材料科学
X射线光电子能谱
锐钛矿
钛
渗氮
表面改性
化学工程
纳米结构
电子顺磁共振
金属
分析化学(期刊)
图层(电子)
纳米技术
光催化
冶金
核磁共振
有机化学
催化作用
化学
物理
工程类
作者
S. M. Prokes,James L. Gole,Xiaobo Chen,Clemens Burda,W. E. Carlos
标识
DOI:10.1002/adfm.200305109
摘要
Abstract The surface modification of TiO 2 nanostructures to incorporate nitrogen and form visible light absorbing titanium oxynitride centers is studied. Anatase TiO 2 structures in the 5–20 nm range, formed by a wet chemical technique, were surface modified and the nitridation of the highly reactive TiO 2 nanocolloid surface, as determined by X‐ray photoelectron spectroscopy (XPS) studies, is achieved by a quick and simple treatment in alkyl ammonium compounds. The nitriding process was also simultaneously accompanied by metal seeding resulting in a metal coating layer on the TiO 2 structures. The structure of the resultant titanium oxynitride nanostructures remains anatase. These freshly prepared samples exhibited a strong emission near 560 nm (2.21 eV), which red‐shifted to 660 nm (1.88 eV) and dropped in intensity with aging in the atmosphere. This behavior was also evident in some of the combined nitrogen doped and metal seeded TiO 2 nanocolloids. Electron spin resonance (ESR) performed on these samples identified a resonance at g = 2.0035, which increased significantly with nitridation. The resonance is attributed to an oxygen hole center created near the surface of the nanocolloid, which correlates well with the observed optical activity.
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