An encapsulated helical one-dimensional cobalt iodide nanostructure

Single-walled carbon nanotubes (SWNTs) can be used as templates for the growth of low-dimensional inorganic materials whose structures and properties often differ greatly from those of the bulk. Here we describe the detailed crystallography of an entire helical one-dimensional cobalt diiodide nanostructure encapsulated within a SWNT. This material has an unprecedented twisted double tetrahedral chain structure arising from a rotation of Co(2)I(4) units along its length. The complete nanostructure comprises two distinct regions with oppositely handed helices separated by a short disordered region. The encapsulating SWNT shows a commensurate ovoid distortion reflecting an unexpectedly strong interaction between the nanostructure and the SWNT.     

Self-assembled zinc/copper hydroxide carbonates with tunable hierarchical nanostructure

Here, we report a synthetic, polymer-mediated method for the self-assembly of zinc/copper hydroxide carbonate superstructures including 3D hierarchical sunflower-like, urchin-like, alga-like, and rotiform-like zinc hydroxide carbonate (ZHC) microstructures, and hierarchical copper hydroxide carbonate (CHC) microspheres with radiating nanoplates and nanorods. As a capping agent, poly(vinylpyrrolidone) (PVP) was found to play an important role in directing the growth and self-assembly of such unique structures. The crystal structure of the products and the resulting hierarchical superstructure morphology, as controlled by the molecular weight and concentration of PVP, were systematically investigated. A possible growth mechanism for the formation of hierarchical superstructures with different morphologies is also proposed.     

聚苯乙烯一维纳米阵列的图案化

采用紫外线光刻技术在阳极氧化铝模板(AAO)上生成预设图案,用物理浸润的方法在图案化的模板上生长聚苯乙烯,最后用NaOH和磷铬酸溶液分别溶解模板.采用扫描电子显微镜(SEM)和电子能谱(EDS)分析.结果表明,制备的图案是直径5μm的圆形组成,圆形图案中心之间距离是10μm,每个圆中长满一维纳米阵列,其纳米特性没有变化.     

ZnS nanostructure arrays: a developing material star

Semiconductor nanostructure arrays are of great scientific and technical interest because of the strong non-linear and electro-optic effects that occur due to carrier confinement in three dimensions. The use of such nanostructure arrays with tailored geometry, array density, and length-diameter-ratio as building blocks are expected to play a crucial role in future nanoscale devices. With the unique properties of a direct wide-bandgap semiconductor, such as the presence of polar surfaces, excellent transport properties, good thermal stability, and high electronic mobility, ZnS nanostructure arrays has been a developing material star. The research on ZnS nanostructure arrays has seen remarkable progress over the last five years due to the unique properties and important potential applications of nanostructure arrays, which are summarized here. Firstly, a survey of various methods to the synthesis of ZnS nanostructure arrays will be introduced. Next recent efforts on exploiting the unique properties and applications of ZnS nanostructure arrays are discussed. Potential future directions of this research field are also highlighted.     

Aligned 1D silicon nanostructure arrays by plasma etching

High-density aligned arrays made of one-dimensional (1D) silicon nanostructures, including nanocone, nanorod, and nanowire, are fabricated by plasma etching in a hot-filament chemical vapor deposition apparatus using the gas mixture of hydrogen, nitrogen and methane. The silicon nanocones are crystalline structure and have a uniform apex angle of about 22°. The cones can be coated in situ with an about 3 nm thick amorphous carbon film by increasing the methane concentration in source gases. With gradually decreasing the plasma intensity, the morphologies of the silicon nanostructures evolve along the nanocone–nanorod–nanowire route, and the nanowire becomes amorphous structure. The model for fabrication process of silicon nanostructures with different morphologies will also be suggested.     

