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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Foster, Jamie Michael
University of Portsmouth
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (6/6 displayed)
- 2018Systematic derivation of a surface polarization model for planar perovskite solar cellscitations
- 2018A fast and robust numerical scheme for solving models of charge carrier transport and ion vacancy motion in perovskite solar cellscitations
- 2017Migration of cations induces reversible performance losses over day/night cycling in perovskite solar cellscitations
- 2017A mathematical model for mechanically-induced deterioration of the binder in lithium-ion electrodescitations
- 2015Improving the long-term stability of perovskite solar cells with a porous Al2O3 buffer-layercitations
- 2015Phosphonic anchoring groups in organic dyes for solid-state solar cellscitations
Places of action
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article
Phosphonic anchoring groups in organic dyes for solid-state solar cells
Abstract
We report the synthesis and the optoelectronic characterization of three new 4<i>H</i>-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 TiO<sub>2</sub> 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 TiO<sub>2</sub>-hole transporter interface, which results in a higher open circuit voltage.