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Anderson localization is the confinement of electron wave functions, or other wave modes, by interference between repeated wave scattering paths in static disorder. A localized eigenstate occupies a limited region even in a much larger sample. Disorder can therefore suppress diffusion without absorbing the wave. In 1958, Philip Warren Anderson studied random site energies and intersite coupling, finding a regime without transport. His paper develops a theoretical model; it does not report an Anderson laboratory measurement.^[ref]

The distinction from ordinary multiple scattering is the retention of wave phases: alternative paths contribute probability amplitudes before their squared modulus is taken. Adding path probabilities alone loses the cross terms responsible for interference. This makes Anderson localization useful as a warning about transport models: repeated deflections need not produce unlimited diffusion. It also connects electron transport with wave propagation in a random medium, although the detailed equations and experimental diagnostics differ between electrons, light and acoustic waves.

Philip Warren Anderson's 1977 lecture distinguishes localized magnetic moments from disorder-localized states. It credits Nevill Francis Mott with recognizing the significance of the mobility edge. A Mott insulator instead requires electron interactions and can exist without disorder.^[ref]

John Hasbrouck Van Vleck developed quantum mechanics explanations of magnetic susceptibility, including its temperature dependence; this is a distinct contribution from Anderson localization.^[ref]

A correlated transition-metal compound whose lowest charge excitation primarily transfers an electron between a ligand orbital and a metal orbital. Its gap is controlled by charge-transfer and Coulomb energies rather than a weakly interacting single-band picture alone. Many cuprate parent compounds are usefully described this way. This distinguishes the orbital character of the low-energy excitation from an idealized single-band Mott insulator.

A Mott insulator is insulating because of electron interactions even where a noninteracting electronic band structure would predict conduction. This mechanism differs from disorder-driven Anderson localization.

A Mott transition is a change between a conducting state and a Mott insulator, driven by the competition between electron motion and electron repulsion. A partially filled energy band need not conduct if repulsion makes moving an electron onto an already occupied site too costly.

The half-filled Hubbard model illustrates the mechanism: hopping lowers the kinetic energy, whereas on-site repulsion $U$ penalizes double occupation. Increasing $U$ relative to the energy-band width can suppress charge motion and open a gap for charge excitations. Changing pressure, composition or carrier concentration can alter that competition, although actual materials may also change their crystal structure or magnetic order. This interaction mechanism differs from a band insulator with filled bands and from disorder-driven Anderson localization.

The clearest examples are the cuprate superconductors. Their unusual properties should be compared with the clean, weak-coupling, fully gapped s-wave electron–phonon limit of BCS theory; that limit is not a definition of all possible BCS-like paired states.

Cuprates are layered copper oxides with strongly anisotropic transport. Their undoped parents are antiferromagnetic Mott insulators or, more specifically for many compounds, charge-transfer insulators, despite partially filled bands in a simple band picture. Doping produces a superconducting dome rather than simply improving an ordinary weakly interacting metal. This points to strong electronic correlations. Near optimal doping, an extended temperature range often shows approximately linear electrical resistivity, termed strange-metal behaviour, instead of the low-temperature $T^2$ law of a conventional Fermi liquid. Neither law applies at every temperature and doping.

The dominant Cooper pair symmetry is spin-singlet $d_{x^2-y^2}$, with a representative gapIt changes sign under a quarter turn and has nodes on the zone diagonals. Phase-sensitive experiments detect that sign change; it is not established by a large transition temperature alone. ^[ref] Clean nodal quasiparticles give power-law low-temperature responses, for example electronic heat capacity $C\propto T^2$ and penetration-depth change $\lambda (T)-\lambda (0)\propto T$, in contrast with activated responses of a fully gapped s-wave state. Disorder, dimensional crossover and competing phases can alter these powers.

The cuprate pseudogap is a partial, momentum-dependent loss of low-energy electronic spectral weight extending above the superconducting transition in underdoped materials. It need not be identical to the superconducting gap, and observing it alone does not identify its microscopic origin or prove preformed pairs. ^[ref]

Short coherence lengths, anisotropy and low phase stiffness in underdoped systems make thermal phase and vortex fluctuations important. Many cuprates are strong type-II superconductors, with large London penetration depths relative to their superconducting coherence lengths. Gap-to-transition-temperature ratios and isotope effects vary with doping and need not obey the simplest weak-coupling benchmarks $2\Delta (0)/(k_{\mathrm{B}}{T}_c)=3.53$ and $T_c\propto M_{\mathrm{ion}}^{-1/2}$. A weak or variable isotope effect by itself does not identify the pairing mechanism.

