电化学沉积Fe单晶纳米线生长中的取向控制

利用电化学沉积方法，发现了一种能够动态地控制铁纳米线生长方向的沉积方法，利用该方法沉积了包括［110］取向，［200］取向及非晶态三种结构和取向的一维Fe纳米线阵列.对于三种纳米线阵列，测量了它们的磁特性，分析发现具有[200]择优取向纳米线阵列的方形度，各向异性特性和矫顽力都比[110]取向阵列有很大的改善. 关键词： 磁性纳米线 电化学沉积 取向控制     

高矫顽力的Co70Cu30合金纳米线阵列的制备及磁性研究

利用直流电化学沉积法, 在多孔阳极氧化铝模板中首次制备出了具有[220]取向的单晶 面心立方结构的CoCu固溶体合金纳米线阵列, 其Co含量高达70%.透射电子显微镜显示纳米线均匀连续, 具有较高的长径比, 约为300. 磁性测量表明所制备的Co₇₀Cu₃₀ 合金纳米线具有超高的矫顽力H_c//=2438 Oe(1 Oe=79.5775 A/m)和较高的矩形比S//=0.76, 远高于以往报道的CoCu合金纳米线的磁性, 分析表明磁性好的主要原因是由于较高Co含量和高形状各向异性. 通过磁性测量和模型计算, 得到Co₇₀Cu₃₀ 合金纳米线阵列在反磁化过程中遵从对称扇型转动的球链模型, 并从结构的角度分析了Co₇₀Cu₃₀合金纳米线阵列的反磁化行为.     

Ni纳米线的结构和性质研究

采用推广模拟退火算法(Generalized Simulated Annealing,GSA)和Sutton-Chen势,研究了初始构型为面心立方(fcc)结构的Ni纳米线,在沿径向压缩时的结构和性质.结果表明:径向压缩程度对Ni纳米线的结构有很大的影响.当Ni纳米线直径大于0.398nm时(初始直径为0.498nm),其结构由fcc结构变为类似fcc结构,但结合能变化很小,表明其结构之间几乎可以实现零能量转换,且稳定性基本不变;当Ni纳米线直径小于0.398nm时,其结构从无定形结构变为缺陷结构,结合能迅速上升,表明其结构稳定性降低;键角的分布也证明了以上结果的正确性.     

磁场对模板法制备的Co纳米线结构和磁性的影响

在用二次氧化法制备的高度有序的氧化铝模板上通过交流电化学方法制备了Co纳米线阵列．研究了外加磁场及电解液pH值对纳米线生长的影响．在pH值为6.0和6.5的电解液中分别在不加磁场和沿纳米线轴向施加0.3 T磁场情况下制备了hcp结构的Co纳米线阵列．实验数据表明,沉积时外加磁场和调节pH值能有效影响纳米线中hcp结构的Co晶粒的易磁化轴沿纳米线长轴方向生长．由于晶粒的磁晶各向异性和纳米线沿长度方向的宏观形状各向异性叠加,制备的Co纳米线阵列具有高垂直各向异性,高矫顽力和较高矩形比． 关键词： Co纳米线阵列 织构 磁性     

铋纳米线中电导的温度依赖性

采用电沉积的方法在多孔氧化铝模板中合成了直径为30 nm且沿着[0112]方向生长的单晶铋纳米线,测量了纳米线电导随着温度78～320 K变化的关系曲线. 结果发现,其半金属半导体转变的温度为230 K,且纳米线的电导有很强的温度依赖性.     

Magnetic nanowire arrays in anodic alumina membranes: Rutherford backscattering characterization

Systematic study of magnetic nanowire arrays grown in anodic alumina membranes (AAM) has been done by means of Rutherford backscattering spectroscopy (RBS). The AAM used as templates were morphologically characterized by using high resolution scanning electron microscopy (HRSEM), fast Fourier transform (FFT) and atomic force microscopy (AFM). The highly ordered templates with a mean pore diameter size of 30 nanometers, a mean inter-pore spacing of 100 nm and lengths ranging from 4 to 180 microns were obtained through two-steps anodization process, and the Ni and Co nanowire arrays were grown by electrodeposition techniques. The main attention is addressed to Ni nanowire arrays. RBS results allowed us to determine the real depth profile of atomic composition of the obtained nanowire arrays. In addition, the RBS spectra fitting showed that the porosity increased from the top to the bottom of the samples. Two phenomenological models are proposed to understand the apparition of that secondary porosity and a linear relation between the total amount of electrodeposited Ni and the electrodeposition time was obtained. As an example, it is also reported the relation between RBS results and magnetic properties, such as coercive field and remanence/saturation magnetization ratio of the samples. Particularly, for Ni nanowires arrays obtained by using voltage pulses, it is demonstrated that the larger the nanowires, the higher the definition for easy axis parallel to the nanowire length is possible. PACS 82.80.Yc; 81.16-c; 75.75.+a     

