Pyridyl vs. bipyridyl anchoring groups of porphyrin sensitizers for dye sensitized solar cells. Issue 26 (24th February 2016)
- Record Type:
- Journal Article
- Title:
- Pyridyl vs. bipyridyl anchoring groups of porphyrin sensitizers for dye sensitized solar cells. Issue 26 (24th February 2016)
- Main Title:
- Pyridyl vs. bipyridyl anchoring groups of porphyrin sensitizers for dye sensitized solar cells
- Authors:
- Angaridis, Panagiotis A.
Ferentinos, Eleftherios
Charalambidis, Georgios
Ladomenou, Kalliopi
Nikolaou, Vasilis
Biswas, Sujit
Sharma, Ganesh D.
Coutsolelos, Athanassios G. - Abstract:
- Abstract : Two D–π–A porphyrins (A = pyridyl, bipyridyl) are synthesized and used as sensitizers in DSSCs. The enhanced photovoltaic performance of the bipyridyl-sensitized device is attributed to its faster electron injection and reduced charge recombination. Abstract : The synthesis of two porphyrins with donor–π–acceptor (D–π–A) molecular architecture is described, namely Znpor-py (3a ) and Znpor-bpy (3b ), which consist of a 4- tert -butyl-phenyl group as donor and either a pyridine or a bipyridine group as acceptor at opposite positions of the porphyrin macrocycle. Photophysical and electrochemical properties of the two compounds, as well as theoretical DFT calculation results suggest that the two porphyrins have the potential to act as sensitizers in dye-sensitized solar cells (DSSCs). Both dyes contain N (pyridyl) atoms able to act as anchors onto the acid sites of TiO2 . A Znpor-py (3a ) sensitized solar cell was found to exhibit power conversion efficiency (PCE) of 3.57%, while the corresponding Znpor-bpy (3b )-functionalized solar cell showed a higher PCE of 5.08%. The enhanced short circuit current J sc and open circuit voltage V oc parameters are the main factors responsible for the improved photovoltaic performance of the latter solar cell. These are attributed to its faster charge injection into the TiO2 photoanode and its reduced charge recombination at the electrode/electrolyte interface, which result from the stronger binding and coordination geometry of theAbstract : Two D–π–A porphyrins (A = pyridyl, bipyridyl) are synthesized and used as sensitizers in DSSCs. The enhanced photovoltaic performance of the bipyridyl-sensitized device is attributed to its faster electron injection and reduced charge recombination. Abstract : The synthesis of two porphyrins with donor–π–acceptor (D–π–A) molecular architecture is described, namely Znpor-py (3a ) and Znpor-bpy (3b ), which consist of a 4- tert -butyl-phenyl group as donor and either a pyridine or a bipyridine group as acceptor at opposite positions of the porphyrin macrocycle. Photophysical and electrochemical properties of the two compounds, as well as theoretical DFT calculation results suggest that the two porphyrins have the potential to act as sensitizers in dye-sensitized solar cells (DSSCs). Both dyes contain N (pyridyl) atoms able to act as anchors onto the acid sites of TiO2 . A Znpor-py (3a ) sensitized solar cell was found to exhibit power conversion efficiency (PCE) of 3.57%, while the corresponding Znpor-bpy (3b )-functionalized solar cell showed a higher PCE of 5.08%. The enhanced short circuit current J sc and open circuit voltage V oc parameters are the main factors responsible for the improved photovoltaic performance of the latter solar cell. These are attributed to its faster charge injection into the TiO2 photoanode and its reduced charge recombination at the electrode/electrolyte interface, which result from the stronger binding and coordination geometry of the bipyridine anchoring group on TiO2 . Electrochemical impedance spectra (EIS) of the two solar cells further support these assumptions, revealing a higher charge recombination resistance R rec and a longer electron lifetime τ e for the Znpor-bpy (3b ) sensitized solar cell. … (more)
- Is Part Of:
- RSC advances. Volume 6:Issue 26(2016)
- Journal:
- RSC advances
- Issue:
- Volume 6:Issue 26(2016)
- Issue Display:
- Volume 6, Issue 26 (2016)
- Year:
- 2016
- Volume:
- 6
- Issue:
- 26
- Issue Sort Value:
- 2016-0006-0026-0000
- Page Start:
- 22187
- Page End:
- 22203
- Publication Date:
- 2016-02-24
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c5ra23445j ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1442.xml