Photoelectrochemical Water Splitting with Triple Junction Polymer Solar Cells
Serkan Esiner a, Robin Willems a, Alice Furlan a, Martijn Wienk a, Rene Janssen a
a Eindhoven University of Technology (TU/e), PO Box 513, Eindhoven, 5600, Netherlands
International Conference on Hybrid and Organic Photovoltaics
Proceedings of 6th International Conference on Hybrid and Organic Photovoltaics (HOPV14)
Ecublens, Switzerland, 2014 May 11th - 14th
Organizers: Michael Graetzel and Mohammad Nazeeruddin
Poster, Serkan Esiner, 375
Publication date: 1st March 2014

Photovoltaic conversion of solar energy into electricity is being successfully employed for many years as a way of sustainable energy generation. One issue about solar power generation is that it does not always occur at desired times and places. So a method to store this energy for future usage is required. Capturing solar energy in chemical bonds of molecular fuels is an effective manner of solar energy storage. A natural example of such a conversion is already observed in photosynthesis. It is possible to convert solar energy directly into a clean fuel also by combining photovoltaic conversion and water splitting for hydrogen generation.

Some examples of solar driven water splitting include the work ofLicht et al.[i] where hydrogen generation through photoelectrochemical water splitting is illustrated with a AlGaAs/Si tandem solar cell using RuO2 and Pt-black as catalysts for a solar-to-fuel conversion efficiency of 18.2%. Nocera et al.[ii] has also shown a stand-alone solar water splitting device with silicon-based triple junction cells and earth-abundant catalysts. Recently, we have also illustrated that photoelectrochemical water splitting is achievable by combining triple junction polymer solar cells with two platinum electrodes[iii].

In practice, water splitting occurs at potentials higher than the theoretical lower limit of E0H2O = 1.229 V for the reaction H2O → H2 + ½O2. The actual water splitting potential depends on the selection of the catalysts, electrolyte and the current density, and typically lies in the range of VH2O = 1.4-1.9 V[iv]. Even though single junction polymer solar cells cannot reach such potentials, series connected triple junction polymer solar cells can.

In this work, we present photoelectrochemical water splitting with triple junction polymer solar cells both using catalysts of precious metal oxides and earth-abundant catalysts. Aiming for the highest efficiency, a previously developed high efficiency triple junction polymer solar cell[v] is first combined with ruthenium oxide (RuO2) both as hydrogen and oxygen evolution catalysts in a 1 M KOH electrolyte. A high solar-to-fuel efficiency of 5.4% is achieved with this configuration. The same solar cell is also combined with cobalt oxide (CoOx) catalyst for oxygen evolution and nickel-molybdenum-zinc (NiMoZn) catalyst for hydrogen evolution in a potassium borate (KBi) electrolyte of near neutral pH conditions (pH9.2). Again, a high solar-to-fuel efficiency of 4.9% is measured. Furthermore, a stand-alone photoelectrochemical water splitting device with a large surface area solar cell connected to RuO2-RuO2 catalysts results in a solar-to-fuel efficiency of 3.6%.



[i] Licht, S.; Wang, B.; Mukerji, S.; Soga, T.; Umeno, M.; Tributsch, H. Int. J. Hydrogen Energy 2001, 26, 653. [ii] Reece, S.Y.; Hamel, J. A.; Sung, K.; Jarvi, T. D.; Esswein, A. J.; Pijpers, J. J. H.; Nocera,D. G. Science, 2011, 334, 645. [iii] Esiner, S.; van Eersel, H.; Wienk, M. M.; and Janssen, R. A. J. Adv. Mater., 2013, 25, 2932–2936 [iv] Cook, T. R.; Dogtuan, D. K.; Reece, S. Y.; Surendranath, Y.; Teets, T. S.; Nocera, D. G. Chem. Rev. 2010, 110, 6474. [v] Li, W.; Furlan, A.; Hendriks, K. H.; Wienk, M. M.; and Janssen, R. A. J. Journal of the American Chemical Society, 2013, 135 (15), 5529-5532
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