Mesoporous α-Fe2O3 thin films synthesized via the sol-gel process for light-driven water oxidationElectronic supplementary information (ESI) available. See DOI: 10.1039/c2cp42535a

• Main Authors: Hamd, Wael, Cobo, Saioa, Fize, Jennifer, Baldinozzi, Gianguido, Schwartz, Wilfrid, Reymermier, Maryse, Pereira, Alexandre, Fontecave, Marc, Artero, Vincent, Laberty-Robert, Christel, Sanchez, Clement
• Format: Journal Article
• Language: English
• Published: 17.09.2012
• ISSN: 1463-9076; 1463-9084
• DOI: 10.1039/c2cp42535a

This work reports a facile and cost-effective method for synthesizing photoactive α-Fe 2 O 3 films as well as their performances when used as photoanodes for water oxidation. Transparent α-Fe 2 O 3 mesoporous films were fabricated by template-directed sol-gel chemistry coupled with the dip-coating approach, followed by annealing at various temperatures from 350 °C to 750 °C in air. α-Fe 2 O 3 films were characterized by X-ray diffraction, XPS, FE-SEM and electrochemical measurements. The photoelectrochemical performance of -Fe 2 O 3 photoanodes was characterized and optimized through the deposition of Co-based co-catalysts via different methods (impregnation, electro-deposition and photo-electro-deposition). Interestingly, the resulting hematite films heat-treated at relatively low temperature (500 C), and therefore devoid of any extrinsic dopant, achieve light-driven water oxidation under near-to-neutral (pH = 8) aqueous conditions after decoration with a Co catalyst. The onset potential is 0.75 V vs. the reversible hydrogen electrode (RHE), thus corresponding to 450 mV light-induced underpotential, although modest photocurrent density values (40 A cm 2 ) are obtained below 1.23 V vs. RHE. These new materials with a very large interfacial area in contact with the electrolyte and allowing for a high loading of water oxidation catalysts open new avenues for the optimization of photo-electrochemical water splitting. Mesostructured hematite films display original photoelectrocatalytic response for water oxidation when coupled with Co-based catalysts.