纳米线
锐钛矿
材料科学
纳米晶材料
白长石
相变
拉曼光谱
相(物质)
化学物理
衍射
化学工程
结晶学
拉曼散射
纳米技术
凝聚态物理
化学
光学
锆石
催化作用
有机化学
光催化
古生物学
工程类
物理
生物
作者
Quanjun Li,Benyuan Cheng,Xue Yang,Ran Liu,Бо Лю,Jing Liu,Zhiqiang Chen,Bo Zou,Tian Cui,Bingbing Liu
摘要
The phase transitions of one-dimensional (1D) anatase TiO2 nanowires were studied by in situ high-pressure synchrotron X-ray diffraction and Raman scattering up to 37 GPa. A direct anatase-to-baddeleyite transformation was observed at ∼9 GPa, which is clearly different from the size-dependent phase transition behaviors for nanocrystalline TiO2. We found the higher compressibility in the c-axis compared to the a-axis for anatase nanowires that may be attributed to both the crystal structural feature and the growth direction of the nanowires. The Ti–O bonds show abnormal changes during the anatase-to-baddeleyite phase transition. This phase transition of the TiO2 nanowires shows obvious morphology-tuned behaviors. Upon decompression, the baddeleyite phase transformed into α-PbO2 phase. The morphology of the TiO2 nanowires shows excellent stability and TiO2 nanowires with α-PbO2 phase were obtained at ambient conditions through a compression–decompression cycle. These results indicate that the nanoscale quasi-1D structure of TiO2 nanowires may contribute to the high-pressure phase transitions showing unique morphology-tuned behaviors.
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