Spectroscopic Engineering toward Near-Infrared Absorption of Materials Containing Perylene Diimide

The ability to tune the dye structure synthetically has been crucial in the development of materials with tailored properties for given applications. In this contribution, a series of discrete molecules are reported, which are constructed from the perylene diimide (PDI) chromophore and three dyes, namely thienyl diketopyrrolopyrrole (DPPTh2), pyridyl diketopyrrolopyrrole (DPPPyr2), and thienoisoindigo (TII). Through the choice of dye molecule and linking of the dye and PDI through conjugated acetylene bridges, the light-harvesting characteristics can be engineered to exhibit optical absorption in the range 300–900 nm. Each molecule shows ambipolar redox behavior, leading to unique electrochromic behavior

Pentaerythritol based push–pull tetramers for organic photovoltaics

The synthesis and characterization of two tetramers based on the functionalization of a central pentaerythritol σ-linker with push–pull chromophores is reported herein. Prepared in only few steps, these original molecules exhibit interesting optical and electrochemical properties. Moreover, once evaluated as donor materials, promising power conversion efficiencies of 4.5% were reached when blended with the [6,6]-phenyl-C71-butyric acid methyl ester (PC71BM) in bulk heterojunction solar cells

Dependence of Crystallite Formation and Preferential Backbone Orientations on the Side Chain Pattern in PBDTTPD Polymers

Alkyl substituents appended to the π-conjugated main chain account for the solution-processability and film-forming properties of most π-conjugated polymers for organic electronic device applications, including field-effect transistors (FETs) and bulk-heterojunction (BHJ) solar cells. Beyond film-forming properties, recent work has emphasized the determining role that side-chain substituents play on polymer self-assembly and thin-film nanostructural order, and, in turn, on device performance. However, the factors that determine polymer crystallite orientation in thin-films, implying preferential backbone orientation relative to the device substrate, are a matter of some debate, and these structural changes remain difficult to anticipate. In this report, we show how systematic changes in the side-chain pattern of poly(benzo[1,2-b:4,5-b′]dithiophene–alt–thieno[3,4-c]pyrrole-4,6-dione) (PBDTTPD) polymers can (i) influence the propensity of the polymer to order in the π-stacking direction, and (ii) direct the preferential orientation of the polymer crystallites in thin films (e.g., “face-on” vs “edge-on”). Oriented crystallites, specifically crystallites that are well-ordered in the π-stacking direction, are believed to be a key contributor to improved thin-film device performance in both FETs and BHJ solar cells

Electron-Deficient N-Alkyloyl Derivatives of Thienopyrrole-4,6-dione Yield Efficient Polymer Solar Cells with Open-Circuit Voltages > 1 V

Poly(benzo[1,2-b:4,5-b′]dithiophene–thieno[3,4-c]pyrrole-4,6-dione) (PBDTTPD) polymer donors yield some of the highest open-circuit voltages (VOC, ca. 0.9 V) and fill factors (FF, ca. 70%) in conventional bulk-heterojunction (BHJ) solar cells with PCBM acceptors. Recent work has shown that the incorporation of ring substituents into the side chains of the BDT motifs in PBDTTPD can induce subtle variations in material properties, resulting in an increase of the BHJ device VOC to ∼1 V. In this contribution, we report on the synthesis of N-alkyloyl-substituted TPD motifs (TPD(CO)) and show that the electron-deficient motifs can further lower both the polymer LUMO and HOMO levels, yielding device VOC > 1 V (up to ca. 1.1 V) in BHJ solar cells with PCBM. Despite the high VOC achieved (i.e., low polymer HOMO), BHJ devices cast from TPD(CO)-based polymer donors can reach power conversion efficiencies (PCEs) of up to 6.7%, making these promising systems for use in the high-band-gap cell of tandem solar cells