紫外光刻法制备图案化聚合物纳米管/线阵列的研究

探讨了紫外光刻技术制备图案化聚合物纳米管/线阵列的方法,研究制备过程中的各种影响因素,并找到了最佳的实验条件。采用溶液浸润法,成功制备了不同图案的聚合物纳米结构阵列。溶液浓度为6%(质量分数),得到的是聚合物纳米管阵列;溶液浓度为10.0%(质量分数),得到的是聚合物纳米线阵列。     

Fiber template approach toward preparing one-dimensional silica nanostructure with rough surface

Silica nanofibers were grown on the surface of chitosan nanofibers used as templates by coating the surface with silica derived from the hydrolysis and condensation of tetraethoxysilane using ammonium hydroxide as a catalyst. This was followed by the decomposition of the chitosan template. The relationship between different processing factors (type of templates as well as amounts of catalyst and template) and the formation of silica nanofibers was examined. Varying the processing factors was found to be effective in controlling the morphology of the silica nanofibers. The use of chitosan nanofibers effectively led to the formation of one-dimensional silica nanofibers as the positively charged chitosan nanofibers promoted the deposition of the negatively charged silica nanoparticles through electrostatic attractive forces. Therefore, the chitosan nanofibers acted as good deposition sites for interacting with silica nanoparticles. Although a large amount of catalyst promoted the sol-gel reaction, the silica nanoparticles grew excessively in the solvent. Therefore, the surface structure of the prepared silica nanofibers could be controlled by varying the amount of chitosan template as this also varied the formation mechanism of the silica nanofibers. The resultant samples had a rough silica wall composed of densely assembled silica nanoparticles, with a high specific surface area (338 m²/g).     

Advances and perspectives on one-dimensional nanostructure electrode materials for potassium-ion batteries

Potassium-ion batteries (PIBs) have aroused considerable interest as a promising next-generation advanced large-scale energy storage system due to the abundant potassium resources and high safety. However, the K⁺ with large ionic radius brings restricted diffusion kinetics and severe volume expansion in electrode materials, resulting in inferior actual rate characteristics and rapid capacity fading. Designing electrode materials with one-dimensional (1D) nanostructure can effectively enhance various electrochemical properties due to the well-guided electron transfer pathways, short ionic diffusion channels and high specific surface areas. In this review, we summarize the recent research progress and achievements of 1D nanostructure electrode materials in PIBs, especially focusing on the development and application of cathode and anode materials. The nanostructure, synthetic methods, electrochemical performances and structure-performance correlation are discussed in detail. The advanced characterizations on the reaction mechanisms of 1D nanostructure electrode materials in PIBs are briefly summarized. Furthermore, the main future research directions of 1D nanostructure electrode materials are also predicted, hoping to accelerate their development into the practical PIBs market.     

Observation of high voltage resonances in one-dimensional arrays

Dynamic states in parallel one-dimensional arrays of small Josephson tunnel junctions are experimentally investigated in the presence of an external magnetic field H. In addition to conventional Fiske modes and flux-flow branches, the current-voltage characteristics exhibit a new type of resonances which appear in higher voltage regions as additional groups of resonant steps. These resonances can be explained in terms of a simple kinematic model, in the limit where the fluxon frequency is higher than the maximum linear wave frequency. The model is in good agreement with reported experiments.     

Characterization of one-dimensional capacitive micromachined ultrasonic immersion transducer arrays

We report on the characterization of 1D arrays of capacitive micromachined ultrasonic transducers (cMUT). A 275×5600 μm 1D CMUT array element is experimentally characterized, and the results are found to be in agreement with theoretical predictions. As a receiver, the transducer has a 0.28-fm/√Hz displacement sensitivity, and, as a transmitter, it produces 5 kPa/V of output pressure at the transducer surface at 3 MHz with a DC bias of 35 V. The transducer has more than 100% fractional bandwidth around 3 MHz, which makes it suitable for ultrasound imaging. The radiation pattern of isolated single elements, as well as those of array elements are measured, and two major sources of acoustical crosstalk are identified. A weakly dispersive non-leaky interface wave (Stoneley wave) is observed to be propagating at the silicon substrate-fluid interface at a speed close to the speed of sound in the fluid. This wave causes internal reflections, spurious resonance, and radiation from the edges of the silicon substrate. The large lateral component of the particle velocity generated by the membranes at the edge of the cMUT array elements is found to be the source of this interface wave. Lowest order Lamb waves in the silicon substrate are also found to contribute to the crosstalk between elements. These waves are excited at the edges of individual vibrating membranes, where they are anchored to the substrate, and result in a narrowing of the beam profile of the array elements. Several methods, such as trench isolation and wafer thinning, are proposed and implemented to modify the acoustical cross coupling between array elements     

