Tuning the Optoelectronic Properties of Nonfullerene Electron Acceptors. Issue 6 (21st October 2014)
- Record Type:
- Journal Article
- Title:
- Tuning the Optoelectronic Properties of Nonfullerene Electron Acceptors. Issue 6 (21st October 2014)
- Main Title:
- Tuning the Optoelectronic Properties of Nonfullerene Electron Acceptors
- Authors:
- Fang, Yuan
Pandey, Ajay K.
Lyons, Dani M.
Shaw, Paul E.
Watkins, Scott E.
Burn, Paul L.
Lo, Shih‐Chun
Meredith, Paul - Abstract:
- Abstract: Broad spectral coverage over the solar spectrum is necessary for photovoltaic technologies and is a focus for organic solar cells. We report a series of small‐molecule, nonfullerene electron acceptors containing the [(benzo[ c ][1, 2, 5]thiadiazol‐4‐yl)methylene]malononitrile unit as a high electron affinity component. The optoelectronic properties of these molecules were fine‐tuned with the objective of attaining strong absorption at longer wavelengths by changing the low‐ionization‐potential moiety. The electron‐accepting function of these materials was investigated with poly(3‐ n ‐hexylthiophene) (P3HT) as a standard electron donor. Significant photocurrent generation in the near infrared region, with an external quantum yield reaching as high as 22 % at 700 nm and an onset >800 nm was achieved. The results support efficient hole transfer to P3HT taking place after light absorption by the acceptor molecules. A Channel II‐dominated power conversion efficiency of up to 1.5 % was, thus, achieved. Abstract : New acceptors: A series of small‐molecule, nonfullerene electron acceptors containing the [(benzo[ c ][1, 2, 5]thiadiazol‐4‐yl)methylene]malononitrile unit is designed to possess different absorption profiles and optical gaps (see picture). When poly(3‐ n ‐hexylthiophene) (P3HT) is used as the standard electron donor, significant photocurrent generation in the near infrared region, with an external quantum yield reaching as high as 22 % at 700 nm and an onsetAbstract: Broad spectral coverage over the solar spectrum is necessary for photovoltaic technologies and is a focus for organic solar cells. We report a series of small‐molecule, nonfullerene electron acceptors containing the [(benzo[ c ][1, 2, 5]thiadiazol‐4‐yl)methylene]malononitrile unit as a high electron affinity component. The optoelectronic properties of these molecules were fine‐tuned with the objective of attaining strong absorption at longer wavelengths by changing the low‐ionization‐potential moiety. The electron‐accepting function of these materials was investigated with poly(3‐ n ‐hexylthiophene) (P3HT) as a standard electron donor. Significant photocurrent generation in the near infrared region, with an external quantum yield reaching as high as 22 % at 700 nm and an onset >800 nm was achieved. The results support efficient hole transfer to P3HT taking place after light absorption by the acceptor molecules. A Channel II‐dominated power conversion efficiency of up to 1.5 % was, thus, achieved. Abstract : New acceptors: A series of small‐molecule, nonfullerene electron acceptors containing the [(benzo[ c ][1, 2, 5]thiadiazol‐4‐yl)methylene]malononitrile unit is designed to possess different absorption profiles and optical gaps (see picture). When poly(3‐ n ‐hexylthiophene) (P3HT) is used as the standard electron donor, significant photocurrent generation in the near infrared region, with an external quantum yield reaching as high as 22 % at 700 nm and an onset >800 nm are achieved. … (more)
- Is Part Of:
- Chemphyschem. Volume 16:Issue 6(2015)
- Journal:
- Chemphyschem
- Issue:
- Volume 16:Issue 6(2015)
- Issue Display:
- Volume 16, Issue 6 (2015)
- Year:
- 2015
- Volume:
- 16
- Issue:
- 6
- Issue Sort Value:
- 2015-0016-0006-0000
- Page Start:
- 1295
- Page End:
- 1304
- Publication Date:
- 2014-10-21
- Subjects:
- energy conversion -- materials science -- organic electronics -- thin films -- solar cells
Chemistry, Physical and theoretical -- Periodicals
541.05 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cphc.201402568 ↗
- Languages:
- English
- ISSNs:
- 1439-4235
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3172.310500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4683.xml