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The ZnO nanobelts were synthesized by a hydrothermal method. The XRD spectrum indicates that the sample is wurtzite (hexagonal) structured ZnO with lattice constants of a = 3.249 A , c = 5.206 A . SEM and TEM images show the nanobelts to have lengths of 10–20 μm, widths of 50–500 nm, thicknesses of about 30–60 nm, and growth direction of [0001]. Gas sensitivity experiments on ZnO nanobelts were carried out under different temperatures. The results indicated high sensitivities with an operating temperature of only 220 ∘C for the oxidative gas O2, and 305 ∘C for the gas N2. The mechanism of gas sensitive effects is analyzed in detail.

Research applications in biomedical science and technology usually require various portable, wearable, easy-to-use, and/or implantable devices that can interface with biological systems. Organic or hybrid organic–inorganic microelectronics and nanoelectronics have long been a possibility. However, these devices require a power source, such as electrochemical cells or piezoelectric, thermoelectric, and pyroelectric transducers, to generate or store the electrical energy created through chemical, mechanical, or thermal processes. Finding a suitable power source has remained a major challenge for many devices in bioengineering and medical fields. ZnO is a typical piezoelectric and pyroelectric inorganic semiconducting material used for electromechanical and thermoelectrical energy conversion. Nanostructures of ZnO, such as nanowires (NWs), nanobelts (NBs), nanotubes, nanorings, nanosprings, and nanohelices, have attracted extensive research interest because of their potential applications as nanoscale sensors and actuators. While most of the current applications focus on its semiconducting properties, only a few efforts have utilized the nanometerscale piezoelectric properties of ZnO. Using ZnO NW arrays grown on a single-crystal sapphire substrate, we have successfully converted mechanical energy into electrical energy at the nanoscale. A conductive atomic force microscopy (AFM) tip was used in contact mode to deflect the aligned NWs. The coupling of piezoelectric and semiconducting properties in ZnO creates a strain field and charge separation across the NWs as a result of their bending. The rectifying characteristic of the Schottky barrier formed between the metal tip and the NW leads to electrical current generation. This is the principle behind piezoelectric nanogenerators. The ceramic and semiconducting substrates used for growing ZnO NWs are hard and brittle and cannot be used in applications that require a foldable or flexible power source, such as implantable biosensors. In this Communication, by using ZnO NW arrays grown on a flexible plastic substrate, we demonstrate the first successful flexible power source built on conducting-polymer films. This approach has two specific advantages: it uses a cost-effective, large-scale, wet-chemistry strategy to grow ZnO NW arrays at temperatures lower than 80 °C, and the growth of aligned ZnO NW arrays can occur on a large assortment of flexible plastic substrates. The latter advantage could play an important role in the flexible and portable electronics industry. Various dimensions, shapes, and orientations of ZnO NWs and microwires on flexible plastic substrates have been shown to be capable of producing piezoelectric voltage output, giving a real advantage for energy harvesting using large-scale ZnO NW arrays. The voltage generated from a single NW can be as high as 50 mV, which is large enough to power many nanoscale devices. The ZnO NWs were grown in solution using a synthetic chemistry approach. Figure 1 shows a series of scanning electron microscopy (SEM) and transmission electron microscopy (TEM) images of typical ZnO NW arrays grown on a conductive plastic substrate. Figure 1a shows a low-resolution, topdown view of the densely aligned NW arrays. The aligned NWs have a uniform diameter of 200–300 nm and a hexagoC O M M U N IC A IO N

Heterogeneous catalysis is among the major solutions and processes for cost-effective and sustainable industrial application and processing. Search and discovery of highly efficient and stable heterogeneous catalysts represent an emergent frontier for overcoming the energy and environmental challenges we are facing. Fortunately, the growing nanotechnology offers one of the solutions through development of nanocatalysts with high activity, selectivity, and stability. Among various nanocatalysts, nano-array catalysts drew a great deal of attention not only owing to its model structure for exploring the origin of catalytic activity and mechanism but also because of its high collective catalytic activity and structural stability. In this chapter, we systematically reviewed recent progresses on the nano-array catalysts and their catalytic performance as oxidation catalysts, electrocatalysts, and photocatalysts.