Bio-inspired design of hierarchical FeP nanostructure arrays for the hydrogen evolution reaction

Hierarchical FeP nanoarray films composed of FeP nanopetals were successfully synthesized via a bio-inspired hydrothermal route followed by phosphorization. Glycerol, as a crystal growth modifier, plays a significant role in controlling the morphology and structure of the FeO(OH) precursor during the biomineralization process, while the following transfer and pseudomorphic transformation of the FeO(OH) film successfully give rise to the FeP array film. The as-prepared FeP film electrodes exhibit excellent hydrogen evolution reaction (HER) performance over a wide pH range. Theoretical calculations reveal that the mixed P/Fe termination in the FeP film is responsible for the high catalytic activity of the nanostructured electrodes. This new insight will promote further explorations of efficient metal phosphoride-based catalysts for the HER. More importantly, this study bridges the gap between biological and inorganic self-assembling nanosystems and may open up a new avenue for the preparation of functional nanostructures with application in energy devices.

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Self-assembled vapor-liquid-solid growth of aligned Cu-SiO2 core-shell nanocable arrays on Cu substrates

The Cu-SiO2 core-shell nanocable arrays on the Cu wafers have been synthesized via a simple thermal evaporation of the SiO powder. The morphology and structure of the as-synthesized Cu-SiO2 core-shell nanocables are characterized by using scanning electron microscopy, high-resolution transmission electron microscopy, and X-ray energy dispersive spectrometer. The growth of amorphous SiO2 shell follows a vapor-liquid-solid mechanism, and then molten metal Cu will be diffused into the SiO2 nanotubes, forming the Cu-SiO2 core-shell nanocable arrays. It is found that the aligned Cu-SiO2 core-shell nanocables prefer to grow along the grooves of the Cu substrate, and the density of the Cu-SiO2 core-shell nanocable arrays can be controlled by adjusting the growth temperature.     

Catalyst-free growth of pyramidal zinc sulfide nanostructure arrays on single walled carbon nanotubes

Uniform and ordered pyramidal zinc sulfide (ZnS) nanostructure arrays have been fabricated on the single walled carbon nanotube (SWNT) films by chemical vapor deposition without using any metal catalyst. Each ZnS pyramid has a 100 nm-sized base, a uniform length of 600 nm, and a sharp tip of 10 nm. The control of interspatial distance between ZnS nanostructures was achieved by creation of selective growth on the SWNTs in voids with the assistance of a close-packed silica particle monolayer as a template. Furthermore, this kind of morphology control of nanostructure arrays can play an important role for potential applications, such as high efficiency of field emission because of the strong correlation between shapes and functionalities of nanostructures.     

Self-assembled colloidal arrays as three-dimensional nanofluidic sieves for separation of biomolecules on microchips

We report on a biomolecular sieving system based on the use of ordered colloidal arrays to define the sieve structure within a microfluidic device. A facile microfluidic colloidal self-assembly strategy has been developed to create ordered, robust, three-dimensional nanofluidic sieves within microfluidic devices, with which fast separation of DNA and proteins of a wide size range was achieved. Compared to conventional colloidal deposition procedures, such as vertical deposition, this approach features much faster assembling speed, the absence of drying-caused cracks that may jeopardize the separation performance, and better flexibility to couple with current microfabrication techniques. The flexibility of pore size enabled by this methodology provides separation of biomolecules with a wide size distribution, ranging from proteins (20-200 kDa) to dsDNA (0.05-50 kbp). Under moderate electric fields, complete separation can be finished in minutes, with separation efficiency comparable to gel/polymer-filled or micro-/nanofabricated microsystems. To our knowledge, this is the first demonstration of size separation of biomolecules within self-assembled ordered colloidal lattices embedded within a microfluidic system.     

