College of the Environment and Ecology, Xiamen University, Xiamen 361102, PR China; College of Chemistry and Environment, Minnan Normal University, Zhangzhou 363000, PR China.
College of Chemistry and Environment, Minnan Normal University, Zhangzhou 363000, PR China.
J Colloid Interface Sci. 2018 Mar 15;514:791-800. doi: 10.1016/j.jcis.2018.01.011. Epub 2018 Jan 4.
The goal of this work was to assess the performance of Pt nanoparticles (NPs) as co-catalysts on the photocatalytic activity of TiO@Pt@CN hollow spheres, which was tested by photodegrading rhodamine B and methyl blue under visible light irradiation. TiO@Pt@CN composites were fabricated by using modified polystyrene balls as templates, hydrothermal reactions, and calcination. Under simulated sunlight irradiation, photocatalytic activity was in the following of TiO@Pt@CN > TiO@CN > CN > P25. The photo-conversion rate of the TiO@Pt@CN increased significantly relative to TiO@CN and the others. The combination of TiO and CN, as well as the sandwiched of Pt NPs reduce electron-hole recombination as a result of having an electron trap site, which can store and shuttle photo-generated electrons, and enhance photo-generation of active radicals. Electron paramagnetic resonance (EPR) spectroscopy, as well as photo-luminescence (PL), and electrochemical measurements were taken to verify this conclusion. Considering the multi-functional combination of precious metals and semiconductor materials, this work may provide new ideas for the design of high-performance catalysts.
这项工作的目的是评估 Pt 纳米粒子 (NPs) 作为 TiO@Pt@CN 空心球光催化活性的共催化剂的性能,该空心球通过可见光照射下罗丹明 B 和亚甲基蓝的光降解来测试。TiO@Pt@CN 复合材料是通过使用改性聚苯乙烯球作为模板、水热反应和煅烧来制备的。在模拟太阳光照射下,光催化活性顺序为 TiO@Pt@CN > TiO@CN > CN > P25。与 TiO@CN 和其他相比,TiO@Pt@CN 的光转化率显著提高。TiO 和 CN 的结合以及 Pt NPs 的夹层减少了电子-空穴复合,因为存在电子陷阱位,可以存储和穿梭光生电子,并增强活性自由基的光生成。电子顺磁共振 (EPR) 光谱以及光致发光 (PL) 和电化学测量被用来验证这一结论。考虑到贵金属和半导体材料的多功能组合,这项工作可能为设计高性能催化剂提供新的思路。