A new method to directly synthesize single-crystalline CeO2 nanoparticles has been developed. The advantages of the method are rapid synthesis, at normal atmosphere, 100% productive ratio and low cost, with a great potential for scale-up. X-ray diffraction (XRD) spectra showed unusual peak width versus particle size, compared with Scherrer equation predictions. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution TEM (HRTEM), electron diffraction and ultraviolet (UV) absorption were used to examine the particle size and microstructure to find out the cause. As a result, ultrafine particles with a size less than 6 nm were found to be self-assembled into a 'coherent interface', so that a large group of particles behave like a large single particle in XRD.

The mechanical resonance behavior of a ZnO nanowire/nanorod at ambient condition has been studied under optical microscope by cutting its length using focused ion beam microscopy. Nanobalance using a ZnO nanowire as the cantilever has been demonstrated for measuring the mass in the order of pico-grams in working atmosphere (see optical microscopy images). The measurement limit of the balance is estimated to be ∼1 pg. The technique demonstrated here has potential for commercial applications in general laboratories, especially for measuring the mass of wet biological cells or species.

Rectifying diodes of single nanobelt/nanowire-based devices have been fabricated by aligning single ZnO nanobelts/nanowires across paired Au electrodes using dielectrophoresis. A current of 0.5 microA at 1.5 V forward bias has been received, and the diode can bear an applied voltage of up to 10 V. The ideality factor of the diode is approximately 3, and the on-to-off current ratio is as high as 2,000. The detailed IV characteristics of the Schottky diodes have been investigated at low temperatures. The formation of the Schottky diodes is suggested due to the asymmetric contacts formed in the dielectrophoresis aligning process.

The low melting point of Zn and the high melting point of ZnO, as well as their hexagonal crystal structures, present great advantages for designing and fabricating various metal/semiconductor core/shell nanostructures. By controlling the kinetics in the Zn and ZnO system, the lower-energy facets, and the oxidation rates of different surfaces, we can control the fabrication of Zn/ZnO core/shell single-crystal, polycrystalline, and mesoporous nanodisks, as well as a variety of ZnO nanotubes. The oxidation of a Zn nano-object leads to the formation of Zn/ZnO core/shell nanodisks. A lower oxidation temperature results in the formation of a single-crystal-like Zn/ZnO core/shell structure, while a higher oxidation temperature leads to the formation of textured and even polycrystalline nanostructures. A re-sublimation process of Zn in the core leaves a ZnO shell structure. This is an approach for synthesizing metal/semiconductor core/shell or composite nanostructures. This article offers a detailed description of the kinetics controlling the procedures, the nanostructures obtained, their morphological and crystal structures, and their formation mechanisms.

Polar surface induced asymmetric growth of single-side teethed ZnO nanocombs was attributed to the self-catalysis of the Zn-terminated (0 0 0 1) surface (Z.L. Wang, X.Y. Kong, J.M. Zuo, Phys. Rev. Lett. 91 (2003) 185502). In this Letter, nanocombs of ZnO with double-sided teeth have been observed. This symmetric growth of the fish-ribbon like teeth has been identified due to the existence of an inversion domain boundary along the ribbon, so that both side surfaces of the ribbon are terminated with the chemically active Zn-(0 0 0 1) plane. A model is also given about the formation of � 110� double-sided nanocombs based on the nucleus composed of multiply twinned pyramids. The data show that the Zn-terminated (0 0 0 1) surface is responsible for the formation of the teeth, while the oxygen-terminated (0 0 0 1) surface is chemically inactive and does not grow teeth. � 2005 Elsevier B.V. All rights reserved.

A previously unknown rigid helical structure of zinc oxide consisting of a superlattice-structured nanobelt was formed spontaneously in a vapor-solid growth process. Starting from a single-crystal stiff nanoribbon dominated by the c -plane polar surfaces, an abrupt structural transformation into the superlattice-structured nanobelt led to the formation of a uniform nanohelix due to a rigid lattice rotation or twisting. The nanohelix was made of two types of alternating and periodically distributed long crystal stripes, which were oriented with their c axes perpendicular to each other. The nanohelix terminated by transforming into a single-crystal nanobelt dominated by nonpolar ( \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(01{\bar{1}}0\) \end{document} ) surfaces. The nanohelix could be manipulated, and its elastic properties were measured, which suggests possible uses in electromechanically coupled sensors, transducers, and resonators.

