(E)-1, 2-Di(thiophen-2-yl)ethene based high mobility polymer for efficient photovoltaic devices without any post treatment. Issue 72 (18th July 2016)
- Record Type:
- Journal Article
- Title:
- (E)-1, 2-Di(thiophen-2-yl)ethene based high mobility polymer for efficient photovoltaic devices without any post treatment. Issue 72 (18th July 2016)
- Main Title:
- (E)-1, 2-Di(thiophen-2-yl)ethene based high mobility polymer for efficient photovoltaic devices without any post treatment
- Authors:
- Ren, Junzhen
Zhang, Yongchao
Liu, Fushuai
Yan, Yan
Qiu, Meng
Roy, V. A. L.
Zheng, Huilin
Sun, Mingliang
Yang, Renqiang - Abstract:
- Abstract : The ethene based polymer shows better photovoltaic performance. Abstract : In order to investigate the effect of an ( E )-1, 2-di(thiophen-2-yl)ethene (TVT) unit on the hole mobility and photovoltaic properties of dithienyl-difluorobenzothiadiazole (DTBT) based polymers, two conjugated polymersPDT-DTBT-DT (thiophene backboned) andPTVT-DTBT-DT (TVT backboned) were synthesized. Compared toPDT-DTBT-DT, the backbone conformation ofPTVT-DTBT-DT could be well modulated by the TVT unit, leading to an extended conjugation length and strengthened intermolecular interaction. Interestingly, it's found that the ultraviolet-visible (UV-vis) absorption peaks of thePTVT-DTBT-DT film was blue-shifted compared to that of the solution. The organic field-effect transistor (OFETs) characterization showed thatPTVT-DTBT-DT possessed a high hole mobility of 0.12 cm 2 V −1 s −1, which was higher than that of the counterpartPDT-DTBT-DT (0.04 cm 2 V −1 s −1 ). Through simplified device optimization without any additives and annealing treatment, a power conversion efficiency (PCE) of 7.86% was achieved forPTVT-DTBT-DT with a short-circuit current density ( J sc ) of 16.33 mA cm −2 and a fill factor (FF) of 68.92%, which is higher the PCE of 7.29% ofPDT-DTBT-DT with a J sc of 15.60 mA cm −2 and a FF of 66.62%. The PCE of 7.86% is among the highest PCEs reported for devices fabricated without any additives and thermal annealing treatment. The results revealed thatPTVT-DTBT-DT as an idealAbstract : The ethene based polymer shows better photovoltaic performance. Abstract : In order to investigate the effect of an ( E )-1, 2-di(thiophen-2-yl)ethene (TVT) unit on the hole mobility and photovoltaic properties of dithienyl-difluorobenzothiadiazole (DTBT) based polymers, two conjugated polymersPDT-DTBT-DT (thiophene backboned) andPTVT-DTBT-DT (TVT backboned) were synthesized. Compared toPDT-DTBT-DT, the backbone conformation ofPTVT-DTBT-DT could be well modulated by the TVT unit, leading to an extended conjugation length and strengthened intermolecular interaction. Interestingly, it's found that the ultraviolet-visible (UV-vis) absorption peaks of thePTVT-DTBT-DT film was blue-shifted compared to that of the solution. The organic field-effect transistor (OFETs) characterization showed thatPTVT-DTBT-DT possessed a high hole mobility of 0.12 cm 2 V −1 s −1, which was higher than that of the counterpartPDT-DTBT-DT (0.04 cm 2 V −1 s −1 ). Through simplified device optimization without any additives and annealing treatment, a power conversion efficiency (PCE) of 7.86% was achieved forPTVT-DTBT-DT with a short-circuit current density ( J sc ) of 16.33 mA cm −2 and a fill factor (FF) of 68.92%, which is higher the PCE of 7.29% ofPDT-DTBT-DT with a J sc of 15.60 mA cm −2 and a FF of 66.62%. The PCE of 7.86% is among the highest PCEs reported for devices fabricated without any additives and thermal annealing treatment. The results revealed thatPTVT-DTBT-DT as an ideal conjugated polymer could provide a greater possibility for the commercial application of PSCs, especially in terms of low cost and manufacturing convenience. … (more)
- Is Part Of:
- RSC advances. Volume 6:Issue 72(2016)
- Journal:
- RSC advances
- Issue:
- Volume 6:Issue 72(2016)
- Issue Display:
- Volume 6, Issue 72 (2016)
- Year:
- 2016
- Volume:
- 6
- Issue:
- 72
- Issue Sort Value:
- 2016-0006-0072-0000
- Page Start:
- 68049
- Page End:
- 68057
- Publication Date:
- 2016-07-18
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c6ra13970a ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
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- 2154.xml