Katoh Masahiro, Aihara Hironori, Horikawa Toshihide, Tomida Tahei
Department of Chemical Science and Technology, Faculty of Engineering, The University of Tokushima, Tokushima 770-8506, Japan.
J Colloid Interface Sci. 2006 Jun 15;298(2):805-9. doi: 10.1016/j.jcis.2006.01.023. Epub 2006 Mar 9.
Yellowish S-containing TiO2 (S-TiO2) powders were prepared by calcination of a mixture of titanium(III) chloride and ammonium thiocyanate solutions. Three kinds of S-TiO2 were prepared by varying the concentration of ammonium thiocyanate (0.5, 1 or 13 M). X-ray photoelectron spectroscopy spectra of the S-TiO2 showed that sulfur atoms existed on the surface of TiO2 powders. But the peaks assigned to S disappeared after Ar+ etching, which means that these atoms were not doped in the bulk of the TiO2 powders. While UV-visible absorption spectra of S-TiO2 showed that the absorption edges of these photocatalysts were seen to shift to a longer wavelength (lower band gap energy) than those of undoped rutile TiO2 prepared and commercial anatase type TiO2 (ST-01). The S-TiO2 (1 M) exhibited higher photocatalytic activity than ST-01 for degradation of methylene blue in aqueous solution under visible light irradiation (lambda > 400 nm). It was also confirmed by IR spectroscopy that acetaldehyde in oxygen under visible light irradiation (lambda > 400 nm) was decomposed to acetic acid by the S-TiO2 and ST-01 at the first decomposition step.
通过煅烧氯化钛(III)和硫氰酸铵溶液的混合物制备了淡黄色含硫二氧化钛(S-TiO₂)粉末。通过改变硫氰酸铵的浓度(0.5、1或13 M)制备了三种S-TiO₂。S-TiO₂的X射线光电子能谱表明硫原子存在于TiO₂粉末表面。但Ar⁺蚀刻后归属于S的峰消失了,这意味着这些原子并未掺杂在TiO₂粉末的本体中。而S-TiO₂的紫外可见吸收光谱表明,这些光催化剂的吸收边相比于制备的未掺杂金红石型TiO₂和商用锐钛矿型TiO₂(ST-01),向更长波长(更低带隙能量)移动。在可见光照射(λ>400 nm)下,S-TiO₂(1 M)对水溶液中亚甲基蓝的降解表现出比ST-01更高的光催化活性。红外光谱也证实,在可见光照射(λ>400 nm)下,氧气中的乙醛在第一步分解时被S-TiO₂和ST-01分解为乙酸。