成核
无定形碳酸钙
无定形固体
溶解
化学物理
透射电子显微镜
碳酸钙
化学工程
材料科学
化学
结晶学
矿物学
方解石
纳米技术
有机化学
工程类
作者
Michael H. Nielsen,Shaul Aloni,James J. De Yoreo
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2014-09-05
卷期号:345 (6201): 1158-1162
被引量:735
标识
DOI:10.1126/science.1254051
摘要
Mechanisms of nucleation from electrolyte solutions have been debated for more than a century. Recent discoveries of amorphous precursors and evidence for cluster aggregation and liquid-liquid separation contradict common assumptions of classical nucleation theory. Using in situ transmission electron microscopy (TEM) to explore calcium carbonate (CaCO3) nucleation in a cell that enables reagent mixing, we demonstrate that multiple nucleation pathways are simultaneously operative, including formation both directly from solution and indirectly through transformation of amorphous and crystalline precursors. However, an amorphous-to-calcite transformation is not observed. The behavior of amorphous calcium carbonate upon dissolution suggests that it encompasses a spectrum of structures, including liquids and solids. These observations of competing direct and indirect pathways are consistent with classical predictions, whereas the behavior of amorphous particles hints at an underlying commonality among recently proposed precursor-based mechanisms.
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