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Phosphonic anchoring groups in organic dyes for solid-state solar cells†
Raquel Pérez-Tejada,Konrad Wojciechowski,Jamie M. Foster,Aditya Sadhanala,Ullrich Steiner,Henry J. Snaith,Santiago Franco,Jesús Orduna
Physical Chemistry Chemical Physics Pub Date : 06/08/2015 00:00:00 , DOI:10.1039/C5CP02671G
Abstract

We report the synthesis and the optoelectronic characterization of three new 4H-pyran-4-ylidene and thiazole derivatives (pyt) as metal-free organic dyes for solid-state dye-sensitized solar cells (DSSCs). We investigate the performance and the long-term stability of devices employing pyt dyes functionalized with carboxylic and phosphonic acids as TiO2 anchoring groups. In contrast to reports on liquid electrolyte DSSCs, we show that solid-state DSSCs prepared with phosphoric pyt derivatives can achieve similar power conversion efficiency to their carboxyl analogues. We make use of the Mott–Schottky analysis and equivalent circuit models to demonstrate that a phosphonic group induces a significant increase in built-in voltage at the TiO2-hole transporter interface, which results in a higher open circuit voltage.

Graphical abstract: Phosphonic anchoring groups in organic dyes for solid-state solar cells
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