Abstract
It is shown that in a simple model of surface dynamics of growing 3D quasicrystals, growth proceeds through the nucleation of steps whose heights hs diverse like (Δμ)1/3 as the growth-driving chemical-potential difference Δμ→0. This large step size leads to very low growth velocities Vg∝exp{-1/3[Δμc(T)/Δμ]4/3}. Δμc(T) defines a rounded kinetic roughening transition and is nonuniversal. For ‘‘perfect-tiling models’’ I find Δμc(T)∝T3/2 at high temperatures T, which fits recent numerical simulations, while in models with bulk phason Debye-Waller disorder, ln(Δμc)∝- √T . The growing interface is algebraically rough.