Scopus İndeksli Yayınlar Koleksiyonu

Permanent URI for this collectionhttps://hdl.handle.net/20.500.12573/395

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  • Book Part
    Citation - Scopus: 19
    Polymeric and Small-Molecule Semiconductors for Organic Field-Effect Transistors
    (wiley, 2015-01-16) Usta, Hakan; Facchetti, A. F.
    This chapter reviews the achievements in the development of molecular and polymeric semiconductors for charge transport in thin-film transistors (TFTs). In particular, it introduces the basic concepts of organic semiconductor structure and organic thin-film transistor (OTFT) operation and then focuses on initial studies and works. Organic semiconductors for OTFTs must possess two essential structural features for their successful implementation in printed electronics. The first feature is a π-conjugated core/chain composed of linked unsaturated units. The second feature is core functionalization with solubilizing substituents, which is essential for inexpensive manufacture by solution methods as well as for enhancing solid-state core interactions. There are several advantages in using polymeric versus molecular p-conjugated semiconductors. Isoindigo has become a popular conjugated moiety in polymer semiconductor design because of its strong electron-withdrawing character. Polymeric p-channel TFTs have reached new heights, with hole mobilities unthinkable only few years back and surpassing 10 cm2V-1 s-1. © 2018 Elsevier B.V., All rights reserved.
  • Article
    Citation - WoS: 13
    Citation - Scopus: 15
    Meso-π-extended/Deficient BODIPYs and Low-Band Donor-Acceptor Copolymers for Organic Optoelectronics
    (Amer Chemical Soc, 2022-02-16) Can, Ayse; Choi, Gi-Seok; Ozdemir, Resul; Park, Soyoon; Park, Jin Su; Lee, Yongchul; Usta, Hakan
    The realization of pi-deficient acceptors and their donor-acceptor copolymers has become a key research focus for the realization of versatile organic optoelectronic materials and devices. Herein, we demonstrate the theoretical design, synthesis, and physicochemical/optoelectronic characterization of two meso-pi-extended/deficient BODIPY building blocks (2OD-T2BDY and 2OD-TTzBDY) and a library of donor-acceptor copolymers with low band gap (E-g = 1.30-1.35 eV) based on these building blocks. These building blocks, to the best of our knowledge, are the first examples of BODIPYs with meso-pi-extension. A library of BODIPY building blocks with varied meso units/substituents is studied to reveal the meso effects on the semiconducting BODIPY's optoelectronic properties. The building blocks showed favorable pi-acceptor electronic/structural properties with meso-pi-delocalized and stabilized LUMOs (ca. -3.6 eV) and large ground-state dipole moments of 4.9-5.5 D. Consistent with the theoretical/experimental pi-electronic structures, all copolymers functioned as p-type semiconductors in field-effect transistors and as donor materials in the bulk heterojunction organic photovoltaics. Power conversion efficiencies of up to 4.4% with a short-circuit current of 12.07 mA cm(-2) were achieved. This study demonstrates a unique meso-pi-extension strategy to realize BODIPYs with favorable pi-acceptor properties, and our findings could open up future materials design avenues in various organic optoelectronic applications.