Sequential crystallization pathways in apatite-wollastonite glass-ceramics

The clinical performance of next generation bioceramics requires precise control over their multi-phase composition, a goal often unachievable with conventional synthesis routes that lead to stochastic crystallization. Here, we establish a deterministic processing-structure paradigm for apatite-wollastonite glass-ceramics (AWGCs) by using a scalable spray pyrolysis technique to create atomically homogeneous amorphous precursors. By systematically controlling the sintering temperature (700-1100 °C), we decouple the kinetic and thermodynamic drivers of phase formation. High-resolution XRD with Rietveld analysis reveals a predictable, three-stage evolution; kinetically driven hydroxylapatite nucleation (<800 °C), followed by a thermodynamic crossover to a whitlockite-dominant regime (900-1000 °C), and finally the diffusion-controlled growth of mechanically robust wollastonite (>1000 °C). This work presents the first quantitative, predictive map for this system, enabling the rational design of AWGCs with bespoke phase assemblages for targeted biomedical applications, from bioactive coatings to load-bearing implants.