Skip to main content

Research Repository

Advanced Search

Ethynyl thiophene-appended unsymmetrical zinc porphyrin sensitizers for dye-sensitized solar cells

Reeta, P. Silviya; Giribabu, Lingamallu; Senthilarasu, Sundaram; Hsu, Min-Hung; Kumar, D. Kishore; Upadhyaya, Hari M.; Robertson, Neil; Hewat, Tracy

Authors

P. Silviya Reeta

Lingamallu Giribabu

Min-Hung Hsu

D. Kishore Kumar

Hari M. Upadhyaya

Neil Robertson

Tracy Hewat



Abstract

Four unsymmetrical porphyrins of A2B donor–π–acceptor type have been designed, synthesized, characterized and their photovoltaic properties explored. Polycyclic aromatic hydrocarbons (PAH), such as pyrene or fluorene, act as a donor, the porphyrin is the π-spacer, appended with an ethynyl thiophene linker, and either cyanoacrylic acid or malonic acid acts as the acceptor. All of the compounds were characterized by 1H NMR and mass spectrometry. UV-Vis absorption spectra and B or Soret (λex at 440 nm for the four sensitizers reported) band-excited fluorescence emission spectra were also obtained. The electrochemical properties suggest that the first oxidation is ring-centred, which is supported by in situ spectro-electrochemical and DFT computational studies. The synthesized porphyrins were applied in dye-sensitized solar cells (DSSCs). A conversion efficiency of up to 3.14%was realized for PYR–Por–MA under our experimental conditions.

Journal Article Type Article
Acceptance Date Jan 27, 2014
Online Publication Date Jan 30, 2014
Publication Date 2014
Deposit Date Mar 14, 2023
Print ISSN 2046-2069
Publisher Royal Society of Chemistry
Peer Reviewed Peer Reviewed
Volume 4
Issue 27
Pages 14165-14175
DOI https://doi.org/10.1039/C3RA47948J