Paramagnetism
Condensed matter physics |
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Paramagnetism is a form of
Paramagnetism is due to the presence of
Unlike
Relation to electron spins
Constituent atoms or molecules of paramagnetic materials have permanent magnetic moments (
If there is sufficient energy exchange between neighbouring dipoles, they will interact, and may spontaneously align or anti-align and form magnetic domains, resulting in
In general, paramagnetic effects are quite small: the magnetic susceptibility is of the order of 10−3 to 10−5 for most paramagnets, but may be as high as 10−1 for synthetic paramagnets such as ferrofluids.
Delocalization
Material | Magnetic susceptibility, [10−5]
(SI units) |
---|---|
Tungsten | 6.8 |
Caesium | 5.1 |
Aluminium | 2.2 |
Lithium | 1.4 |
Magnesium | 1.2 |
Sodium | 0.72 |
In conductive materials, the electrons are
The effect always competes with a
s and p electrons
Generally, strong delocalization in a solid due to large overlap with neighboring wave functions means that there will be a large
d and f electrons
Stronger magnetic effects are typically only observed when d or f electrons are involved. Particularly the latter are usually strongly localized. Moreover, the size of the magnetic moment on a lanthanide atom can be quite large as it can carry up to 7 unpaired electrons in the case of
Molecular localization
The above picture is a generalization as it pertains to materials with an extended lattice rather than a molecular structure. Molecular structure can also lead to localization of electrons. Although there are usually energetic reasons why a molecular structure results such that it does not exhibit partly filled orbitals (i.e. unpaired spins), some non-closed shell moieties do occur in nature. Molecular oxygen is a good example. Even in the frozen solid it contains di-radical molecules resulting in paramagnetic behavior. The unpaired spins reside in orbitals derived from oxygen p wave functions, but the overlap is limited to the one neighbor in the O2 molecules. The distances to other oxygen atoms in the lattice remain too large to lead to delocalization and the magnetic moments remain unpaired.
Theory
The Bohr–Van Leeuwen theorem proves that there cannot be any diamagnetism or paramagnetism in a purely classical system. The paramagnetic response has then two possible quantum origins, either coming from permanent magnetic moments of the ions or from the spatial motion of the conduction electrons inside the material. Both descriptions are given below.
Curie's law
For low levels of magnetization, the magnetization of paramagnets follows what is known as Curie's law, at least approximately. This law indicates that the susceptibility, , of paramagnetic materials is inversely proportional to their temperature, i.e. that materials become more magnetic at lower temperatures. The mathematical expression is:
- is the resulting magnetization, measured in amperes/meter (A/m),
- is the volume magnetic susceptibility (dimensionless),
- is the auxiliary magnetic field (A/m),
- is absolute temperature, measured in kelvins (K),
- is a material-specific Curie constant(K).
Curie's law is valid under the commonly encountered conditions of low magnetization (μBH ≲ kBT), but does not apply in the high-field/low-temperature regime where saturation of magnetization occurs (μBH ≳ kBT) and magnetic dipoles are all aligned with the applied field. When the dipoles are aligned, increasing the external field will not increase the total magnetization since there can be no further alignment.
For a paramagnetic ion with noninteracting magnetic moments with angular momentum J, the Curie constant is related to the individual ions' magnetic moments,
where n is the number of atoms per unit volume. The parameter μeff is interpreted as the effective magnetic moment per paramagnetic ion. If one uses a classical treatment with molecular magnetic moments represented as discrete magnetic dipoles, μ, a Curie Law expression of the same form will emerge with μ appearing in place of μeff.
Curie's Law can be derived by considering a substance with noninteracting magnetic moments with angular momentum J. If orbital contributions to the magnetic moment are negligible (a common case), then in what follows J = S. If we apply a magnetic field along what we choose to call the z-axis, the energy levels of each paramagnetic center will experience
Where is the z-component of the magnetic moment for each Zeeman level, so is called the Bohr magneton and gJ is the Landé g-factor, which reduces to the free-electron g-factor, gS when J = S. (in this treatment, we assume that the x- and y-components of the magnetization, averaged over all molecules, cancel out because the field applied along the z-axis leave them randomly oriented.) The energy of each Zeeman level is . For temperatures over a few K, , and we can apply the approximation :
When orbital angular momentum contributions to the magnetic moment are small, as occurs for most organic radicals or for octahedral transition metal complexes with d3 or high-spin d5 configurations, the effective magnetic moment takes the form ( with g-factor ge = 2.0023... ≈ 2),
When Curie constant is null, second order effects that couple the ground state with the excited states can also lead to a paramagnetic susceptibility independent of the temperature, known as Van Vleck susceptibility.
