2
I. INTRODUCTION
The electronic properties of quasicrystals have continued to pose fundamental problems ever since the dis-
covery of these materials by Schechtman et al [1]. The question of what constitutes “intrinsic” behavior of
quasicrystals, and how it is affected by disorder is not yet clearly understood. The reasons for this deficit of
understanding lie in the fact that the complexity of real materials – both chemical and structural – render
numerical computations difficult, and that analytical tools lack for even the simplest two or three dimensional
cases. Many numerical studies have been carried out for simplified tight-binding models on quasiperiodic
tilings. These indicate that single particle electronic states are, typically, multifractal for undisordered tilings
(see review in [2]). The generalized dimensions can in fact be exactly computed for the ground states of two
well-known tilings [3]. However, it is not understood what happens to such multifractal states in the pres-
ence of disorder. The nature of electronic states in real quasicrystals, where a certain amount of disorder is
inevitably present, has remained an open question. While the transition to Anderson localization has been
studied in detail for a 1D quasicrystal, the Fibonacci chain [4, 5], the effects of disorder on eigenstates have
not been analyzed in detail for 2D and 3D quasicrystals. This paper fills the gap by presenting a comprehensive
numerical study of the effects of disorder on eigenstates of an eight-fold symmetric 2D tiling, the Ammann-
Beenker (AB) tiling [6]. A patch of this tiling, composed of squares and 45◦rhombuses is shown in Fig. 1,
along with a typical critical state, represented by colored circles whose radii are proportional to the amplitude
on each site. We will address here in detail the question of how such multifractal or critical states evolve as a
function of disorder into strongly Anderson localized states.
In the study of disordered quasiperiodic tilings the extensive literature on a variety of disordered systems
provides a valuable guide. Random matrix models [7]are important reference systems which predict certain
universal properties. In particular, as we will describe, the Gaussian orthogonal ensemble (GOE) which has
the symmetry of the Hamiltonians we will consider here describes some spectral properties of tilings for both
the pure case and for weakly disordered tilings of finite size. The best known reference system for condensed
matter is the Anderson model for localization in random lattices [8]. In the Anderson model, it is well-known
that a metal-insulator transition occurs for three dimensional lattices, in contrast to 2D or 1D lattices, where
any disorder, however small, suffices to localize all of the eigenstates [9]. These statements hold in an infinite
system. However, if one considers a finite system of linear dimension L, one can distinguish between two
regimes of disorder – a weak disorder regime, where states appear to be extended on the scale of the system
size, and a strong disorder regime, where the states are clearly localized. The crossover occurs for a disorder
strength W?which corresponds to the localization length ξloc(W?)∼L. Since in 2D the localization length
diverges exponentially as W→0, the apparent metallic-like regime at weak disorder extends up to very large
system sizes.
We show here that, within the weak disorder regime, most states display a non-monotonic behavior as a
function of the disorder strength W. That is, states tend at first to delocalize for very small W. Localization
occurs only when the disorder exceeds a crossover value W?, which depends on the energy and system size.
The non-monotonic evolution of the localization properties only exists for finite systems, since the value of
the cross-over disorder strength vanishes in the thermodynamic limit. However the characteristic disorder W?
decreases logarithmically with the system size and hence the non-monotonicity is observed also for very large
approximants. The non-monotonic behavior can be seen by plotting the inverse participation ratio (IPR) as a
function of disorder, but also in the f(α)curve, which describes multifractal properties of wave-functions, and
in the generalized dimensions of the wave functions Dψ
q. This non-monotonicity is particularly pronounced for
the states around zero energy, in the middle of the spectrum. This is due to the fact that there is a zero-width
band of localized states at E=0 in this model, analogous to the E=0 states present in the well-known Penrose
rhombus tiling [10, 11]. All of these degenerate states are mixed as soon as disorder is introduced, and they
delocalize rapidly for W6=0. In contrast, the states lying near band edges and the main pseudogap behave
differently. They are the fastest to localize and, upto numerical accuracy, their evolution under disorder is
monotonic.
To complete the description of electronic properties in the disordered quasicrystal, we have carried out
detailed studies of two-point spatial correlation functions C(r,ω;E). These describe correlations of the ampli-
tudes of two eigenstates of energies close to E, having an energy separation ω, as a function of spatial distance
r. We obtain these correlation functions for increasing values of disorder, and show that for a large range of
disorder strength across the crossover regime, correlations follow power laws over a broad range of distances.