Facet-dependent spatial charge separation with rational cocatalyst deposition on BiVO4

Rational assembly of cocatalyst on the photocatalyst with exposed functional crystal facets has been demonstrated to be viable in enhancing the photocatalytic activity. However, greater attention is paid to the property of the loaded cocatalyst while the effect of varied functional facet exposure is relatively less discussed. Herein, dual-faceted BiVO4 with well-defined {010} and {110} facets but with varied {010}/ {110} exposure extent ratios are coupled with CoOx which is known as a cocatalyst for water oxidation. The enhancement induced by the cocatalyst loading depends on both its deposit location and the ratio of {010}/{110} facet exposure. When selectively deposited on oxidation {110} facet, CoOx generates over two-fold enhancement on BiVO4 in photocatalytic oxygen evolution as compared to its randomly deposited analogue. Meanwhile, the {010}-dominant BiVO4 is more obviously benefited from the cocatalyst loading to both photocatalytic water oxidation and hydrogen peroxide generation reactions with respect to the {110}-dominant BiVO4. Further investigation reveals that CoOx functions more effectively in PL quenching and generating greater band bending on {010}-dominant BiVO4, substantiating the better enhancement in reducing charge recombination and forming larger space charge region width for charge separation, which deliver greater photocatalytic activity enhancement on {010} dominant BiVO4. (C)& nbsp;2022 Elsevier Ltd. All rights reserved.

Automated summary

It has been demonstrated that loading a cocatalyst onto a photocatalyst with exposed crystal facets can enhance photocatalytic activity. In this study, dual-faceted BiVO4 with different {010}/{110} exposure ratios was coupled with CoOx as a water oxidation cocatalyst. The location of cocatalyst deposition and the ratio of {010}/{110} facet exposure were found to determine the enhancement induced by the cocatalyst loading. Additionally, it was found that {010}-dominant BiVO4 benefitted more from the cocatalyst loading in both photocatalytic water oxidation and hydrogen peroxide generation reactions compared to {110}-dominant BiVO4.