Zhou Xiaofeng, Shen Bo, Zhai Jiwei, Yuan Jiayin, Hedin Niklas
School of Materials Science and Engineering, Tongji University, Shanghai 201804, China.
Department of Materials and Environmental Chemistry, Stockholm University, Stockholm SE-106 91, Sweden.
ACS Appl Mater Interfaces. 2024 Apr 24;16(16):20472-20484. doi: 10.1021/acsami.4c01283. Epub 2024 Apr 9.
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 BiVO 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, ·O, and O) as compared to isolated BiVO and BiOI. Also, the piezocatalytic rate of HO production with the BiOI/BiVO heterojunction reaches 480 μmol g h, which is 1.6- and 12-fold higher than those of BiVO and BiOI, respectively. Furthermore, the p-n heterojunction maintains a highly stable HO 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.
通过内置电场调节电荷转移过程是加速电催化和光催化反应动力学的有效方法。然而,p-n异质结的内置电场与微应变诱导极化对压电催化影响的耦合尚未得到充分研究。在此,我们展示了p型BiOI/n型BiVO异质结的内置电场在增强其压电催化行为中的作用。通过在环境水条件下使用共沉淀法合成了高结晶度的p-n异质结。在暴露于空气中的水中进行超声辐照时,与孤立的BiVO和BiOI相比,p-n异质结表现出显著更高的活性物种(·OH、·O和O)生成速率。此外,BiOI/BiVO异质结产生HO的压电催化速率达到480 μmol g h,分别比BiVO和BiOI高1.6倍和12倍。此外,p-n异质结在超声辐照下长达5小时内保持高度稳定的HO生成速率。应变和压电势分布的实验结果以及方程驱动模拟表明,p-n异质结的压电催化反应活性源于周期性超声诱导的极化强度,p-n异质结的内置电场增强了该极化强度。本研究为压电催化剂的设计提供了新的见解,并为医学、环境修复和声化学传感器等应用开辟了新的前景。