锐钛矿
材料科学
无定形固体
衍射
原位
同步加速器
相变
X射线晶体学
同步辐射
相(物质)
化学工程
结晶学
纳米技术
光学
凝聚态物理
化学
物理
催化作用
有机化学
工程类
光催化
作者
Yao Lu,Jiatang Chen,Zhiqiang Wang,Yu‐Chun Chuang,Lo-Yeuh Chang,Tsun‐Kong Sham
标识
DOI:10.1021/acs.jpclett.4c02233
摘要
TiO2 nanotubes (NTs) with amorphous and crystalline structures have attracted interest due to their wide range of applications, particularly black TiO2, which addresses the limitations of conventional TiO2 (a wide band gap of 3.0-3.2 eV). Understanding the amorphous-to-anatase phase transition is crucial for phase control of crystalline TiO2. This study investigates the size-dependent phase transition behavior of TiO2 and black TiO2 NTs using temperature-dependent synchrotron-based X-ray diffraction. Thermal treatments reveal that phase transitions occur in the ranges of 210-240 °C for normal NTs and 270-300 °C for black NTs. The onset temperature and crystallization growth are dependent on size, especially NT length, at least in the system under investigation. We observe anisotropic crystallization in quantum confinement, with the unit cell undergoing compression in the a-axis and expansion in the c-axis during crystallization. The longest black NTs (BV50T4) show a significant difference in the c/a ratio. Defects, such as oxygen vacancies, localize on specific NT planes.
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