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Antiferromagnetism AI simulator
(@Antiferromagnetism_simulator)
Hub AI
Antiferromagnetism AI simulator
(@Antiferromagnetism_simulator)
Antiferromagnetism
In materials that exhibit antiferromagnetism, the magnetic moments of atoms or molecules, usually related to the spins of electrons, align in a regular pattern with neighboring spins (on different sublattices) pointing in opposite directions. This is, like ferromagnetism and ferrimagnetism, a manifestation of ordered magnetism. The phenomenon of antiferromagnetism was first introduced by Lev Landau in 1933.
Generally, antiferromagnetic order may exist at sufficiently low temperatures, but vanishes at and above the Néel temperature – named after Louis Néel, who had first identified this type of magnetic ordering. Above the Néel temperature, the material is typically paramagnetic.
When no external field is applied, the antiferromagnetic structure corresponds to a vanishing total magnetization. In an external magnetic field, a kind of ferrimagnetic behavior may be displayed in the antiferromagnetic phase, with the absolute value of one of the sublattice magnetizations differing from that of the other sublattice, resulting in a nonzero net magnetization. Although the net magnetization should be zero at a temperature of absolute zero, the effect of spin canting often causes a small net magnetization to develop, as seen for example in hematite.
The magnetic susceptibility of an antiferromagnetic material typically shows a maximum at the Néel temperature. In contrast, at the transition between the ferromagnetic to the paramagnetic phases the susceptibility will diverge. In the antiferromagnetic case, a divergence is observed in the staggered susceptibility.
Various microscopic (exchange) interactions between the magnetic moments or spins may lead to antiferromagnetic structures. In the simplest case, one may consider an Ising model on a bipartite lattice, e.g. the simple cubic lattice, with couplings between spins at nearest neighbor sites. Depending on the sign of that interaction, ferromagnetic or antiferromagnetic order will result. Geometrical frustration or competing ferro- and antiferromagnetic interactions may lead to different and, perhaps, more complicated magnetic structures.
The relationship between magnetization and the magnetizing field is non-linear like in ferromagnetic materials. This fact is due to the contribution of the hysteresis loop, which for ferromagnetic materials involves a residual magnetization.
Antiferromagnetic structures were first shown through neutron diffraction of transition metal oxides such as nickel, iron, and manganese oxides. The experiments, performed by Clifford Shull, gave the first results showing that magnetic dipoles could be oriented in an antiferromagnetic structure.
Antiferromagnetic materials occur commonly among transition metal compounds, especially oxides. Examples include hematite, metals such as chromium, alloys such as iron manganese (FeMn), and oxides such as nickel oxide (NiO). There are also numerous examples among high nuclearity metal clusters. Organic molecules can also exhibit antiferromagnetic coupling under rare circumstances, as seen in radicals such as 5-dehydro-m-xylylene.
Antiferromagnetism
In materials that exhibit antiferromagnetism, the magnetic moments of atoms or molecules, usually related to the spins of electrons, align in a regular pattern with neighboring spins (on different sublattices) pointing in opposite directions. This is, like ferromagnetism and ferrimagnetism, a manifestation of ordered magnetism. The phenomenon of antiferromagnetism was first introduced by Lev Landau in 1933.
Generally, antiferromagnetic order may exist at sufficiently low temperatures, but vanishes at and above the Néel temperature – named after Louis Néel, who had first identified this type of magnetic ordering. Above the Néel temperature, the material is typically paramagnetic.
When no external field is applied, the antiferromagnetic structure corresponds to a vanishing total magnetization. In an external magnetic field, a kind of ferrimagnetic behavior may be displayed in the antiferromagnetic phase, with the absolute value of one of the sublattice magnetizations differing from that of the other sublattice, resulting in a nonzero net magnetization. Although the net magnetization should be zero at a temperature of absolute zero, the effect of spin canting often causes a small net magnetization to develop, as seen for example in hematite.
The magnetic susceptibility of an antiferromagnetic material typically shows a maximum at the Néel temperature. In contrast, at the transition between the ferromagnetic to the paramagnetic phases the susceptibility will diverge. In the antiferromagnetic case, a divergence is observed in the staggered susceptibility.
Various microscopic (exchange) interactions between the magnetic moments or spins may lead to antiferromagnetic structures. In the simplest case, one may consider an Ising model on a bipartite lattice, e.g. the simple cubic lattice, with couplings between spins at nearest neighbor sites. Depending on the sign of that interaction, ferromagnetic or antiferromagnetic order will result. Geometrical frustration or competing ferro- and antiferromagnetic interactions may lead to different and, perhaps, more complicated magnetic structures.
The relationship between magnetization and the magnetizing field is non-linear like in ferromagnetic materials. This fact is due to the contribution of the hysteresis loop, which for ferromagnetic materials involves a residual magnetization.
Antiferromagnetic structures were first shown through neutron diffraction of transition metal oxides such as nickel, iron, and manganese oxides. The experiments, performed by Clifford Shull, gave the first results showing that magnetic dipoles could be oriented in an antiferromagnetic structure.
Antiferromagnetic materials occur commonly among transition metal compounds, especially oxides. Examples include hematite, metals such as chromium, alloys such as iron manganese (FeMn), and oxides such as nickel oxide (NiO). There are also numerous examples among high nuclearity metal clusters. Organic molecules can also exhibit antiferromagnetic coupling under rare circumstances, as seen in radicals such as 5-dehydro-m-xylylene.