首页> 外文期刊>Separation and Purification Technology >Enhanced photocatalytic degradation of tetracycline under visible light by using a ternary photocatalyst of Ag3PO4/AgBr/g-C3N4 with dual Z-scheme heterojunction
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Enhanced photocatalytic degradation of tetracycline under visible light by using a ternary photocatalyst of Ag3PO4/AgBr/g-C3N4 with dual Z-scheme heterojunction

机译:通过使用双Z-Schement异质结的Ternary光催化剂,通过使用Ag3PO4 / Agbr / G-C3n4的三元光催化来增强光催化降解四环素。

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摘要

A ternary dual Z-scheme heterojunction photocatalyst composed of Ag3PO4, AgBr and g-C3N4 was prepared by a facile chemical deposition method. Scanning electron microscope equipped with energy-dispersive X-ray, X-ray diffraction, diffusive reflective spectrophotometry and X-ray photoelectron spectroscopy were carried out to characterize the morphology, element and structure properties of the photocatalysts. The photocatalytic activity was evaluated by the photoelectrochemical tests and the degradation of tetracycline (TC). The results indicated that the composite Ag3PO4/AgBr-20%g-C3N4 exhibited the best photocatalytic activity in terms of the photocurrent response and the degradation of TC under visible light irradiation. The degradation rate of TC over the ternary photocatalyst was 0.12 min(-1), which was 2.55 and 3.24 times faster than that over Ag3PO4/AgBr and Ag3PO4, respectively. During photocatalysis, metallic Ag could be formed and served as the electron transfer mediator to build the dual Z-scheme heterojunction by bridging the recombination of electrons and holes. By this manner, more efficient separation of photo-generated carriers and better redox ability could be obtained, consequently promoting the photocatalytic activity. Additionally, the trapping experiments verified that O-center dot(2)- and h(+) played prominent roles in the photocatalytic processes, while the impact of (OH)-O-center dot on the removal efficiency was relatively small.
机译:由Ag3PO4,AgBr和G-C3N4组成的三元双Z方案异质结光催化剂是通过容易的化学沉积方法制备的。扫描电子显微镜配有能量分散X射线,X射线衍射,衍射反射分光光度法和X射线光电子能谱,表征光催化剂的形态,元素和结构性质。通过光电化学测试评估光催化活性和四环素(Tc)的降解。结果表明,复合Ag3PO4 / AgBr-20%G-C3N4在光电流响应和可见光照射下TC的降解表现出最佳的光催化活性。 TC在三元光催化剂上的降解率为0.12分钟(-1),分别比Ag3PO4 / Agbr和Ag3PO4更快的2.55%和3.24倍。在光催化期间,可以通过桥接电子和孔的重组来形成和用作电子传递介体以构建双Z方案异质结的金属AG。通过这种方式,可以获得光产生的载体和更好的氧化还原能力的更有效的分离,因此促进光催化活性。另外,诱捕实验验证了O中心点(2) - 和H(+)在光催化过程中起着突出的作用,而(OH)-o中心点对去除效率的影响相对较小。

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