Ordered tellurium nanowire arrays and their optical properties

High-density tellurium (Te) nanowire arrays were prepared in the nanochannels of an anodic aluminum membrane (AAM) template using the electrochemical deposition method. The as-synthesized Te nanowires, typically 60 nm in diameter and up to 40 μm in length, possess a hexagonal single crystalline structure following [001] growth direction. The optical polarization properties of Te nanowire arrays embedded in AAM were investigated using an optic parameter oscillator in the wavelength range from 0.7 to 1 μm. The high optical polarization of the Te nanowire arrays embedded in the AAM assembly system was observed. PACS 81.05.Cy; 78.67.-n; 82.80.Fk.     

Al纳米线不同晶向力学行为和变形机制的模拟

采用分子动力学模拟计算方法,考察具有较高层错能的Al纳米线沿不同晶向的力学行为和变形机制。在相同计算条件下与具有较低层错能的Ni、Cu、Au和Ag等FCC金属纳米线进行比较。结果表明：在力学行为方面,Al纳米线的弹性模量呈现明显的结构各向异性,满足E_[111] > E_[110] > E_[100]的关系,这一关系在FCC金属纳米线中普遍成立;Al纳米线的屈服应力随晶向呈现σ_y[100] > σ_y[111] > σ_y[110]的关系,这一关系在具有较低层错能的FCC金属纳米线中不具有普遍性,这与体系中位错形成机制密切相关。根据拉伸变形过程微观结构的演变规律,阐明Al纳米线不同晶向的变形机制,并与具有较低层错能的Ni、Cu、Au和Ag等FCC金属纳米线的变形机制进行比较。结果表明,对于尺度较小的高层错能Al纳米线,Schmid因子和广义层错能均难以准确预测其变形机制。     

Electrodeposition and magnetic properties of Ni nanowire arrays on anodic aluminum oxide/Ti/Si substrate

Ni nanowire arrays with different diameters have now been extended to directly fabricate in porous anodic alumina oxide (AAO) templates on Ti/Si substrate by direct current (DC) electrodeposition. An aluminum film is firstly sputter-deposited on a silicon substrate coated with a 300 nm Ti film. AAO/Ti/Si substrate is synthesized by a two-step electrochemical anodization of the aluminum film on the Ti/Si substrate and then used as template to grow Ni nanowire arrays with different diameters. The coercivity and the squareness in parallel direction of Ni nanowires with about 10 nm diameters are 664 Oe and 0.90, respectively. The Ni nanowire arrays fabricated on AAO/Ti/Si substrates should lead to practical applications in ultrahigh-density magnetic storage devices because of the excellent properties.     

The effect of structure on magnetic properties of Co nanowire arrays

Co nanowire arrays with three typical diameters of 20, 50 and 120 nm have been fabricated into anodic alumina oxide templates using an ac electrodeposition method. It is found that the crystal texture of the Co nanowires depends on the pH value of the deposition electrolyte. X-ray diffraction results show that the (1 0 0) texture appears at pH 6.2, while the diffraction peaks of (1 0 0) and (1 0 1) appear at pH 6.4 with the diameter of 20 nm. In addition, the (0 0 2), (1 0 0) and (1 0 1) peaks appear with an increase of pH value for the nanowire arrays with diameters of 50 and 120 nm, respectively. Magnetic measurements indicate the effect of structure on the magnetic properties of the nanowire arrays, which depend strongly on the different diffraction peaks, as adjusted by the pH value.     

