Benzo[1, 2-b:4, 5-b′]diselenophene-fused nonfullerene acceptors with alternative aromatic ring-based and monochlorinated end groups: a new synergistic strategy to simultaneously achieve highly efficient organic solar cells with the energy loss of 0.49 eV. Issue 19 (3rd May 2019)
- Record Type:
- Journal Article
- Title:
- Benzo[1, 2-b:4, 5-b′]diselenophene-fused nonfullerene acceptors with alternative aromatic ring-based and monochlorinated end groups: a new synergistic strategy to simultaneously achieve highly efficient organic solar cells with the energy loss of 0.49 eV. Issue 19 (3rd May 2019)
- Main Title:
- Benzo[1, 2-b:4, 5-b′]diselenophene-fused nonfullerene acceptors with alternative aromatic ring-based and monochlorinated end groups: a new synergistic strategy to simultaneously achieve highly efficient organic solar cells with the energy loss of 0.49 eV
- Authors:
- Wan, Shi-Sheng
Xu, Xiaopeng
Wang, Jin-Liang
Yuan, Gui-Zhou
Jiang, Zhao
Ge, Gao-Yang
Bai, Hai-Rui
Li, Zheng
Peng, Qiang - Abstract:
- Abstract : The PCE of 13.68% with the E loss of 0.49 eV were obtained, which were the highest values obtained to date in binary PSCs with monochlorinated NF-SMAs. Abstract : Herein, a new synergistic strategy using electron-rich core units and alternative aromatic structure-based 1, 1-dicyanomethylene-3-indanone (IC) end-groups for nonfullerene PSCs was reported and investigated in an attempt to simultaneously obtain excellent PCE with extremely low E loss . Specifically, two benzo[1, 2- b :4, 5- b ′]diselenophene-based, A–D–A-type chlorinated NF-SMAs (BDSeThCl andBDSePhCl ) were synthesized, which were linked with a new 2-chlorothienyl-based IC and a conventional monochlorinated phenyl-based IC as end-groups, respectively.BDSePhCl exhibited a wider and red-shifted absorption and downshifted energy levels thanBDSeThCl . The blend films ofBDSePhCl :PM7 exhibited better charge generation properties, more suitable phase separation, and more balanced charge mobilities as compared to those ofBDSeThCl :PM7 . Therefore, compared to theBDSeThCl :PM7 blends with the best PCE of 11.91% and the E loss of 0.58 eV, the optimalBDSePhCl :PM7 blends showed the enhanced PCE of 13.68% with the reduced E loss of 0.49 eV. Notably, the excellent PCE of 13.68% is the highest value recorded to date for A–D–A-type NF-SMAs with a monochlorinated IC group in binary PSCs. The E loss of 0.49 eV is the lowest value reported to date for A–D–A-type NF-SMAs in binary PSCs with the PCE > 13%. These resultsAbstract : The PCE of 13.68% with the E loss of 0.49 eV were obtained, which were the highest values obtained to date in binary PSCs with monochlorinated NF-SMAs. Abstract : Herein, a new synergistic strategy using electron-rich core units and alternative aromatic structure-based 1, 1-dicyanomethylene-3-indanone (IC) end-groups for nonfullerene PSCs was reported and investigated in an attempt to simultaneously obtain excellent PCE with extremely low E loss . Specifically, two benzo[1, 2- b :4, 5- b ′]diselenophene-based, A–D–A-type chlorinated NF-SMAs (BDSeThCl andBDSePhCl ) were synthesized, which were linked with a new 2-chlorothienyl-based IC and a conventional monochlorinated phenyl-based IC as end-groups, respectively.BDSePhCl exhibited a wider and red-shifted absorption and downshifted energy levels thanBDSeThCl . The blend films ofBDSePhCl :PM7 exhibited better charge generation properties, more suitable phase separation, and more balanced charge mobilities as compared to those ofBDSeThCl :PM7 . Therefore, compared to theBDSeThCl :PM7 blends with the best PCE of 11.91% and the E loss of 0.58 eV, the optimalBDSePhCl :PM7 blends showed the enhanced PCE of 13.68% with the reduced E loss of 0.49 eV. Notably, the excellent PCE of 13.68% is the highest value recorded to date for A–D–A-type NF-SMAs with a monochlorinated IC group in binary PSCs. The E loss of 0.49 eV is the lowest value reported to date for A–D–A-type NF-SMAs in binary PSCs with the PCE > 13%. These results demonstrate that tailoring of the monochlorinated aromatic ring-based IC is an effective strategy to simultaneously improve the PCE and reduce the E loss in binary PSCs. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 7:Issue 19(2019)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 7:Issue 19(2019)
- Issue Display:
- Volume 7, Issue 19 (2019)
- Year:
- 2019
- Volume:
- 7
- Issue:
- 19
- Issue Sort Value:
- 2019-0007-0019-0000
- Page Start:
- 11802
- Page End:
- 11813
- Publication Date:
- 2019-05-03
- 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/c9ta03177d ↗
- 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:
- 10397.xml