4.8 Article

Rutile TiO2 single crystals delivering enhanced photocatalytic oxygen evolution performance

Journal

NANOSCALE
Volume 13, Issue 18, Pages 8591-8599

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1nr01544c

Keywords

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Funding

  1. National Natural Science Foundation of China [21972028]
  2. Strategic Priority Research Program of Chinese Academy of Sciences [XDB36000000]

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A simple and environmentally friendly synthetic method was developed to synthesize regulable reductive and oxidative facets of rutile TiO2 single crystals. Sodium fluoride and glycolic acid played crucial roles in this process, serving as effective phase and facet controlling agents.
Owing to their scientific and technological importance, the development of highly efficient photocatalytic water oxidation systems with rapid photogenerated charge separation and high surface catalytic activity is highly desirable for the storage and conversion of solar energy. A promising candidate is rutile phase titanium dioxide (TiO2), which has been widely studied over half a century. Specifically, oriented single-crystalline TiO2 surfaces with high oxidative reactivity would be most desirable, but achieving these structures has been limited by the availability of synthetic techniques. In this study, a facile and green synthetic approach was developed for the first time to synthesize rutile TiO2 single crystals with regulable reductive and oxidative facets. Glycolic acid (GA) and sodium fluoride (NaF) are used as the crucial and effective phase and facet controlling agents, respectively. The selective adsorption of F- ions on the facets of rutile TiO2 crystals not only plays a key role in driving the nucleation and preferential growth of the crystals with desired facets but also significantly affects their photocatalytic gas evolution reactivity. With heat treatment, the highly stable F--free rutile TiO2 single crystals with a high percentage of oxidative facets exhibit a superior photocatalytic gas evolution rate (approximate to 116 mu mol h(-1) per 0.005 g catalyst), 8.5 times higher than that of previous F--containing samples.

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