated conjugated polymer (PBDB-T-2Cl)] and two acceptor materials [A(1) = a non-fullerene (ITIC-F) and A(2) = a fullerene (PCBM)]. …”
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  2. 1002
    por Zhu, Xinyao, Zhang, Nan, Wang, Zuobin, Liu, X.
    Publicado 2016
    “…In this study, we presented an investigation of mechanical properties by AFM nanoindentation on human hepatocellular carcinoma cells treated with fullerenol for 24, 48 and 72 h. AFM nanoindentation was routinely applied to investigate the morphology and biomechanical properties of living carcinoma cells, and adhesion phenomena (negative force) were detected in the obtained force-displacement curves. …”
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  3. 1003
    por Zhong, Peng, Ma, Xiaohua, Xi, He
    Publicado 2017
    “…However, the inert charge transfer between conducting polymer and ZnO limits the performance enhancement of this type of hybrid solar cells. In this work, a fullerene derivative named C60 pyrrolidine tris-acid is used to modify the interface of ZnO/poly(3-hexylthiophene) (P3HT). …”
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  4. 1004
  5. 1005
    “…These results support the idea that in these samples, aerobic photodegradation proceeds via superoxide formation by the photogenerated polaron on the fullerene, followed by further chemical reaction. In the absence of air, photodegradation rate is correlated with molecular structure, supporting the mechanism of microstructural degradation via fullerene dimerization. …”
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  6. 1006
    por Ismael, Ali K.
    Publicado 2023
    “…Through comprehensive theoretical investigations involving electronic structure and electric transport, we report 20 molecular switching states that can be statistically recognized employing the endohedral fullerene Li@C(60) complex. We propose a switching technique that counts on the location of the alkali metal that encapsulates inside a fullerene cage. …”
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  7. 1007
  8. 1008
  9. 1009
    “…An introduction of fullerene molecules into the non-fullerene acceptor-based blend may further improve the photovoltaic performance of the resultant ternary PSCs. …”
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  10. 1010
  11. 1011
    “…Here we investigated the thermodynamics of binding of a model EMF (Gd@C(60)) with a protein (lysozyme) that is known to act as a host for the empty fullerene. As a rule, even if the shape of an EMF is exactly the same as that of the related fullerene, the interactions with a protein are significantly different. …”
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  12. 1012
  13. 1013
    “…The impact of fullerene side chain functionalization with thiophene and carbazole groups on the device properties of bulk-heterojunction polymer:fullerene solar cells is discussed through a systematic investigation of material blends consisting of the conjugated polymer poly[(5,6-difluoro-2,1,3-benzothiadiazol-4,7-diyl)-alt-(3,3‴-di(2-octyldodecyl)-2,2′;5′,2″;5″,2‴-quaterthiophen-5,5‴-diyl)] (PffBT4T-2OD) as donor and C(60) or C(70) fulleropyrrolidines as acceptors. …”
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  14. 1014
  15. 1015
    “…A benefit of the combined fibril network morphology and non-fullerene acceptor properties was that a high efficiency of 16.5% (certified as 16.1%) was achieved. …”
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  16. 1016
    “…A supramolecular complex, formed by encapsulation of C(60) fullerene in a molecular container built from two resorcin[4]arene rims zipped together by peptidic arms hydrogen bonded into a cylindrical β-sheet, was studied by X-ray crystallography, solid-state and solution NMR, EPR spectroscopy and differential scanning calorimetry (DSC). …”
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  17. 1017
    “…A new side-chain C(60)-fullerene functionalized thiophene copolymer bearing tributylphosphine-substituted hexylic lateral groups was successfully synthesized by means of a fast and effective post-polymerization reaction on a regioregular ω-alkylbrominated polymeric precursor. …”
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  18. 1018
    “…With the recent development of non-fullerene acceptors, wide attention has been paid to improve miscibility, solubility and nanoscale separation by laborious molecular design processes and by the use of additives. …”
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  19. 1019
    “…Due to the partially reduced π-conjugation of the fullerene cage, multi-functionalized fullerene derivatives exhibit remarkable fluorescent properties compared to pristine fullerenes, which have high potential for application in organic light-emitting diodes (OLEDs). …”
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  20. 1020
    “…The introduction of heteroatoms, such as electropositive silicon atoms, to fullerene cages is a novel functionalization method that remarkably affects the electronic characteristics of fullerenes. …”
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