A novel D–π–A small molecule with N-heteroacene as acceptor moiety for photovoltaic application. (November 2015)
- Record Type:
- Journal Article
- Title:
- A novel D–π–A small molecule with N-heteroacene as acceptor moiety for photovoltaic application. (November 2015)
- Main Title:
- A novel D–π–A small molecule with N-heteroacene as acceptor moiety for photovoltaic application
- Authors:
- Wang, Chengyuan
Okabe, Takuya
Long, Guankui
Kuzuhara, Daiki
Zhao, Yang
Aratani, Naoki
Yamada, Hiroko
Zhang, Qichun - Abstract:
- Abstract: Organic π -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 π -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. Highlights: A novel D– π –A small molecule has been synthesized and characterized. The standard BHJ-structured OPV device using this small molecule as the donor has been fabricated. The efficiency of theAbstract: Organic π -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 π -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. Highlights: A novel D– π –A small molecule has been synthesized and characterized. The standard BHJ-structured OPV device using this small molecule as the donor has been fabricated. The efficiency of the as-fabricated devices can be as high as 1.97%. … (more)
- Is Part Of:
- Dyes and pigments. Volume 122(2015)
- Journal:
- Dyes and pigments
- Issue:
- Volume 122(2015)
- Issue Display:
- Volume 122, Issue 2015 (2015)
- Year:
- 2015
- Volume:
- 122
- Issue:
- 2015
- Issue Sort Value:
- 2015-0122-2015-0000
- Page Start:
- 231
- Page End:
- 237
- Publication Date:
- 2015-11
- Subjects:
- Small molecule-based photovoltaics -- D–π–A structure -- N-heteroacenes -- Molybdenum trioxide -- Synthesis -- Devices' fabrication
Dyes and dyeing -- Periodicals
Pigments -- Periodicals
667.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01437208 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.dyepig.2015.06.029 ↗
- Languages:
- English
- ISSNs:
- 0143-7208
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3635.600000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 8340.xml