Abstract

The surface modification of semiconductor photoelectrodes with passivation overlayers has attracted great attention as an effective strategy to improve the charge separation and charge transfer processes across the semiconductor-electrolyte interface. In this work, a thin Fe2 TiO5 layer was decorated on nanostructured hematite nanoflake and nanocoral photoanodes (by thermal oxidation of iron foils) by a facile water-based solution method. Photoelectrochemical measurements show that the Fe2 O3 /Fe2 TiO5 heterostructure exhibits an obvious enhancement in photoelectrochemical water oxidation performance compared to the pristine hematite. For example, at 1.23 V versus the reversible hydrogen electrode (VRHE ) in 1 m KOH under AM 1.5 G (100 mW cm(-2) ) illumination, a 4-8× increase in the water oxidation photocurrent is achieved for Fe2 O3 /Fe2 TiO5 , and a considerable cathodic shift of the onset potential up to 0.53-0.62 VRHE is obtained. Moreover, the performance of the Fe2 O3 /Fe2 TiO5 heterostructure can be further improved by decoration with a SnOx layer. The enhancement in photocurrent can be attributed to the synergistic effect of Fe2 TiO5 /SnOx overlayers passivating surface states, and thus reducing surface electron-hole recombination.

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