In this Letter, three-dimensional (3D) interconnected networks of ZnO nanowires and nanorods are synthesized by a high temperature solid–vapor deposition process. The nanorods and nanowires have diameters of 20–100 nm and they grow along the c-axis. Due to the diverse orientation of the nanowires grown from a polycrystalline substrate, the networks are formed by a sintering process of the crossed nanowires during growth. The thickness of the multilayer nano-network could be as thick as � 30 lm. The sharp nanowire tips, the high degree of networking, and high surface area of these unique nanonetworks make them a potential candidate for field emission, ultra-sensitive gas sensing, catalysts and filtering. � 2005 Elsevier B.V. All rights reserved.

We demonstrate a novel approach for the large-scale, shape-controlled synthesis of one-dimensional (1D) corrugated nanoarrays of Pb(1-x)Mn(x)Se nanocrystals (0.002 < or = x < or = 0.008) through an in-situ self-assembly without using either capping polymer or ionic surfactant. The one-step-prepared 1D nanoarrays exhibit a well-defined morphology, single-crystal orientation, and clean surface without amorphous contamination. The average diameter of the 1D nanoarrays can be controlled and varied from

Zinc oxide, an important semiconducting and piezoelectric material, has three key characteristics. First, it is a semiconductor, with a direct bandgap of 3.37 eV and a large excitation binding energy (60 meV), and exhibits near-UV emission and transparent conductivity. Secondly, due to its non-centrosymmetric symmetry, it is piezoelectric, which is a key phenomenon in building electro-mechanical coupled sensors and transducers. Finally, ZnO is bio-safe and bio-compatible, and can be used for biomedical applications without coating. With these unique advantages, ZnO is one of the most important nanomaterials for integration with microsystems and biotechnology. Structurally, due to the three types of fastest growth directions— , , and —as well as the ±(0001) polar surfaces, a diverse group of ZnO nanostructures have been grown in our laboratory. These include nanocombs, nanosaws, nanosprings, nanorings, nanobows, and nanopropellers. This article reviews our recent progress in the synthesis and characterization of polar-surface-induced ZnO nanostructures, their growth mechanisms, and possible applications as sensors, transducers, and resonators. It is suggested that ZnO could be the next most important nanomaterial after carbon nanotubes.

Vapor-liquid-solid (VLS) is a well-established process in catalyst-guided growth of nanowires. The catalyst particle is generally believed to be in liquid state during growth, and it is the site for adsorbing incoming molecules; the crystalline structure of the catalyst may not have any influence on the structure of the grown one-dimensional nanostructures. In this paper, using tin particle guided growth of ZnO nanostructures as a model system, we show that the interfacial region of the tin particle with the ZnO nanowire/nanobelt could be ordered (or partially crystalline) during the VLS growth, although the local growth temperature is much higher than the melting point of tin, and the crystallographic lattice structure at the interface is important in defining the structural characteristics of the grown nanowires and nanobelts. The interface prefers to take the least lattice mismatch; thus, the crystalline orientation of the tin particle may determine the growth direction and the side surfaces of the nanowires and nanobelts. This result may have important impact on the understanding of the physical chemical process in the VLS growth.

Well-aligned ZnO nanorods with identical crystallographic orientation have been synthesized using a vapor transport deposition process. Orientation-ordered nanorods grow normal to the c planes of t...

The work function at the tips of individual ZnO nanobelts has been measured by an electromechanical resonant method using in-situ transmission electron microscopy. The work function of the ZnO nanobelts is ∼5.2 eV, which shows no significant dependence on the geometrical size. Using a ZnO nanobelt as a carrier beam, the work function of a single nanoparticle of a different material has also been measured.

We report the synthesis and characterization of nanowire−nanoribbon junction arrays of ZnO, which were grown by thermal evaporation of the mixture of ZnO and SnO2 powders at 1300 °C through a vapor−liquid−solid process. The Sn particles produced by the reduction of SnO2 act as the catalyst; the structure is formed due to a fast growth of ZnO nanowires along [0001] and the subsequent “epitaxial” radial growth of the ZnO nanoribbons along the six 〈0110〉 directions around the nanowire. The “liana” shape nanostructure could be a candidate for fabricating ultrahigh sensitive sensors.

