一维长程关联无序系统中的电子态

利用傅里叶滤波法在一维Anderson无序系统中产生了具有幂律谱密度公式s(q)∝q^-p形式的长程关联随机能量序列，并利用传输矩阵方法计算了系统中引入了长程关联后的局域长度，同时应用负本征值理论对系统中的电子态密度进行了分析，并分别把计算结果与系统中不具有长程关联时的局域长度与电子态密度进行了比较.结果表明，长程幂律关联的引入对电子态的性质产生了很大的影响，当关联指数p≥2.0时，在系统能带中心范围内发生了部分局域态向退局域态的转变，而同时电子态密度也发生了很大的变化，出现了六个范霍夫奇点，系统的能带范围也相应地得到展宽. 关键词： 无序系统 长程关联 局域长度 电子态密度     

一维长程关联无序系统的局域性

研究了在紧束缚近似下,由de Moura和Lyra提出的一维长程关联无序模型的局域性. 分布在［-W/2,W/2］区间的格点位能,其关联函数〈ε_iεj〉的傅里叶变换满足S(k)∝k^-α,其中关联强度α>0. 利用participation ratio不仅证实了在α>2和W<4 关键词： 安德森局域化 长程关联 扩展态     

一维二元非对角关联无序体系交流跳跃电导特性

在单电子紧束缚无序模型基础上，建立了一维二元非对角关联无序体系电子跳跃输运交流电导模型，并推导了其交流电导公式，通过计算其交流电导率，探讨了格点能量无序度、格点原子组分、非对角关联及温度、外场对体系交流跳跃电导的影响.计算结果表明，一维二元非对角关联无序体系的交流电导率随格点能量无序度的增大而减小.同时，体系中两种原子的组分的变化实际代表着体系成分无序程度的变化，因而对其交流电导率的影响很大，表现为随A类原子含量p的增加而先减小后增大.当引入非对角关联时，体系出现退局域化现象，电子波函数由局 关键词： 二元无序体系 交流跳跃电导 格点能量无序度 非对角关联     

准一维纳米线电子输运的梯度无序效应

考虑实际体系的梯度无序和结散射,发展格林函数矩阵分解消元方法,研究了准一维纳米线的电子输运性质. 结果表明,由于结散射,电导随能量呈现振荡行为,无序的引入破坏了电子相干性,在低无序度区平均电导呈现异常增加,呈现一个新的电导峰. 当表面存在无序但无梯度衰减时,体系的平均电导随无序度增强先减后增,出现类局域-退局域性转变. 当表面无序线性衰减时,平均电导在强无序区稍有增加,而当表面无序高斯型衰减时,平均电导指数衰减,类局域-退局域性转变消失,不同于以前的理论预言. 研究结果对准一维纳米线电子器件的结构设计和应用有指导作用. 关键词： 准一维纳米线 梯度无序 电子输运     

准二维无序系统的电子结构

对形如N_t×N_l型准二维无序系统，只考虑格点之间的最近邻跳跃积分，采用特殊的格点编号方案，在单电子近似下，系统的哈密顿量可表示为简明对称矩阵，借助豪斯荷尔德变换将其约化为对称三对角矩阵，再利用负本征值理论及传输矩阵等方法,对系统态密度、局域长度及电导等电子结构特性进行数值计算. 重点研究了准一维四平行链和五平行链无序系统， 将结果与一维单链、准一维双链及三链系统进行对比，发现随维度的增加，系统的能带有所展宽，能态密度分布发生很大的变化，其峰值数量呈偶数规律增加. 并且在能带中心处存在有局域长度大于系统大小的扩展态，处于这些态下的系统具有较大电导. 从单链到多链，相当于扩大了系统的关联范围，使系统出现了类似非对角长程关联的行为. 关键词： 准二维无序系统 态密度 局域长度 电导     

Sb掺杂引起Ru1222体系中的空穴局域化

本利用X射线衍射、电阻率测量等实验手段对Rul-xSbxSr2Gdl．4Ce0.6Cu2O10-δ（Ru1222)体系的结构和正常态性质进行了研究．结果表明，Sb掺杂明显抑制超导电性，这可能是由于Sb掺杂引起体系无序度增加，另一方面，Sb在Ru位的掺杂可加剧RuO6八面体的变形，从而使CuO2面的空穴载流子被磁捕获或磁散射的程度增加．Sb掺杂导致载流子被无序散射和磁捕获或磁散射，这些都会阻碍载流子的运动，使载流子局域化．样品在铁磁转变点温度以下的正常态电阻率可由可变程跃迁模型很好地描述．发现局域化长度随着掺杂而降低，这表明空穴局域化程度随着无序度的增加而提高．样品在铁磁转变点温度以上的正常态电阻率可由小极化子跃迁模型很好地描述．     

