Ultrahigh Responsivity UV Photodetector Based on Cu Nanostructure/ZnO QD Hybrid Architectures

Strong near‐surface electromagnetic field formed by collective oscillation of electrons on Cu nanostructure a shows a strong dependence on geometry, offering a promising approach to boost the light absorption of ZnO photoactive layers with enhanced plasmon scattering. Here, a facile way to fabricate UV photodetectors with tunable configuration of the self‐assembled Cu nanostructures on ZnO thin films is reported. The incident lights are effectively confined in ZnO photoactive layers with the existence of the uplayer Cu nanostructures, and the interdiffusion of Cu atoms during fabrication of the Cu nanostructures can improve the carrier transfer in ZnO thin films. The optical properties of the hybrid architectures are successfully tailored over a control of the geometric evolution of the Cu nanostructures, resulting in significantly enhanced photocurrent and responsivity of 2.26 mA and 234 A W^?1 under a UV light illumination of 0.62 mW cm^?2 at 10 V, respectively. The photodetectors also exhibit excellent reproducibility, stability, and UV–visible rejection ratio (R_{370 nm}/R_{500 nm}) of ≈370, offering an approach of high‐performance UV photodetectors for practical applications.     

Rapid chemical synthesis and optical properties of ZnO ellipsoidal nanostructures

ZnO ellipsoidal nanostructures were rapidly synthesized using a chemical synthesis method at 90 °C without the assistance of aging procedure, calcination, sonication, microwave, laser or any organic additives. The effects of pH values and Zn²⁺ concentration on the morphologies of ZnO nanostructures were investigated. The instantaneous underdeveloped ZnO nanostructures were successfully obtained by using the electrophoretic deposition (EPD). Based on the experimental results, growth mechanism of ellipsoidal ZnO nanostructures was proposed. The ellipsoidal nanostructures are self-assembled by the oriented-attachment growth of primary nanoparticles, involving the end-to-end oriented-attachment along the major axis and the side-by-side oriented-attachment along the minor axis. Two half-ellipsoids of the ZnO nanostructures germinate in sequence. The UV–vis absorption and photoluminescence of the ellipsoidal nanostructures was also studied. This work presents a simple and ultra-fast route for large-scale fabrication of ZnO ellipsoidal nanostructures.     

Controlled synthesis of ZnO branched nanorod arrays by hierarchical solution growth and application in dye-sensitized solar cells

We demonstrate the controlled synthesis of ZnO branched nanorod arrays on fluorine-doped SnO₂-coated glass substrates by the hierarchical solution growth method. In the secondary growth, the concentration of Zn(NO₃)₂/hexamethylenetetramine plays an important role in controlling the morphology of the branched nanorod arrays, besides that of diaminopropane used as a structure-directing agent to induce the growth of branches. The population density and morphology of the branched nanorod arrays depend on those of the nanorod arrays obtained from the primary growth, which can be modulated though the concentration of Zn(NO₃)₂/hexamethylenetetramine in the primary growth solution. The dye-sensitized ZnO branched nanorod arrays exhibit much stronger optical absorption as compared with its corresponding primary nanorod arrays, suggesting that the addition of the branches improves light harvesting. The dye-sensitized solar cell based on the optimized ZnO branched nanorod array reaches a conversion efficiency of 1.66% under the light radiation of 1000 W/m². The branched nanorod arrays can also be applied in other application fields of ZnO.     

Heteroepitaxial growth of ZnO nanosheet bands on ZnCo2O4 submicron rods toward high-performance Li ion battery electrodes

We report the direct synthesis of ZnCo₂O₄ and ZnO/ZnCo₂O₄ submicron rod arrays grown on Ni foil current collectors via an ammonia-evaporation-induced method by controlling the ratio of Zn to Co. These three-dimensional (3D) hierarchical self-supported nanostructures are composed of one-dimensional (1D) ZnCo₂O₄ rods and two-dimensional (2D) ZnO nanosheet bands perpendicular to the axis of the each ZnCo₂O₄ rod. We carefully deal with the heteroepitaxial growth mechanisms of hexagonal ZnO nanosheets from a crystallographic point of view. Furthermore, we demonstrate the ability of these high-surface-area ZnO/ZnCo₂O₄ heterostructured rods to enable improved electrolyte permeability and Li ion transfer, thereby enhancing their Li storage capability (～900 mA·h·g^?1 at a rate of 45 mA·h·g^?1) for Li ion battery electrodes.      

Dendritic and epitaxial growths of ZnO particle-rod and rod-rod nanostructures with quasi-one-dimensional and two-dimensional configurations

Quasi-one-dimensional and two-dimensional ZnO nanostructures have been fabricated through thermal evaporation approach. The microstructures of the ZnO nanostructures have been studied using scanning electron microscopy and high-resolution electron microscopy. Quasi-one-dimensional ZnO nanostructures are formed by dendritic growths of ZnO nanoparticles from the stem nanorods surfaces, forming particle-rod nanostructures. While epitaxial growths of branch nanorods from the stem nanorods configure two-dimensional ZnO nanostructures. The epitaxial growth orientation relationship can be described as [2? 110]_R1 || [2? 110]_R2 and (0001) _R1 || (011?0)_R2. The growth mechanism of the quasi-one-dimensional and two-dimensional ZnO nanostructures has been discussed.     