The monolithic catalyst, namely the structured catalyst, is one of the important categories of catalysts used in various fields, especially in catalytic exhaust after-treatment. Despite its successful application in conventional wash-coated catalysts in both mobile and stationary catalytic converters, washcoat-based technologies are facing multi-fold challenges, including: (1) high Pt-group metals (PGM) material loading being required, driving the market prices; (2) less-than ideal distribution of washcoats in typically square-shaped channels associated with pressure drop sacrifice; and (3) far from clear correlations between macroscopic washcoat structures and their catalytic performance. To tackle these challenges, the well-defined nanostructure array (nano-array)-integrated structured catalysts which we invented and developed recently have been proven to be a promising class of cost-effective and efficient devices that may complement or substitute wash-coated catalysts. This new type of structured catalysts is composed of honeycomb-structured monoliths, whose channel surfaces are grown in situ with a nano-array forest made of traditional binary transition metal oxide support such as Al2O3, CeO2, Co3O4, MnO2, TiO2, and ZnO, or newer support materials including perovskite-type ABO3 structures, for example LaMnO3, LaCoO3, LaNiO, and LaFeO3. The integration strategy parts from the traditional washcoat technique. Instead, an in situ nanomaterial assembly method is utilized, such as a hydro (solva-) thermal synthesis approach, in order to create sound structure robustness, and increase ease and complex-shaped substrate adaptability. Specifically, the critical fabrication procedures for nano-array structured catalysts include deposition of seeding layer, in situ growth of nano-array, and loading of catalytic materials. The generic methodology utilization in both the magnetic stirring batch process and continuous flow reactor synthesis offers the nano-array catalysts with great potential to be scaled up readily and cost-effectively. The tunability of the structure and catalytic performance could be achieved through morphology and geometry adjustment and guest atoms and defect manipulation, as well as composite nano-array catalyst manufacture. Excellent stabilities under various conditions were also present compared to conventional wash-coated catalysts.

Using a combination of vapor and solution phase deposition methods, scalable heterostrutured nanowire arrays have been successfully fabricated composed of metal oxide nanowire cores ~100-300 nm in diameter, ~1-30 nm thick shells of perovskite, metal oxide and noble metal nanoparticles on ceramic substrates. The nanowire structure features tuned composition, density, geometry, and dimensions through varying the deposition temperature, concentration, pH, substrate temperature, time, etc.. Multi-mode chemical sensing platform has been achieved at both room temperature and elevated temperature to include photocurrent, electrical resistance and electrochemical impedance modes. Depending on the selections of comprising materials, dimensions and post-treatment processes, trace amount decoration of perovskite, metal oxide and noble metal nanoparticle shells may enable formations of catalytic filters, sensitizers and hetero-junctions that can drastically enhance nanosensor performance in both oxidative and reductive gas atmospheres. Specifically the materials-synergy effect in metal oxide/perovskite, and metal oxide/noble metal nanowire array sensors are discussed toward sensing of various gaseous species such as O2, CO, HCs, SOx, and NOx. Toward mixture gas conditions, this new type of multi-mode nanowire array sensors allows selective and sensitive detection of multiple chemical species in a single-device platform.

Monitoring and control of the gaseous combustion process are critically important in advanced energy systems such as power plants, gas turbines, and automotive engines. However, very limited gas sensing solutions are available in the market for such applications due to the inherent high temperature of the combustion gaseous atmosphere. In this study, we fabricated and demonstrated high-performance metal oxide based nanorod array sensors assisted with ultra-violet (UV) illumination for in situ and real-time high-temperature gas detection. Without UV-illumination, it was found that surface decoration of either 5 nm LSFO or 1 nm Pt nanoparticles can enhance the sensitivity over CO at 500 °C by an order of magnitude. Under the 254 nm UV illumination, the CO gas-sensing performance of Ga2O3-based nanorod array sensors was further enhanced with the sensitivity boosted by 125% and the response time reduced by 30% for the La0.8Sr0.2FeO3(LSFO)-decorated sample. The UV-enhanced detection of CO might be due to the i...

Helical nanomaterials represent an emerging group of nanostructures with unique spiral geometry as well as multiple functionalities owing to their enriched physical and chemical properties. With the novel properties enabled by their nanoscale dimension and unique geometry, the helical nanostructures may open opportunities to develop our understanding of new physics, chemistry and biology, and enable new nanodevice design and fabrication. This review article presents a comprehensive and in-depth overview of the latest progress in helical nanostructures synthesis, properties and potential applications. Specific attention is concentrated on the crystal growth theory for helical nanostructures, summary of the helical nanomaterials obtained so far, and their fabrication techniques as well as typical physical properties that can be potentially utilized for various applications.

