首页> 外文期刊>International journal of hydrogen energy >Fabrication of S-scheme ZnO/Zn_3(PO_4)_2 heterojunction photocatalyst toward photodegradation of tetracycline antibiotic and photocatalytic mechanism insight
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Fabrication of S-scheme ZnO/Zn_3(PO_4)_2 heterojunction photocatalyst toward photodegradation of tetracycline antibiotic and photocatalytic mechanism insight

机译:S型ZnO/Zn_3(PO_4)_2异质结光催化剂的制备及其对四环素类抗生素光降解的分析及光催化机理见解

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摘要

In this work, a S-scheme ZnO/Zn-3(PO4)(2) heterojunction photocatalyst was fabricated by a simple co-precipitation manner under reflux condition. The ZnO/Zn-3(PO4)(2) heterostructured nanocomposite was employed for the degradation of tetracycline antibiotic under UV and visible light irradiation. The structure, composition, morphology, and optical properties of the as-synthesized ZnO/Zn-3(PO4)(2) products were characterized by XRD, EDS, FESEM, TEM, UV-Vis DRS, and PL measurements. The hybrid ZnO/Zn-3(PO4)(2) nanoparticles exhibited the highest photocatalytic efficiency in the degradation of tetracycline under ultraviolet (97) and visible (82) light irradiation, which was similar to 1.5 times more than sole Zn-3(PO4)(2) nanostructures. The promoted light harvesting and generated heterojunction interfaces between ZnO and Zn-3(PO4)(2) can obviously reduce the recombination rate of charge carriers in the ZnO/Zn-3(PO4)(2) heterostructure. Moreover, a reasonable photocatalytic mechanism of the UV and visible light-induced degradation of antibiotic over ZnO/Zn-3(PO4)(2) nanocomposites is suggested. The results indicated that under UV, the mechanism follows from the S-scheme in the presence of O-center dot(2)- and (OH)-O-center dot as predominant species, while upon visible, the type-II heterojunction utilizing O-center dot(2)- as prevailing radical is possible.
机译:本工作采用简单的共沉淀方式在回流条件下制备了S型ZnO/Zn-3(PO4)(2)异质结光催化剂。采用ZnO/Zn-3(PO4)(2)异质结构纳米复合材料在紫外和可见光照射下降解四环素类抗生素。采用XRD、EDS、FESEM、TEM、紫外-可见光DRS和PL等手段对ZnO/Zn-3(PO4)(2)产物的结构、组成、形貌和光学性能进行了表征。杂化ZnO/Zn-3(PO4)(2)纳米颗粒在紫外(97%)和可见光(82%)光照射下降解四环素的光催化效率最高,是单纯Zn-3(PO4)(2)纳米结构的1.5倍。ZnO与Zn-3(PO4)(2)异质结界面的促进光捕获和异质结界面的产生可以明显降低ZnO/Zn-3(PO4)(2)异质结中载流子的复合速率。此外,提出了紫外光和可见光诱导ZnO/Zn-3(PO4)(2)纳米复合材料降解抗生素的合理光催化机理。结果表明,在紫外光下,在O-中心点(2)-和(OH)-O-中心点为主要物种的情况下,其机理遵循S-方案,而在可见光下,利用O-中心点(2)-作为主要自由基的II型异质结是可能的。

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