Laboratory of Environmental Sciences and Technology, Xinjiang Technical Institute of Physics & Chemistry, Key Laboratory of Functional Materials and Devices for Special Environments, Chinese Academy of Sciences , Urumqi, 830011, China.
Nano Institute of Utah and Department of Materials Science and Engineering, University of Utah , Salt Lake City, Utah 84112, United States.
ACS Nano. 2016 Feb 23;10(2):2386-91. doi: 10.1021/acsnano.5b07197. Epub 2016 Jan 13.
Because of the lack of experimental evidence, much confusion still exists on the nucleation and growth dynamics of a nanostructure, particularly of metal. The situation is even worse for nanodroplets because it is more difficult to induce the formation of a nanodroplet while imaging the dynamic process with atomic resolution. Here, taking advantage of an electron beam to induce the growth of Bi nanodroplets on a SrBi2Ta2O9 platelet under a high resolution transmission electron microscope (HRTEM), we directly observed the detailed growth pathways of Bi nanodroplets from the earliest stage of nucleation that were previously inaccessible. Atomic scale imaging reveals that the dynamics of nucleation involves a much more complex trajectory than previously predicted based on classical nucleation theory (CNT). The monatomic Bi layer was first formed in the nucleation process, which induced the formation of the prenucleated clusters. Following that, critical nuclei for the nanodroplets formed both directly from the addition of atoms to the prenucleated clusters by the classical growth process and indirectly through transformation of an intermediate liquid film based on the Stranski-Krastanov growth mode, in which the liquid film was induced by the self-assembly of the prenucleated clusters. Finally, the growth of the Bi nanodroplets advanced through the classical pathway and sudden droplet coalescence. This study allows us to visualize the critical steps in the nucleation process of an interfacial nanodroplet, which suggests a revision of the perspective of CNT.
由于缺乏实验证据,纳米结构(尤其是金属)的成核和生长动力学仍然存在很多混淆。对于纳米液滴来说,情况更糟,因为在原子分辨率下成像动态过程时,更难以诱导纳米液滴的形成。在这里,我们利用电子束在高分辨透射电子显微镜(HRTEM)下诱导 Bi 纳米液滴在 SrBi2Ta2O9 薄片上生长,直接观察到了以前无法获得的从最早成核阶段开始的 Bi 纳米液滴的详细生长途径。原子尺度成像揭示了成核动力学涉及的轨迹比基于经典成核理论(CNT)预测的复杂得多。在成核过程中,首先形成了单原子 Bi 层,这诱导了预成核团簇的形成。随后,通过经典生长过程从预成核团簇添加原子直接形成纳米液滴的临界核,以及通过基于 Stranski-Krastanov 生长模式的中间液相的间接转变形成纳米液滴的临界核,其中通过预成核团簇的自组装诱导了液相。最后,Bi 纳米液滴通过经典途径和突然的液滴聚合并继续生长。这项研究使我们能够直观地了解界面纳米液滴成核过程中的关键步骤,这表明需要对 CNT 的观点进行修正。