Ferrimagnetism

A ferrimagnetic material is a material that has populations of atoms with opposing magnetic moments, as in antiferromagnetism, but these moments are unequal in magnitude, so a spontaneous magnetization remains.^[1] This can for example occur when the populations consist of different atoms or ions (such as Fe²⁺ and Fe³⁺).

Magnetic orders: comparison between ferro, antiferro and ferrimagnetism

Like ferromagnetic substances, ferrimagnetic substances are attracted by magnets and can be magnetized to make permanent magnets. The oldest known magnetic substance, magnetite (Fe₃O₄), is ferrimagnetic, but was classified as a ferromagnet before Louis Néel discovered ferrimagnetism in 1948.^[2] Since the discovery, numerous uses have been found for ferrimagnetic materials, such as hard-drive platters and biomedical applications.

History

Until the twentieth century, all naturally occurring magnetic substances were called ferromagnets. In 1936, Louis Néel published a paper proposing the existence of a new form of cooperative magnetism he called antiferromagnetism.^[3] While working with Mn₂Sb, French physicist Charles Guillaud discovered that the current theories on magnetism were not adequate to explain the behavior of the material, and made a model to explain the behavior.^[4] In 1948, Néel published a paper about a third type of cooperative magnetism, based on the assumptions in Guillaud's model. He called it ferrimagnetism. In 1970, Néel was awarded for his work in magnetism with the Nobel Prize in Physics.^[5]

Physical origin

➀ Below the magnetization compensation point, ferrimagnetic material is magnetic. ➁ At the compensation point, the magnetic components cancel each other, and the total magnetic moment is zero. ➂ Above the Curie temperature, the material loses magnetism.

Ferrimagnetism has the same physical origins as ferromagnetism and antiferromagnetism. In ferrimagnetic materials the magnetization is also caused by a combination of dipole–dipole interactions and exchange interactions resulting from the Pauli exclusion principle. The main difference is that in ferrimagnetic materials there are different types of atoms in the material's unit cell. An example of this can be seen in the figure above. Here the atoms with a smaller magnetic moment point in the opposite direction of the larger moments. This arrangement is similar to that present in antiferromagnetic materials, but in ferrimagnetic materials the net moment is nonzero because the opposed moments differ in magnitude.

Ferrimagnets have a critical temperature above which they become paramagnetic just as ferromagnets do.^[6] At this temperature (called the Curie temperature) there is a second-order phase transition,^[7] and the system can no longer maintain a spontaneous magnetization. This is because at higher temperatures the thermal motion is strong enough that it exceeds the tendency of the dipoles to align.

Derivation

There are various ways to describe ferrimagnets, the simplest of which is with mean-field theory. In mean-field theory the field acting on the atoms can be written as

{\vec {H}}={\vec {H}}_{0}+{\vec {H}}_{m},

where ${\vec {H}}_{0}$ is the applied magnetic field, and ${\vec {H}}_{m}$ is field caused by the interactions between the atoms. The following assumption then is ${\vec {H}}_{m}=\gamma {\vec {M}}.$

Here ${\vec {M}}$ is the average magnetization of the lattice, and $\gamma$ is the molecular field coefficient. When we allow ${\vec {M}}$ and $\gamma$ to be position- and orientation-dependent, we can then write it in the form

{\vec {H}}_{i}={\vec {H}}_{0}+\sum _{k=1}^{n}\gamma _{ik}{\vec {M}}_{k},

where ${\vec {H}}_{i}$ is the field acting on the i-th substructure, and $\gamma _{ik}$ is the molecular field coefficient between the i-th and k-th substructures. For a diatomic lattice we can designate two types of sites, a and b. We can designate $N$ the number of magnetic ions per unit volume, $\lambda$ the fraction of the magnetic ions on the a sites, and $\mu =1-\lambda$ the fraction on the b sites. This then gives

{\vec {H}}_{aa}=\gamma _{aa}{\vec {M}},\quad {\vec {H}}_{ab}=\gamma _{ab}{\vec {M}}_{b},\quad {\vec {H}}_{ba}=\gamma _{ba}{\vec {M}}_{a},\quad {\vec {H}}_{bb}=\gamma _{bb}{\vec {M}}_{b}.

It can be shown that $\gamma _{ab}=\gamma _{ba}$ and that $\gamma _{aa}\neq \gamma _{bb},$ unless the structures are identical. $\gamma _{ab}>0$ favors a parallel alignment of ${\vec {M}}_{a}$ and ${\vec {M}}_{b}$ , while $\gamma _{ab}<0$ favors an anti-parallel alignment. For ferrimagnets, $\gamma _{ab}<0$ , so it will be convenient to take $\gamma _{ab}$ as a positive quantity and write the minus sign explicitly in front of it. For the total fields on a and b this then gives

{\vec {H}}_{a}={\vec {H}}_{0}+\gamma _{aa}{\vec {M}}_{a}-\gamma _{ab}{\vec {M}}_{b},

{\vec {H}}_{b}={\vec {H}}_{0}+\gamma _{bb}{\vec {M}}_{b}-\gamma _{ab}{\vec {M}}_{a}.

