Asymmetric, efficient π-conjugated organic semiconducting chromophore for bulk-heterojunction organic photovoltaics. (February 2018)
- Record Type:
- Journal Article
- Title:
- Asymmetric, efficient π-conjugated organic semiconducting chromophore for bulk-heterojunction organic photovoltaics. (February 2018)
- Main Title:
- Asymmetric, efficient π-conjugated organic semiconducting chromophore for bulk-heterojunction organic photovoltaics
- Authors:
- Nazim, M.
Ameen, Sadia
Shaheer Akhtar, M.
Shin, Hyung Shik - Abstract:
- Abstract: A novel, asymmetric benzothiadiazole-core π-conjugated organic semiconducting chromophore (CF-BTz-ThR) containing an alkyl bithiophene donor and 3, 5-bis (trifluoromethyl) benzene as acceptor unit was synthesized via Suzuki cross-coupling in a relatively cost-effective way. The synthesized chromophore was applied as an acceptor material in the solution-processed fabrication of bulk heterojunction (BHJ) organic photovoltaics (OPVs). The presence of terminal hexyl chain in CF-BTz-ThR induced its solubility in common organic solvents. The energy levels of CF-BTz-ThR were calculated as −5.22 eV and −3.19 eV for HOMO and LUMO, respectively. The fabricated devices attained power conversion efficiency (PCE) of ∼3.52% for CF-BTz-ThR: PC61 BM (1:3, w/w) ratio with the short circuit current (JSC ) of ∼10.38 mA/cm 2 and the open-circuit voltage (VOC ) of ∼0.68 V. The reasonable JSC and VOC of the devices might be attributed to strong absorption and emission properties as well as the electrochemical properties due to the presence of strong electron-withdrawing benzothiadiazole as well as –CF3 unit as electron-acceptor. Highlights: An asymmetric benzothiadiazole-core π-conjugated organic (CF-BTz-ThR) semiconducting chromophore. It is applied as an electron-donor material in the solution-processed organic solar cells. CF-BTz-ThR presents the good HOMO (−5.22 eV) and LUMO (−3.19 eV) values. Device with CF-BTz-ThR:PC61 BM (1:3, w/w) ratio attains reasonable power conversionAbstract: A novel, asymmetric benzothiadiazole-core π-conjugated organic semiconducting chromophore (CF-BTz-ThR) containing an alkyl bithiophene donor and 3, 5-bis (trifluoromethyl) benzene as acceptor unit was synthesized via Suzuki cross-coupling in a relatively cost-effective way. The synthesized chromophore was applied as an acceptor material in the solution-processed fabrication of bulk heterojunction (BHJ) organic photovoltaics (OPVs). The presence of terminal hexyl chain in CF-BTz-ThR induced its solubility in common organic solvents. The energy levels of CF-BTz-ThR were calculated as −5.22 eV and −3.19 eV for HOMO and LUMO, respectively. The fabricated devices attained power conversion efficiency (PCE) of ∼3.52% for CF-BTz-ThR: PC61 BM (1:3, w/w) ratio with the short circuit current (JSC ) of ∼10.38 mA/cm 2 and the open-circuit voltage (VOC ) of ∼0.68 V. The reasonable JSC and VOC of the devices might be attributed to strong absorption and emission properties as well as the electrochemical properties due to the presence of strong electron-withdrawing benzothiadiazole as well as –CF3 unit as electron-acceptor. Highlights: An asymmetric benzothiadiazole-core π-conjugated organic (CF-BTz-ThR) semiconducting chromophore. It is applied as an electron-donor material in the solution-processed organic solar cells. CF-BTz-ThR presents the good HOMO (−5.22 eV) and LUMO (−3.19 eV) values. Device with CF-BTz-ThR:PC61 BM (1:3, w/w) ratio attains reasonable power conversion efficiency (PCE) of ∼3.52%. … (more)
- Is Part Of:
- Dyes and pigments. Volume 149(2018)
- Journal:
- Dyes and pigments
- Issue:
- Volume 149(2018)
- Issue Display:
- Volume 149, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 149
- Issue:
- 2018
- Issue Sort Value:
- 2018-0149-2018-0000
- Page Start:
- 141
- Page End:
- 148
- Publication Date:
- 2018-02
- Subjects:
- Benzothiadiazole -- 3, 5-bis (trifluoromethyl) benzene -- Electrochemical properties -- Semiconducting chromophore -- Organic photovoltaics
Dyes and dyeing -- Periodicals
Pigments -- Periodicals
667.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01437208 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.dyepig.2017.09.048 ↗
- Languages:
- English
- ISSNs:
- 0143-7208
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3635.600000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 5477.xml