Gerrard Nikki, Gattinoni Chiara, McBride Fiona, Michaelides Angelos, Hodgson Andrew
Surface Science Research Centre and Department of Chemistry , University of Liverpool , Liverpool L69 3BX , United Kingdom.
Materials Theory , ETH Zürich , Wolfgang-Pauli-Str. 27 , 8093 Zürich , Switzerland.
J Am Chem Soc. 2019 May 29;141(21):8599-8607. doi: 10.1021/jacs.9b03311. Epub 2019 May 14.
Heterogeneous ice nucleation at solid surfaces impacts many areas of science, from environmental processes, such as precipitation, to microbiological systems and food processing, but the microscopic mechanisms underpinning nucleation remain unclear. Discussion of ice growth has often focused around the role of the surface in templating the structure of water, forcing the first layer to adopt the registry of the underlying substrate rather than that of ice. To grow a thick ice film, water in the first few ice layers must accommodate this strain, but understanding how this occurs requires detailed molecular-scale information that is lacking. Here we combine scanning tunneling microscopy, low-energy electron diffraction, and work-function measurements with electronic structure calculations to investigate the initial stages of ice growth on a Pt alloy surface, having a lattice spacing 6% larger than ice. Although the first layer of water forms a strictly commensurate hexagonal network, this behavior does not extend to the second layer. Instead, water forms a 2D structure containing extended defect rows made from face-sharing pentamer and octamer rings. The defect rows allow the majority of second-layer water to remain commensurate with the solid surface while compensating lateral strain by increasing the water density close to that of an ice surface. The observation of octamer-pentamer rows in ice films formed on several surfaces suggests that the octamer-pentamer defect motif acts as a flexible strain relief mechanism in thin ice films, providing a mechanism that is not available during the growth of strained films in other materials, such as semiconductors.
固体表面的异质冰核化影响着许多科学领域,从降水等环境过程到微生物系统和食品加工,但冰核化的微观机制仍不清楚。关于冰生长的讨论通常集中在表面在水结构模板化中的作用,迫使第一层采用下层基底的晶格排列而非冰的晶格排列。要生长出厚冰膜,最初几层冰层中的水必须适应这种应变,但要理解这是如何发生的,就需要目前尚缺乏的详细分子尺度信息。在这里,我们将扫描隧道显微镜、低能电子衍射和功函数测量与电子结构计算相结合,以研究在晶格间距比冰大6%的铂合金表面上冰生长的初始阶段。尽管第一层水形成了严格匹配的六边形网络,但这种行为并未延伸到第二层。相反,水形成了一种二维结构,其中包含由面共享五聚体和八聚体环构成的延伸缺陷行。这些缺陷行使得大部分第二层水能够与固体表面保持匹配,同时通过将水密度提高到接近冰表面的密度来补偿横向应变。在几个表面上形成的冰膜中观察到八聚体 - 五聚体行,这表明八聚体 - 五聚体缺陷基序在薄冰膜中起到了灵活的应变缓解机制,提供了一种在其他材料(如半导体)的应变膜生长过程中不存在的机制。