Effects of including electron-withdrawing atoms on the physical and photovoltaic properties of indacenodithieno[3, 2-b]thiophene-based donor–acceptor polymers: towards an acceptor design for efficient polymer solar cells. Issue 33 (7th April 2017)
- Record Type:
- Journal Article
- Title:
- Effects of including electron-withdrawing atoms on the physical and photovoltaic properties of indacenodithieno[3, 2-b]thiophene-based donor–acceptor polymers: towards an acceptor design for efficient polymer solar cells. Issue 33 (7th April 2017)
- Main Title:
- Effects of including electron-withdrawing atoms on the physical and photovoltaic properties of indacenodithieno[3, 2-b]thiophene-based donor–acceptor polymers: towards an acceptor design for efficient polymer solar cells
- Authors:
- Cai, Ping
Xu, Xiaofeng
Sun, Jiangman
Chen, Junwu
Cao, Yong - Abstract:
- Abstract : Three new D–A polymers using indacenodithieno[3, 2- b ]thiophene (IDTT) as an electron-rich unit and benzoxadiazole (BO), benzodiathiazole (BT) or difluorobenzothiadiazole (FBT) as an electron-deficient unit were synthesized and applied in solar cells. Abstract : Three new D–A polymersPIDTT-DTBO, PIDTT-DTBT andPIDTT-DTFBT, using indacenodithieno[3, 2- b ]thiophene (IDTT ) as the electron-rich unit and benzoxadiazole (BO ), benzodiathiazole (BT ) or difluorobenzothiadiazole (FBT ) as the electron-deficient unit, were synthesized via a Pd-catalyzed Stille polymerization. The included electron-withdrawing atoms of the acceptor portion were varied between O, S, and F for tailoring the optical and electrochemical properties and the geometry of structures. Their effects on the film topography, photovoltaic and hole-transporting properties of the polymers were thoroughly investigated via a range of techniques. As expected, the stronger electron-withdrawingBO unit affords red-shifted absorption, low-lying HOMO and LUMO levels for the polymerPIDTT-DTBO . However, it depicts lower hole mobility and a less efficient charge collection in the active layer compared to the polymerPIDTT-DTBT . In addition, degradation of the solubility is observed in the fluorinated polymerPIDTT-DTFBT . As a result, a BHJ PSC (ITO/PEDOT:PSS/polymer:PC71 BM/interlayer/Al) fabricated withPIDTT-DTBT attains the best power conversion efficiency (PCE) of 4.91%. These results thus demonstrate theAbstract : Three new D–A polymers using indacenodithieno[3, 2- b ]thiophene (IDTT) as an electron-rich unit and benzoxadiazole (BO), benzodiathiazole (BT) or difluorobenzothiadiazole (FBT) as an electron-deficient unit were synthesized and applied in solar cells. Abstract : Three new D–A polymersPIDTT-DTBO, PIDTT-DTBT andPIDTT-DTFBT, using indacenodithieno[3, 2- b ]thiophene (IDTT ) as the electron-rich unit and benzoxadiazole (BO ), benzodiathiazole (BT ) or difluorobenzothiadiazole (FBT ) as the electron-deficient unit, were synthesized via a Pd-catalyzed Stille polymerization. The included electron-withdrawing atoms of the acceptor portion were varied between O, S, and F for tailoring the optical and electrochemical properties and the geometry of structures. Their effects on the film topography, photovoltaic and hole-transporting properties of the polymers were thoroughly investigated via a range of techniques. As expected, the stronger electron-withdrawingBO unit affords red-shifted absorption, low-lying HOMO and LUMO levels for the polymerPIDTT-DTBO . However, it depicts lower hole mobility and a less efficient charge collection in the active layer compared to the polymerPIDTT-DTBT . In addition, degradation of the solubility is observed in the fluorinated polymerPIDTT-DTFBT . As a result, a BHJ PSC (ITO/PEDOT:PSS/polymer:PC71 BM/interlayer/Al) fabricated withPIDTT-DTBT attains the best power conversion efficiency (PCE) of 4.91%. These results thus demonstrate the potential effects of electronegative atoms onIDTT -based polymers and the structure–function correlations of such electron-donor materials for efficient PSCs. … (more)
- Is Part Of:
- RSC advances. Volume 7:Issue 33(2017)
- Journal:
- RSC advances
- Issue:
- Volume 7:Issue 33(2017)
- Issue Display:
- Volume 7, Issue 33 (2017)
- Year:
- 2017
- Volume:
- 7
- Issue:
- 33
- Issue Sort Value:
- 2017-0007-0033-0000
- Page Start:
- 20440
- Page End:
- 20450
- Publication Date:
- 2017-04-07
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c7ra01049d ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 2278.xml