Su Wenyue, Zhang Yongfan, Li Zhaohui, Wu Ling, Wang Xuxu, Li Junqian, Fu Xianzhi
Research Institute of Photocatalysis, State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, PR China.
Langmuir. 2008 Apr 1;24(7):3422-8. doi: 10.1021/la701645y. Epub 2008 Feb 27.
Multivalency iodine (I(7)+/I(-)) doped TiO(2) were prepared via a combination of deposition-precipitation process and hydrothermal treatment. The as-prepared samples were characterized by X-ray diffraction, transmission electron microscopy, Brunauer-Emmett-Teller surface area, UV-vis diffuse reflectance spectra, X-ray photoelectron spectroscopy, surface photovoltage spectroscopy, and electric-field-induced surface photovoltage spectroscopy. The electronic structure calculations based on the density functional theory revealed that upon doping, new states that originated from the I atom of the IO(4) group are observed near the conduction-band bottom region of TiO(2), and the excitation from the valence band of TiO(2) to the surface IO(4-) is responsible for the visible-light response of the I-doped TiO(2). The as-prepared I-doped TiO(2) showed high efficiency for the photocatalytic decomposition of gaseous acetone under visible light irradiation (lambda > 420 nm). A possible mechanism for the photocatalysis on this multivalency iodine (I(7)+/I(-)) doped TiO(2) under visible light was also proposed.
通过沉积沉淀法和水热处理相结合的方法制备了多价碘(I(7)+/I(-))掺杂的TiO(2)。采用X射线衍射、透射电子显微镜、Brunauer-Emmett-Teller比表面积、紫外-可见漫反射光谱、X射线光电子能谱、表面光电压光谱和电场诱导表面光电压光谱对所制备的样品进行了表征。基于密度泛函理论的电子结构计算表明,掺杂后,在TiO(2)的导带底部区域附近观察到源于IO(4)基团中I原子的新态,并且从TiO(2)的价带激发到表面IO(4-)是I掺杂TiO(2)可见光响应的原因。所制备的I掺杂TiO(2)在可见光照射(λ>420nm)下对气态丙酮的光催化分解表现出高效率。还提出了这种多价碘(I(7)+/I(-))掺杂TiO(2)在可见光下光催化的可能机理。