A series of large scale Mx Co3-x O4 (M=Co, Ni, Zn) nanoarray catalysts have been cost-effectively integrated onto large commercial cordierite monolithic substrates to greatly enhance the catalyst utilization efficiency. The monolithically integrated spinel nanoarrays exhibit tunable catalytic performance (as revealed by spectroscopy characterization and parallel first-principles calculations) toward low-temperature CO and CH4 oxidation by selective cation occupancy and concentration, which lead to controlled adsorption-desorption behavior and surface defect population. This provides a feasible approach for scalable fabrication and rational manipulation of metal oxide nanoarray catalysts applicable at low temperatures for various catalytic reactions.

This review presents a comprehensive overview of the hierarchical nanostructured materials with either geometry or composition complexity in environmental applications. The hierarchical nanostructures offer advantages of high surface area, synergistic interactions, and multiple functionalities toward water remediation, biosensing, environmental gas sensing and monitoring as well as catalytic gas treatment. Recent advances in synthetic strategies for various hierarchical morphologies such as hollow spheres and urchin-shaped architectures have been reviewed. In addition to the chemical synthesis, the physical mechanisms associated with the materials design and device fabrication have been discussed for each specific application. The development and application of hierarchical complex perovskite oxide nanostructures have also been introduced in photocatalytic water remediation, gas sensing, and catalytic converter. Hierarchical nanostructures will open up many possibilities for materials design and device fabrication in environmental chemistry and technology.

This final report to the Department of Energy (DOE) and National Energy Technology Laboratory (NETL) for DE-EE0000210 covers the period from October 1, 2009 to July 31, 2013. Under this project, DOE awarded UConn about $1,248,242 to conduct the research and development on a new class of 3D composite nanostructure based catalysts for lean NOx emission control. Much of the material presented here has already been submitted to DOE/NETL in quarterly technical reports. In this project, through a scalable solution process, we have successfully fabricated a new class of catalytic reactors, i.e., the composite nanostructure array (nano-array) based catalytic converters. These nanocatalysts, distinct from traditional powder washcoat based catalytic converters, directly integrate monolithic substrates together with nanostructures with well-defined size and shape during the scalable hydrothermal process. The new monolithic nanocatalysts are demonstrated to be able to save raw materials including Pt-group metals and support metal oxides by an order of magnitude, while perform well at various oxidation (e.g., CO oxidation and NO oxidation) and reduction reactions (H{sub 2} reduction of NOx) involved in the lean NOx emissions. The size, shape and arrangement of the composite nanostructures within the monolithic substrates are found to be the key in enabling the drastically reduced materials usage while maintaining the good catalytic reactivity in the enabled devices. The further understanding of the reaction kinetics associated with the unique mass transport and surface chemistry behind is needed for further optimizing the design and fabrication of good nanostructure array based catalytic converters. On the other hand, the high temperature stability, hydrothermal aging stability, as well as S-poisoning resistance have been investigated in this project on the nanocatalysts, which revealed promising results toward good chemical and mechanical robustness, as well as S-poisoning resistance. Further investigation is needed for unraveling the understanding, design and selection principles of this new class of nanostructure based monolithic catalysts.

This final report to the Department of Energy/National Energy Technology Laboratory for DE-FE0000870 covers the period from 2009 to June, 2013 and summarizes the main research accomplishments, which can be divided in sensing materials innovation, bimodular sensor demonstration, and new understanding and discoveries. As a matter of fact, we have successfully completed all the project tasks in June 1, 2013, and presented the final project review presentation on the 9th of July, 2013. Specifically, the major accomplishments achieved in this project include: 1) Successful development of a new class of high temperature stable gas sensor nanomaterials based on composite nano-array strategy in a 3D or 2D fashion using metal oxides and perovskite nanostructures. 2) Successful demonstration of bimodular nanosensors using 2D nanofibrous film and 3D composite nanowire arrays using electrical resistance mode and electrochemical electromotive force mode. 3) Series of new discoveries and understandings based on the new composite nanostructure platform toward enhancing nanosensor performance in terms of stability, selectivity, sensitivity and mass flux sensing. In this report, we highlight some results toward these accomplishments.

