成核
经典成核理论
化学物理
Crystal(编程语言)
化学
动力学
扩散
热力学
物理
计算机科学
经典力学
程序设计语言
出处
期刊:ChemPhysChem
[Wiley]
日期:2015-04-27
卷期号:16 (10): 2069-2075
被引量:88
标识
DOI:10.1002/cphc.201500231
摘要
Recent observations of prenucleation species and multi-stage crystal nucleation processes challenge the long-established view on the thermodynamics of crystal formation. Here, we review and generalize extensions to classical nucleation theory. Going beyond the conventional implementation as has been used for more than a century now, nucleation inhibitors, precursor clusters and non-classical nucleation processes are rationalized as well by analogous concepts based on competing interface and bulk energy terms. This is illustrated by recent examples of species formed prior to/instead of crystal nucleation and multi-step nucleation processes. Much of the discussed insights were obtained from molecular simulation using advanced sampling techniques, briefly summarized herein for both nucleation-controlled and diffusion-controlled aggregate formation.
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