Krueger Brenda J, Ross Jean L, Grassian Vicki H
Department of Chemistry and the Central Microscopy Research Facility, The University of Iowa, Iowa City, Iowa 52242.
Langmuir. 2005 Sep 13;21(19):8793-801. doi: 10.1021/la051378j.
In this study, atomic force microscopy (AFM) is used to image freshly cleaved MgO(100) and CaCO3(104) as these surfaces undergo reaction with water and nitric acid under ambient conditions of temperature, pressure, and relative humidity. The reaction of water and nitric acid results in the formation of hydroxylated and nitrated surfaces, respectively. It is clear from the AFM images that there are spatial inhomogenieties and surface features that form on micrometer and nanometer length scales as these reactions proceed. These features, which include hillocks, patches, microcrystallites, and micropuddles, are due to surface and phase segregation as a result of facile ion mobility in the presence of adsorbed water. In addition, instabilities and oscillations in the AFM images provide an indication of liquid formation and the deliquescence (i.e., a solid to liquid-phase transition) of nitrate salts as a function of relative humidity.
在本研究中,使用原子力显微镜(AFM)对刚解理的MgO(100)和CaCO3(104)表面进行成像,因为这些表面在温度、压力和相对湿度的环境条件下与水和硝酸发生反应。水和硝酸的反应分别导致形成羟基化和硝化表面。从AFM图像可以清楚地看出,随着这些反应的进行,在微米和纳米长度尺度上会形成空间不均匀性和表面特征。这些特征包括小丘、斑块、微晶和微水坑,是由于在存在吸附水的情况下离子易于迁移导致的表面和相分离。此外,AFM图像中的不稳定性和振荡表明了液体的形成以及硝酸盐作为相对湿度函数的潮解(即从固相到液相的转变)。