4.7 Article

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

期刊

NANOMATERIALS
卷 10, 期 1, 页码 -

出版社

MDPI
DOI: 10.3390/nano10010053

关键词

perovskite-type hydroxide; photocatalysis; tetracycline; photoelectrochemistry; type-II heterojunction

资金

  1. National Natural Science Foundation of China [11904039]
  2. Basic and Frontier Research Project of Chongqing Science and Technology Commission [cstc2018jcyjAX0827, cstc2019jcyj-msxmX0187]
  3. project of Scientific and Technological Research Program of Chongqing Municipal Education Commission [KJQN201801135]
  4. Children's Research Institute of National Center for Schooling Development Program
  5. Chongqing University of Education [CSDP19FS01109]
  6. project of Science and Technology Collaborative Innovation Platform Construction of Chongqing University of Education [2017XJPT01]
  7. Cultivation for National Science Foundation of Chongqing University of Education [18GZKP01]

向作者/读者索取更多资源

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)(6)/SnO2, was successfully prepared via a facile one-pot in situ hydrothermal method at 220 degrees 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)(6) and SnO2 compounds. Among them, the obtained MgSn(OH)(6)/SnO2 heterojunction with MgCl(2)6H(2)O:SnCl(4)5H(2)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.

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