Double D–π–A Dye Linked by 2, 2′‐Bipyridine Dicarboxylic Acid: Influence of para‐ and meta‐Substituted Carboxyl Anchoring Group. Issue 5 (5th February 2015)
- Record Type:
- Journal Article
- Title:
- Double D–π–A Dye Linked by 2, 2′‐Bipyridine Dicarboxylic Acid: Influence of para‐ and meta‐Substituted Carboxyl Anchoring Group. Issue 5 (5th February 2015)
- Main Title:
- Double D–π–A Dye Linked by 2, 2′‐Bipyridine Dicarboxylic Acid: Influence of para‐ and meta‐Substituted Carboxyl Anchoring Group
- Authors:
- Ganesan, Paramaguru
Chandiran, Aravind Kumar
Gao, Peng
Rajalingam, Renganathan
Grätzel, Michael
Nazeeruddin, Mohammad Khaja - Abstract:
- Abstract: Starting from 2, 2′‐bipyridine dicarboxylic acid, two new (D –π–A)2 sensitizers, including m ‐DA with the carboxyl anchoring group substituted meta to the donor‐bridge moiety and p ‐DA with a para ‐substituted anchoring group, were synthesized in order to evaluate the impact of the position of the anchoring group on the optical, electrochemical, and photovoltaic properties of dye‐sensitized solar cells. p ‐DA exhibits red‐shifted absorption behavior compared to m ‐DA, owing to the more efficiently extended π‐conjugation with para substitution. Both m ‐DA and p ‐DA are adsorbed on the mesoporous TiO2 surface by using both of their carboxylic acid groups in a bianchoring mode, which is confirmed through attenuated total reflectance FTIR analysis. Red‐shifted absorption of p ‐DA assists the achievement of a red‐shifted incident photon‐to‐electron conversion efficiency and a higher short‐circuit current density than m ‐DA. The photogenerated electron lifetime in TiO2 is also found to be higher for para substituted p ‐DA than the meta ‐substituted m ‐DA, which results in a higher open‐circuit voltage. All of the results suggest that dicarboxyl‐2, 2′‐bipyridine can be used as an acceptor for metal‐free organic sensitizers. However, the anchoring segments should be adjusted to the favorable position of the corresponding donor‐bridge moieties for better conjugation. Abstract : On the bench: Two new (D –π–A)2 organic sensitizers ( m ‐DA, p ‐DA) employing a 2, 2′‐bipyridineAbstract: Starting from 2, 2′‐bipyridine dicarboxylic acid, two new (D –π–A)2 sensitizers, including m ‐DA with the carboxyl anchoring group substituted meta to the donor‐bridge moiety and p ‐DA with a para ‐substituted anchoring group, were synthesized in order to evaluate the impact of the position of the anchoring group on the optical, electrochemical, and photovoltaic properties of dye‐sensitized solar cells. p ‐DA exhibits red‐shifted absorption behavior compared to m ‐DA, owing to the more efficiently extended π‐conjugation with para substitution. Both m ‐DA and p ‐DA are adsorbed on the mesoporous TiO2 surface by using both of their carboxylic acid groups in a bianchoring mode, which is confirmed through attenuated total reflectance FTIR analysis. Red‐shifted absorption of p ‐DA assists the achievement of a red‐shifted incident photon‐to‐electron conversion efficiency and a higher short‐circuit current density than m ‐DA. The photogenerated electron lifetime in TiO2 is also found to be higher for para substituted p ‐DA than the meta ‐substituted m ‐DA, which results in a higher open‐circuit voltage. All of the results suggest that dicarboxyl‐2, 2′‐bipyridine can be used as an acceptor for metal‐free organic sensitizers. However, the anchoring segments should be adjusted to the favorable position of the corresponding donor‐bridge moieties for better conjugation. Abstract : On the bench: Two new (D –π–A)2 organic sensitizers ( m ‐DA, p ‐DA) employing a 2, 2′‐bipyridine dicarboxylic acid unit as an acceptor and anchoring group are designed. The m ‐DA has the anchoring part substituted meta to the donor moiety and p ‐DA has a para ‐substituted anchoring moiety. Overall, para ‐substituted p ‐DA exhibits better photovoltaic performance than meta ‐substituted m ‐DA. … (more)
- Is Part Of:
- Chemphyschem. Volume 16:Issue 5(2015)
- Journal:
- Chemphyschem
- Issue:
- Volume 16:Issue 5(2015)
- Issue Display:
- Volume 16, Issue 5 (2015)
- Year:
- 2015
- Volume:
- 16
- Issue:
- 5
- Issue Sort Value:
- 2015-0016-0005-0000
- Page Start:
- 1035
- Page End:
- 1041
- Publication Date:
- 2015-02-05
- Subjects:
- 2, 2′‐bipyridine -- bianchoring -- double acceptor -- dyes/pigments -- solar cells
Chemistry, Physical and theoretical -- Periodicals
541.05 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cphc.201402822 ↗
- Languages:
- English
- ISSNs:
- 1439-4235
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3172.310500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4534.xml