Single‐Crystal Ferroelectric‐Based (K,Na)NbO3 Microcuboid/CuO Nanodot Heterostructures with Enhanced Photo–Piezocatalytic Activity

材料科学 异质结 单晶 光催化 氧化还原 罗丹明B 纳米点 微晶 Crystal(编程语言) 载流子 催化作用 反应速率常数 化学工程 纳米技术 光电子学 结晶学 化学 动力学 量子力学 物理 工程类 生物化学 冶金 程序设计语言 计算机科学
作者
Eunmi Im,Seonhwa Park,Geon‐Tae Hwang,Dong Choon Hyun,Yuho Min,Geon Dae Moon
出处
期刊:Small [Wiley]
卷期号:20 (1) 被引量:6
标识
DOI:10.1002/smll.202304360
摘要

Abstract Developing single‐crystal‐based heterostructured ferroelectrics with high‐performance photo–piezocatalytic activity is highly desirable to utilize large piezopotentials and more reactive charges that can trigger the desired redox reactions. To that end, a single‐crystal‐based (K,Na)NbO 3 (KNN) microcuboid/CuO nanodot heterostructure with enhanced photo–piezocataytic activity, prepared using a facile strategy that leveraged the synergy between heterojunction formation and an intense single‐crystal‐based piezoelectric effect, is reported herein. The catalytic rhodamine B degrading activity of KNN/CuO is investigated under light irradiation, ultrasonication, or co‐excitation with both stimulations. Compared to polycrystalline KNN powders and bare KNN single‐crystals, single‐crystal‐based KNN/CuO exhibits a higher piezocurrent density and an optimal energy band structure, resulting in 5.23 and 2.37 times higher piezocatalytic degradation activities, respectively. Furthermore, the maximum photo–piezocatalytic rate constant (≈0.093 min −1 ) of KNN/CuO under 25 min ultrasonication and light irradiation is superior to that of other KNN‐based catalysts, and 1.6 and 48.6 times higher than individual piezocatalytic and photocatalytic reaction rate constants, respectively. The excellent photo–piezocatalytic activity is attributed to the enhanced charge‐carrier separation and proper alignment of band structure to the required redox levels by the appropriate p–n heterojunction and high piezoelectric potential. This report provides useful insight into the relationships between heterojunctions, piezoelectric responses, and catalytic mechanisms for single‐crystal‐based heterostructured catalysts.
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