Piezo-photocatalytic H 2 O 2 production faces a central challenge: inadequate visible-light absorption and insufficient driving forces for charge separation, especially in wide-bandgap nonpolar semiconductors. To address this, we propose a strategy that constructs Cu + -oxygen vacancy defect dipoles within nonpolar ZrO 2 to enable piezo-photo coupling. Under ultrasonic excitation, these defect dipoles produce a robust piezoelectric polarization field that facilitates directional separation of photogenerated carriers. As a result, charge recombination at visible-light-absorbing defect states is effectively suppressed, enabling synergistic utilization of mechanical and optical energy. The optimized catalyst exhibits a remarkable H 2 O 2 production rate of 415.36 μmol·g −1 ·hour −1 under ambient air/water conditions and achieves near-complete degradation (88.7%) of rhodamine B in continuous-flow wastewater treatment (1 liter within 60 min). Theoretical calculations further reveal that the defect dipoles lower the d-band center of the active sites, thereby promoting *OH desorption and accelerating H 2 O 2 formation kinetics. This study offers a viable strategy for inducing piezoelectricity in nonpolar semiconductors, thereby establishing design principles for high-performance piezo-photocatalytic systems.
Chen et al. (Fri,) studied this question.