Scopus İndeksli Yayınlar Koleksiyonu

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

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  • Conference Object
    Citation - WoS: 25
    Citation - Scopus: 26
    Semiconducting Copolymers Based on Meso-Substituted BODIPY for Inverted Organic Solar Cells and Field-Effect Transistors
    (Wiley, 2017-12-11) Ozdemir, Mehmet; Kim, Sang Woo; Kim, Hyungsug; Kim, Myung-Gil; Kim, Bumjoon J.; Kim, Choongik; Usta, Hakan
    The synthesis, physicochemical, and optoelectronic properties of a new class of low band-gap (approximate to 1.3 eV) donor-acceptor copolymers based on a highly electron-deficient meso-5-(2-octyldodecyl)thiophene-substituted BODIPY pi-unit are presented. The polymeric solutions exhibit strong aggregation-dependent excitonic properties indicating the presence of enhanced pi-coherence as a result of strong interchain interactions. The polymeric semiconductor thin films prepared by spin coating show isotropic nodule-like grains with essentially no ordering in the out-of-plane direction. Field-effect hole mobilities of 0.005 cm(2) V-1.s(-1) are observed in bottom-gate top-contact organic field-effect transistors, and inverted bulk-heterojunction organic photovoltaics employing the polymer:PC71BM active layer exhibit excellent power conversion efficiencies of 6.2% with a short-circuit current of 16.6 mA cm(-2). As far as it is known, this is a record high value achieved to date for a boron-containing donor polymer in the photovoltaic literature indicating a significant enhancement in power conversion efficiency (>3-4 times). The findings clearly present that rationally designed BODIPY-based donor-acceptor copolymers can be a key player in photovoltaic applications.
  • Article
    Citation - WoS: 10
    Citation - Scopus: 11
    Interplay Between Charge Injection, Electron Transport, and Quantum Efficiency in Ambipolar Trilayer Organic Light-Emitting Transistors
    (Wiley, 2022-01-15) Moschetto, Salvatore; Benvenuti, Emilia; Usta, Hakan; Ozdemir, Resul; Facchetti, Antonio; Muccini, Michele; Toffanin, Stefano
    The fascinating characteristic of organic light-emitting transistors (OLETs) of being electrical switches with an intrinsic light-emitting capability makes them attractive candidates for a wide variety of applications, ranging from sensors to displays. To date, the OLET ambipolar trilayer heterostructure is the most developed architecture for maximizing device performance. However, a major challenge of trilayer OLETs remains the inverse correlation between external quantum efficiency and brightness under ambipolar conditions. The complex interconnection between electroluminescent and ambipolar charge transport properties, in conjunction with the limited availability of electron transport semiconducting materials, has indeed hampered the disruptive evolution of the OLET technology. Here, an in-depth study of the interplay of the key fundamental features that determine the device performance is reported by exploring electron transport semiconductors with different properties in ambipolar trilayer OLETs. Through the selection of compounds with tailored chemical structures, the relation between intrinsic optoelectronic characteristics of the electron transport semiconductor, energy level alignment within the structure, and morphological features is unraveled. Furthermore, the introduction of a suitable electron injector at the emissive/semiconducting layers interface sheds light into the bidimensional nature of OLETs that is a distinguishing factor of this class of devices with respect to prototypical organic light-emitting diodes.