Photoelectrochemical water splitting is one of the most interesting alternatives to produce hydrogen in a clean way by solar energy conversion.(1) Despite the huge potential and great advances, new materials need to be developed in order to take this technology to a commercial level. At present, different materials as oxides, oxisulfides and metal chalcogenides are being investigated as photoelectrodes in photoelectrochemical cells. However, achieving high energy conversion efficiencies by using a single material is a very tricky objective. Therefore, hybrid materials are getting a lot of attention lately. (2)

In this work, we present a hybrid material formed by the heterojunction of a novel synthesized organic conductive polymer and TiO2 nanocrystals. The nanostructured conjugated porous polymer is based on dithiothiophene moiety (Nano-CMPDTT) and was synthesized by Sonogashira cross coupling reaction from precursors in mini-emulsion conditions. In order to elucidate the electronic structure and the ability of this material to be used as a photocatalyst, HOMO and LUMO positions were determined by cyclic voltammetry. The energy diagram shows an ideal position of the energy bands in order to use the synthesized polymer as an electron injector to TiO2 in photocatalytic reactions. TiO2 NCs and organic polymer suspensions have been deposited by spin coating in ITO glasses. The formed films have been characterized by X-ray diffraction, SEM, EDX and AFM. Photoelectrochemical measurements were performed in a three electrode cell configuration, using the hybrid material as the working electrode. The hybrid material presents an enhancement in photovoltages and photocurrents values. Electrochemical Impedance Spectroscopy (EIS) was performed to confirm the improved charge transfer observed when illuminating the hybrid material in comparison to the TiO2 nanocrystals alone. In fact, a decrease in the resistance associated with this phenomenon was found. This confirms that the presence of the polymer in the hybrid material increases the absorption of light, charge transfer and reduces electron-hole recombination, making this hybrid a good candidate to be used as a photoelectrode for the hydrogen evolution reaction. In fact, recent results show an improvement in the energy conversion efficiency by using this new hybrid material as electrode compared with regular TiO2.

[1] Z. Chen, H. N. Dinh, E. Miller, Photoelectrochemical Water Splitting (Springer New York, New York, NY, 2013; http://link.springer.com/10.1007/978-1-4614-8298-7), SpringerBriefs in Energy.

[2] M. P. Arciniegas et al., Self-Assembled Dense Colloidal Cu2Te Nanodisk Networks in P3HT Thin Films with Enhanced Photocurrent. Adv. Funct. Mater. 26, 4535–4542 (2016).