Pauli paramagnetism
For some alkali metals and noble metals, conduction electrons are weakly interacting and delocalized in space forming a Fermi gas. For these materials one contribution to the magnetic response comes from the interaction between the electron spins and the magnetic field known as Pauli paramagnetism. For a small magnetic field , the additional energy per electron from the interaction between an electron spin and the magnetic field is given by:
where is the vacuum permeability, is the electron magnetic moment, is the Bohr magneton, is the reduced Planck constant, and the g-factor cancels with the spin . The indicates that the sign is positive (negative) when the electron spin component in the direction of is parallel (antiparallel) to the magnetic field.
For low temperatures with respect to the Fermi temperature (around 104 kelvins for metals), the number density of electrons () pointing parallel (antiparallel) to the magnetic field can be written as:
with the total free-electrons density and the electronic density of states (number of states per energy per volume) at the Fermi energy .
In this approximation the magnetization is given as the magnetic moment of one electron times the difference in densities:
which yields a positive paramagnetic susceptibility independent of temperature:
The Pauli paramagnetic susceptibility is a macroscopic effect and has to be contrasted with
The magnetic response calculated for a gas of electrons is not the full picture as the magnetic susceptibility coming from the ions has to be included. Additionally, these formulas may break down for confined systems that differ from the bulk, like
Pauli paramagnetism is named after the physicist Wolfgang Pauli. Before Pauli's theory, the lack of a strong Curie paramagnetism in metals was an open problem as the leading Drude model could not account for this contribution without the use of quantum statistics. Pauli paramagnetism and Landau diamagnetism are essentially applications of the spin and the free electron model, the first is due to intrinsic spin of electrons; the second is due to their orbital motion.[5][6]
Examples of paramagnets
Materials that are called "paramagnets" are most often those that exhibit, at least over an appreciable temperature range, magnetic susceptibilities that adhere to the Curie or Curie–Weiss laws. In principle any system that contains atoms, ions, or molecules with unpaired spins can be called a paramagnet, but the interactions between them need to be carefully considered.
Systems with minimal interactions
The narrowest definition would be: a system with unpaired spins that do not interact with each other. In this narrowest sense, the only pure paramagnet is a dilute gas of
A gas of lithium atoms already possess two paired core electrons that produce a diamagnetic response of opposite sign. Strictly speaking Li is a mixed system therefore, although admittedly the diamagnetic component is weak and often neglected. In the case of heavier elements the diamagnetic contribution becomes more important and in the case of metallic gold it dominates the properties. The element hydrogen is virtually never called 'paramagnetic' because the monatomic gas is stable only at extremely high temperature; H atoms combine to form molecular H2 and in so doing, the magnetic moments are lost (quenched), because of the spins pair. Hydrogen is therefore diamagnetic and the same holds true for many other elements. Although the electronic configuration of the individual atoms (and ions) of most elements contain unpaired spins, they are not necessarily paramagnetic, because at ambient temperature quenching is very much the rule rather than the exception. The quenching tendency is weakest for f-electrons because f (especially 4f) orbitals are radially contracted and they overlap only weakly with orbitals on adjacent atoms. Consequently, the lanthanide elements with incompletely filled 4f-orbitals are paramagnetic or magnetically ordered.[7]
Material | μeff/μB |
---|---|
[Cr(NH3)6]Br3 | 3.77 |
K3[Cr(CN)6] | 3.87 |
K3[MoCl6] | 3.79 |
K4[V(CN)6] | 3.78 |
[Mn(NH3)6]Cl2 | 5.92 |
(NH4)2[Mn(SO4)2]·6H2O | 5.92 |
NH4[Fe(SO4)2]·12H2O | 5.89 |
Thus, condensed phase paramagnets are only possible if the interactions of the spins that lead either to quenching or to ordering are kept at bay by structural isolation of the magnetic centers. There are two classes of materials for which this holds:
- Molecular materials with a (isolated) paramagnetic center.
- Good examples are coordination complexes of d- or f-metals or proteins with such centers, e.g. myoglobin. In such materials the organic part of the molecule acts as an envelope shielding the spins from their neighbors.