Furthermore, we will introduce the parameters $\alpha =\gamma _{aa}/\gamma _{ab}$ and $\beta =\gamma _{bb}/\gamma _{ab},$ which give the ratio between the strengths of the interactions. At last we will introduce the reduced magnetizations

{\vec {\sigma }}_{a}={\vec {M}}_{a}/\lambda Ng\mu _{B}S_{a},

{\vec {\sigma }}_{b}={\vec {M}}_{b}/\mu Ng\mu _{B}S_{b}

with $S_{i}$ the spin of the i-th element. This then gives for the fields:

{\vec {H}}_{a}={\vec {H}}_{0}+Ng\mu _{B}S_{a}\gamma _{ab}(\lambda \alpha {\vec {\sigma }}_{a}-\mu {\vec {\sigma }}_{b}),

{\vec {H}}_{b}={\vec {H}}_{0}+Ng\mu _{B}S_{b}\gamma _{ab}(-\lambda {\vec {\sigma }}_{a}+\mu \beta {\vec {\sigma }}_{b}).

The solutions to these equations (omitted here) are then given by

\sigma _{a}=B_{S_{a}}(g\mu _{b}S_{a}H_{a}/k_{\text{B}}T),

\sigma _{b}=B_{S_{b}}(g\mu _{b}S_{b}H_{b}/k_{\text{B}}T).

where $B_{J}(x)$ is the Brillouin function. The simplest case to solve now is $S_{a}=S_{b}=1/2$ . Since $B_{1/2}(x)=\tanh(x)$ , this then gives the following pair of equations:

\lambda \sigma _{a}={\frac {\tau F(\lambda ,\alpha ,\beta )}{\alpha \beta -1}}(\beta \tanh ^{-1}\sigma _{a}+\tanh ^{-1}\sigma _{b}),

\mu \sigma _{b}={\frac {\tau F(\lambda ,\alpha ,\beta )}{\alpha \beta -1}}(\tanh ^{-1}\sigma _{a}+\alpha \tanh ^{-1}\sigma _{b})

with $\tau =T/T_{\text{c}}$ and $F(\lambda ,\alpha ,\beta )={\frac {1}{2}}\left(\lambda \alpha +\mu \beta +{\sqrt {(\lambda \alpha -\mu \beta )^{2}+4\lambda \mu }}\right)$ . These equations do not have a known analytical solution, so they must be solved numerically to find the temperature dependence of $\mu$ .

Effects of temperature

Unlike ferromagnetism, the magnetization curves of ferrimagnetism can take many different shapes depending on the strength of the interactions and the relative abundance of atoms. The most notable instances of this property are that the direction of magnetization can reverse while heating a ferrimagnetic material from absolute zero to its critical temperature, and that strength of magnetization can increase while heating a ferrimagnetic material to the critical temperature, both of which cannot occur for ferromagnetic materials. These temperature dependencies have also been experimentally observed in NiFe_2/5Cr_8/5O₄^[8] and Li_1/2Fe_5/4Ce_5/4O₄.^[9]

A temperature lower than the Curie temperature, but at which the opposing magnetic moments are equal (resulting in a net magnetic moment of zero) is called a magnetization compensation point. This compensation point is observed easily in garnets and rare-earth–transition-metal alloys (RE-TM). Furthermore, ferrimagnets may also have an angular momentum compensation point, at which the net angular momentum vanishes. This compensation point is crucial for achieving fast magnetization reversal in magnetic-memory devices.

Effect of external fields

Theoretical model of magnetization

m

against magnetic field

h

. Starting at the origin, the upward curve is the initial magnetization curve. The downward curve after saturation, along with the lower return curve, form the main loop. The intercepts

h c

and

m rs

are the coercivity and saturation remanence.

