We report the synthesis of a library of colloidal Zr4+-, Ti4+-, and Si4+-based A2BF6 (A = Na+, Cs+, NH4+, and N(CH3)4+) nanocrystals. These lattices are synthesized without the use of aqueous HF but instead are prepared using safer fluoride salt precursors dissolved in nonpolar solutions. We show that nanocrystal morphologies, including shape anisotropy, are altered when various synthetic parameters are adjusted, including reaction temperature, time, and solvent polarity. Nucleation and growth pathways of A2ZrF6 compositions are compared. An in situ A-site cation exchange requiring internal anion sublattice reorganization is described that allows for conversion of anisotropic (NH4)2ZrF6 nanorods into Cs2ZrF6 nanorods that could not be prepared directly. The development of colloidal nanocrystals as a new form factor for A2BF6 lattices addresses fundamental synthesis challenges in inorganic nanoscience and lays the groundwork for future work into doping such nanocrystals for solution-phase photonic applications, processing, or printing.
Tzanetopoulos et al. (Thu,) studied this question.