Live Visualization of the Nucleation and Growth of Needle-Like Hydroxyapatite Crystals in Solution by In Situ TEM

结晶 生物矿化 成核 无定形磷酸钙 透射电子显微镜 无定形固体 材料科学 纳米团簇 相(物质) 结晶学 纳米颗粒 粒子(生态学) 磷灰石 化学工程 纳米技术 化学 工程类 有机化学 冶金 地质学 海洋学
作者
Gisele M. L. Dalmônico,Dris Ihiawakrim,Nathaly Ortiz Peña,Evaristo C. Biscaia,Caio Felippe Curitiba Marcellos,Marcos Farina,Ovidiu Ersen,André L. Rossi
出处
期刊:Crystal Growth & Design [American Chemical Society]
卷期号:22 (8): 4828-4837 被引量:8
标识
DOI:10.1021/acs.cgd.2c00296
摘要

Calcium phosphate materials are widely investigated for the study of biomineralization processes and for the development of new biomaterials. It has been proposed that the crystallization of hydroxyapatite in aqueous media occurs in steps and not directly by ion-by-ion accretion. Prenucleation nanoclusters aggregate to form amorphous spheres and further crystallize into hydroxyapatite. However, conventional analytical techniques cannot visualize phase transformations over time continuously, and the nonclassical crystallization of hydroxyapatite is still under debate. In situ liquid-phase transmission electron microscopy (TEM) is a novel technique that allows us to follow reactions occurring during TEM in real time and thus to visualize the formation of calcium phosphate crystals from the formation of the first mineral nucleus to the final crystallized phase. In this work, in situ TEM was performed, and videos showed the exact moment of hydroxyapatite nucleation and crystallization. During the experiment, different amorphous calcium phosphate nanoparticles were identified prior to the formation of the plate/needle-like hydroxyapatite particles. Crystallization was achieved only after particle elongation. A combined kinetic model that considered the thermodynamic nonideality of the electrolyte solution was applied. Sensitivity analyses were performed to interpret the thermodynamic environment of the liquid cell and the possible species formed over time.
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