Achieving high-performance non-halogenated nonfullerene acceptor-based organic solar cells with 13.7% efficiency via a synergistic strategy of an indacenodithieno[3, 2-b]selenophene core unit and non-halogenated thiophene-based terminal group. Issue 42 (9th October 2019)
- Record Type:
- Journal Article
- Title:
- Achieving high-performance non-halogenated nonfullerene acceptor-based organic solar cells with 13.7% efficiency via a synergistic strategy of an indacenodithieno[3, 2-b]selenophene core unit and non-halogenated thiophene-based terminal group. Issue 42 (9th October 2019)
- Main Title:
- Achieving high-performance non-halogenated nonfullerene acceptor-based organic solar cells with 13.7% efficiency via a synergistic strategy of an indacenodithieno[3, 2-b]selenophene core unit and non-halogenated thiophene-based terminal group
- Authors:
- Liu, Kai-Kai
Xu, Xiaopeng
Wang, Jin-Liang
Zhang, Chao
Ge, Gao-Yang
Zhuang, Fang-Dong
Zhang, Han-Jian
Yang, Can
Peng, Qiang
Pei, Jian - Abstract:
- Abstract : The combination of indacenodithieno[3, 2- b ]selenophene core unit and thiophene-containing IC is a successful synergistic strategy with PCE of 13.7%, which is the highest value in NFAs with thiophene-containing IC for binary OSCs. Abstract : An outmost selenophene-functionalized electron-rich central core (indacenodithieno[3, 2- b ]selenophene) and a new non-halogenated A–D–A architecture non-fullerene small molecular acceptor (NF-SMA) (TSeTIC ) based on indacenodithieno[3, 2- b ]selenophene as the central unit and thiophene-fused IC as a terminal group was designed and synthesized for high performance organic solar cells. In contrast to the similar NF-SMA (TTTIC ) with an indacenodithieno[3, 2- b ]thiophene unit, TSeTIC exhibited a stronger and red-shifted absorption spectrum, higher highest occupied molecular orbital (HOMO) energy level, and enhanced electron mobility in neat thin films. Furthermore, a TSeTIC /PM6 -based device presented higher hole/electron mobility, better phase separation features with favorable morphology, and higher charge dissociation and collection efficiency than a TTTIC /PM6 -based device, resulting in remarkably improved J sc and FF without sacrificing the V oc . Therefore, compared to the best PCE of 12.05% with an energy loss ( E loss ) of 0.64 eV for the PM6 /TTTIC device, the optimized PM6 /TSeTIC device yields a significantly higher PCE of 13.71% with a higher FF of 75.9% and decreased E loss of 0.60 eV. It is worth noting thatAbstract : The combination of indacenodithieno[3, 2- b ]selenophene core unit and thiophene-containing IC is a successful synergistic strategy with PCE of 13.7%, which is the highest value in NFAs with thiophene-containing IC for binary OSCs. Abstract : An outmost selenophene-functionalized electron-rich central core (indacenodithieno[3, 2- b ]selenophene) and a new non-halogenated A–D–A architecture non-fullerene small molecular acceptor (NF-SMA) (TSeTIC ) based on indacenodithieno[3, 2- b ]selenophene as the central unit and thiophene-fused IC as a terminal group was designed and synthesized for high performance organic solar cells. In contrast to the similar NF-SMA (TTTIC ) with an indacenodithieno[3, 2- b ]thiophene unit, TSeTIC exhibited a stronger and red-shifted absorption spectrum, higher highest occupied molecular orbital (HOMO) energy level, and enhanced electron mobility in neat thin films. Furthermore, a TSeTIC /PM6 -based device presented higher hole/electron mobility, better phase separation features with favorable morphology, and higher charge dissociation and collection efficiency than a TTTIC /PM6 -based device, resulting in remarkably improved J sc and FF without sacrificing the V oc . Therefore, compared to the best PCE of 12.05% with an energy loss ( E loss ) of 0.64 eV for the PM6 /TTTIC device, the optimized PM6 /TSeTIC device yields a significantly higher PCE of 13.71% with a higher FF of 75.9% and decreased E loss of 0.60 eV. It is worth noting that the excellent PCE of 13.71% is the highest recorded for A–D–A structural NF-SMAs with thiophene-containing terminal groups for binary organic solar cells. These results demonstrate that the synergistic strategy of using an indacenodithieno[3, 2- b ]selenophene core unit and thiophene-containing IC end group is a promising avenue to enhance the PCE of non-halogenated NF-SMAs with high V oc and FF as well as low E loss . … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 7:Issue 42(2019)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 7:Issue 42(2019)
- Issue Display:
- Volume 7, Issue 42 (2019)
- Year:
- 2019
- Volume:
- 7
- Issue:
- 42
- Issue Sort Value:
- 2019-0007-0042-0000
- Page Start:
- 24389
- Page End:
- 24399
- Publication Date:
- 2019-10-09
- Subjects:
- Materials -- Research -- Periodicals
Chemistry, Analytic -- Periodicals
Environmental sciences -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/ta ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9ta08328f ↗
- Languages:
- English
- ISSNs:
- 2050-7488
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205100
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 12017.xml