Efficient piezo-photocatalysis of 0D/2D α-FeO/BiWO: Synergy of weak force-driven piezoelectric polarization and Z-scheme junction.

J Colloid Interface Sci

Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences, Beijing 100083, China. Electronic address:

Published: November 2023

Photocatalysis shows huge potential in environmental purification, but suffers from fast photocharge recombination and finite photoabsorption. Piezoelectric polarization is perceived as a promising approach to drive charge separation, but it always relies on the energy-guzzling ultrasonic vibration. Herein, a piezo-photocatalytic system integrating dual electric fields constructed by weak force-driven piezoelectric polarization and Z-scheme junction is developed in 0D/2D α-FeO/BiWO. The introduction of low-frequency water flow-induced piezoelectric polarization field accelerates the migration of bulk photoexcited carriers of polar BiWO, and forming Z-scheme junction with intimate interface guarantees the spatial separation of interfacial charges and strong visible light response. Benefiting from these merits, water flow-triggered α-FeO/BiWO delivers a superb tetracycline hydrochloride photodegradation efficiency of 82% within 20 min, which outperforms related piezo-photocatalysts in previous reports, even those driven by high-frequency ultrasound. KPFM and DFT calculations provide forceful evidence for the Z-scheme transfer pathway between α-FeO and BiWO. Additionally, the synergetic effect of constructing the Z-scheme junction and introducing piezoelectric polarization is well confirmed by PFM, COMSOL simulation, ESR and photoelectrochemical characterization. This work offers a novel strategy to design the piezo-photocatalytic system and maybe realize the in-situ treatment of sewage taking full advantage of hydrodynamic characteristics.

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Source
http://dx.doi.org/10.1016/j.jcis.2023.07.122DOI Listing

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