Abstract
To begin with, let us first define the term “surface”. We mean by it, simply the termination of the bulk state, that is to say, the region of a solid or liquid phase where the equations based on three-dimensionality are no longer sufficient to describe the complete physical state of the system. This definition implies that a surface is not necessarily confined to the topmost layer of atoms of a liquid or a crystal, but may consist of several such layers extending into the bulk, i.e., that region at or near the surface where the symmetry of the bulk is perturbed so as to give rise to altered interaction forces. This asymmetry is illustrated in Fig. 2.1 and is actually responsible for the peculiar behavior of surfaces and interfaces that lead to phenomena such as surface tension, capillary pressure or enhanced chemical reactivity of surfaces in general.
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Christmann, K. (1991). Macroscopic Treatment of Surface Phenomena: Thermodynamics and Kinetics of Surfaces. In: Introduction to Surface Physical Chemistry. Topics in Physical Chemistry, vol 1. Steinkopff, Heidelberg. https://doi.org/10.1007/978-3-662-08009-2_2
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DOI: https://doi.org/10.1007/978-3-662-08009-2_2
Publisher Name: Steinkopff, Heidelberg
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