Peng Xinxing, Zhu Fu-Chun, Jiang You-Hong, Sun Juan-Juan, Xiao Liang-Ping, Zhou Shiyuan, Bustillo Karen C, Lin Long-Hui, Cheng Jun, Li Jian-Feng, Liao Hong-Gang, Sun Shi-Gang, Zheng Haimei
State Key Laboratory for Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005, China.
Materials Science Division, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, USA.
Nat Commun. 2022 Jun 23;13(1):3601. doi: 10.1038/s41467-022-31075-z.
An understanding of solid-liquid interfaces is of great importance for fundamental research as well as industrial applications. However, it has been very challenging to directly image solid-liquid interfaces with high resolution, thus their structure and properties are often unknown. Here, we report a quasi-liquid phase between metal (In, Sn) nanoparticle surfaces and an aqueous solution observed using liquid cell transmission electron microscopy. Our real-time high-resolution imaging reveals a thin layer of liquid-like materials at the interfaces with the frequent appearance of small In nanoclusters. Such a quasi-liquid phase serves as an intermediate for the mass transport from the metal nanoparticle to the liquid. Density functional theory-molecular dynamics simulations demonstrate that the positive charges of In ions greatly contribute to the stabilization of the quasi-liquid phase on the metal surface.
理解固液界面对于基础研究和工业应用都非常重要。然而,直接对固液界面进行高分辨率成像一直极具挑战性,因此它们的结构和属性常常未知。在此,我们报告了使用液体池透射电子显微镜观察到的金属(铟、锡)纳米颗粒表面与水溶液之间的准液相。我们的实时高分辨率成像揭示了界面处存在一层类似液体的薄材料,且频繁出现小的铟纳米团簇。这种准液相充当了从金属纳米颗粒到液体的质量传输中间体。密度泛函理论 - 分子动力学模拟表明,铟离子的正电荷对金属表面准液相的稳定起到了很大作用。