Unraveling the role of Ti3C2 MXene underlayer for enhanced photoelectrochemical water oxidation of hematite photoanodes

Abstract

Hematite is regarded as a promising photoanode for photoelectrochemical (PEC) water splitting. However, the charge recombination occurred at the interface of FTO/hematite strictly limits the PEC performance of hematite. Herein, we reported a Ti3C2 MXene underlayer modified hematite (Ti–Fe2O3) photoanode via a simple drop-casting followed by hydrothermal and annealing processes. Owing to the bifunctional role of Ti3C2 MXene underlayer in improving the interfacial properties of FTO/hematite and providing Ti source for the construction of Fe2TiO5/Fe2O3 heterostructure in hematite nanostructure, the bulk and interfacial charge transfer dynamics of hematite are significantly enhanced, and consequently enhancing the PEC performance. Compared with the pristine hematite, the as-prepared Ti–Fe2O3 photoanode shows an increased photocurrent density from 0.80 mA/cm2 to 1.30 mA/cm2 at 1.23 V vs. RHE. Moreover, a further promoted PEC performance including a dramatically increased photocurrent density of 2.49 mA/cm2 at 1.23 V vs. RHE and an obviously lowered onset potential is achieved for the Ti–Fe2O3 sample after the subsequent surface F-treatment and the loading of FeNiOOH cocatalyst. Such results suggest that the introduction of Ti3C2 MXene underlayer is a facile but effective approach to improve the PEC water splitting activity of hematite.