双层石墨烯材料中无序导致超导-绝缘体相变的数值研究

本文利用一种新的数值方法研究了在较大的双层石墨烯样品中杂质的无序 效应对超导态特性的影响. 采用核多项式方法 (Kernel Polynomial Method) 来自洽求解双层石墨烯系统的Bogoliubov-de-Gennes (BdG) 方程, 从而得到了由无序效应所引起的超导序参量的空间涨落精确解. 进一步, 计算了系统处于超导态时的态密度、光电导和广义逆参与率 (inverse participation ratio) 等物理量, 并发现随着无序强度的不断增大态密度中的能隙被 完全抑制, 同时光电导的Drude权重也迅速减小并最终降为零, 这表明双层石墨烯中的低能电子态发生了安德森局域化, 系统因而发生了由无序效应诱导的超导-绝缘体相变. 关键词： 双层石墨烯 安德森局域化 超导-绝缘体相变 核多项式方法     

无序系统中电子局域态分布

本文应用一种计算无序系统中电子本征态的方法,求得了含有2000个粒子的无序系统中电子局域态的分布,并结合态密度、计算误差进行了分析讨论。所得结果表明,在不同的能量范围内局域态的分布不同,分布可遍及整个系统,且与无序度有关。 关键词：     

DNA分子链电子结构特性研究

在单电子紧束缚近似下，建立了一维无序二元DNA分子链模型，计算了链长为2×10⁴个碱基对的DNA分子链的电子态密度、局域化特性，并探讨了碱基对的不同组分、格点能量无序度对电子局域态的影响.结果表明：由于DNA分子链中格点能量无序及碱基对的不同组分的存在，其电子波函数呈现出局域化的特性，而局域长度作为衡量电子局域化程度的一个尺度，受碱基对的组分及格点能量无序度的影响. 关键词： DNA分子链 电子结构 电子局域态 局域长度     

非晶光子晶体中的光子局域化

利用多重散射方法计算并研究了二维光子晶体随着无序度变化的光子局域化.通过控制方形单元随机旋转角度以控制光子晶体的无序度.研究发现，随着无序度的增加光子通带的透过率逐渐降低，而光子禁带中的透过率逐渐上升，即无序导致的局域化逐渐由光子带边向光子禁带中心和光子通带的中心扩展.而且光子通带中的平均透过率随无序度的增加呈e指数下降. 关键词： 非晶 光子晶体 无序 光子局域     

Localization-delocalization transition in chains with long-range correlated disorder

We investigated numerically localization properties of electron eigenstates in a chain with long-range correlated diagonal disorder. A tight-binding one-dimensional model with on-site energies exhibiting long-range correlated disorder (LCD) was used with various disorder strength W. LCD was defined so that it gave a power-law spectral density of the form S(k)αk^-p, where p determines the roughness of the potential landscape. Numerical results on the correlation length ξ of eigenstates shows the existence of the localization-delocalization transition at p=2. It is found that the critical values for disorder strength W_c and also the critical exponent ν for localization length change with the values of p.     

Localization-delocalization transition in one-dimensional system with long-range correlated diagonal disorder

We show that the electronic states in a one-dimensional (1D) Anderson model of diagonal disorder with long-range correlation proposed by de Moura and Lyra exhibit localization-delocalization phase transition in varying the energy of electrons. Using transfer matrix method, we calculate the average resistivity and investigate how it changes with the size of the system N. For given value of α (> 2) we find critical energies E_c1 and E_c2 such that the resistivity decreases with N as a power law ∝ N ^{- γ} for electron energies within the range of [E _c1, E _c2], and exponentially grows with N outside this range. Such behaviors persist in approaching the transition points and the exponent γ is in the range from 0.92 to 0.96. The origin of the delocalization in this 1D model is discussed. Received 18 December 2001 / Received in final form 2 May 2002 Published online 14 October 2002 RID="a" ID="a"e-mail: sjxiong@nju.edu.cn     

Numerical studies on the anderson localization problem

The electron localization is studied for Anderson's tight-binding model with diagonal and off-diagonal disorder for a very large square lattice (10,000 sites) and diamond lattice (27,000 sites). The numerical investigations are based on the Lanczos recursion method. The convergence of the recursion coefficientsa _n ,b _n is discussed with regard to the electron localization.From Anderson's criterion and an exact real space renormalization method the energy of the localization edge is found as a function of the degree of disorder. Also the dependence of the spatial decay rate of localized wave functions on the energy and the degree of disorder is evaluated. Near the Anderson transition, where all states become localized, we get two critical exponentsv _E andv _W , which lead us to the tentative suggestion of multicritical scaling laws for this transition.     

