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Synthesis and Controlled Self-Assembly of Covalently Linked Hexa-peri-hexabenzocoronene/Perylene Diimide Dyads as Models To Study Fundamental Energy and Electron Transfer Processes

Doessel, L. F., Kamm, V., Howard, I. A., Laquai, F., Pisula, W., Feng, X., Li, C., Takase, M., Kudernac, T., De Feyter, S. & Muellen, K., 4-Apr-2012, In : Journal of the American Chemical Society. 134, 13, p. 5876-5886 11 p.

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  • Synthesis and Controlled Self-Assembly of Covalently Linked Hexa-peri-hexabenzocoronene/Perylene Diimide Dyads as Models To Study Fundamental Energy and Electron Transfer Processes Lukas F. Dössel, Valentin Kamm, Ian A. Howard, Frédéric Laquai, Wojciech Pisula, Xinliang Feng, Che

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DOI

  • Lukas F. Doessel
  • Valentin Kamm
  • Ian A. Howard
  • Frederic Laquai
  • Wojciech Pisula
  • Xinliang Feng
  • Chen Li
  • Masayoshi Takase
  • Tibor Kudernac
  • Steven De Feyter
  • Klaus Muellen

We report the synthesis and photophysical characterization of a series of hexa-peri-hexabenzocoronene (HBC)/perylenetetracarboxy diimide (PDI) dyads that are covalently linked with a rigid bridge. Both the ratio of the vs. two components and the conjugation of the bridging element are systematically modified to study the influence on self-assembly and energy and electron transfer between electron donor HBC and acceptor PDI. STM and 2D-WAXS experiments reveal that both in solution and in bulk solid state the dyads assemble into well-ordered two-dimensional supramolecular structures with controllable mutual orientations and distances between donor and acceptor at a nanoscopic scale. Depending on the symmetry of the dyads, either columns with nanosegregated stacks of HBC and PDI or interdigitating networks with alternating HBC and PDI moieties are observed. UV-vis, photoluminescence, transient photoluminescence, and transient absorption spectroscopy confirm that after photoexcitation of the donor HBC a photoinduced electron transfer between HBC and PDI can only compete with the dominant Forster resonance energy transfer, if facilitated by an intimate stacking of HBC and PDI with sufficient orbital overlap. However, while the alternating stacks allow efficient electron transfer, only the nanosegregated stacks provide charge transport channels in bulk state that are a prerequisite for application as active components in thin film electronic devices. These results have important implications for the further design of functional donor acceptor dyads, being promising materials for organic bulk heterojunction solar cells and field-effect transistors.

Original languageEnglish
Pages (from-to)5876-5886
Number of pages11
JournalJournal of the American Chemical Society
Volume134
Issue number13
Publication statusPublished - 4-Apr-2012

    Keywords

  • PERYLENE BISIMIDE DYES, POLYMER SOLAR-CELLS, PHOTOPHYSICAL PROPERTIES, ORGANIC SEMICONDUCTORS, MORPHOLOGY, TRANSPORT, DONOR, TRANSISTORS, COPOLYMERS

ID: 136167172