Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences, 72 Wenhua Road, Shenyang 110016, China.
J Colloid Interface Sci. 2010 Sep 15;349(2):477-83. doi: 10.1016/j.jcis.2010.05.076. Epub 2010 Jun 1.
Extending the response range of wide-bandgap (3.2 eV) anatase TiO(2) photocatalysts into the visible light range can play an important role in promoting the practical applications of photocatalysts. Here, we report a route to prepare sulfur doped anatase TiO(2) single crystal sheets with a high percentage of {0 0 1} facets. The resultant TiO(2) sheets were investigated by a combination of experimental characterizations and electronic structure calculations. The synthesized sulfur doped anatase samples show an additional visible light absorption band from 400 nm to ca. 550 nm and some visible-light photocatalytic activity in *OH radical generation and photodecomposition of organic dyes. The Ti-S bond structure causes not only visible light absorption but also changes to an extent the surface structures of doped anatase TiO(2) sheets. Theoretically, localized 3p states of S formed in the bandgap are implicated for the visible light absorption of the sulfur doped anatase TiO(2).
将宽带隙(3.2eV)锐钛矿 TiO(2) 光催化剂的响应范围扩展到可见光范围,可以在促进光催化剂的实际应用方面发挥重要作用。在这里,我们报告了一种制备具有高比例{001}面的硫掺杂锐钛矿 TiO(2)单晶片的方法。通过实验表征和电子结构计算的结合,对所得的 TiO(2)片进行了研究。合成的硫掺杂锐钛矿样品在 400nm 至约 550nm 处显示出额外的可见光吸收带,并在*OH 自由基生成和有机染料的光解方面表现出一定的可见光光催化活性。Ti-S 键结构不仅引起可见光吸收,而且在一定程度上改变了掺杂锐钛矿 TiO(2)片的表面结构。从理论上讲,在带隙中形成的 S 的局域 3p 态被认为是硫掺杂锐钛矿 TiO(2)可见光吸收的原因。