Polar surface dominated ZnO nanopropeller arrays were synthesized by a two-step high temperature solid-vapor deposition process. The axis of the nanopropellers is a straight nanowire along the c axis and enclosed by {2110} surfaces, which grew first; the sixfold symmetric nanoblades are later formed along the crystallographic equivalent a axes (〈2110〉) perpendicular to the nanowire; and the array is formed by epitaxial growth of nanoblades on the nanowire. The top surface of the nanoblade is the Zn terminated +c plane, showing surface steps and possible secondary growth of nanowires due to higher self-catalytic activity, while the back surface is the oxygen-terminated −c plane, which is smooth and inert.

Zinc oxide (ZnO) nanobelts synthesized by thermal evaporation have been ion implanted with 30 keV Mn+ ions. Both transmission electron microscopy and photoluminescence investigations show highly defective material directly after the implantation process. Upon annealing to 800 °C, the implanted Mn remains in the ZnO nanobelts and the matrix recovers both in structure and luminescence. The produced high-quality ZnO:Mn nanobelts are potentially useful for spintronics.

The increasing human demand for clean and renewable energy and a cleaner environment has stimulated various materials related research and development for efficient solar energy conversion and utilization, photocatalytic environmental remediation, and photoassisted selective conversion of organic compounds. Among the various candidate solutions to improving the efficiency of these processes, semiconductor nanowire (NW) and nanorod (NR) array structures have been offering a unique tool box combining desirable characteristics in structure, function, and applicability. Efficient photocatalytic energy conversion requires excellent light absorption, readily charge separation, transport, and collection, as well as fast kinetics of interfacial reactions and mass transport of reactants. The long axis of the NW enables adequate light absorption, while the radical axis provides short electron–hole separation distance. Additionally, the NW arrays have relatively high surface area to facilitate interfacial kinetics while their open pore structure allows good mass transport properties. This study reviews the current status of research on NW and NR array structures of some most popular semiconducting materials for photocatalytic energy conversion and utilization including photocatalytic water splitting and CO2 reduction/fixation, dye/quantum dot sensitized solar cells, and other photoassisted reactive applications such as pollutant degradation, selective conversion of organic compounds, and biological disinfection.

The mechanical resonance of a single ZnO nanobelt, induced by an alternative electric field, was studied by in situ transmission electron microscopy. Due to the rectangular cross section of the nanobelt, two fundamental resonance modes have been observed corresponding to two orthogonal transverse vibration directions, showing the versatile applications of nanobelts as nanocantilevers and nanoresonators. The bending modulus of the ZnO nanobelts was measured to be ∼52 GPa and the damping time constant of the resonance in a vacuum of 5×10−8 Torr was ∼1.2 ms and quality factor Q=500.

Self-assembled composite nanostructures integrate various basic nano-elements such as nanoparticles, nanofilms and nanowires toward realizing multifunctional characteristics, which promises an important route with potentially high reward for the fast evolving nanoscience and nanotechnology. A broad array of hierarchical metal oxide based nanostructures have been designed and fabricated in our research group, involving semiconductor metal oxides, ternary functional oxides such as perovskites and spinels and quaternary dielectric hydroxyl metal oxides with diverse applications in efficient energy harvesting/saving/utilization, environmental protection/control, chemical sensing and thus impacting major grand challenges in the area of materials and nanotechnology. Two of our latest research activities have been highlighted specifically in semiconductor oxide alloy nanowires and metal oxide/perovskite composite nanowires, which could impact the application sectors in ultraviolet/blue lighting, visible solar absorption, vehicle and industry emission control, chemical sensing and control for vehicle combustors and power plants.

In nature, three-dimensional (3D) helical structure is the most fundamental structural configuration of DNAs, proteins, and bio-functional groups, such as cytoplasm and periplasm [1]. Synthetically, many 3D helical structures with micro- and nano-features have been fabricated from a number of inorganic materials. Typical examples include ZnO nanohelices/nanosprings [2–7], SiO2 nanohelices [8, 9], carbon-based nano-/microcoils [10–12], and some other nanohelices based on III–V and II–VI semiconductors [13–16]. Because of their nanoscale 3D spiral symmetric geometry, as well as unique mechanical, electrical, and electromagnetic properties, helically nanostructured materials are attracting considerable attention and have potential applications in electronics, optics, nano- and micro-electromechanical system (NEMS and MEMS), energy and environment-related technologies, and biomedicine.

