Better Together: Ilmenite/Hematite Junctions for Photoelectrochemical Water Oxidation

High Resolution Image Download MS PowerPoint Slide Hematite (α-Fe 2 O 3 ) is an earth-abundant indirect n-type semiconductor displaying a band gap of about 2.2 eV, useful for collecting a large fraction of visible photons, with frontier energy levels suitably aligned for carrying out the photoelectrochemical water oxidation reaction under basic conditions. The modification of hematite mesoporous thin-film photoanodes with Ti(IV), as well as their functionalization with an oxygen-evolving catalyst, leads to a 6-fold increase in photocurrent density with respect to the unmodified electrode. In order to provide a detailed understanding of this behavior, we report a study of Ti-containing phases within the mesoporous film structure. Using X-ray absorption fine structure and high-resolution transmission electron microscopy coupled with electron energy loss spectroscopy, we find that Ti(IV) ions are incorporated within ilmenite (FeTiO 3 ) near-surface layers, thus modifying the semiconductor–electrolyte interface. To the best of our knowledge, this is the first time that an FeTiO 3 /α-Fe 2 O 3 composite is used in a photoelectrochemical setup for water oxidation. In fact, previous studies of Ti(IV)-modified hematite photoanodes reported the formation of pseudobrookite (Fe 2 TiO 5 ) at the surface. By means of transient absorption spectroscopy, transient photocurrent experiments, and electrochemical impedance spectroscopy, we show that the formation of the Fe 2 O 3 /FeTiO 3 interface passivates deep traps at the surface and induces a large density of donor levels, resulting in a strong depletion field that separates electron and holes, favoring hole injection in the electrolyte. Our results provide the identification of a phase coexistence with enhanced photoelectrochemical performance, allowing for the rational design of new photoanodes with improved kinetics.