4.7 Article

Solvothermal preparation and characterization of ordered-mesoporous ZrO2/TiO2 composites for photocatalytic degradation of organic dyes

期刊

CERAMICS INTERNATIONAL
卷 47, 期 6, 页码 7632-7641

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.ceramint.2020.11.104

关键词

ZrO2/TiO2 composites; Solvothermal method; Ink-bottle structure; Heterostructure; Enhanced photocatalytic activity

资金

  1. National Natural Science Foundation of China [51672070]
  2. China Scholarship Council [201808410578]
  3. Opening Project of National Joint Engineering Research Center for Abrasion Control and Molding of Metal Materials, Henan Key Laboratory of High-temperature Structural and Functional Materials, Henan University of Science and Technology [HKDNM2019013]

向作者/读者索取更多资源

The ZrO2/TiO2 composites with an ink-bottle mesoporous structure were synthesized without high-temperature calcination, and their catalytic performance was investigated. The TiO2-10 wt% ZrO2 composite showed outstanding photocatalytic performance under simulated sunlight, especially with ZrO2 particle size on the submicron scale. Combining ZrO2 and TiO2 to form a new heterostructure inhibited electron-hole recombination, thereby improving photocatalytic activity.
ZrO2/TiO2 composites with an ink-bottle mesoporous structure were synthesized by a mild solvothermal method without high-temperature calcination. Many caves in this ink-bottle structure can adsorb organic groups, making them suitable for catalytic materials. The effects of ZrO2 additions and particle size on the morphology and catalytic performance of composite powders were investigated. Comparative experiments on changing the particle size and the content of ZrO2 show that the TiO2-10 wt% ZrO2 composite has outstanding photocatalytic performance under simulated sunlight, especially when the particle size of as-prepared ZrO2 is on the submicron scale. By mixing two different n-type semiconductors of ZrO2 and TiO2, a new heterostructure is formed to hinder the autonomous recombination of excited electron-hole pairs, improving photocatalytic activity.

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