Constructing
facet junction in semiconductor photocatalysts has
been demonstrated as an effective method to promote charge-carrier
separation and suppress carrier recombination. Herein, we proposed
a novel but facile self-doping strategy to regulate the crystal facet
exposure ratio in ferroelectric Bi3Ti
x
Nb2–x
O9 single-crystalline
nanosheets, thereby optimizing its facet junction effect. Through
tuning the atomic ratio of Ti and Nb, the exposure ratio of {001}
and {110} crystal planes in Bi3Ti
x
Nb2–x
O9 nanosheets
can be delicately modulated, and more {110} facets were exposed with
the increase of the Ti/Nb atomic ratio as evidenced by the X-ray diffraction
and scanning electron microscopy results. A facet junction between
{110} and {001} crystal planes was verified based on the density functional
theory calculation and photodeposition experiment results. Photogenerated
electrons tend to accumulate in {110}, while holes gathered in {001}
crystal planes. Owing to the optimal facet junction effect, the sample
of Ti1.05 shows the most efficient charge-carrier separation and transportation
compared to Ti0.95 and Ti1.00 as supported by the photoluminescence,
surface photovoltage, photoelectrochemistry, and electron paramagnetic
resonance (EPR) results. In addition, the oxygen vacancy arising from
the inequivalent substitution of Nb5+ by Ti4+ as proved by X-ray photoelectron spectroscopy and EPR results and
the enhanced ferroelectricity supported by P–E loops can also assist charge-carrier separation and migration.
Benefiting from these properties, Ti1.05 outperformed Ti0.95 and Ti1.00
in the photodegradation of organic dye and antibiotic molecules. Meanwhile,
the excellent antibacterial activity of Ti1.05 under visible light
was also demonstrated by the Escherichia coli sterilization experiment. This work not only presents a novel pathway
to adjust the facet junction but also provides new deep insights into
the crystal facet engineering in ferroelectrics as photocatalysts.