Synthesis of new D-A1–D-A2 type low bandgap terpolymers based on different thiadiazoloquinoxaline acceptor units for efficient polymer solar cells. Issue 75 (26th July 2016)
- Record Type:
- Journal Article
- Title:
- Synthesis of new D-A1–D-A2 type low bandgap terpolymers based on different thiadiazoloquinoxaline acceptor units for efficient polymer solar cells. Issue 75 (26th July 2016)
- Main Title:
- Synthesis of new D-A1–D-A2 type low bandgap terpolymers based on different thiadiazoloquinoxaline acceptor units for efficient polymer solar cells
- Authors:
- Keshtov, M. L.
Kuklin, S. A.
Radychev, N. A.
Ostapov, I. E.
Nikolaev, A. Y.
Konstantinov, I. O.
Krayushkin, M. M.
Koukaras, E. N.
Sharma, Abhishek
Sharma, G. D. - Abstract:
- Abstract : Two low bandgap D-A1–D-A2 conjugated (with/without fluorine substitution) copolymers, with benzothiadiazole and thiadiazoloquinoxaline acceptors, were used to fabricate BHJ polymer solar cells that achieved up to 7.21% power conversion efficiency. Abstract : Two low bandgap D-A1–D-A2 conjugated copolymers, namely denoted asP1 (non-fluorine substituted thiadiazoloquinoxaline A2) andP2 (fluorine substituted thiadiazoloquinoxaline A2) with the same D (thiophene) and A1 (benzothiadiazole) groups were synthesized in order to investigate the effect of fluorine atoms on the photovoltaic performance of polymer solar cells. The electrochemical properties demonstrate that the highest occupied molecular orbital (HOMO) energy level lowered from −5.08 eV (forP1 ) to −5.16 eV (forP2 ), whereas the lowest unoccupied molecular orbital (LUMO) energy levels remain nearly the same. These copolymers showed strong absorption in the wavelength range 300–1100 nm and have a bandgap of around 1.08 and 1.11 eV forP1 andP2, respectively. After the optimization of the weight ratio and concentration of solvent additives 1-chloronaphathalene (CN), the highest power conversion efficiencies of bulk heterojunction polymer solar cells achieved were up to 5.30% and 7.21% forP1 andP2 as donor and PC71 BM as acceptor. The enhanced V oc and J sc for theP2 based device can be mainly ascribed to the lower HOMO energy levels and higher hole mobility and better morphology of the fluorinated copolymerP2Abstract : Two low bandgap D-A1–D-A2 conjugated (with/without fluorine substitution) copolymers, with benzothiadiazole and thiadiazoloquinoxaline acceptors, were used to fabricate BHJ polymer solar cells that achieved up to 7.21% power conversion efficiency. Abstract : Two low bandgap D-A1–D-A2 conjugated copolymers, namely denoted asP1 (non-fluorine substituted thiadiazoloquinoxaline A2) andP2 (fluorine substituted thiadiazoloquinoxaline A2) with the same D (thiophene) and A1 (benzothiadiazole) groups were synthesized in order to investigate the effect of fluorine atoms on the photovoltaic performance of polymer solar cells. The electrochemical properties demonstrate that the highest occupied molecular orbital (HOMO) energy level lowered from −5.08 eV (forP1 ) to −5.16 eV (forP2 ), whereas the lowest unoccupied molecular orbital (LUMO) energy levels remain nearly the same. These copolymers showed strong absorption in the wavelength range 300–1100 nm and have a bandgap of around 1.08 and 1.11 eV forP1 andP2, respectively. After the optimization of the weight ratio and concentration of solvent additives 1-chloronaphathalene (CN), the highest power conversion efficiencies of bulk heterojunction polymer solar cells achieved were up to 5.30% and 7.21% forP1 andP2 as donor and PC71 BM as acceptor. The enhanced V oc and J sc for theP2 based device can be mainly ascribed to the lower HOMO energy levels and higher hole mobility and better morphology of the fluorinated copolymerP2 : PC71 BM blend. … (more)
- Is Part Of:
- RSC advances. Volume 6:Issue 75(2016)
- Journal:
- RSC advances
- Issue:
- Volume 6:Issue 75(2016)
- Issue Display:
- Volume 6, Issue 75 (2016)
- Year:
- 2016
- Volume:
- 6
- Issue:
- 75
- Issue Sort Value:
- 2016-0006-0075-0000
- Page Start:
- 71232
- Page End:
- 71244
- Publication Date:
- 2016-07-26
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c6ra14537j ↗
- 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:
- 5630.xml