Large scale dendritic MgO/ZnO composite nanowire arrays have been successfully synthesized on Si substrates using a two-step sequential hydrothermal synthesis at low temperature for the first time. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), scanning transmission electron microscopy (STEM), and x-ray photoelectron spectroscopy (XPS) were systematically carried out to confirm and elaborate the potentially localized Mg surface alloying process into the ZnO nanowire arrays. Both room temperature and low temperature (40 K) photoluminescence results revealed an enhanced and blue-shifted near-band-edge (NBE) ultraviolet (UV) emission for the MgO/ZnO nanowires compared to those of the pure ZnO nanowire arrays, indicating the success of Mg alloying into ZnO nanowires. This enhancement might be due to the 155 degrees C hydrothermal process and the amorphous MgO layer in the MgO/ZnO nanowires. The specific template of densely packed ZnO nanowire arrays was suggested to be instrumental in enabling this type of MgO/ZnO composite nanowire growth.

Superlattice-structured ZnO nanohelix is a structure that is made of a coiling nanobelt, which is composed of ZnO nanostripes oriented alternatively in two different orientations (Science 2005, 309, 1700). The nanostripes run almost in parallel to the nanobelt direction but at an offset angle of approximately 5 degrees . We have measured the transport properties of a nanohelix and found its abnormal nonlinear characteristic. In comparison to the Ohmic transport property of a single crystal ZnO nanobelt measured under the same experimental conditions, the symmetric "Schottky-type" I-V property of the nanohelix is suggested due to nanostripe boundaries and surfaces, where built-in periodic back-to-back energy barriers might occur across the nanostripe interfaces as a result of polar charges and interface-strain-induced piezoelectric effect. The effective potential barrier across the nanostripe boundary is estimated to be approximately 24 meV. With the increasing of bias voltage, electrons can effectively tunnel through and thermionic emission across nanostripe boundaries, leading to a fast increase in transport current. It is suggested that the ZnO nanohelix could form a new type of band structure modulated superlattice for fabricating novel electronic devices.

In this Paper we present growth and characterization of ZnO nanowires on wideband gap substrates, such as SiC and GaN. Experimental results on the ZnO nanowires grown on p-SiC and p-GaN are presented with growth morphology, structure analysis, and dimensionality control. We also present experimental results on individual nanowires such as I-V measurements and UV sensitivity measurements with use of polymer coating on ZnO nanowires. The ZnO nanowires can be used for a variety of nanoscale optical and electronics applications.

In this Paper we present growth and characterization of ZnO nanowires on a variety of substrates, such as Silicon and SiC. Experimental results on the ZnO nanowires grown on Si and SiC are presented with growth morphology, structure analysis, and dimensionality control. The ZnO nanowires can be used for a variety of nanoscale optical and electronics sensors.

A superelasticity (shape memory) behavior has been discovered for the superlattice-structured ZnO nanohelices. By in situ manipulation using a nanoprobe, the nanohelix could elastically recover its shape after an extremely large axial stretching to a degree close to the theoretical limit, while suffering little residual plastic deformation. As a result, its spring constant can be increased continuously for up to 300-800%. A shape memory/recovery of the nanohelix was observed after subjecting to a buckling deformation. The superelastic deformation and fracture process of a nanohelix have been studied by transversely compressing under an AFM tip. A two-step mechanism is suggested for explaining the measured force-displacement curve. It is suggested that the small thickness and the superlattice structure of the nanohelix might be the keys for the observed superelasticity. The ZnO nanohelices may be a new category of shape-memory ceramic nanostructures, which could be of great interest for investigating nanoscale fracture process and application in MEMS and NEMS. The elastic recovery of the nanohelix after extremely large deformation makes it a potential structure for nanoscale elastic energy storage.

We report a new structure, mesoporous structured polyhedral drum and spherical cages and shells formed by textured self-assembly of ZnO nanocrystals, which are made by a novel self-assembly process during epitaxial surface oxidation. The cages/shells exhibit unique geometrical shapes, and their walls are composed of mesoporous and textured ZnO nanocrystals. The structures of the cages and shells are studied, and a growth mechanism is proposed to be a process following solidification of the Zn liquid droplets, surface oxidation, and sublimation.