A facile chemical route to synthesize ZnO nanoarrays: one-dimensional nanowire arrays and two-dimensional porous nanosheet arrays

A facile chemical route is presented to synthesize ZnO nanoarrays including one-dimensional nanowire arrays and two-dimensional porous nanosheet arrays. Large-scale ZnO nanowire arrays with the length of 5 microm and aspect ratio of 42 were achieved by cyclic growth in aqueous solution. After being immerged in the zinc acetate solution for 24 h, the ZnO nanowire arrays converted to sheet-like Zn5(OH)8(CH3COO)2 arrays. Subsequently, the sheet-like Zn5(OH)8(CH3COO)2 arrays converted to the porous ZnO nanosheet arrays by annealing treatment. As demonstrated by the performance of dye-sensitized solar cells (DSC), the porous ZnO nanosheet arrays can improve the efficiency of DSC effectively. In addition, the synthesized ZnO nanoarrays have potential applications in solar cells, catalysis, sensors and other nanodevices.     

Platinum plasmonic nanostructure arrays for massively parallel single-molecule detection based on enhanced fluorescence measurements

We fabricated platinum bowtie nanostructure arrays producing fluorescence enhancement and evaluated their performance using two-photon photoluminescence and single-molecule fluorescence measurements. A comprehensive selection of suitable materials was explored by electromagnetic simulation and Pt was chosen as the plasmonic material for visible light excitation near 500 nm, which is preferable for multicolor dye-labeling applications like DNA sequencing. The observation of bright photoluminescence (λ = 500-600 nm) from each Pt nanostructure, induced by irradiation at 800 nm with a femtosecond laser pulse, clearly indicates that a highly enhanced local field is created near the Pt nanostructure. The attachment of a single dye molecule was attempted between the Pt triangles of each nanostructure by using selective immobilization chemistry. The fluorescence intensities of the single dye molecule localized on the nanostructures were measured. A highly enhanced fluorescence, which was increased by a factor of 30, was observed. The two-photon photoluminescence intensity and fluorescence intensity showed qualitatively consistent gap size dependence. However, the average fluorescence enhancement factor was rather repressed even in the nanostructure with the smallest gap size compared to the large growth of photoluminescence. The variation of the position of the dye molecule attached to the nanostructure may influence the wide distribution of the fluorescence enhancement factor and cause the rather small average value of the fluorescence enhancement factor.     

Effects of Lévy-type distribution on transverse localization in one-dimensional disordered waveguide arrays

In this paper, we analyse a one-dimensional disordered waveguide array in which the refractive indices of the waveguides are selected to be random numbers drawn from a Lévy-type distribution characterized by the exponent α. We study the effect of changing the exponent α on the transverse localization effect. It is shown that the quality of transverse localization is improved by decreasing the exponent α. Furthermore, we study this effect for several refractive index ranges. The design of disordered waveguide arrays in this way permits control of the degree of transverse localization.     

Self-assembled nanoscale ferroelectrics

Multifunctional ferroelectric materials offer a wide range of useful properties, from switchable polarization that can be applied in memory devices to piezoelectric and pyroelectric properties used in actuators, transducers and thermal sensors. At the nanometer scale, however, material properties are expected to be different from those in bulk. Fundamental problems such as the super-paraelectric limit, the influence of the free surface, and of interfacial and bulk defects on ferroelectric switching, etc., arise when scaling down ferroelectrics to nanometer sizes. In order to study these size effects, fabrication methods of high quality nanoscale ferroelectric crystals have to be developed. The present paper briefly reviews self-patterning and self-assembly fabrication methods, including chemical routes, morphological instability of ultrathin films, microemulsion, and self-assembly lift-off, employed up to the date to fabricate ferroelectric structures with lateral sizes in the range of few tens of nanometers.     

Self-assembled virus-membrane complexes

Anionic polyelectrolytes and cationic lipid membranes can self-assemble into lamellar structures ranging from alternating layers of membranes and polyelectrolytes to 'missing layer' superlattice structures. We show that these structural differences can be understood in terms of the surface-charge-density mismatch between the polyelectrolyte and membrane components by examining complexes between cationic membranes and highly charged M13 viruses, a system that allowed us to vary the polyelectrolyte diameter independently of the charge density. Such virus-membrane complexes have pore sizes that are about ten times larger in area than DNA-membrane complexes, and can be used to package and organize large functional molecules; correlated arrays of Ru(bpy)(3)(2+) macroionic dyes have been directly observed within the virus-membrane complexes using an electron-density reconstruction. These observations elucidate fundamental design rules for rational control of self-assembled polyelectrolyte-membrane structures, which have applications ranging from non-viral gene therapy to biomolecular templates for nanofabrication.