Tuning
the charge transfer processes through a built-in electric
field is an effective way to accelerate the dynamics of electro- and
photocatalytic reactions. However, the coupling of the built-in electric
field of p–n heterojunctions and the microstrain-induced polarization
on the impact of piezocatalysis has not been fully explored. Herein,
we demonstrate the role of the built-in electric field of p-type BiOI/n-type
BiVO4 heterojunctions in enhancing their piezocatalytic
behaviors. The highly crystalline p–n heterojunction is synthesized
by using a coprecipitation method under ambient aqueous conditions.
Under ultrasonic irradiation in water exposed to air, the p–n
heterojunctions exhibit significantly higher production rates of reactive
species (·OH, ·O2–, and 1O2) as compared to isolated BiVO4 and
BiOI. Also, the piezocatalytic rate of H2O2 production
with the BiOI/BiVO4 heterojunction reaches 480 μmol
g–1 h–1, which is 1.6- and 12-fold
higher than those of BiVO4 and BiOI, respectively. Furthermore,
the p–n heterojunction maintains a highly stable H2O2 production rate under ultrasonic irradiation for up
to 5 h. The results from the experiments and equation-driven simulations
of the strain and piezoelectric potential distributions indicate that
the piezocatalytic reactivity of the p–n heterojunction resulted
from the polarization intensity induced by periodic ultrasound, which
is enhanced by the built-in electric field of the p–n heterojunctions.
This study provides new insights into the design of piezocatalysts
and opens up new prospects for applications in medicine, environmental
remediation, and sonochemical sensors