Interstitial defect

Interstitials are a variety of crystallographic defects where atoms assume a normally unoccupied site in the crystal structure. In interstitial defects two or more atoms may share one lattice site, thereby increasing its total energy.[1] Alternatively small atoms in some crystals may occupy interstitial sites in energetically favorable configurations, such as hydrogen in palladium. Interstitials can be produced by bombarding a crystal with elementary particles having energy above the displacement threshold for that crystal, but they may also exist in small concentrations in thermodynamic equilibrium.

Self-interstitials

Self-interstitial defects are interstitial defects which contain only atoms which are the same as those already present in the lattice.

Structure of self-interstitial in some common metals. The left-hand side of each crystal type shows the perfect crystal and the right-hand side the one with a defect.

The structure of interstitial defects has been experimentally determined in some metals and semiconductors.

Contrary to what one might intuitively expect, most self-interstitials in metals with a known structure have a 'split' structure, in which two atoms share the same lattice site.[1][2] Typically the center of mass of the two atoms is at the lattice site, and they are displaced symmetrically from it along one of the principal lattice directions. For instance, in several common face-centered cubic (fcc) metals such as copper, nickel and platinum, the ground state structure of the self-interstitial is the split [100] interstitial structure, where two atoms are displaced in a positive and negative [100] direction from the lattice site. In body-centered cubic (bcc) iron the ground state interstitial structure is similarly a [110] split interstitial.

These split interstitials are often called dumbbell interstitials, because plotting the two atoms forming the interstitial with two large spheres and a thick line joining them makes the structure resemble a dumbbell weight-lifting device.

In other bcc metals than iron, the ground state structure is believed based on recent density-functional theory calculations to be the [111] crowdion interstitial,[3] which can be understood as a long chain (typically some 10–20) of atoms along the [111] lattice direction, compressed compared to the perfect lattice such that the chain contains one extra atom.

Structure of dumbbell self-interstitial in silicon. Note that the structure of the interstitial in silicon may depend on charge state and doping level of the material.

In semiconductors the situation is more complex, since defects may be charged and different charge states may have different structures. For instance, in silicon, the interstitial may either have a split [110] structure or a tetrahedral truly interstitial one.[4]

Impurity interstitials

Small impurity interstitial atoms are usually on true off-lattice sites between the lattice atoms. Such sites can be characterized by the symmetry of the interstitial atom position with respect to its nearest lattice atoms. For instance, an impurity atom I with 4 nearest lattice atom A neighbours (at equal distances) in an fcc lattice is in a tetrahedral symmetry position, and thus can be called a tetrahedral interstitial.

Large impurity interstitials can also be in split interstitial configurations together with a lattice atom, similar to those of the self-interstitial atom.

Octahedral (red) and tetrahedral (blue) interstitial symmetry polyhedra in a face-centered cubic lattice. The actual interstitial atom would ideally be in the middle of one of the polyhedra.

Effects of interstitials

Interstitials modify the physical and chemical properties of materials.

References

  1. 1 2 Ehrhart, P. (1991) Properties and interactions of atomic defects in metals and alloys, H. Ullmaier (ed.), Landolt-Börnstein, New Series III vol. 25 ch. 2, pp. 88 ff. Springer, Berlin.
  2. Schilling, W. (1978). "Self-interstitial atoms in metals". Journal of Nuclear Materials. 69–70: 465. Bibcode:1978JNuM...69..465S. doi:10.1016/0022-3115(78)90261-1.
  3. Derlet, P. M.; D. Nguyen-Manh; S. L. Dudarev (2007). "Multiscale modeling of crowdion and vacancy defects in body-centered-cubic transition metals". Phys. Rev. B. 76 (5): 054107. Bibcode:2007PhRvB..76e4107D. doi:10.1103/physrevb.76.054107.
  4. Watkins, G. D. (1991) "Native defects and their interactions with impurities in silicon", p. 139 in Defects and Diffusion in Silicon Processing, T. Diaz de la Rubia, S. Coffa, P. A. Stolk and C. S. Rafferty (eds.), MRS Symposium Proceedings vol. 469. Materials Research Society, Pittsburg.
  5. Seidman, D. N.; Averback, R. S.; Okamoto, P. R.; Baily, A. C. (1987). "Amorphization Processes in Electron- and/or Ion-Irradiated Silicon". Phys. Rev. Lett. 58 (9): 900–903. Bibcode:1987PhRvL..58..900S. doi:10.1103/PhysRevLett.58.900. PMID 10035067.
  6. Cerofilini, G. F.; Meda, L.; Volpones, C. (1988). "A model for damage release in ion-implanted silicon". J. Appl. Phys. 63 (10): 4911. Bibcode:1988JAP....63.4911C. doi:10.1063/1.340432.
  7. Rehn, L. E.; Holder, J.; Granato, A. V.; Coltman, R. R.; Young, J. F. W. (1974). "Effects of thermal-neutron irradiation on the elastic constants of copper". Phys. Rev. B. 10 (2): 349. Bibcode:1974PhRvB..10..349R. doi:10.1103/PhysRevB.10.349.
  8. Granato, A. V. (1992). "Interstitialcy Model for Condensed Matter States of Face-Centered-Cubic Metals". Phys. Rev. Lett. 68 (7): 974–977. Bibcode:1992PhRvL..68..974G. doi:10.1103/PhysRevLett.68.974. PMID 10046046.
  9. Forsblom, M.; Grimvall, G. (2005). "Homogeneous melting of superheated crystals: Molecular dynamics simulations". Phys. Rev. B. 72 (5): 054107. Bibcode:2005PhRvB..72e4107F. doi:10.1103/PhysRevB.72.054107.
  10. Nordlund, K.; Ashkenazy, Y.; Averback, R. S.; Granato, A. V. (2005). "Strings and interstitials in liquids, glasses and crystals" (PDF). Europhys. Lett. 71 (4): 625. Bibcode:2005EL.....71..625N. doi:10.1209/epl/i2005-10132-1.
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