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动力学结晶途径的直接成像:模拟与液相透射电子显微镜观察

Direct Imaging of the Kinetic Crystallization Pathway: Simulation and Liquid-Phase Transmission Electron Microscopy Observations.

作者信息

Xu Zhangying, Ou Zihao

机构信息

Qian Weichang College, Shanghai University, Shanghai 200444, China.

Department of Materials Science and Engineering, Stanford University, Stanford, CA 94305, USA.

出版信息

Materials (Basel). 2023 Mar 1;16(5):2026. doi: 10.3390/ma16052026.

Abstract

The crystallization of materials from a suspension determines the structure and function of the final product, and numerous pieces of evidence have pointed out that the classical crystallization pathway may not capture the whole picture of the crystallization pathways. However, visualizing the initial nucleation and further growth of a crystal at the nanoscale has been challenging due to the difficulties of imaging individual atoms or nanoparticles during the crystallization process in solution. Recent progress in nanoscale microscopy had tackled this problem by monitoring the dynamic structural evolution of crystallization in a liquid environment. In this review, we summarized several crystallization pathways captured by the liquid-phase transmission electron microscopy technique and compared the observations with computer simulation. Apart from the classical nucleation pathway, we highlight three nonclassical pathways that are both observed in experiments and computer simulations: formation of an amorphous cluster below the critical nucleus size, nucleation of the crystalline phase from an amorphous intermediate, and transition between multiple crystalline structures before achieving the final product. Among these pathways, we also highlight the similarities and differences between the experimental results of the crystallization of single nanocrystals from atoms and the assembly of a colloidal superlattice from a large number of colloidal nanoparticles. By comparing the experimental results with computer simulations, we point out the importance of theory and simulation in developing a mechanistic approach to facilitate the understanding of the crystallization pathway in experimental systems. We also discuss the challenges and future perspectives for investigating the crystallization pathways at the nanoscale with the development of in situ nanoscale imaging techniques and potential applications to the understanding of biomineralization and protein self-assembly.

摘要

材料从悬浮液中结晶决定了最终产物的结构和功能,并且大量证据指出经典的结晶途径可能无法涵盖结晶途径的全貌。然而,由于在溶液结晶过程中对单个原子或纳米颗粒进行成像存在困难,在纳米尺度上可视化晶体的初始成核和进一步生长一直具有挑战性。纳米尺度显微镜的最新进展通过监测液体环境中结晶的动态结构演变解决了这个问题。在这篇综述中,我们总结了液相透射电子显微镜技术捕捉到的几种结晶途径,并将观察结果与计算机模拟进行了比较。除了经典的成核途径外,我们重点介绍了在实验和计算机模拟中都观察到的三种非经典途径:在临界核尺寸以下形成无定形聚集体、从无定形中间体结晶相的成核以及在获得最终产物之前多种晶体结构之间的转变。在这些途径中,我们还强调了从原子结晶单个纳米晶体的实验结果与由大量胶体纳米颗粒组装胶体超晶格的实验结果之间的异同。通过将实验结果与计算机模拟进行比较,我们指出了理论和模拟在开发一种有助于理解实验系统中结晶途径的机理方法方面的重要性。我们还讨论了随着原位纳米尺度成像技术的发展以及在理解生物矿化和蛋白质自组装方面的潜在应用,在纳米尺度研究结晶途径所面临的挑战和未来前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35ba/10004038/6ba709d800ba/materials-16-02026-g002.jpg

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