An asymmetrical thieno[2, 3-f]benzofuran (TBF)-based conjugated polymer for organic solar cells with high fill factor. (7th April 2017)
- Record Type:
- Journal Article
- Title:
- An asymmetrical thieno[2, 3-f]benzofuran (TBF)-based conjugated polymer for organic solar cells with high fill factor. (7th April 2017)
- Main Title:
- An asymmetrical thieno[2, 3-f]benzofuran (TBF)-based conjugated polymer for organic solar cells with high fill factor
- Authors:
- He, Dingjun
Qiu, Lixia
Yuan, Jun
Zhang, Zhi-Guo
Li, Yongfang
Zou, Yingping - Abstract:
- Abstract: An asymmetrical building block-TBF modified with alkylthio phenyl as the side chain, polymerization with 4, 7-di (5-bromothiophen-2-yl)-5, 6-dioctyloxybenzo[c] [1, 2, 5]thiadiazole (BT), a new polymer-TBFPS-BT was obtained. As described in the UV-Vis spectrum, TBFPS-BT exhibited good absorption covering from 300 to 750 nm. Benefited from the alkylthio phenyl substitution, the polymer possessed deep HOMO level of −5.39 eV. The photoluminescence (PL) spectra indicated the generated excitons could be almost completely dissociation at the polymer/PC71 BM interface. Furthermore, the high and balanced mobility (1.49 × 10 −4 cm 2 V −1 s −1 for hole and 1.07 × 10 −4 cm 2 V −1 s −1 for electron) greatly contributed to enhance the fill factor (FF) and short-circuit current density ( J sc ) of device. PSC with different electron transporting layers (ETLs) were investigated, the results showed that when using perylene diimide (PDI) derivative with amino terminal substituent (PDIN) as ETL companied with 2% 1, 8-Diiodooctane (DIO), the device delivered a best PCE of 6.55% ( V oc = 0.8 V, J sc = 11.93 mA cm −2 and FF = 0.69). It is worth noting that all of the devices with ETLs and 2% DIO have shown high FFs over 0.65. So, the suitable modification on TBF and selection of ETLs were valid methods to improve device efficiency. Graphical abstract: With a new alkylthio phenyl substituted TBF polymer and PC[71]BM as the active layer, the best PCE for device of 6.55% wasAbstract: An asymmetrical building block-TBF modified with alkylthio phenyl as the side chain, polymerization with 4, 7-di (5-bromothiophen-2-yl)-5, 6-dioctyloxybenzo[c] [1, 2, 5]thiadiazole (BT), a new polymer-TBFPS-BT was obtained. As described in the UV-Vis spectrum, TBFPS-BT exhibited good absorption covering from 300 to 750 nm. Benefited from the alkylthio phenyl substitution, the polymer possessed deep HOMO level of −5.39 eV. The photoluminescence (PL) spectra indicated the generated excitons could be almost completely dissociation at the polymer/PC71 BM interface. Furthermore, the high and balanced mobility (1.49 × 10 −4 cm 2 V −1 s −1 for hole and 1.07 × 10 −4 cm 2 V −1 s −1 for electron) greatly contributed to enhance the fill factor (FF) and short-circuit current density ( J sc ) of device. PSC with different electron transporting layers (ETLs) were investigated, the results showed that when using perylene diimide (PDI) derivative with amino terminal substituent (PDIN) as ETL companied with 2% 1, 8-Diiodooctane (DIO), the device delivered a best PCE of 6.55% ( V oc = 0.8 V, J sc = 11.93 mA cm −2 and FF = 0.69). It is worth noting that all of the devices with ETLs and 2% DIO have shown high FFs over 0.65. So, the suitable modification on TBF and selection of ETLs were valid methods to improve device efficiency. Graphical abstract: With a new alkylthio phenyl substituted TBF polymer and PC[71]BM as the active layer, the best PCE for device of 6.55% was obtained with PDIN as ETL. Highlights: A new asymmetrical polymer based on alkylthio phenyl substituted TBF (TBFPS-BT) was designed and synthesized. TBFPS-BT/PC71 BM equipped with high and balanced mobilities for hole and electron under the optimized conditions. The device with PDIN as electron transporting layer, the PCE was increased to 6.55% with a high FF up to 0.69. … (more)
- Is Part Of:
- Polymer. Volume 114(2017)
- Journal:
- Polymer
- Issue:
- Volume 114(2017)
- Issue Display:
- Volume 114, Issue 2017 (2017)
- Year:
- 2017
- Volume:
- 114
- Issue:
- 2017
- Issue Sort Value:
- 2017-0114-2017-0000
- Page Start:
- 348
- Page End:
- 354
- Publication Date:
- 2017-04-07
- Subjects:
- Thieno[2, 3-f]benzofuran -- Alkylthio phenyl substitution -- Electron transporting layer -- Organic solar cells
Polymers -- Periodicals
Polymerization -- Periodicals
Polymères -- Périodiques
Polymérisation -- Périodiques
547.7 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00323861 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.polymer.2017.03.001 ↗
- Languages:
- English
- ISSNs:
- 0032-3861
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6547.700000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 521.xml