| Autor: |
Gao, Zhonghui, Hao, Zhangxiang, Yi, Min, Huang, Ying, Xu, Yiming, Zhao, Ying, Li, Zhaoyang, Zhu, Shengli, Xu, Baixiang, Liu, Porun, Wang, Feng Ryan, Huang, Yunhui, Zhao, Huijun, Yang, Xianjin |
| Zdroj: |
ChemistrySelect; 10/17/2018, Vol. 3 Issue 38, p10711-10716, 6p |
| Abstrakt: |
Developing TiO2 crystals with specific morphologies and nanostructured architectures is highly desirable in energy storage, conversion and catalysis applications. Thermally activated amorphous‐to‐crystal transition provides effective growth of poly or monocrystalline TiO2, while an in‐depth understanding of different crystallization pathways at the solid state is still lacking. Herein, we report a close correlation between mechanical strength of the TiO2 precursors and their different crystallization pathways. Two different morphologies, i. e., well‐defined anatase TiO2 single nanocrystals and anatase polycrystalline nanotubes are obtained via rapid heating of two amorphous TiO2 precursors with distinctive mechanical strengths. The mechanical‐strength‐dependent crystallization from amorphous solid‐state precursors provides additional control on the crystallization pathway and thus the desirable properties of the resultant nanostructures. In this study, the well‐defined anatase nanocrystals with controlled morphology show higher storage capacity of sodium ion than that of polycrystalline ones in sodium ion batteries. We have successfully demonstrated the correlation between mechanical strength of precursors and their solid‐state crystallization pathways, this suggesting a new way to predict and optimize solid‐state synthesis of nanomaterials. Well‐defined anatase TiO2 single nanocrystals or anatase polycrystalline nanotubes are obtained via rapid heating of two amorphous TiO2 precursors with significant difference in mechanical strength. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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