Department of Physics and Astronomy, University of California, Los Angeles, CA, USA.
California NanoSystems Institute, University of California, Los Angeles, CA, USA.
Nature. 2019 Jun;570(7762):500-503. doi: 10.1038/s41586-019-1317-x. Epub 2019 Jun 26.
Nucleation plays a critical role in many physical and biological phenomena that range from crystallization, melting and evaporation to the formation of clouds and the initiation of neurodegenerative diseases. However, nucleation is a challenging process to study experimentally, especially in its early stages, when several atoms or molecules start to form a new phase from a parent phase. A number of experimental and computational methods have been used to investigate nucleation processes, but experimental determination of the three-dimensional atomic structure and the dynamics of early-stage nuclei has been unachievable. Here we use atomic electron tomography to study early-stage nucleation in four dimensions (that is, including time) at atomic resolution. Using FePt nanoparticles as a model system, we find that early-stage nuclei are irregularly shaped, each has a core of one to a few atoms with the maximum order parameter, and the order parameter gradient points from the core to the boundary of the nucleus. We capture the structure and dynamics of the same nuclei undergoing growth, fluctuation, dissolution, merging and/or division, which are regulated by the order parameter distribution and its gradient. These experimental observations are corroborated by molecular dynamics simulations of heterogeneous and homogeneous nucleation in liquid-solid phase transitions of Pt. Our experimental and molecular dynamics results indicate that a theory beyond classical nucleation theory is needed to describe early-stage nucleation at the atomic scale. We anticipate that the reported approach will open the door to the study of many fundamental problems in materials science, nanoscience, condensed matter physics and chemistry, such as phase transition, atomic diffusion, grain boundary dynamics, interface motion, defect dynamics and surface reconstruction with four-dimensional atomic resolution.
成核在许多物理和生物现象中起着关键作用,这些现象的范围从结晶、熔化和蒸发到云的形成和神经退行性疾病的发生。然而,成核是一个具有挑战性的实验研究过程,特别是在其早期阶段,当几个原子或分子开始从母体相中形成新相时。已经使用了许多实验和计算方法来研究成核过程,但实验确定三维原子结构和早期核的动力学是无法实现的。在这里,我们使用原子电子断层扫描技术在原子分辨率下以四维度(即包括时间)研究早期成核。使用 FePt 纳米颗粒作为模型系统,我们发现早期核是不规则形状的,每个核都有一个到几个原子的核心,最大序参量,并且序参量梯度从核心指向核的边界。我们捕获了相同核的结构和动力学,这些核经历了生长、波动、溶解、合并和/或分裂,这些过程受序参量分布及其梯度的调节。这些实验观察结果得到了 Pt 液-固相变中异质和同质成核的分子动力学模拟的证实。我们的实验和分子动力学结果表明,需要超越经典成核理论的理论来描述原子尺度上的早期成核。我们预计,所报道的方法将为研究材料科学、纳米科学、凝聚态物理和化学中的许多基本问题打开大门,例如相变、原子扩散、晶界动力学、界面运动、缺陷动力学和表面重建,具有四维度的原子分辨率。