Analysis of localization-delocalization transitions in corner-sharing tetrahedral lattices

We study the critical behavior of the Anderson localization-delocalization transition in corner-sharing tetrahedral lattices. We compare our results obtained by three different numerical methods namely the multifractal analysis, the Green resolvent method, and the energy-level statistics which yield the singularity strength, the decay length of the wave functions, and the (integrated) energy-level distribution, respectively. From these measures a finite-size scaling approach allows us to determine the critical parameters simultaneously. With particular emphasis we calculate the propagation of the statistical errors by a Monte-Carlo method. We find a high agreement between the results of all methods and we can estimate the highest critical disorder W _c = 14.474 (8) at energy E _c = ? 4.0 and the critical exponent ν = 1.565 (11). Our results agree with a previous study by Fazileh et al. [F. Fazileh, X. Chen, R.J. Gooding, K. Tabunshchyk, Phys. Rev. B 73, 035124 (2006)] but improve accuracy significantly.     

Inverse Anderson transition caused by flatbands

We propose a new disorder-induced insulator-metal transition of one-electron states, which may be called the "inverse Anderson transition." We first make a highly degenerated localized states by constructing a three-dimensional periodic system possessing only flat dispersion relations. When we introduce a disorder into it, a finite-size scaling of the level statistics shows two clear (localization-delocalization and delocalization-localization) transitions for a wide range of the energy, with increasing the degree of disorder. These transitions are confirmed also by finding the system-size-independent characteristic of the wave function.     

Finite-size scaling of the level compressibility at the Anderson transition

We compute the number level variance Σ ₂ and the level compressibility χ from high precision data for the Anderson model of localization and show that they can be used in order to estimate the critical properties at the metal-insulator transition by means of finite-size scaling. With N, W, and L denoting, respectively, linear system size, disorder strength, and the average number of levels in units of the mean level spacing, we find that both χ(N, W) and the integrated Σ ₂ obey finite-size scaling. The high precision data was obtained for an anisotropic three-dimensional Anderson model with disorder given by a box distribution of width W/2. We compute the critical exponent as ν≈ 1.45±0.12 and the critical disorder as W _c≈ 8.59±0.05 in agreement with previous transfer-matrix studies in the anisotropic model. Furthermore, we find χ≈ 0.28±0.06 at the metal-insulator transition in very close agreement with previous results. Received 1st November 2001 and Received in final form 8 March 2002 Published online 6 June 2002     

Delocalization in one-dimensional tight-binding models with fractal disorder

In the present work, we investigated the correlation-induced localization-delocalization transition in the one-dimensional tight-binding model with fractal disorder. We obtained a phase transition diagram from localized to extended states based on the normalized localization length by controlling the correlation and the disorder strength of the potential. In addition, the transition of the diffusive property of wavepacket dynamics is shown around the critical point.     

Electronic properties of one-dimensional systems with long-range correlated binary potentials

We study numerically the electronic properties of one-dimensional systems with long-range correlated binary potentials.The potentials are mapped from binary sequences with a power-law power spectrum over the entire frequency range,which is characterized by correlation exponent β.We find the localization length ξ increases with β.At system sizes N →∞,there are no extended states.However,there exists a transition at a threshold β c.When β > β c,we obtain ξ > 0.On the other hand,at finite system sizes,ξ≥ N may happen at certain β,which makes the system "metallic",and the upper-bound system size N (β) is given.     

Simple-Complex Fluid Transition in Microemulsions

The aim of this work was to study the rheological behavior of water in-oil microemulsion formulated with AOT (sodium bis(2-ethylhexyl) sulfoccinate) in isooctane over a temperature range from 25°C to 55°C for the oil/AOT volume fraction φ _m =0.1 and various AOT and H₂O molar ratios, W₀, ranging from 0 to 45. The apparent viscosity was measured vs. shear rate by a rotational concentric cylinder viscometer. It was shown that above s^?1, the solutions utilized behaved as Newtonian liquids. The absolute viscosities were deduced from the shear stress- shear rate rheograms. For W₀ < 17, the solutions behaved as simple fluids, where the viscosities decrease as the temperature increases. However, an opposite behavior was observed for W₀ > 17; the viscosity remained constant and then increased above a critical temperature, T_c, depending on W₀. For the molar ratio W_0,c = 17; the studied viscosity remained constant, η(W_0,c) = (1.17 ± 0.04) cP, for the temperature range studied. Thus, a simple–complex fluid transition was evident in the studied system. For the simple fluids, W₀ < W_0,c, the total activation energy vs. W₀ showed three linear parts. The different slopes were attributed to the change of the microscopic structure of the formed micelles. For the critical molar ratio W_0,c = 17, the total activation energy vanished. So, according to the Eyring lattice model, the jump of the formed micelles from one site to another was not permitted and the entire molecular groups were in vibration and rotation motions. For W₀ > W_0,c, where the formed micelles were fully hydrated, the relative viscosity of the studied solutions vs. temperature was fitted according a polynomial law, where the exponent was found to be dependent on W₀.