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In Situ Construction of a MgSn(OH)6 Perovskite/SnO2 Type-II Heterojunction: A Highly Efficient Photocatalyst towards Photodegradation of Tetracycline

机译:MgSn(OH)6钙钛矿/ SnO2 II型异质结的原位构建:高效的光催化剂对四环素的光降解

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摘要

Using solar energy to remove antibiotics from aqueous environments via photocatalysis is highly desirable. In this work, a novel type-II heterojunction photocatalyst, MgSn(OH) /SnO was successfully prepared via a facile one-pot in situ hydrothermal method at 220 °C for 24 h. The obtained heterojunctions were characterized via powder X-ray diffraction, Fourier-transform infrared spectroscopy, transmission electron microscopy, and ultraviolet-visible diffuse reflectance spectroscopy. The photocatalytic performance was evaluated for photodegradation of tetracycline solution under ultraviolet irradiation. The initial concentration of tetracycline solution was set to be 20 mg/L. The prepared heterojunctions exhibited superior photocatalytic activity compared with the parent MgSn(OH) and SnO compounds. Among them, the obtained MgSn(OH) /SnO heterojunction with MgCl ·6H O:SnCl ·5H O = 4:5.2 (mmol) displayed the highest photocatalytic performance and the photodegradation efficiency conversion of 91% could be reached after 60 min under ultraviolet irradiation. The prepared heterojunction maintained its performance after four successive cycles of use. Active species trapping experiments demonstrated that holes were the dominant active species. Hydroxyl radicals and superoxide ions had minor effects on the photocatalytic oxidation of tetracycline. Photoelectrochemical measurements were used to investigate the photocatalytic mechanism. The enhancement of photocatalytic activity could be assigned to the formation of a type-II junction photocatalytic system, which was beneficial for efficient transfer and separation of photogenerated electrons and holes. This research provides an in situ growth strategy for the design of highly efficient photocatalysts for environmental restoration.
机译:非常需要使用太阳能通过光催化从水性环境中去除抗生素。在这项工作中,一种新型的II型异质结光催化剂MgSn(OH)/ SnO通过一种简便的一锅原位水热方法在220°C下成功制备了24 h。通过粉末X射线衍射,傅立叶变换红外光谱,透射电子显微镜和紫外可见漫反射光谱来表征获得的异质结。评价四环素溶液在紫外线照射下的光催化性能。四环素溶液的初始浓度设定为20mg / L。与母体MgSn(OH)和SnO化合物相比,制备的异质结表现出优异的光催化活性。其中,所得到的MgCl·6H O:SnCl·5H O = 4:5.2(mmol)的MgSn(OH)/ SnO异质结表现出最高的光催化性能,在紫外光下60 min达到91%的光降解效率。辐射。连续四个使用周期后,制备的异质结保持其性能。活性物种捕获实验表明,空穴是主要的活性物种。羟自由基和超氧离子对四环素的光催化氧化作用较小。使用光电化学测量来研究光催化机理。光催化活性的增强可以归因于II型结光催化体系的形成,这对光生电子和空穴的有效转移和分离是有利的。该研究为设计用于环境修复的高效光催化剂提供了原位生长策略。

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