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  • Wiley  (3)
  • Chang, Dongdong  (3)
  • Zhao, Yan  (3)
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  • Wiley  (3)
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  • 1
    In: Advanced Functional Materials, Wiley, Vol. 32, No. 33 ( 2022-08)
    Abstract: The molecular packing and resultant charge transport behaviors of semiconducting polymers are widely known to be temperature‐dependent. Due to the limitation of measurement methods, previous studies on molecular packing behavior have been mainly focused on a very limited temperature range, and therefore cannot support the understanding of charge transport behaviors. In this study, with a homemade temperature‐dependent grazing incidence XRD measurement chamber, the relationship between molecular packing structure and charge transport properties of diketopyrrolopyrrole‐based polymers is investigated across a wide temperature range of 98–623 K. Glass transition temperatures of the alkyl side‐chain and aromatic backbone are identified through the observation of clear transitions in the thermal expansion coefficients of d − d packing and π−π stacking, respectively. A correlation between the π−π stacking distance and charge transport properties is then established using an extended Miller−Abrahams model. The turning point of the charge transport and the failure of the polymer‐based devices are proved to be caused by packing structure changes due to increased temperatures. Such an examination over a wide range of temperatures improves the understanding of the charge transport properties of semiconducting polymers and helps construct thermally stable devices to be used in extreme conditions.
    Type of Medium: Online Resource
    ISSN: 1616-301X , 1616-3028
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2022
    detail.hit.zdb_id: 2029061-5
    detail.hit.zdb_id: 2039420-2
    SSG: 11
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  • 2
    In: Small, Wiley, Vol. 18, No. 44 ( 2022-11)
    Abstract: Adjusting the local coordination environment of single‐atom electrocatalysts is a viable way to improve catalytic performance. The diversity of coordination geometric structures is limited to the traditional in‐plane configuration, with only a little consideration paid to out‐of‐plane configurations due to the lack of suitable carriers and fabrication methods. This study reports out‐of‐plane coordination of Co‐based single‐atom catalysts mediated by the conjugated bipyridine‐rich covalent organic framework (COF). The bipyridine nitrogen on the COF layer backbone of these catalysts serves as the linker center for cobalt sites anchoring, while the complementary moieties are coordinated at the other side of the Co metal and reside beyond the COF backbone plane, thus yielding out‐of‐plane coordination. The electrochemical experiments and density functional theory calculations reveal that catalysts with multiple out‐of‐plane coordinations exhibit different electrocatalytic oxygen evolution activities and catalytic pathways. The out‐of‐plane coordination enabled by COFs provides a strategy for designing single‐atom electrocatalysts, expanding the application of COFs in the field of electrocatalysis.
    Type of Medium: Online Resource
    ISSN: 1613-6810 , 1613-6829
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2022
    detail.hit.zdb_id: 2168935-0
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  • 3
    In: Aggregate, Wiley
    Abstract: A series of new π ‐conjugated macrocycles ( AzoM‐n‐ E , n = 1–3) incorporating azobenzene units have been synthesized by a facile strategy in one‐pot reaction. The resultant azobenzene‐embedded macrocycles feature intrinsic photoresponsive behaviors and intriguing supramolecular assembling properties. The smallest macrocycle AzoM‐1‐ E with a rigid planar conjugated backbone structure is used to prepare the single crystal transistors, showing reversible optical tunability. The moderate size macrocycle AzoM‐2‐ E assembles into a dimer in the form of interpenetration through π‐π stacking between azobenzene units. The largest macrocycle AzoM‐3‐ E with enhanced flexibility can adaptively assemble with various types of electron‐deficient guests accompanied by distortion of azobenzene. Typically, AzoM‐3‐ E assembles with the planar F4‐TCNQ to form a tetragonal geometry by C‐F···π and π‐π interactions, while the assembly with ellipsoidal C 70 via π‐π interactions induces AzoM‐3‐ E to form a boat‐shaped geometry. This work will shed new light on the development of functional conjugated macrocycles in organic electronics.
    Type of Medium: Online Resource
    ISSN: 2692-4560 , 2692-4560
    Language: English
    Publisher: Wiley
    Publication Date: 2023
    detail.hit.zdb_id: 3045361-6
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