Center for Electron Microscopy, Wuhan University, Wuhan 430072, People's Republic of China.
ACS Appl Mater Interfaces. 2010 Apr;2(4):1173-6. doi: 10.1021/am100011c.
The photocatalytic activity of TiO(2) is enhanced mainly through heightening absorption of UV-vis light and improving the separation efficiency of photoinduced electrons and holes. The recent new theoretical research revealed that the TiO(2) codoped with Mo + C is considered to be an optimal doping system. On the basis of this theory, the Mo + C codoped TiO(2) powders were first experimentally synthesized by thermal oxidizing a mixture of TiC and MoO(3) powders in the air. The XRD patterns and the XPS survey spectrum showed that carbon (C) acted as a Ti-O-C band structure and molybdenum (Mo) existed as Mo(6+) in anatase TiO(2). The Mo+C codoped TiO(2) had a 32 nm red shift of the spectrum onset compared with pure anatase TiO(2), and its band gap was reduced from 3.20 to 2.97 eV. The photocurrent of the Mo + C codoped TiO(2) was about 4 times as high as that of pure anatase TiO(2), and its photocatalytic activity on decomposition of methylene blue was enhanced.
TiO(2)的光催化活性主要通过提高对紫外-可见光的吸收和提高光生电子和空穴的分离效率来增强。最近的新理论研究表明,TiO(2)共掺杂 Mo+C 被认为是一种最佳的掺杂体系。在此理论基础上,首次通过在空气中热氧化 TiC 和 MoO(3)粉末的混合物实验合成了 Mo+C 共掺杂 TiO(2)粉末。XRD 图谱和 XPS 全谱表明,碳 (C) 作为 Ti-O-C 带结构,钼 (Mo) 以锐钛矿 TiO(2)中的 Mo(6+)形式存在。Mo+C 共掺杂 TiO(2)的光谱起始处有 32nm 的红移,其带隙从 3.20eV 降低到 2.97eV。Mo+C 共掺杂 TiO(2)的光电流约为纯锐钛矿 TiO(2)的 4 倍,其对亚甲基蓝分解的光催化活性增强。