| Autor: |
Durelle M; CEA, DES, ISEC, DMRC, Univ. Montpellier, 30207 Marcoule, France.; Université Paris-Saclay, CNRS, CEA, NIMBE, LIONS, 91191 Gif-sur-Yvette, France., Charton S; CEA, DES, ISEC, DMRC, Univ. Montpellier, 30207 Marcoule, France., Gobeaux F; Université Paris-Saclay, CNRS, CEA, NIMBE, LIONS, 91191 Gif-sur-Yvette, France., Chevallard C; Université Paris-Saclay, CNRS, CEA, NIMBE, LIONS, 91191 Gif-sur-Yvette, France., Belloni L; Université Paris-Saclay, CNRS, CEA, NIMBE, LIONS, 91191 Gif-sur-Yvette, France., Testard F; Université Paris-Saclay, CNRS, CEA, NIMBE, LIONS, 91191 Gif-sur-Yvette, France., Trépout S; Institut Curie, Université PSL, CNRS UMS2016, Inserm US43, Université Paris-Saclay, Multimodal Imaging Center, 91400 Orsay, France., Carriere D; Université Paris-Saclay, CNRS, CEA, NIMBE, LIONS, 91191 Gif-sur-Yvette, France. |
| Abstrakt: |
Crystallization from solution often occurs via "nonclassical" routes; that is, it involves transient, non-crystalline states like reactant-rich liquid droplets and amorphous particles. However, in mineral crystals, the well-defined thermodynamic character of liquid droplets and whether they convert─or not─into amorphous phases have remained unassessed. Here, by combining cryo-transmission electron microscopy and X-ray scattering down to a 250 ms reaction time, we unveil that crystallization of cerium oxalate involves a metastable chemical equilibrium between transient liquid droplets and solid amorphous particles: contrary to the usual expectation, reactant-rich droplets do not evolve into amorphous solids. Instead, at concentrations above 2.5 to 10 mmol L -1 , both amorphous and reactant-rich liquid phases coexist for several tens of seconds and their molar fractions remain constant and follow the lever rule in a multicomponent phase diagram. Such a metastable chemical equilibrium between solid and liquid precursors has been so far overlooked in multistep nucleation theories and highlights the interest of rationalizing phase transformations using multicomponent phase diagrams not only when designing and recycling rare earths materials but also more generally when describing nonclassical crystallization. |
