期刊
SCIENCE ADVANCES
卷 8, 期 35, 页码 -出版社
AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/sciadv.abn7087
关键词
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资金
- U.S. Department of Energy (DOE), Office of Basic Energy Sciences, Division of Materials Science and Engineering, Synthesis, and Processing Science Program at Pacific Northwest National Laboratory (PNNL)
- US DOE Office of Science Distinguished Scientist Fellows award at PNNL
- Engineering and Physical Sciences Research Council (EPSRC) [EP/S028234/1]
- DOE [DE-AC05-76RL01830]
In this study, the growth process of an aluminum hydroxide film from an aqueous solution was directly observed using high-speed atomic force microscopy. The results showed that the dynamically fluctuating nanostructures preceding the formation of the film exhibited similar characteristics to those predicted by classical nucleation theory. However, the cluster energy landscape deviated from classical expectations. Kinetic Monte Carlo simulations revealed that these deviations were caused by electrostatic interactions between the clusters and the underlying substrate, resulting in microphase separation and the formation of a nanostructured surface phase.
Crystal nucleation is facilitated by transient, nanoscale fluctuations that are extraordinarily difficult to observe. Here, we use high-speed atomic force microscopy to directly observe the growth of an aluminum hydroxide film from an aqueous solution and characterize the dynamically fluctuating nanostructures that precede its formation. Nanoscale cluster distributions and fluctuation dynamics show many similarities to the predictions of classical nucleation theory, but the cluster energy landscape deviates from classical expectations. Kinetic Monte Carlo simulations show that these deviations can arise from electrostatic interactions between the clusters and the underlying substrate, which drive microphase separation to create a nanostructured surface phase. This phase can evolve seamlessly from a low-coverage state of fluctuating clusters into a high-coverage nanostructured network, allowing the film to grow without having to overcome classical nucleation barriers.
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