International
Tables for
Crystallography
Volume C
Mathematical, physical and chemical tables
Edited by E. Prince

International Tables for Crystallography (2006). Vol. C. ch. 9.2, p. 752

Section 9.2.1.1.2. Close-packed structures

D. Pandeyc and P. Krishnab

9.2.1.1.2. Close-packed structures

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A three-dimensional close-packed structure results from stacking the hexagonal close-packed layers in the A, B, or C position with the restriction that no two successive layers are in identical positions. Thus, any sequence of the letters A, B, and C, with no two successive letters alike, represents a possible manner of stacking the hexagonal close-packed layers. There are thus infinite possibilities for close-packed layer stackings. The identity period n of these layer stackings is determined by the number of layers after which the stacking sequence starts repeating itself. Since there are two possible positions for a new layer on the top of the preceding layer, the total number of possible layer stackings with a repeat period of n is 2n−1.

In all the close-packed layer stackings, each sphere is surrounded by 12 other spheres. However, it is touched by all 12 spheres only if the axial ratio h/a is [\sqrt{2/3}], where h is the separation between two close-packed layers and a is the diameter of the spheres (Verma & Krishna, 1966[link]). Deviations from the ideal value of the axial ratio are common, especially in hexagonal metals (Cottrell, 1967[link]). The arrangement of spheres described above provides the highest packing density of 0.7405 in the ideal case for an infinite lattice (Azaroff, 1960[link]). There are, however, other arrangements of a finite number of equal spheres that have a higher packing density (Boerdijk, 1952[link]).

References

First citation Azaroff, L. V. (1960). Introduction to solids. London: McGraw-Hill.Google Scholar
First citation Boerdijk, A. H. (1952). Some remarks concerning close-packing of equal spheres. Philips Res. Rep. 7, 303–313.Google Scholar
First citation Cottrell, A. (1967). An introduction to metallurgy. London: Edward Arnold.Google Scholar
First citation Verma, A. R. & Krishna, P. (1966). Polymorphism and polytypism in crystals, New York: John Wiley.Google Scholar








































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