Bi2YO4Cl is a robust mixed-anion
compound
suitable for solar water splitting but generally delivers a mediocre
catalytic level due to poor separation of photocarriers (e– and h+). In this work, we have modified Bi2YO4Cl by facet-engineering techniques, which generate
plate-like single crystals dominantly exposing {001} and {100} crystal
facets. These two sets of crystal facets are of diverse energy states,
thereby setting up an internal built-in electric field that can readily
separate and guide the flow of photocarriers. Thanks to this facet-aided
charge separation mechanism, the faceted Bi2YO4Cl single crystals deliver much higher activities for solar water
splitting reactions than conventional counterparts. Notably, the faceted
Bi2YO4Cl single crystals can achieve apparent
quantum efficiency as high as 7.51 and 2.52% at 420 ± 20 nm for
photocatalytic O2- and H2-evolution from water,
respectively. Stable overall water splitting under visible light illumination
(λ ≥ 420 nm) has also been attained by merging the faceted
Bi2YO4Cl single crystals into a Z-scheme system.
As a photoanode material, the faceted Bi2YO4Cl single crystals can reach a high photocurrent density of ∼1.57
mA·cm–2 at 1.23 V vs RHE under
AM 1.5G with a Faradic efficiency of almost unity.