Microscopic kinetics pathway of salt crystallization in graphene nanocapillaries
arXiv:2103.05987 · doi:10.1103/PhysRevLett.126.136001
Abstract
The fundamental understanding of crystallization, in terms of microscopic kinetic and thermodynamic details, remains a key challenge in the physical sciences. Here, by using in situ graphene liquid cell transmission electron microscopy, we reveal the atomistic mechanism of NaCl crystallization from solutions confined within graphene cells. We find that rock salt NaCl forms with a peculiar hexagonal morphology. We also see the emergence of a transitory graphite-like phase, which may act as an intermediate in a two-step pathway. With the aid of density functional theory calculations, we propose that these observations result from a delicate balance between the substrate-solute interaction and thermodynamics under confinement. Our results highlight the impact of confinement on both the kinetics and thermodynamics of crystallization, offering new insights into heterogeneous crystallization theory and a potential avenue for materials design.
arXiv commentMain: 7 pages, 4 figures; Supplemental Material: 12 pages, 7 figures
References in corpus (8)
- Van der Waals density functionals applied to solids
- Implicit solvation model for density-functional study of nanocrystal surfaces and reaction pathways
- Crystal Nucleation in Liquids: Open Questions and Future Challenges in Molecular Dynamics Simulations
- Square ice in graphene nanocapillaries
- 2D ice from first principles: structures and phase transitions
- Nucleation in aqueous NaCl solutions shifts from 1-step to 2-step mechanism on crossing the spinodal
- Structural and configurational properties of nanoconfined monolayer ice from first principles
- Phase transitions in fluctuations and their role in two-step nucleation