In situ liquid transmission electron microscopy captures mineralization processes on titanium dioxide, highlighting bioactivity implications.
The integration of titanium dioxide (TiO 2 ) with calcium phosphate (CaP)‐based hydroxyapatite (HAP) is a promising strategy for enhancing the bioactivity of bone implants. However, a fundamental understanding of the interfacial reactions governing CaP mineralization on TiO 2 remains limited due to lack of characterization techniques with sufficient spatial and temporal resolution in hydrated state. In this study, in situ liquid transmission electron microscopy (TEM) imaging and correlative ex situ TEM analyses are combined to investigate the nucleation, aggregation, and crystallization of the CaP layer on TiO 2 nanoparticle surfaces. The findings reveal a three‐step mineralization process: 1) aggregation of TiO 2 nanoparticles in solution, 2) formation of an amorphous CaP‐like (ACP‐like) layer, leading to an ACP‐like coated TiO 2 nanoparticle structure, and 3) progressive crystallization of ACP into HAP, forming a HAP‐like coated TiO 2 nanoparticle structure. Liquid‐TEM imaging captured dynamic transformations, including nanoparticle aggregation, structural evolution, and phase transitions, providing unprecedented insights into the physicochemical interactions underlying mineralization. Additionally, the effects of electron beam exposure on TiO 2 nanoparticles are evaluated, demonstrating that high electron flux densities can induce morphological instability. This study advances the understanding of CaP‐TiO 2 interfacial mineralization and offers valuable guidance for optimizing bioactive coatings to improve osseointegration and the stability of bone implants.
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Zhang et al. (2025) studied this question.
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