Polymers for application in organic solar cells: Bithiophene can work better than thienothiophene when coupled to benzodithiophene

TitoloPolymers for application in organic solar cells: Bithiophene can work better than thienothiophene when coupled to benzodithiophene
Tipo di pubblicazioneArticolo su Rivista peer-reviewed
Anno di Pubblicazione2016
AutoriParenti, F., Ricciardi Rosa, Diana R., Morvillo P., Fontanesi C., Tassinari F., Schenetti L., Minarini Carla, and Mucci A.
RivistaJournal of Polymer Science, Part A: Polymer Chemistry
Volume54
Paginazione1603-1614
ISSN0887624X
Parole chiaveBulk heterojunction (BHJ), Characterization, Conjugated polymers, Energy gap, External quantum efficiency, Heteroatom-containing polymers, Heterojunctions, Low band-gap copolymers, Organic polymers, Photophysical properties, Polymer solar cell (PSCs), Solar cells, Structure property relation, Synthesis (chemical), Synthesis and characterizations
Astratto

The synthesis and characterization of two low band gap copolymers (P1 and P2) incorporating benzo[1,2-b:4,5-b']dithiophene unit substituted with octylsulfanylthienyl groups (OSBT) are here reported. These materials, designed to be employed in polymer solar cells (PSCs), were obtained from alternating OSBT and bithiophene (P1) or thienothiophene (P2) units. Their structural electrochemical and photophysical properties were investigated. They are thermally stable and soluble in organic solvents from which they easily form films. They also form π-stacks in solution, in film and display a moderate solvatochromism. These polymers were tested with [70]PCBM in bulk-heterojunction (BHJ) PSCs where they act as donor materials and [70]PCBM is the electron acceptor. The best device, obtained using a 1:3 weight ratio for the P1:[70]PCBM blend, shows a PCE around 1.5%. A broad response from 350 to 700 nm is also observed in the external quantum efficiency (EQE) curves, wider for P1 with respect to P2. © 2015 Wiley Periodicals, Inc.

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URLhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84952690920&doi=10.1002%2fpola.28014&partnerID=40&md5=e5f06cdc5d7b16db6554d153991c72b7
DOI10.1002/pola.28014