Thermally activated magnetization reversal process of self-assembled Fe55Co45 nanowire arrays

We have investigated the temperature dependence of the magnetic properties and the magnetic relaxation of the Fe₅₅Co₄₅ nanowire arrays electrodeposited into self-assembled porous alumina templates with the diameter about 10 nm. X-ray diffraction (XRD) pattern indicates that the nanowire arrays are BCC structure with [1 1 0] orientation along the nanowire axes. Owing to the strong shape anisotropy, the nanowire arrays exhibit uniaxial magnetic anisotropy with the easy magnetization direction along the nanowire axes. The coercivity at 5 K can be explained by the sphere chains of the symmetric fanning mechanism. The temperature dependence of coercivity can be interpreted by thermally activated reversal mechanism as being the localized nucleation reversal mechanism with the activation volume much smaller than the wire volume. Strong field and temperature-dependent magnetic viscosity effects were also observed.     

Pulsed electrodeposition of monocrystalline Ni nanowire array and its magnetic properties

By means of a porous template without removing the aluminium substrate, a technique of pulsed electrodeposition with an intermittent symmetric square pulse has successfully been applied to fabricate Ni nanowire array. The as-obtained nanowires have a diameter of about 60 nm and exhibit high aspect ratio of more than 50. The electron diffraction pattern investigation demonstrates that the nanowires are single crystal. Moreover, a highly preferential orientation [2 2 0] of the as-obtained Ni nanowires with high purity decided by XRD has been obtained, and the preferred orientation is weakened remarkably by an annealing process. Furthermore, the investigation of magnetic properties by VSM indicates that the as-obtained Ni nanowire array has an obvious magnetic anisotropy and exhibits a good thermal stability.     

第一性原理研究[112]硅锗异质结纳米线的电子结构与光学性质

基于密度泛函理论体系下的广义梯度近似,本文利用第一性原理方法着重研究了[112]晶向硅锗异质结纳米线的电子结构与光学性质.能带结构计算表明:随着锗原子数的增加,[112]晶向硅锗纳米线的带隙逐渐减小;对Si_(36)Ge_(24)H_(32)纳米线施加单轴应变,其能量带隙随拉应变的增加而单调减小.光学性质计算则表明:随着锗原子数的增加,[112]硅锗纳米线介电函数的峰位和吸收谱的吸收边均向低能量区移动;而随着拉应变的增大,吸收系数峰值呈现出逐渐减小的趋势,且峰位不断向低能量区移动,上述结果说明锗原子数的增加与施加拉应变均导致[112]硅锗纳米线的吸收谱产生红移.本文的研究为硅锗异质结纳米线光电器件研究与设计提供一定的理论参考.     

Electron transport in dye-sensitized solar cells based on TiO2 nanowires

Anatase titanium dioxide nanowire arrays were prepared by hydrothermally oxidizing titanium foils in aqueous alkali and transferred onto fluorinated tin oxide(FTO)glass for use as the photoanodes of front side illuminated dye-sensitized solar cells(DSCs).Electrochemical impedance spectroscopy(EIS)measurement was applied to compare the electron transport and recombination properties of DSCs using TiO2nanowire films and TiO2nanoparticle films as photoanodes.It was found that the nanowire array films possess smaller electron transport resistance(Rt)and larger electron diffusion length(Le)in the photoanodes,suggesting that the nanowire arrays can enhance the electron transport rate and have a potential to improve the charge collection efficiency of DSCs.     

Nanowire manipulation on surfaces through electrostatic self‐assembly and magnetic interactions

A method for fabricating aligned nanowire arrays on surfaces is shown. Gold and segmented Au/Ni/Au nanowires of high aspect ratio have been prepared by template electrosynthesis, and functionalized with charged short alkanethiols that can be ionized in aqueous solutions. Different distributions of funtionalized nanowires could be obtained on large surfaces from nanowire aqueous suspensions, avoiding aggregation due to electrical repulsion. Due to the high magnetic anisotropy of segmented Au/Ni/Au nanowires chaining of aligned nanowires could be obtained by applying a low magnetic field. While electrostatics favours side wire interactions due to the high aspect ratio, concurrent electrostatics and applied magnetic field yields end‐to‐end interaction and linear alignment without bifunctionalization. (© 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Magnetostatic interaction in electrodeposited Ni/Au multilayer nanowire arrays

Ordered Ni/Au multilayer nanowire arrays are successfully fabricated inside the nanochannels of anodic aluminum oxide template by pulse electrodeposition method. The thickness of the alternating layers is controlled to examine the magnetostatic interaction in Ni/Au multilayer nanowires. The magnetic easy axis parallel to the nanowires indicates that here the magnetostatic coupling along the wire axis dominates over the interactions perpendicular to the nanowires. However,the magnetostatic interaction between adjacent nanowires with larger magnetic layers is enhanced, leading to the existence of an optimum coercivity value.     

