异质结
材料科学
光催化
铋
三元运算
光电子学
纳米技术
氧化还原
降级(电信)
光致发光
带隙
四环素
化学工程
复合数
可见光谱
宽禁带半导体
半导体
纳米颗粒
电子转移
猝灭(荧光)
载流子
热液循环
纳米复合材料
对偶(语法数字)
阻塞(统计)
作者
Liang Gaoyan,Hongxia Jing,Jingqi Jia,Bingge Chen,Yunkai Zhang,Pei Wangjun,Liang Gaoyan,Hongxia Jing,Jingqi Jia,Bingge Chen,Yunkai Zhang,Pei Wangjun
出处
期刊:Langmuir
[American Chemical Society]
日期:2025-11-14
卷期号:41 (46): 31595-31607
标识
DOI:10.1021/acs.langmuir.5c04799
摘要
Tetracycline antibiotics pose persistent ecological risks, underscoring the urgent need for sustainable remediation strategies. Bismuth oxyiodide (BiOI) is attractive for photocatalysis owing to its visible-light responsiveness, yet its narrow band gap (1.8 eV) and rapid charge recombination hinder efficiency. Here, a ternary CeO2/BiOI/PANI heterostructure was fabricated via hydrothermal synthesis and in situ polymerization. The design exploits Ce3+/Ce4+ redox cycling to generate oxygen vacancies, establishes a dual Z-scheme heterojunction among CeO2, BiOI, and PANI to preserve high redox potentials, and leverages PANI's π-conjugated framework to accelerate interfacial electron transfer. These synergistic effects narrow the band gap to 1.30 eV, suppress photoluminescence by 75%, and markedly reduce interfacial resistance, thereby enhancing charge separation and migration. The optimized composite achieved 92% tetracycline degradation within 120 min under visible light─approximately double that of pristine BiOI─and retained 79% activity after five cycles, demonstrating excellent stability. Radical quenching and band structure analyses confirmed a dual Z-scheme charge transfer pathway. This work provides a robust strategy for constructing organic-inorganic heterostructures toward efficient photocatalytic degradation of antibiotics and other recalcitrant pollutants.
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