Aggregation induced light harvesting of molecularly engineered D-A-π-A carbazole dyes for dye-sensitized solar cells. (1st November 2018)
- Record Type:
- Journal Article
- Title:
- Aggregation induced light harvesting of molecularly engineered D-A-π-A carbazole dyes for dye-sensitized solar cells. (1st November 2018)
- Main Title:
- Aggregation induced light harvesting of molecularly engineered D-A-π-A carbazole dyes for dye-sensitized solar cells
- Authors:
- Hemavathi, B.
Jayadev, V.
Pradhan, Sourava C.
Gokul, G.
Jagadish, Kusuma
Chandrashekara, G.K.
Ramamurthy, Praveen C.
Pai, Ranjith Krishna
Narayanan Unni, K.N.
Ahipa, T.N.
Soman, Suraj
Geetha Balakrishna, R. - Abstract:
- Graphical abstract: Highlights: Dyes with cyanopyridine auxiliary acceptor were synthesized. J-aggregation leads to broader absorption spectra. Aggregation assisted in better performance. Abstract: Novel class of metal free organic dyes (CCTh andCCBz ) with D-A-π-A configuration, having carbazole as donor and 3-cyanopyridine as auxiliary acceptor replacing conventional benzannulated heterocycles along with variable π-linkers were synthesized and used in dye-sensitized solar cells (DSSCs). Both the dyes are having cyanoacrylic acid as the anchoring group with thiophene (CCTh ) and phenylene (CCBz ) as π-linkers. The photophysical, electrochemical, theoretical and photovoltaic properties of the dyes were investigated in detail. The absorption spectra of dyes on TiO2 showed broader absorption band forCCTh in comparison to the solution spectra indicating aggregation in solid state. The aggregation studies in varied THF/water fraction indicates J -aggregation for both the dyes.CCTh with thiophene linker showed broader absorption compared toCCBz, and the photovoltaic performance recorded forCCTh directly indicates better light harvesting ability corresponding to the red shifted J- aggregated states. Hence, solar cells fabricated withCCTh gave a power conversion efficiency of 3.39% andCCBz delivered an efficiency of 2.03% under full sun condition. A detailed investigation of device dynamics have been carried out employing charge extraction (CE), intensity-modulated photovoltageGraphical abstract: Highlights: Dyes with cyanopyridine auxiliary acceptor were synthesized. J-aggregation leads to broader absorption spectra. Aggregation assisted in better performance. Abstract: Novel class of metal free organic dyes (CCTh andCCBz ) with D-A-π-A configuration, having carbazole as donor and 3-cyanopyridine as auxiliary acceptor replacing conventional benzannulated heterocycles along with variable π-linkers were synthesized and used in dye-sensitized solar cells (DSSCs). Both the dyes are having cyanoacrylic acid as the anchoring group with thiophene (CCTh ) and phenylene (CCBz ) as π-linkers. The photophysical, electrochemical, theoretical and photovoltaic properties of the dyes were investigated in detail. The absorption spectra of dyes on TiO2 showed broader absorption band forCCTh in comparison to the solution spectra indicating aggregation in solid state. The aggregation studies in varied THF/water fraction indicates J -aggregation for both the dyes.CCTh with thiophene linker showed broader absorption compared toCCBz, and the photovoltaic performance recorded forCCTh directly indicates better light harvesting ability corresponding to the red shifted J- aggregated states. Hence, solar cells fabricated withCCTh gave a power conversion efficiency of 3.39% andCCBz delivered an efficiency of 2.03% under full sun condition. A detailed investigation of device dynamics have been carried out employing charge extraction (CE), intensity-modulated photovoltage spectroscopy (IMVS) and open-circuit voltage decay (OCVD) measurements. … (more)
- Is Part Of:
- Solar energy. Volume 174(2018)
- Journal:
- Solar energy
- Issue:
- Volume 174(2018)
- Issue Display:
- Volume 174, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 174
- Issue:
- 2018
- Issue Sort Value:
- 2018-0174-2018-0000
- Page Start:
- 1085
- Page End:
- 1096
- Publication Date:
- 2018-11-01
- Subjects:
- Cyanopyridine -- Carbazole -- D-A-π-A -- DSSC
Solar energy -- Periodicals
Solar engines -- Periodicals
621.47 - Journal URLs:
- http://www.sciencedirect.com/science/journal/0038092X ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.solener.2018.09.073 ↗
- Languages:
- English
- ISSNs:
- 0038-092X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8327.200000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11132.xml