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Enhanced Photocatalytic Degradation of Tetracycline by Agl/BiVO4 Heterojunction under Visible-Light Irradiation: Mineralization Efficiency and Mechanism

机译:可见光照射下Agl / BiVO4异质结增强四环素的光催化降解作用:成矿效率和机理

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Recently, visible-light-driven photocatalysis is of great interest in the environmental pollutant remediation. In the present study, a novel heterostructured photocatalyst AgI/BiVO4 was synthesized by an in situ precipitation procedure. The AgI/BiVO4 heterojunctions exhibited excellent photoactivity for the refractory pollutant (tetracycline (TC), a typical antibiotic) decomposition under visible light illumination. The synthetic sample with 1:4 mass ratio of AgI:BiVO4 possessed the highest photocatalytic performance in all of the as-prepared catalysts. The TC molecules were substantially eliminated (94.91%) within 60 min, and degradation efficiency was considerably better than those of bare BiVO4 (62.68%) and AgI (75.43%) under identical conditions. Simultaneously, 90.46% of TOC removal was also achieved within 120 min, suggesting that the mineralization was superior and further confirmed by three-dimensional excitation emission matrix fluorescence spectroscopy (3D EEMs). The XRD, XPS, DRS, and PL measurements revealed that a small amount of Ag nanoparticles was produced at the early photodegradation process. The structure transformation from AgI/BiVO4 (double-type) to AgI/Ag/BiVO4 (sandwich-like) improved the corresponding visible-light absorption performance. The self-assembly Z-scheme heterojunction that consisted of AgI, Ag, and BiVO4 also efficiently accelerated photoinduced electron hole pairs' separation and ultimately improved the efficiency of TC degradation. The responsible photocatalytic mechanism was discussed in detail on the basis of the reactive species capturing tests and ESR analysis, and the experimental results had been validated that superoxide radicals and holes played a vital role during the photocatalytic process. Furthermore, TC degradation efficiency was not of significant loss after four consecutive cycles, suggesting the excellent photostability of AgI/BiVO4 nanocomposite. These features demonstrate that the AgI/BiVO4 heterojunction has great application potential for refractory pollutants' removal from wastewater.
机译:近来,可见光驱动的光催化在环境污染物的修复中引起了极大的兴趣。在本研究中,通过原位沉淀法合成了一种新型的异质结构光催化剂AgI / BiVO4。 AgI / BiVO4异质结在可见光照射下对难降解污染物(四环素(TC),一种典型的抗生素)的分解显示出优异的光活性。质量比为1:4的AgI:BiVO4的合成样品在所有制备的催化剂中具有最高的光催化性能。在相同条件下,TC分子在60分钟内基本消失(94.91%),降解效率明显好于裸BiVO4(62.68%)和AgI(75.43%)。同时,在120分钟内还达到了90.46%的TOC去除率,这表明矿化作用优越,并通过三维激发发射矩阵荧光光谱法(3D EEM)进一步证实。 XRD,XPS,DRS和PL测量表明,在早期光降解过程中产生了少量的Ag纳米颗粒。从AgI / BiVO4(双重型)到AgI / Ag / BiVO4(三明治型)的结构转变提高了相应的可见光吸收性能。由AgI,Ag和BiVO4组成的自组装Z型异质结也有效地加速了光致电子空穴对的分离,并最终提高了TC降解的效率。在反应物种捕获试验和ESR分析的基础上,详细讨论了负责的光催化机理,并验证了实验结果,表明超氧自由基和空穴在光催化过程中起着至关重要的作用。此外,TC降解效率在连续四个周期后没有显着损失,表明AgI / BiVO4纳米复合材料具有出色的光稳定性。这些特征表明,AgI / BiVO4异质结在从废水中去除难降解污染物方面具有巨大的应用潜力。

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