Zhang Xiaolei, Hu Cheng, Zhu Zijian, Zhang Yingge, Tu Shuchen, Zhang Yihe, Ma Tianyi, Chen Fang, Huang Hongwei
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.
SCNU Environmental Research Institute, Guangdong Provincial Key Laboratory of Chemical Pollution and Environmental Safety & MOE Key Laboratory of Theoretical Chemistry of Environment, School of Environment, South China Normal University, Guangzhou 510006, China.
J Colloid Interface Sci. 2023 Nov 15;650(Pt B):1536-1549. doi: 10.1016/j.jcis.2023.07.122. Epub 2023 Jul 20.
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.
光催化在环境净化方面显示出巨大潜力,但存在光电荷快速复合和光吸收有限的问题。压电极化被认为是一种驱动电荷分离的有前景的方法,但它总是依赖于耗能的超声振动。在此,在0D/2D α-FeO/BiWO中开发了一种由弱力驱动的压电极化和Z型结构建的集成双电场的压电光催化系统。低频水流诱导的压电极化场的引入加速了极性BiWO的体相光激发载流子的迁移,与紧密界面形成Z型结保证了界面电荷的空间分离和强可见光响应。受益于这些优点,水流触发的α-FeO/BiWO在20分钟内实现了82%的优异盐酸四环素光降解效率,优于先前报道中的相关压电光催化剂,甚至优于那些由高频超声驱动的催化剂。KPFM和DFT计算为α-FeO和BiWO之间的Z型转移途径提供了有力证据。此外,PFM、COMSOL模拟、ESR和光电化学表征很好地证实了构建Z型结和引入压电极化的协同效应。这项工作为设计压电光催化系统提供了一种新策略,并可能充分利用流体动力学特性实现污水的原位处理。