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Spin glass

Disordered magnetic state

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Through Spin (physics), Ferromagnetism and Entropy

The term "glass" comes from an analogy between the magnetic disorder in a spin glass and the positional disorder of a conventional, chemical glass (e.g., a window glass). In any amorphous solid, such as window glass, the atomic bond structure is highly irregular; in contrast, a crystal has a uniform pattern of atomic bonds. In ferromagnetic solids, magnetic spins all align in the same direction; this is analogous to a crystal's lattice-based structure.

The individual atomic bonds in a spin glass are a mixture of roughly equal numbers of ferromagnetic bonds (where neighbors have the same orientation) and antiferromagnetic bonds (where neighbors have exactly the opposite orientation, where north and south poles are flipped 180 degrees). These patterns of aligned and misaligned atomic magnets create what are known as frustrated interactions – distortions in the geometry of atomic bonds compared to what would be seen in a regular, fully aligned solid. They may also create situations where more than one geometric arrangement of atoms is stable.

There are two main aspects of spin glass. On the physical side, spin glasses are real materials with distinctive properties, a review of which was published in 1982. On the mathematical side, models from statistical mechanics inform the study of both real spin glasses and analogous systems (e.g., human social systems).

Spin glasses and the complex internal structures that arise within them are termed "metastable" because they are "stuck" in stable configurations other than the lowest-energy configuration (which would be aligned and ferromagnetic). While difficult, the study of spin glasses has yielded valuable results in fields outside of physics, including chemistry, computer science and neural networks, pure mathematics, complex systems science, and even sociology.

Magnetic behavior

The key methods of determining whether a material is a spin glass are rooted in its magnetic behavior. Because of the underlying disordered structure of the magnetic moments, a spin glass is expected to exhibit a unique combination of features. A list of necessary criteria is proposed by Mydosh in a review paper:

  1. The ac susceptibility χac=χ′+iχ″=∂M∂Bac is the response of the spin glass to an alternating magnetic field. It consists of an (reactive) in-phase component χ′ and an (absorptive) out-of-phase component χ″. The expectation for a spin glass is that χ″(T) peaks sharply at the freezing temperature Tf. It is, furthermore expected that the freezing temperature is only weakly dependent on the excitation frequency. An explanation for this is that during the freezing process, the fluctuations lead to a slowing down of the spin dynamics and thus a higher absorption χ″.
  2. The temperature dependent magnetization M(T) in the frozen state must depend on the magnetic history: A pronounced splitting between the magnetization in heating must occur where a constant M is expected up to Tf when the sample was cooled across the transition in a magnetic field (so called field cooled FC). This is opposed to a field-free cooling and application of the magnetic field only in the frozen state (zero-field cooling ZFC). Underlying this is that the glass is frozen into a (partially) magnetized state in a FC protocol.
  3. The magnetic specific heat cm shows a broad, field-dependent maximum at Tf, whereas it is sharp at the transition to an ordered state (like a ferro- or antiferromagnet).
  4. Because spin glasses are based on disorder, there is a decay of the magnetized state, it ages. This means that a zero-field cooled magnetized state will decay back into an unmagnetized one. There will be a maximum in the quantity S(t)=(1/H)∂M∂ln⁡t.

Above the spin glass transition temperature, Tc, the spin glass exhibits typical magnetic behaviour (such as paramagnetism).

If a magnetic field is applied as the sample is cooled to the transition temperature, magnetization of the sample increases as described by the Curie law.

Surprisingly, the sum of the two complicated functions of time (the zero-field-cooled and remanent magnetizations) is a constant, namely the field-cooled value, and thus both share identical functional forms with time, at least in the limit of very small external fields.

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