Near-IR organic sensitizers containing squaraine and phenothiazine units for dye-sensitized solar cells. (February 2015)
- Record Type:
- Journal Article
- Title:
- Near-IR organic sensitizers containing squaraine and phenothiazine units for dye-sensitized solar cells. (February 2015)
- Main Title:
- Near-IR organic sensitizers containing squaraine and phenothiazine units for dye-sensitized solar cells
- Authors:
- Bae, Seong Hee
Seo, Kang Deuk
Choi, Won Seok
Hong, Ji Yeoun
Kim, Hwan Kyu - Abstract:
- Abstract: Unsymmetrical squaraine near-infrared (NIR) sensitizers with variable π-bridge units, based on the donor-π-squaraine core-acceptor structural motif, were synthesized and used as sensitizers for dye-sensitized solar cells. The phenothiazine as a donor group was linked to a squaraine core unit using various thiophene derivatives. Among them, three squaraine-based sensitizers have a carboxylic acid group as an electron-accepting group directly attached to the squaraine component, while one of four squaraine-based sensitizers has a cyanoacrylic acid as a more strongly electron-accepting group directly attached to the squaraine component. The sensitizers exhibited intense absorption in the NIR region and strong luminescence. The LUMO levels of the present squaraine-based sensitizers were slightly more negative than the conduction band edge of TiO2 photoanode. As a result, a solar cell based on the squaraine-based sensitizer containing a thiophene unit as a π-bridge unit and a carboxylic acid group as an electron-accepting group exhibited better photovoltaic performance with a J SC of 6.0 mA cm −2, a V OC of 448 mV, and an FF of 0.73, corresponding to an overall conversion efficiency η of 2.0%. Graphical abstract: Highlights: The squaraine-based dyes were synthesized and used as sensitizer for DSSCs. The phenothaizine donor was linked to a squaraine core unit using thiophene units. The sensitizers exhibited intense absorption in the NIR region. The LUMO levels ofAbstract: Unsymmetrical squaraine near-infrared (NIR) sensitizers with variable π-bridge units, based on the donor-π-squaraine core-acceptor structural motif, were synthesized and used as sensitizers for dye-sensitized solar cells. The phenothiazine as a donor group was linked to a squaraine core unit using various thiophene derivatives. Among them, three squaraine-based sensitizers have a carboxylic acid group as an electron-accepting group directly attached to the squaraine component, while one of four squaraine-based sensitizers has a cyanoacrylic acid as a more strongly electron-accepting group directly attached to the squaraine component. The sensitizers exhibited intense absorption in the NIR region and strong luminescence. The LUMO levels of the present squaraine-based sensitizers were slightly more negative than the conduction band edge of TiO2 photoanode. As a result, a solar cell based on the squaraine-based sensitizer containing a thiophene unit as a π-bridge unit and a carboxylic acid group as an electron-accepting group exhibited better photovoltaic performance with a J SC of 6.0 mA cm −2, a V OC of 448 mV, and an FF of 0.73, corresponding to an overall conversion efficiency η of 2.0%. Graphical abstract: Highlights: The squaraine-based dyes were synthesized and used as sensitizer for DSSCs. The phenothaizine donor was linked to a squaraine core unit using thiophene units. The sensitizers exhibited intense absorption in the NIR region. The LUMO levels of sensitizers were more negative than the conduction band of TiO2 . … (more)
- Is Part Of:
- Dyes and pigments. Volume 113(2015)
- Journal:
- Dyes and pigments
- Issue:
- Volume 113(2015)
- Issue Display:
- Volume 113, Issue 2015 (2015)
- Year:
- 2015
- Volume:
- 113
- Issue:
- 2015
- Issue Sort Value:
- 2015-0113-2015-0000
- Page Start:
- 18
- Page End:
- 26
- Publication Date:
- 2015-02
- Subjects:
- Squaraine dye -- Near-IR sensitization -- Phenothiazine -- Dye-sensitized solar cell -- π−Bridge units -- Metal-free organic dyes
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.2014.07.031 ↗
- 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:
- 5437.xml