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Slater–Pauling rule

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Rule in condensed matter physics

In condensed matter physics, the Slater–Pauling rule states that adding an element to a metal alloy will reduce the alloy's saturation magnetization by an amount proportional to the number of valence electrons outside of the added element's d shell. Conversely, elements with a partially filled d shell will increase the magnetic moment by an amount proportional to number of missing electrons. Investigated by the physicists John C. Slater and Linus Pauling in the 1930s, the rule is a useful approximation for the magnetic properties of many transition metals.

Application

The use of the rule depends on carefully defining what it means for an electron to lie outside of the d shell. The electrons outside a d shell are the electrons which have higher energy than the electrons within the d shell. The Madelung rule (incorrectly) suggests that the s shell is filled before the d shell. For example, it predicts Zinc has a configuration of 4s 3d. However, Zinc's 4s electrons actually have more energy than the 3d electrons, putting them outside the d shell. Ordered in terms of energy, the electron configuration of Zinc is 3d 4s. (see: the n+ℓ energy ordering rule)

Slater–Pauling rule (nearest integer)
Element Electron configuration Magnetic valence Predicted moment per atom
Tin 4d 5s 5p -4 -4 μ B {\displaystyle \mu _{\mathrm {B} }}
Aluminum 3s 3p -3 -3 μ B {\displaystyle \mu _{\mathrm {B} }}
Zinc 3d 4s -2 -2 μ B {\displaystyle \mu _{\mathrm {B} }}
Copper 3d 4s -1 -1 μ B {\displaystyle \mu _{\mathrm {B} }}
Palladium 4d 0 0 μ B {\displaystyle \mu _{\mathrm {B} }}
Cobalt 3d 4s +1 +1 μ B {\displaystyle \mu _{\mathrm {B} }}
Iron 3d 4s +2 +2 μ B {\displaystyle \mu _{\mathrm {B} }}
Manganese 3d 4s +3 +3 μ B {\displaystyle \mu _{\mathrm {B} }}

The basic rule given above makes several approximations. One simplification is rounding to the nearest integer. Because we are describing the number of electrons in a band using an average value, the s and d shells can be filled to non-integer numbers of electrons, allowing the Slater–Pauling rule to give more accurate predictions. While the Slater–Pauling rule has many exceptions, it is often a useful as an approximation to more accurate, but more complicated physical models.

Building on further theoretical developments done by physicists such as Jacques Friedel, a more widely applicable version of the rule, known as the generalized Slater–Pauling rule was developed.

See also

References

  1. Kittel, Charles (2005). Introduction to Solid State Physics (8th ed.). United States: John Wiley & Sons. p. 335-336. ISBN 0-471-41526-X.
  2. Slater, J. C. (1936-06-15). "The Ferromagnetism of Nickel. II. Temperature Effects". Physical Review. 49 (12). American Physical Society (APS): 931–937. Bibcode:1936PhRv...49..931S. doi:10.1103/physrev.49.931. ISSN 0031-899X.
  3. Pauling, Linus (1938-12-01). "The Nature of the Interatomic Forces in Metals". Physical Review. 54 (11). American Physical Society (APS): 899–904. Bibcode:1938PhRv...54..899P. doi:10.1103/physrev.54.899. ISSN 0031-899X.
  4. Friedel, J. (1958). "Metallic alloys". Il Nuovo Cimento. 7 (S2). Springer Science and Business Media LLC: 287–311. Bibcode:1958NCim....7S.287F. doi:10.1007/bf02751483. ISSN 0029-6341. S2CID 189771420.
  5. Williams, A.; Moruzzi, V.; Malozemoff, A.; Terakura, K. (1983). "Generalized Slater-Pauling curve for transition-metal magnets". IEEE Transactions on Magnetics. 19 (5). Institute of Electrical and Electronics Engineers (IEEE): 1983–1988. Bibcode:1983ITM....19.1983W. doi:10.1109/tmag.1983.1062706. ISSN 0018-9464.
  6. Malozemoff, A. P.; Williams, A. R.; Moruzzi, V. L. (1984-02-15). ""Band-gap theory" of strong ferromagnetism: Application to concentrated crystalline and amorphous Fe- and Co-metalloid alloys". Physical Review B. 29 (4). American Physical Society (APS): 1620–1632. Bibcode:1984PhRvB..29.1620M. doi:10.1103/physrevb.29.1620. ISSN 0163-1829.
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