A crystal is never a perfect lattice at T > 0 — thermal agitation constantly creates and destroys point defects. The equilibrium number present at a given temperature is set purely by minimising free energy F = E − TS: making n defects costs energy nEf but gains configurational entropy from the huge number of ways to arrange them among the N available sites, and balancing dF/dn = 0 gives an Arrhenius law. That combinatorial argument never uses the lattice's dimensionality, so the same law governs the 2D cross-section drawn here as it does the full 3D crystal.
Schottky vacancy:
n/N = exp(−E_f / k_BT)
Frenkel pair (vacancy + interstitial):
n_F = √(N·N_i) · exp(−E_f / 2k_BT)
k_B = 8.617×10⁻⁵ eV/K
- Schottky — an atom leaves its lattice site entirely (migrates to the surface/grain boundary), leaving one empty site (red wire ring) per defect.
- Frenkel — an atom is displaced into a nearby interstitial gap instead of leaving the crystal, so a vacancy (ring) and an interstitial atom (orange dot, off-lattice) always appear together. The extra freedom of "which interstitial site" halves the effective exponent, so at equal Ef Frenkel pairs are always more numerous than Schottky vacancies.
- The lattice relaxes the live defect count toward whichever equilibrium value the sliders currently predict — exactly the kinetic process (vacancy diffusion driven by the same Boltzmann factor) that lets a real crystal re-equilibrate after a temperature change. The relaxation-speed slider only changes how fast it visibly catches up, not the target it is chasing.
- The Arrhenius panel plots ln(n/N) against 1000/T for both defect types at the current Ef; the highlighted dot is where your sliders currently sit on that line.
This is why quenching a metal from high temperature "freezes in" excess vacancies, and why ionic crystals (which favour Frenkel/Schottky disorder depending on the ion size ratio) become significantly more conductive as they approach their melting point.