When ferrimagnets are exposed to an external magnetic field, they display what is called magnetic hysteresis, where magnetic behavior depends on the history of the magnet. They also exhibit a saturation magnetization $M_{\text{rs}}$ ; this magnetization is reached when the external field is strong enough to make all the moments align in the same direction. When this point is reached, the magnetization cannot increase, as there are no more moments to align. When the external field is removed, the magnetization of the ferrimagnet does not disappear, but a nonzero magnetization remains. This effect is often used in applications of magnets. If an external field in the opposite direction is applied subsequently, the magnet will demagnetize further until it eventually reaches a magnetization of $-M_{\text{rs}}$ . This behavior results in what is called a hysteresis loop.^[10]

Properties and uses

Ferrimagnetic materials have high resistivity and have anisotropic properties. The anisotropy is actually induced by an external applied field. When this applied field aligns with the magnetic dipoles, it causes a net magnetic dipole moment and causes the magnetic dipoles to precess at a frequency controlled by the applied field, called Larmor or precession frequency. As a particular example, a microwave signal circularly polarized in the same direction as this precession strongly interacts with the magnetic dipole moments; when it is polarized in the opposite direction, the interaction is very low. When the interaction is strong, the microwave signal can pass through the material. This directional property is used in the construction of microwave devices like isolators, circulators, and gyrators. Ferrimagnetic materials are also used to produce optical isolators and circulators. Ferrimagnetic minerals in various rock types are used to study ancient geomagnetic properties of Earth and other planets. That field of study is known as paleomagnetism. In addition, it has been shown that ferrimagnets such as magnetite can be used for thermal energy storage.^[11]

Examples

The oldest known magnetic material, magnetite, is a ferrimagnetic substance. The tetrahedral and octahedral sites of its crystal structure exhibit opposite spin. Other known ferrimagnetic materials include yttrium iron garnet (YIG); cubic ferrites composed of iron oxides with other elements such as aluminum, cobalt, nickel, manganese, and zinc; and hexagonal or spinel type ferrites, including rhenium ferrite, ReFe₂O₄, PbFe₁₂O₁₉ and BaFe₁₂O₁₉ and pyrrhotite, Fe_1−xS.^[12]

Ferrimagnetism can also occur in single-molecule magnets. A classic example is a dodecanuclear manganese molecule with an effective spin S = 10 derived from antiferromagnetic interaction on Mn(IV) metal centers with Mn(III) and Mn(II) metal centers.^[13]

References

^ Spaldin, Nicola A. (2011). Magnetic materials : fundamentals and applications (2nd ed.). Cambridge: Cambridge University Press. ISBN 978-0-521-88669-7. OCLC 607986416.
^ Néel, M. Louis (1948). "Propriétés magnétiques des ferrites ; ferrimagnétisme et antiferromagnétisme" (PDF). Annales de Physique. 12 (3): 137–198. Bibcode:1948AnPh...12..137N. doi:10.1051/anphys/194812030137. ISSN 0003-4169. S2CID 126111103.
^ Néel, Louis (1936). "Propriétés magnétiques de l'état métallique et énergie d'interaction entre atomes magnétiques". Annales de Physique. 11 (5): 232–279. Bibcode:1936AnPh...11..232N. doi:10.1051/anphys/193611050232. ISSN 0003-4169.
^ Smart, J. Samuel (September 1955). "The Néel Theory of Ferrimagnetism". American Journal of Physics. 23 (6): 356–370. Bibcode:1955AmJPh..23..356S. doi:10.1119/1.1934006. ISSN 0002-9505.
^ "The Nobel Prize in Physics 1970". NobelPrize.org. Retrieved 2021-01-26.
^ Simon, Steven H. (21 June 2013). The Oxford Solid State Basics (1st ed.). Oxford. ISBN 978-0-19-150210-1. OCLC 851099021.{{cite book}}: CS1 maint: location missing publisher (link)
^ Blundell, Stephen; Blundell, Katherine M. (2010). Concepts in thermal physics (2nd ed.). Oxford: Oxford University Press. ISBN 978-0-19-956209-1. OCLC 607907330.
^ Tsushima, Tachiro (August 1963). "Magnetic Properties of Ferrite-Chromite Series of Nickel and Cobalt". Journal of the Physical Society of Japan. 18 (8): 1162–1166. Bibcode:1963JPSJ...18.1162T. doi:10.1143/jpsj.18.1162. ISSN 0031-9015.
^ Gorter, E. W.; Schulkes, J. A. (1953-05-01). "Reversal of Spontaneous Magnetization as a Function of Temperature in LiFeCr Spinels". Physical Review. 90 (3): 487–488. Bibcode:1953PhRv...90..487G. doi:10.1103/physrev.90.487.2. ISSN 0031-899X.
^ Soler, M. A. G.; Paterno, L. G. (2017-01-01), Da Róz, Alessandra L.; Ferreira, Marystela; de Lima Leite, Fábio; Oliveira, Osvaldo N. (eds.), "Chapter 6. Magnetic Nanomaterials", Nanostructures, William Andrew Publishing, pp. 147–186, doi:10.1016/b978-0-323-49782-4.00006-1, ISBN 978-0-323-49782-4, retrieved 2021-01-25.
^ Grosu, Yaroslav; Faik, Abdessamad; Ortega-Fernández, Iñigo; D'Aguanno, Bruno (March 2017). "Natural Magnetite for thermal energy storage: Excellent thermophysical properties, reversible latent heat transition and controlled thermal conductivity". Solar Energy Materials and Solar Cells. 161: 170–176. doi:10.1016/j.solmat.2016.12.006.
^ Klein, C. and Dutrow, B., Mineral Science, 23rd ed., Wiley, p. 243.
^ Sessoli, Roberta; Tsai, Hui Lien; Schake, Ann R.; Wang, Sheyi; Vincent, John B.; Folting, Kirsten; Gatteschi, Dante; Christou, George; Hendrickson, David N. (1993). "High-spin molecules: [Mn₁₂O₁₂(O₂CR)₁₆(H₂O)₄]". J. Am. Chem. Soc. 115 (5): 1804–1816. doi:10.1021/ja00058a027.

