Built in electric field boosted photocatalytic performance in a ferroelectric layered material SrBi2Ta2O9 with oriented facets: Charge separation and mechanism insights

材料科学 铁电性 光催化 电场 降级(电信) 可见光谱 极化(电化学) 化学工程 光电子学 纳米技术 化学物理 有机化学 电介质 物理化学 催化作用 化学 电子工程 物理 工程类 量子力学
作者
Biru Liao,Xiaomin Liao,Huiyuan Xie,Yuanchu Qin,Yi Zhu,Yang Yu,Sen Hou,Yuanming Zhang,Xiaoyun Fan
出处
期刊:Journal of Materials Science & Technology [Elsevier]
卷期号:123: 222-233 被引量:32
标识
DOI:10.1016/j.jmst.2022.01.023
摘要

Antibiotics have received increasing attention due to their potential adverse effects on aquatic life and human health. How to efficiently degrade them into harmless substances is a challenging subject. Ferroelectric materials with a built-in electric field can offer a strong separation ability for the photoinduced-charge pairs and are now found to be used as photocatalysts. Herein, a series of different morphologies of SrBi2Ta2O9 ferroelectric photocatalysts with high antibiotic degradation efficiency have been successfully synthesized through a molten salt method. With the addition of KCl, SrBi2Ta2O9 (SBTO 3) with exposed (001) facets shows the most excellent photocatalytic activity for decomposing tetracycline (TC) and ciprofloxacin (CIP) under visible light illumination (λ > 420 nm). The rate constants of SBTO 3 for TC and CIP degradation are 1.38 × 10–1 and 4.54 × 10–2 min–1, which are 18 and 138 times that of the unmodified sample, respectively. The enhancement of photocatalytic performance is mainly attributed to the spontaneous polarization electric field along the [001] direction which provides a strong driven force for the separation of photoinduced charges. The KPFM results also confirm that the superior photocatalytic activity is consistent with the big large surface potential changes before and after light irradiation. The possible degradation pathways and intermediates of TC and CIP were well analyzed by DFT calculation and LC-MS. The results highlight that morphology control of the ferroelectric materials exhibits enhanced photocatalytic performance for the degradation of the antibiotic.
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