Exploring the Synthesis, Band Edge Insights, and Photoelectrochemical Water Splitting Properties of Lead Vanadates

Exploring the ideal and stable semiconductor material for the efficient photoelectrochemical (PEC) overall water splitting reaction has remained a major challenge. Herein, we develop a facile hydrothermal method for the fabrication of monoclinic Pb-3[VO4](2) and orthorhombic PbV2O6 thin films for the efficient and stable PEC overall water splitting applications. Detailed characterization was performed to study the crystal structure and optical, electrical, and electrochemical properties. The band edge positions of Pb-3[VO4](2) and PbV2O6 are determined using spectroscopic data, revealing the conduction band edge positioned near the water reduction potential [similar to 0 V vs reversible hydrogen electrode (RHE)] and the valence band edge positioned well above the water oxidation potential, indicating the possible utilization of photogenerated electrons and holes for efficient reduction and oxidation, respectively. With the optimized PbV2O6 thin films, a maximum photocurrent of 0.35 mA cm(-2) was obtained at 1.23 V versus RHE and the stable production of both O-2 and H-2 is observed with >90% Faradaic efficiency. Importantly, this work demonstrates the possibility of utilizing lead vanadate materials for PEC water splitting applications.

Automated summary

This study developed Pb-3[VO4](2) and PbV2O6 thin films for efficient and stable photoelectrochemical water splitting. Characterization showed that these films have suitable band edge positions for efficient reduction and oxidation. The optimized PbV2O6 thin films achieved a maximum photocurrent of 0.35 mA cm(-2), with stable production and high Faradaic efficiency for both O-2 and H-2.