High performance alternating polymers based on two-dimensional conjugated benzo[1, 2-b:4, 5-b′]dithiophene and fluorinated dithienylbenzothiadiazole for solar cells. Issue 81 (16th August 2016)
- Record Type:
- Journal Article
- Title:
- High performance alternating polymers based on two-dimensional conjugated benzo[1, 2-b:4, 5-b′]dithiophene and fluorinated dithienylbenzothiadiazole for solar cells. Issue 81 (16th August 2016)
- Main Title:
- High performance alternating polymers based on two-dimensional conjugated benzo[1, 2-b:4, 5-b′]dithiophene and fluorinated dithienylbenzothiadiazole for solar cells
- Authors:
- Cong, Zhiyuan
Liu, Shuo
Zhao, Baofeng
Wang, Weiping
Liu, Hongli
Su, Jin
Guo, Zhaoqi
Wei, Wei
Gao, Chao
An, Zhongwei - Abstract:
- Abstract : Three D–A polymers based on alkylthienyl substituted benzo[1, 2- b :4, 5- b ′]dithiophene (BDTT) and fluorinated 4, 7-dialkylthienyl-2, 1, 3-benzothiadiazole (DTBT) derivatives were synthesized and applied as donors in BHJ solar cells. Abstract : Three donor–acceptor polymers based on two-dimensional conjugated alkylthienyl substituted benzo[1, 2- b :4, 5- b ′]dithiophene (BDTT) and fluorinated 4, 7-dialkylthienyl-2, 1, 3-benzothiadiazole (DTBT) derivatives were synthesized and applied as donor materials for bulk heterojunction solar cells. The effects of fluorine substitution on the absorption properties, energy levels, dielectric constants and photovoltaic properties of the polymers were investigated. We found that the incorporation of fluorine atoms on the DTBT unit can effectively deepen the highest occupied molecular orbital (HOMO) energy level and increase the dielectric constant of the polymers. As a result of these improved properties, a high open-circuit voltage ( V oc ) of 0.85 V was obtained for the optimal conventional polymer solar cells (PSCs) based on a two-fluorine-substituted analogueP3 blended with [6, 6]-phenyl-C71 butyric acid methyl ester (PC71 BM) as the active layer (1 : 1.5), giving rise to a high power conversion efficiency (PCE) of 7.48%. The influences of the molecular weight (MW) ofP3 on the device performances were further studied and enhanced photovoltaic parameters were achieved for the medium molecular weightP3 based device, with aAbstract : Three D–A polymers based on alkylthienyl substituted benzo[1, 2- b :4, 5- b ′]dithiophene (BDTT) and fluorinated 4, 7-dialkylthienyl-2, 1, 3-benzothiadiazole (DTBT) derivatives were synthesized and applied as donors in BHJ solar cells. Abstract : Three donor–acceptor polymers based on two-dimensional conjugated alkylthienyl substituted benzo[1, 2- b :4, 5- b ′]dithiophene (BDTT) and fluorinated 4, 7-dialkylthienyl-2, 1, 3-benzothiadiazole (DTBT) derivatives were synthesized and applied as donor materials for bulk heterojunction solar cells. The effects of fluorine substitution on the absorption properties, energy levels, dielectric constants and photovoltaic properties of the polymers were investigated. We found that the incorporation of fluorine atoms on the DTBT unit can effectively deepen the highest occupied molecular orbital (HOMO) energy level and increase the dielectric constant of the polymers. As a result of these improved properties, a high open-circuit voltage ( V oc ) of 0.85 V was obtained for the optimal conventional polymer solar cells (PSCs) based on a two-fluorine-substituted analogueP3 blended with [6, 6]-phenyl-C71 butyric acid methyl ester (PC71 BM) as the active layer (1 : 1.5), giving rise to a high power conversion efficiency (PCE) of 7.48%. The influences of the molecular weight (MW) ofP3 on the device performances were further studied and enhanced photovoltaic parameters were achieved for the medium molecular weightP3 based device, with a corresponding open circuit voltage ( V oc ) of 0.80 V, short-circuit current density ( J sc ) of 14.7 mA cm −2, high fill factor (FF) of 71.9% and the resulting best PCE of 8.47%, verifying thatP3 with an appropriate MW should be a promising polymer for highly efficient photovoltaic application. … (more)
- Is Part Of:
- RSC advances. Volume 6:Issue 81(2016)
- Journal:
- RSC advances
- Issue:
- Volume 6:Issue 81(2016)
- Issue Display:
- Volume 6, Issue 81 (2016)
- Year:
- 2016
- Volume:
- 6
- Issue:
- 81
- Issue Sort Value:
- 2016-0006-0081-0000
- Page Start:
- 77525
- Page End:
- 77534
- Publication Date:
- 2016-08-16
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c6ra13595a ↗
- 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:
- 356.xml