- Small molecules can be stable in radical form, oxygen O2 is a good example. Such systems are quite rare because they tend to be rather reactive.
- Dilute systems.
- Dissolving a paramagnetic species in a diamagnetic lattice at small concentrations, e.g. Nd3+ in CaCl2 will separate the neodymium ions at large enough distances that they do not interact. Such systems are of prime importance for what can be considered the most sensitive method to study paramagnetic systems: EPR.
Systems with interactions
As stated above, many materials that contain d- or f-elements do retain unquenched spins. Salts of such elements often show paramagnetic behavior but at low enough temperatures the magnetic moments may order. It is not uncommon to call such materials 'paramagnets', when referring to their paramagnetic behavior above their Curie or Néel-points, particularly if such temperatures are very low or have never been properly measured. Even for iron it is not uncommon to say that iron becomes a paramagnet above its relatively high Curie-point. In that case the Curie-point is seen as a phase transition between a ferromagnet and a 'paramagnet'. The word paramagnet now merely refers to the linear response of the system to an applied field, the temperature dependence of which requires an amended version of Curie's law, known as the Curie–Weiss law:
This amended law includes a term θ that describes the exchange interaction that is present albeit overcome by thermal motion. The sign of θ depends on whether ferro- or antiferromagnetic interactions dominate and it is seldom exactly zero, except in the dilute, isolated cases mentioned above.
Obviously, the paramagnetic Curie–Weiss description above TN or TC is a rather different interpretation of the word "paramagnet" as it does not imply the absence of interactions, but rather that the magnetic structure is random in the absence of an external field at these sufficiently high temperatures. Even if θ is close to zero this does not mean that there are no interactions, just that the aligning ferro- and the anti-aligning antiferromagnetic ones cancel. An additional complication is that the interactions are often different in different directions of the crystalline lattice (anisotropy), leading to complicated magnetic structures once ordered.
Randomness of the structure also applies to the many metals that show a net paramagnetic response over a broad temperature range. They do not follow a Curie type law as function of temperature however; often they are more or less temperature independent. This type of behavior is of an itinerant nature and better called Pauli-paramagnetism, but it is not unusual to see, for example, the metal aluminium called a "paramagnet", even though interactions are strong enough to give this element very good electrical conductivity.
Superparamagnets
Some materials show induced magnetic behavior that follows a Curie type law but with exceptionally large values for the Curie constants. These materials are known as superparamagnets. They are characterized by a strong ferromagnetic or ferrimagnetic type of coupling into domains of a limited size that behave independently from one another. The bulk properties of such a system resembles that of a paramagnet, but on a microscopic level they are ordered. The materials do show an ordering temperature above which the behavior reverts to ordinary paramagnetism (with interaction). Ferrofluids are a good example, but the phenomenon can also occur inside solids, e.g., when dilute paramagnetic centers are introduced in a strong itinerant medium of ferromagnetic coupling such as when Fe is substituted in TlCu2Se2 or the alloy AuFe. Such systems contain ferromagnetically coupled clusters that freeze out at lower temperatures. They are also called mictomagnets.
See also
References
- ISBN 0-13-035471-6.
- ^ paramagnetism. Encyclopædia Britannica
- ^ "Magnetic Properties". Chemistry LibreTexts. 2013-10-02. Retrieved 2020-01-21.
- ^ Nave, Carl L. "Magnetic Properties of Solids". HyperPhysics. Retrieved 2008-11-09.
- ^ Pauli, Z.Phys. 41, 81, 1927
- ^ Landau, Z.Phys. 64, 629, 1930
- ^ Jensen, J. & MacKintosh, A. R. (1991). Rare Earth Magnetism. Oxford: Clarendon Press. Archived from the original on 2010-12-12. Retrieved 2009-07-12.
- ^ Orchard, A. F. (2003) Magnetochemistry. Oxford University Press.
Further reading
- The Feynman Lectures on Physics Vol. II, Ch. 35: "Paramagnetism and Magnetic Resonance
- Charles Kittel, Introduction to Solid State Physics (Wiley: New York, 1996).
- John David Jackson, Classical Electrodynamics (Wiley: New York, 1999).
External links
- "Magnetism: Models and Mechanisms" in E. Pavarini, E. Koch, and U. Schollwöck: Emergent Phenomena in Correlated Matter, Jülich, 2013, ISBN 978-3-89336-884-6