External links

Media related to Ferrimagnetism at Wikimedia Commons

[1] Spaldin, Nicola A. (2011). Magnetic materials : fundamentals and applications (2nd ed.). Cambridge: Cambridge University Press. ISBN 978-0-521-88669-7. OCLC 607986416.

[2] Néel, M. Louis (1948). "Propriétés magnétiques des ferrites ; ferrimagnétisme et antiferromagnétisme" (PDF). Annales de Physique. 12 (3): 137–198. Bibcode:1948AnPh...12..137N. doi:10.1051/anphys/194812030137. ISSN 0003-4169. S2CID 126111103.

[3] Néel, Louis (1936). "Propriétés magnétiques de l'état métallique et énergie d'interaction entre atomes magnétiques". Annales de Physique. 11 (5): 232–279. Bibcode:1936AnPh...11..232N. doi:10.1051/anphys/193611050232. ISSN 0003-4169.

[4] Smart, J. Samuel (September 1955). "The Néel Theory of Ferrimagnetism". American Journal of Physics. 23 (6): 356–370. Bibcode:1955AmJPh..23..356S. doi:10.1119/1.1934006. ISSN 0002-9505.

[5] "The Nobel Prize in Physics 1970". NobelPrize.org. Retrieved 2021-01-26.

[6] Simon, Steven H. (21 June 2013). The Oxford Solid State Basics (1st ed.). Oxford. ISBN 978-0-19-150210-1. OCLC 851099021.{{cite book}}: CS1 maint: location missing publisher (link)

[7] Blundell, Stephen; Blundell, Katherine M. (2010). Concepts in thermal physics (2nd ed.). Oxford: Oxford University Press. ISBN 978-0-19-956209-1. OCLC 607907330.

[8] Tsushima, Tachiro (August 1963). "Magnetic Properties of Ferrite-Chromite Series of Nickel and Cobalt". Journal of the Physical Society of Japan. 18 (8): 1162–1166. Bibcode:1963JPSJ...18.1162T. doi:10.1143/jpsj.18.1162. ISSN 0031-9015.

[9] Gorter, E. W.; Schulkes, J. A. (1953-05-01). "Reversal of Spontaneous Magnetization as a Function of Temperature in LiFeCr Spinels". Physical Review. 90 (3): 487–488. Bibcode:1953PhRv...90..487G. doi:10.1103/physrev.90.487.2. ISSN 0031-899X.

[10] Soler, M. A. G.; Paterno, L. G. (2017-01-01), Da Róz, Alessandra L.; Ferreira, Marystela; de Lima Leite, Fábio; Oliveira, Osvaldo N. (eds.), "Chapter 6. Magnetic Nanomaterials", Nanostructures, William Andrew Publishing, pp. 147–186, doi:10.1016/b978-0-323-49782-4.00006-1, ISBN 978-0-323-49782-4, retrieved 2021-01-25.

[11] Grosu, Yaroslav; Faik, Abdessamad; Ortega-Fernández, Iñigo; D'Aguanno, Bruno (March 2017). "Natural Magnetite for thermal energy storage: Excellent thermophysical properties, reversible latent heat transition and controlled thermal conductivity". Solar Energy Materials and Solar Cells. 161: 170–176. doi:10.1016/j.solmat.2016.12.006.

[12] Klein, C. and Dutrow, B., Mineral Science, 23rd ed., Wiley, p. 243.

[13] Sessoli, Roberta; Tsai, Hui Lien; Schake, Ann R.; Wang, Sheyi; Vincent, John B.; Folting, Kirsten; Gatteschi, Dante; Christou, George; Hendrickson, David N. (1993). "High-spin molecules: [Mn₁₂O₁₂(O₂CR)₁₆(H₂O)₄]". J. Am. Chem. Soc. 115 (5): 1804–1816. doi:10.1021/ja00058a027.

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