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  • A crystalline D-π-A organic small molecule with naphtho[1,2-b:5,6-b′]dithiophene-core for solution processed organic solar cells

  • Add time:09/30/2019    Source:infona.pl

    In this work, we have designed and synthesized a new naphtho[1,2-b:5,6-b′]dithiophene-containing enlarged π-conjugated donor–acceptor (D–A) small molecule, NDT(TTz) 2 , for use in solution-processed organic photovoltaics. NDT(TTz) 2 , which contains a thiophene-bridged naphtho[1,2-b:5,6-b′]dithiophene as the central fused core and triphenylamine-flanked thiophene thiazolothiazole as a spacer, was synthesized via sequential Suzuki and Stille coupling reactions. The thermal, physiochemical, and electrochemical properties of NDT(TTz) 2 have been evaluated by differential scanning calorimetry, thermogravimetry, UV–Vis spectroscopy, photoluminescence spectroscopy, X-ray diffraction, and cyclic voltammetry. As desired for photovoltaic applications, NDT(TTz) 2 possesses good solubility, thermal stability, and a well-ordered, π–π stacked, crystallinity. The optical band gap and HOMO level of NDT(TTz) 2 were determined to be 2.0eV and −5.23eV, respectively. In addition to organic thin film transistor studies, application of NDT(TTz) 2 to preliminary photovoltaic devices has also been investigated by fabricating solution-processed bulk heterojunction solar cells together with PC 71 BM in a typical layered device structure, ITO/PEDOT:PSS/NDT(TTz) 2 :PC 71 BM/LiF/Al. Without extensive optimization of the device, NDT(TTz) 2 in these devices shows a maximum power conversion efficiency of 1.44% under AM 1.5 illumination at a 100mW/cm 2 intensity.

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    Prev:New acceptor–donor–acceptor-type conjugated molecules bearing naphtho[1,2-b:5,6-b′]dithiophene and (E)-1,2-di(thiophen-2-yl)ethene and their applications in thin-film transistors and photovoltaic cells
    Next:Discogens Possessing Aryl Side Groups Synthesized by Suzuki Coupling of Triphenylene (cas 217-59-4) Triflates and Their Self‐Organization Behavior)

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