Triphenylamine-functionalized corrole sensitizers for solar-cell applications

New corrole sensitizers having a triphenylamine moiety at the –meso position and a carboxylic anchoring group at the pyrrole‐β position, in both free‐base and copper complex forms, have been designed, synthesized, and tried as sensitizers in dye‐sensitized solar cells. All the substituted carboxy‐co...

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Published inPhysica status solidi. A, Applications and materials science Vol. 212; no. 1; pp. 194 - 202
Main Authors Sudhakar, Kolanu, Giribabu, Lingamallu, Salvatori, Paolo, Angelis, Filippo De
Format Journal Article
LanguageEnglish
Published Weinheim Blackwell Publishing Ltd 01.01.2015
Wiley Subscription Services, Inc
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Summary:New corrole sensitizers having a triphenylamine moiety at the –meso position and a carboxylic anchoring group at the pyrrole‐β position, in both free‐base and copper complex forms, have been designed, synthesized, and tried as sensitizers in dye‐sensitized solar cells. All the substituted carboxy‐corroles were completely characterized from structural, optical and electrochemical points of view. Computational investigations by means of density functional theory (DFT) and time‐dependent‐DFT (TD‐DFT) calculations have been carried out, in order to give a deep insight into the charge‐injection process. Quite low photovoltaic performances were obtained, particularly for the investigated copper complexes, possibly due to an unfavorable energy‐level alignment between the dye's injecting states and TiO2 conduction band, limiting the charge injection and thus the photocurrent extracted from the devices. Our study may provide the guidelines for future development of more efficient solar‐cell sensitizers. Scheme of a dye‐sensitized solar cell (DSC) based on a triphenylamine‐corrole dye and a I–/I3– electrolyte.
Bibliography:ark:/67375/WNG-1MG4WLX6-6
DST-EU ESCORT (FP7-ENERGY-2010) - No. 261920
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ArticleID:PSSA201431169
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1862-6300
1862-6319
DOI:10.1002/pssa.201431169