Xu Jiaoxing, Li Liping, Yan Youjun, Wang Hui, Wang Xuxu, Fu Xianzhi, Li Guangshe
State Key Structural Chemistry Laboratory, Fujian Institute of Research on the Structure of Matter, Graduate School of Chinese Academy of Science, Fujian 350002, People's Republic of China.
J Colloid Interface Sci. 2008 Feb 1;318(1):29-34. doi: 10.1016/j.jcis.2007.10.004. Epub 2007 Nov 7.
High-purity anatase TiO(2) nanoparticles were prepared using a low-temperature sol-gel route. The as-prepared sample was characterized by X-ray diffraction, transmission electron microscopy, infrared spectroscopy, thermogravimetric analysis, UV-vis spectroscopy, and photoluminescence. It is shown that the as-prepared sample crystallized in a pure anatase phase with an average crystallite size of about 7 nm, and the surfaces were highly hydrated. These nanoparticles were stabilized as a water suspension via the cooperation of DLVO force and surface hydration force. These suspensions showed characteristic band-gap emission at 397+/-1.5 nm, which is a little red-shifted compared with the band-gap energy of indirect electronic transition measured in the UV-vis absorption spectrum. These observations were explained by the light-induced relaxation of polar water molecules in the surface hydration layer.
采用低温溶胶-凝胶法制备了高纯度锐钛矿型TiO₂纳米颗粒。通过X射线衍射、透射电子显微镜、红外光谱、热重分析、紫外-可见光谱和光致发光对所制备的样品进行了表征。结果表明,所制备的样品结晶为纯锐钛矿相,平均晶粒尺寸约为7 nm,且表面高度水合。通过DLVO力和表面水化力的协同作用,这些纳米颗粒作为水悬浮液得以稳定。这些悬浮液在397±1.5 nm处显示出特征带隙发射,与紫外-可见吸收光谱中测量的间接电子跃迁的带隙能量相比有轻微的红移。这些观察结果通过表面水化层中极性水分子的光致弛豫来解释。