Photocatalytic Hydrogen Evolution from Substoichiometric Colloidal WO3–x Nanowires

Abstract

We report direct photocatalytic hydrogen evolution from substoichiometric highly reduced tungsten oxide (WO x ) nanowires (NWs) using sacrificial alcohol. WO x NWs are synthesized via nonaqueous colloidal synthesis with a diameter of about 4 nm and an average length of about 250 nm. As-synthesized WO x NWs exhibit a broad absorption across the visible to infrared regions attributed to the presence of oxygen vacancies. The optical band gap is increased in these WO x NWs compared to stoichiometric bulk tungsten oxide (WO 3 ) powders as a result of the Burstein–Moss shift. As a consequence of this increase, we demonstrate direct photocatalytic hydrogen production from WO x NWs through alcohol photoreforming. The stable H 2 evolution on platinized WO x NWs is observed under conditions in which platinized bulk WO 3 and bulk WO 2.9 powders either do not show activity or show very low rates, suggesting that increased surface area and specific exposed facets are key for the improved performance of WO x NWs. This work demonstrates that control of size and composition can lead to unexpected and beneficial changes in the photocatalytic properties of semiconductor materials.