4.8 Article

Double-Cable Conjugated Polymers with Linear Backbone toward High Quantum Efficiencies in Single-Component Polymer Solar Cells

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 139, Issue 51, Pages 18647-18656

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.7b10499

Keywords

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Funding

  1. National Key R&D Program of China [2017YFA0204702]
  2. NSFC of China [51773207, 21574138, 51603209, 91633301]
  3. Strategic Priority Research Program of the Chinese Academy of Sciences [XDB12030200]
  4. Open Research Fund of State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, CAS
  5. Recruitment Program of Global Youth Experts of China
  6. European Research Council (ERC) [339031]
  7. Ministry of Education, Culture and Science [024.001.035]
  8. European Union [747422]
  9. Swedish Research Council [VR621-2013-5561]
  10. Swedish Government Strategic Research Area in Materials Science on Functional Materials at Linkoping University [200900971]
  11. China Scholarship Council [CSC201606920028]
  12. Marie Curie Actions (MSCA) [747422] Funding Source: Marie Curie Actions (MSCA)

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A series of double-cable conjugated polymers were developed for application in efficient single-component polymer solar cells, in which high quantum efficiencies could be achieved due to the optimized nanophase separation between donor and acceptor parts. The new double-cable polymers contain electron-donating poly(benzodithiophene) (BDT) as linear conjugated backbone for hole transport and pendant electron-deficient perylene bisimide (PBI) units for electron transport, connected via a dodecyl linker. Sulfur and fluorine substituents were introduced to tune the energy levels and crystallinity of the conjugated polymers. The double-cable polymers adopt a face-on orientation in which the conjugated BDT backbone and the pendant PBI units have a preferential pi-pi stacking direction perpendicular to the substrate, favorable for interchain charge transport normal to the plane. The linear conjugated backbone acts as a scaffold for the crystallization of the PBI groups, to provide a double-cable nanophase separation of donor and acceptor phases. The optimized nanophase separation enables efficient exciton dissociation as well as charge transport as evidenced from the high-up to 80%-internal quantum efficiency for photon-to-electron conversion. In single-component organic solar cells, the double-cable polymers provide power conversion efficiency up to 4.18%. This is one of the highest performances in single-component organic solar cells. The nanophase-separated design can likely be used to achieve high-performance single-component organic solar cells.

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