These features motivate strongly correlated pairing descriptions, often involving spin fluctuations, but do not uniquely establish a microscopic pairing glue. Other high-temperature families need not share every cuprate property: iron-based superconductors are multiband and may be nodeless. The robust distinction is the observed combination of correlated normal states, unusual gap symmetry and important collective fluctuations, rather than high $T_c$ alone.

Put $N=N_x{N}_y{N}_z$ primitive cells in a periodic box. In each reciprocal-space direction, the allowed Bloch wavevectors are spaced by $2\pi /L_i$, giving $N_i$ independent values in the first Brillouin zone. There are consequently $N$ wavevectors per band and, including two electron spin states at each wavevector,The total and per-atom counts are different; a factor $N$ cannot remain in the per-atom count for this monatomic lattice.

In independent-electron band theory, a partially occupied band permits low-energy changes of occupancy and gives a metal. Filled bands separated from empty bands by a finite band gap give a band insulator at zero temperature. An odd number of electrons per primitive cell cannot fill spin-degenerate bands, whereas an even number can; even filling alone does not ensure an insulator if bands overlap. Magnetic symmetry breaking and strong correlations, such as a Mott insulator, go beyond this simple counting criterion.

The Hubbard model combines band motion and local repulsion:Hopping favors itinerant states, while positive $U$ penalizes simultaneous opposite-spin occupation on one site. In a uniform mean-field treatment, a spin imbalance reduces the interaction cost but raises the band-filling energy. The Stoner criterion for instability of the unpolarized metal is $U{g}_{\uparrow }(E_F)>1$ when $g_{\uparrow }$ is the density of states per site, per energy, for one spin. Using a total two-spin density of states changes the displayed numerical convention.

The ordered mean-field state has exchange-split spin bands and a spontaneous magnetization, with the kinetic and interaction costs balancing at equilibrium. This is a model of itinerant ferromagnetism, not a guarantee that every repulsive Hubbard system becomes ferromagnetic. Filling, lattice structure and competing order matter: near half filling on a bipartite lattice, antiferromagnetism and a Mott insulator can be favored instead. The approximation also omits important spin fluctuations and strong-correlation effects.

The Hubbard model combines hopping with a local repulsion,Hopping favours a broad itinerant band; the interaction penalizes opposite-spin double occupancy. For uniform Stoner decoupling of the Hubbard interaction, let $s=n_{\uparrow }-n_{\downarrow }$ be the spin imbalance per site. The interaction is $U(n^2-s^2)/4$, so polarization lowers it by $U{s}^2/4$, at the expense of kinetic energy.

If $D(E_F)$ is the noninteracting density of states per spin per site, small polarization costs $s^2/[4D(E_F)]$. Thereforeis the mean-field ferromagnetic instability criterion. The exchange splitting is $\Delta =Us$, and the paramagnetic response is enhanced as $\chi ={\chi }_0/[1-UD(E_F)]$. A density of states including both spins changes the written factor in the criterion.

The model explains how itinerant bands can polarize without imposing pre-existing localized atomic spins. It is not a claim that every large-$U$ metal becomes ferromagnetic: near half filling the Hubbard model can instead form a Mott insulator with antiferromagnetic superexchange of scale $4t^2/U$. Band filling, bandwidth and fluctuations matter.^[ref] The interaction-energy and kinetic-cost expansion above is the stated mean-field derivation of the enhancement.^[ref]

For state counting in a Bloch band, take a primitive cubic lattice of spacing $a$ and impose periodic boundary conditions on lengths $L_i=N_{i}a$. The allowed wavevectors are $k_i=2\pi l_i/L_i$. The first Brillouin zone has side $2\pi /a$, so it contains $N_i$ distinct values in each direction and hence $N_x{N}_y{N}_z=N$ wavevectors. Each orbital-derived energy band has one state per wavevector per spin orientation. ThereforeThe phrase “per atom” attached to $2N$ in the PDF is a counting error: $2N$ is the total, not the per-atom count.

By the Pauli exclusion principle, a monovalent crystal supplies $N$ valence electrons and half-fills a spin-degenerate band; its Fermi level lies within allowed states, giving a metal in the independent-electron picture. Two electrons per atom can fill one band. If a band gap separates it from all empty bands, the crystal is a band insulator. An even valence count only permits insulation: overlapping bands can still produce a metal. Conversely, electron interactions can produce a Mott insulator, and symmetry breaking can permit insulation outside this simple spin-degenerate electronic band structure criterion. The relevant count in a crystal with a basis is per primitive unit cell.