367
Views
9
CrossRef citations to date
0
Altmetric
Articles

A new 1H-pyridin-(2E)-ylidene ruthenium complex as sensitizer for a dye-sensitized solar cell

, , , &
Pages 1384-1395 | Received 02 Aug 2012, Accepted 17 Jan 2013, Published online: 09 Apr 2013
 

Abstract

The new heteroleptic ruthenium(II) complex containing a 1H-pyridin-(2E)-ylidene (PYE) ligand was synthesized and characterized using UV/Vis, FTIR, and NMR spectroscopies, mass spectrometry, elemental analysis, and cyclic voltammetry. The photovoltaic performance of the ruthenium complex as a charge transfer photosensitizer in nc-titanium dioxide based dye-sensitized solar cell was studied and compared with cis-bis(isothiocyanato)(2,2′-bipyridyl-4,4′-dicarboxylato)(2,2′-bipyridyl-4,4′-di-nonyl)ruthenium(II) (Z907) under standard AM 1.5 sunlight. The complex CS90 gave a photocurrent density of 1.80 mA cm−2, 400 mV open-circuit potential, and 0.58 fill factor yielding an efficiency of 0.42% where the reference Z907 yielded an efficiency of 4.12%. The decrease in conversion efficiency observed for CS90 is attributed to a steric interaction between PYE and the TiO2 surface that prevents optimum binding and also restricts ligand dynamics that are associated with oxidation state changes.

Acknowledgements

We acknowledge the project support funds of State Planning Organization (DPT), Ege University, University of York, and Pamukkale University.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.