College of Chemistry and Chemical Engineering, Ocean University of China, Qingdao, Shandong 266100, China.
Nanoscale. 2013 Jun 7;5(11):4986-92. doi: 10.1039/c3nr01033c. Epub 2013 May 2.
A unique nanocomposite C-TiO2 was prepared by the growth of TiO2 on carbon nanoparticles using a simple hydrothermal procedure. Transmission electron microscopic (TEM) measurements showed that the nanocomposites exhibited an average core diameter of approximately 5 nm with a rather well-defined lattice space (0.4 nm) that was somewhat larger than that (0.38 nm) of the (100) crystalline planes of anatase TiO2. This lattice expansion was accounted for by the formation of surface defect dipoles of the nanosized TiO2 particles. X-ray photoelectron spectroscopic (XPS) measurements suggested that partial charge transfer occurred from carbon nanoparticles to TiO2 by the interfacial Ti-O-C linkages, which led to effective diminishment of the C-TiO2 photoluminescence as compared to that of pure TiO2 or carbon nanoparticles, suggesting intimate electronic interactions between the carbon and TiO2 components in the nanocomposites. Such unique characteristics were then exploited for the effective photocatalytic degradation of organic pollutants, as exemplified by methylene blue, by C-TiO2 under UV photoirradiation. Experimental measurements showed that the photocatalytic activity of C-TiO2 nanocomposites was about twice that of TiO2 alone, whereas little activity was observed with carbon nanoparticles. This was attributed to the electron-accepting sites on the carbon nanoparticles that facilitated interfacial charge separation.
一种独特的纳米复合材料 C-TiO2 通过使用简单的水热程序在碳纳米粒子上生长 TiO2 来制备。透射电子显微镜 (TEM) 测量表明,纳米复合材料表现出约 5nm 的平均核直径,并且具有相当明确的晶格空间(0.4nm),略大于锐钛矿 TiO2 的(100)晶面的晶格空间(0.38nm)。这种晶格膨胀是由纳米 TiO2 颗粒的表面缺陷偶极子的形成引起的。X 射线光电子能谱 (XPS) 测量表明,通过界面 Ti-O-C 键合,部分电荷从碳纳米粒子转移到 TiO2,这导致 C-TiO2 的光致发光与纯 TiO2 或碳纳米粒子相比有效减少,表明在纳米复合材料中碳和 TiO2 成分之间存在紧密的电子相互作用。然后,利用这些独特的特性来有效光催化降解有机污染物,例如亚甲基蓝,通过 C-TiO2 在 UV 光照射下进行。实验测量表明,C-TiO2 纳米复合材料的光催化活性约为 TiO2 单独使用的两倍,而碳纳米粒子的活性则很小。这归因于碳纳米粒子上的电子接受位点,它们促进了界面电荷分离。