The elastic properties and energy characteristics of Au nanowires: an atomistic simulation study

This paper have performed molecular static calculations with the quantum corrected Sutten Chen type many body potential to study size effects on the elastic modulus of Au nanowires with [100], [110] and [111] crystallographic directions, and to explore the preferential growth orientation of Au nanowires. The main focus of this work is the size effects on their surface characteristics. Using the common neighbour analysis, this paper deduces that surface region approximately consists of two layer atoms. Further, it extracts the elastic modulus of surface, and calculate surface energy of nanowire. The results show that for all three directions the Young＇s modulus of nanowire increases as the diameter increases. Similar trend has been observed for the Young＇s modulus of surface. However, the atomic average potential energy of nanowire shows an opposite change. Both the potential and surface energy of [110] nanowire are the lowest among all three orlentational nanowires, which helps to explain why Au nanowires possess a [110] preferred orientation during the experimental growth proceeds.     

The effects of annealing on the structure and magnetic properties of CoNi patterned nanowire arrays

NiCo alloy nanowire arrays were fabricated by using an electrochemical method in a porous anodic aluminum oxide (PAO) template. X-ray-diffraction results showed that there was a preferred orientation in the CoNi nanowire arrays with Ni content ranging from 0.2 to 0.8 in the as-electro-deposited state, while a random orientation was observed after the sample was heat treated in an argon atmosphere. When the shape anisotropy is very high in the sample, it is found that the squareness (Mr/Ms) of the hysteresis loops for the samples is only about 0.6 before annealing, but increases to about 0.9 after annealing. All the results are discussed qualitatively and an explanation for the magnetic reversal mechanism in terms of a localized magnetization model is given. As the CoNi alloy nanowire arrays have high bit densities, they can be used as perpendicular magnetic recording media of high-density quantum magnetic disks. Received: 8 January 2001 / Accepted: 6 June 2001 / Published online: 30 August 2001     

Control growth of catalyst-free high-quality ZnO nanowire arrays on transparent quartz glass substrate by chemical vapor deposition

ZnO nanowire arrays have been successfully synthesized on transparent quartz glass substrate by chemical vapor deposition technique. Our work demonstrates the critical role of the growth temperature and the buffer layer on the effective control of the morphology of ZnO nanowires. A proper growth temperature and the thicker buffer layer could promise the good alignment and high density of the nanowires. The room-temperature photoluminescence spectrum shows that the buffer layer has also great effects on optical properties of ZnO nanowire arrays. The integrated intensity ratio [I_UV/I_{Visible band}] of the ZnO UV emission peak to visible band emission decreases with the increase of the thickness of the buffer layers. The obtained nanowire arrays have transmittance of above 50% in the visible region.     

Growth mechanism studies of ZnO nanowire arrays via hydrothermal method

Well-controlled ZnO nanowire arrays have been synthesized using the hydrothermal method, a low temperature and low cost synthesis method. The process consists of two steps: the ZnO buffer layer deposition on the substrate by spin-coating and the growth of the ZnO nanowire array on the seed layer. We demonstrated that the microstructure and the morphology of the ZnO nanowire arrays can be significantly influenced by the main parameters of the hydrothermal method, such as pH value of the aqueous solution, growth time, and solution temperature during the ZnO nanowire growth. Scanning electron microscopy observations showed that the well oriented and homogeneous ZnO nanowire arrays can be obtained with the optimized synthesis parameters. Both x-ray diffraction spectra and high-resolution transmission electron microscopy (HRTEM) observations revealed a preferred orientation of ZnO nanowires toward the c-axis of the hexagonal Wurtzite structure, and HRTEM images also showed an excellent monocrystallinity of the as-grown ZnO nanowires. For a deposition temperature of 90 °C, two growth stages have been identified during the growth process with the rates of 10 and 3 nm/min, respectively, at the beginning and the end of the nanowire growth. The ZnO nanowires obtained with the optimized growth parameters owning a high aspect ratio about 20. We noticed that the starting temperature of seed layer can seriously influence the nanowire growth morphology; two possible growth mechanisms have been proposed for the seed layer dipped in the solution at room temperature and at a high temperature, respectively.