4.7 Article

A novel D-π-A small molecule with N-heteroacene as acceptor moiety for photovoltaic application

Journal

DYES AND PIGMENTS
Volume 122, Issue -, Pages 231-237

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.dyepig.2015.06.029

Keywords

Small molecule-based photovoltaics; D-pi-A structure; N-heteroacenes; Molybdenum trioxide; Synthesis; Devices' fabrication

Funding

  1. MOE [RG133/14, ARC 20/12, ARC 2/13]
  2. CREATE program (Nanomaterials for Energy and Water Management) from NRF
  3. New Initiative Fund from NTU, Singapore
  4. Japan Society for the Promotion of Science (JSPS) [25288092, 26105004, 25107519]
  5. Grants-in-Aid for Scientific Research [15H00876, 25107519, 26105001, 25288092, 26288038] Funding Source: KAKEN

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Organic pi-conjugated small molecules have attracted much attention for developing high performance organic photovoltaics (OPVs) due to their well-defined molecular structure, easily controlled energy levels and absorption, and more accurate simulation-experiment match. A novel small molecule combing a N-heteroacene (acceptor moiety) and benzo[1,2-b:4,5-b']dithiophene (donor unit) together through a pi-conjugated bridge (3,3 ''-dioctyl-2,2':5',2 ''-terthiophene), has been synthesized and characterized. The blended films of this small molecule with different acceptors have a wide absorption in visible region, which makes it possible for application in OPVs. The as-fabricated devices with PEDOT:PSS as an anode buffer layer show the power conversion efficiency at around 1%. By replacing PEDOT:PSS with MoO3, the power conversion efficiency is almost doubled up to 1.97%. AFM images and XRD patterns are employed to investigate the morphologies of the active layer. Consistent with the J-V curves and EQE spectra, the higher power conversion efficiency probably comes from the good alignment of the HOMO energy level of the small molecule with the work function of anode buffer layer and reduced chemical interactions between active layer and anode buffer layer. (C) 2015 Elsevier Ltd. All rights reserved.

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