亚稳态
成核
水溶液
溶解
相(物质)
Crystal(编程语言)
离子键合
透射电子显微镜
卤化物
材料科学
原位
化学物理
傅里叶变换
结晶学
碱金属
相变
化学
傅里叶变换红外光谱
结晶
单晶
转化(遗传学)
动力学
动能
X射线晶体学
晶体结构
分析化学(期刊)
化学工程
钙钛矿(结构)
非平衡态热力学
作者
Lu Jin,Xia Song,T. D. Xu,Di Wu,An Bai,Wei Tu,Wei J,Haoyang Li,Haihua Wang,Zhiguo Zhang,Fengjiao Zhang,Zhiyong Yu,Bo Guan,Yao Yang,Xianhu Sun
出处
期刊:Nano Letters
[American Chemical Society]
日期:2026-07-13
卷期号:26 (28): 9234-9241
标识
DOI:10.1021/acs.nanolett.6c02166
摘要
Directly resolving the atomic-scale dynamics of phase transitions in alkali halide crystals after nucleation from saturated solutions remains challenging but is essential for understanding crystal growth. Here, in situ liquid-phase transmission electron microscopy (LP-TEM) was used to visualize the early stage structural evolution of KCl in aqueous solution. We observe the dissolution of [110]-oriented KCl domains followed by reprecipitation into [100]-oriented domains. Time-resolved radial distribution function (RDF) analysis derived from sequential fast Fourier transform (FFT) diffractograms quantitatively maps the kinetic pathway of this transformation. A previously unreported metastable hexagonal phase (h-KCl) is identified as a transient intermediate connecting two cubic domains. These results provide direct evidence for a cubic-hexagonal-cubic transformation pathway in a prototypical ionic crystal and reveal how nonequilibrium intermediates govern solution-mediated solid-state phase transitions.
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