金红石
介孔材料
锐钛矿
光催化
材料科学
化学工程
纳米技术
相(物质)
比表面积
微球
多孔性
催化作用
化学
复合材料
有机化学
工程类
作者
Wei Zhang,Haili He,Yong Tian,Kun Lan,Qi Liu,Changyao Wang,Yang Liu,Ahmed A. Elzatahry,Renchao Che,Wei Li,Dongyuan Zhao
出处
期刊:Chemical Science
[Royal Society of Chemistry]
日期:2018-11-21
卷期号:10 (6): 1664-1670
被引量:144
摘要
As a benchmark photocatalyst, commercial P25-TiO2 has been widely used for various photocatalytic applications. However, the low surface area and poorly porous structure greatly limit its performance. Herein, uniform ordered mesoporous TiO2 microspheres (denoted as Meso-TiO2-X; X represents the rutile percentage in the resultant microspheres) with controllable anatase/rutile phase junctions and radially oriented mesochannels are synthesized by a coordination-mediated self-assembly approach. The anatase/rutile ratio in the resultant microspheres can be facilely adjusted as desired (rutile percentage: 0-100) by changing the concentration of hydrochloric acid. As a typical one, the as-prepared Meso-TiO2-25 microspheres have a similar anatase/rutile ratio to commercial P25. But the surface area (78.6 m2 g-1) and pore volume (0.39 cm3 g-1) of the resultant microspheres are larger than those of commercial P25. When used as the photocatalyst for H2 generation, the Meso-TiO2-25 delivers high solar-driven H2 evolution rates under air mass 1.5 global (AM 1.5 G) and visible-light (λ > 400 nm), respectively, which are significantly larger than those of commercial P25. This coordination-mediated self-assembly method paves a new way toward the design and synthesis of high performance mesoporous photocatalysts.
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