Understanding the Growth Mechanism of α-Fe2O3 Nanoparticles through a Controlled Shape Transformation

铁酸盐 奥斯特瓦尔德成熟 成核 纳米颗粒 溶解 赤铁矿 化学工程 材料科学 结晶 过饱和度 纳米技术 化学 结晶学 化学物理 矿物学 物理化学 有机化学 吸附 工程类
作者
Ming Lin,Hui Ru Tan,Joyce Pei Ying Tan,Shi‐Qiang Bai
出处
期刊:Journal of Physical Chemistry C [American Chemical Society]
卷期号:117 (21): 11242-11250 被引量:68
标识
DOI:10.1021/jp402281a
摘要

The growth mechanism of α-Fe2O3 nanoparticles in solution has been elucidated from a comprehensive analysis on the shape and morphology of obtained particles. It is found that the hydrothermal synthesis of α-Fe2O3 nanoparticles from ferric chloride precursor follows two stages: the initial nucleation of α-Fe2O3 nuclei and the subsequent ripening of nuclei into various shapes. The initial nucleation involves the formation of polynuclears from hydrolysis of Fe3+ salt precursors, followed by the growth of β-FeOOH nanowires with an akaganeite structure, and then into two-line ferrihydrite nanoparticles through a dissolution–recrystallization process. In the subsequent ripening process, we suggest that the formation of large α-Fe2O3 particles follows the dissolution of two-line ferrihydrite and then precipitation and oriented aggregation of α-Fe2O3 nuclei rather than the oriented aggregation of ferrihydrite nanoparticles followed by phase transformation. The oriented attachment of {104} facets between α-Fe2O3 nuclei results in the formation of oblate spheroid nanocrystals (nanoflower-like particles) either in ethanol or in the beginning stage where the particles first undergo oriented aggregation. With the addition of water, Ostwald ripening process (dissolution–reprecipitation) will play an important role to convert the assembly of nanoflowers into a 3D rhombohedral shape with well-defined edges and surfaces. The proposed mechanism in this article not only allows us to better control the synthesis of iron oxide particles with designed shapes and structures but also provides guidance for theoretical simulations on the oriented attachment process for hematite formation.
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