Abstract

Charge separation and transfer kinetics play a significant role in photocatalytic water oxidation, which is sensitive to the crystal facets. Herein, the bismuth tungstate (Bi2WO6) films were used as a model photoanode to investigate how the photogenerated charges react on {131} and {200} facets under constantly applied bias in a photoelectrochemical (PEC) cell. On the WO3 electron transport layer, the Bi2WO6 films have a {200} orientation while possessing a {131} orientation on the fluorine-doped tin oxide substrate. It is discovered that {200} facets on the WO3/Bi2WO6 heterojunction display a low overpotential of PEC water oxidation, showing a 1st-order reaction behavior and faster charge transfer rate constant. Differently, water oxidation on the {131} facet on Bi2WO6 displays a 2nd-order reaction behavior. Further, density functional theory calculations were applied to demonstrate how the rate-determining step and the major formed intermediate correlate with the charge accumulation and reaction orders. The findings of this work shed fundamental light on how to rationally design and precisely modulate surface charge density and reaction kinetics for efficient (photo)electrocatalysts.

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