赤铁矿
化学
磁铁矿
结晶学
透射电子显微镜
成核
八面体
相(物质)
电子衍射
过渡金属
粒子(生态学)
相变
图层(电子)
化学物理
晶体结构
衍射
纳米技术
矿物学
凝聚态物理
材料科学
冶金
光学
催化作用
生物化学
物理
海洋学
有机化学
地质学
作者
Xiaoben Zhang,Chuanchuan Jin,Shaobo Han,Peiyao Guo,Yan Zhou,Wei Liu,Wenjie Shen
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2023-07-20
卷期号:62 (30): 12111-12118
被引量:7
标识
DOI:10.1021/acs.inorgchem.3c01653
摘要
Phase transition between iron oxides practically defines their functionalities in both physical and chemical applications. Direct observation of the atomic rearrangement and a quantitative description of the dynamic behavior of the phase transition, however, are rare. Here, we monitored the structure evolution from a rod-shaped hematite nanoparticle to magnetite during H2 reduction at elevated temperatures. Environmental transmission electron microscopy observations, along with selected area electron diffraction experiments, identified that the reduction preferentially commenced with Fe3O4 nucleation on the surface defective sites, followed by laterally growing into a Fe3O4 film until fully covering the particle surface. The Fe3O4 phase then propagated toward the bulk particle via a Fe3O4/α-Fe2O3 interface with the relationship α-Fe2O3(0001)//Fe3O4(111) in an aligned orientation of [112]Fe3O4||[112̅0]α-Fe2O3. Upon this Fe3O4/α-Fe2O3 interface, the Fe-O octahedra in Fe3O4(111) (as layer A) matches that of α-Fe2O3(0001) at a rotation angle of 30°, and the reduction proceeds in such a pattern that two-thirds of the FeOh in the adjacent layer (layer B) is transformed into FeTe.
科研通智能强力驱动
Strongly Powered by AbleSci AI