In Situ Synthesis of CuO and Cu Nanostructures with Promising Electrochemical and Wettability Properties

A strategy is presented for the in situ synthesis of single crystalline CuO nanorods and 3D CuO nanostructures, ultra‐long Cu nanowires and Cu nanoparticles at relatively low temperature onto various substrates (Si, SiO₂, ITO, FTO, porous nickel, carbon cotton, etc.) by one‐step thermal heating of copper foam in static air and inert gas, respectively. The density, particle sizes and morphologies of the synthesized nanostructures can be effectively controlled by simply tailoring the experimental parameters. A compressive stress based and subsequent structural rearrangements mechanism is proposed to explain the formation of the nanostructures. The as‐prepared CuO nanostructures demonstrate promising electrochemical properties as the anode materials in lithium‐ion batteries and also reversible wettability. Moreover, this strategy can be used to conveniently integrate these nanostructures with other nanostructures (ZnO nanorods, Co₃O₄ nanowires and nanowalls, TiO₂ nanotubes, and Si nanowires) to achieve various hybrid hierarchical (CuO‐ZnO, CuO‐Co₃O₄, CuO‐TiO₂, CuO‐Si) nanocomposites with promising properties. This strategy has the potential to provide the nano society with a general way to achieve a variety of nanostructures.     

Structured ZnO-based contacts deposited by non-reactive rf magnetron sputtering on ultra-thin SiO2/Si through a stencil mask

In this paper, we study the localized deposition of ZnO micro and nanostructures deposited by non-reactive rf-magnetron sputtering through a stencil mask on ultra-thin (10 nm) SiO₂ layers containing a single plane of silicon nanocrystals (NCs), synthetized by ultra-low energy ion implantation followed by thermal annealing. The localized ZnO-deposited areas are reproducing the exact stencil mask patterns. A resistivity of around 5 × 10^− 3 Ω cm is measured on ZnO layer. The as-deposited ZnO material is 97% transparent above the wavelength at 400 nm. ZnO nanostructures can thus be used as transparent electrodes for Si NCs embedded in the gate-oxide of MOS devices.     

Controlled synthesis and photoluminescence properties of hierarchical BaXO4 (X = Mo, W) nanostructures at room temperature

Controlled synthesis of hierarchical Barium molybdate (BaMoO₄) nanostructures with different morphologies, such as peanut-like, cube-like and flower-like, was successfully achieved in aqueous solution at room temperature. The obtained products were characterized by a scanning electron microscope (SEM) and an X-ray power diffractometer (XRD). The morphologies of the obtained products were found to be greatly dependent on reaction time, EDTA concentration and the [Ba²⁺]/[MoO₄²⁻] ratio. This controllable method could be readily extended to produce hierarchical Barium tungstate (BaWO₄) nanostructures with peanut-like, dumbbell-like, sphere-like and flower-like morphologies. The photoluminescence (PL) properties of the obtained BaMoO₄ and BaWO₄ nanostructures exhibited strong dependence on the morphologies and sizes, respectively.     

Morphological syntheses of ZnO nanostructures under microwave irradiation

ZnO nanostructures with flower-, rod-, and flake-like morphologies have been controllably synthesized using Zn(acac)₂·H₂O (acac = acetylacetonate) as a single-source precursor through a facile and fast microwave-assisted method. The morphologies of ZnO nanostructures can be systematically adjusted by using various surfactants. The ZnO products are characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and selected area electron diffraction. The results show that all ZnO nanostructures are of single-crystalline nature with hexagonal wurtzite structure. The possible formation mechanism for these ZnO nanostructures is proposed and their photoluminescence properties are also investigated.     

Controllable fabrication of various ZnO micro/nanostructures from a wire-like Zn-EG-AC precursor via a facile solution-based route

In this paper, ZnO particles with various morphologies were prepared though a facile solution-based route. The complexes Zn-EG-AC (EG: ethylene glycol; AC: CH₃COO⁻ groups) obtained by reaction of anhydrous zinc acetate and EG were used as precursors. It is found that the precursor could transform into ZnO in water with no need of assistant of additional alkali as it is sensitive to water. At the same time, it is well dispersed in reaction medium (water and ethanol). Experimental results showed that ZnO particles with various morphologies, such as the hexagonal rings, the hexagonal plates, the tubes, the prisms, and some interesting hierarchical structures, could be obtained by controlling hydrolysis of precursor in water and water/ethanol medium through finely tuning the experimental parameters. The success of shape-controllable fabrication was related intimately with the Zn-EG-AC precursor used in our synthesis.     

Hierarchical nanostructures of ZnO obtained by spray pyrolysis

A two step spray pyrolysis deposition method was applied in order to grow ZnO nanorod core/ZnO shell hierarchical nanostructures with various surface morphologies, such as a highly organised platelet network on the side facets of the ZnO rod and bundles of nanoneedles on the top plane of the rod. First, well-shaped ZnO nanorods with lengths of ca. 1 μm and average diameters of 150–300 nm were deposited from zinc chloride (ZnCl₂·2H₂O) aqueous solutions onto TCO/glass substrates. Then, zinc acetate (Zn(CH₃COO)₂·2H₂O) solution was pulverised over the surface of the sprayed ZnO nanorods at a growth temperature of approximately 330 °C within 6–10 min. The obtained structures were characterised by high resolution SEM, UV–VIS and XRD. To estimate the surface areas and photocatalytic ability of the bare rods and hierarchical structures, their adsorption ability and activity of photocatalytic oxidation of doxycycline were measured. It was found that the surface area of hierarchical structures comprised of a network of platelets is at least 4 times larger than that of a bare rod. The structural and morphological properties of sprayed hierarchical structures largely depend on the spraying rate of the zinc acetate solution and on the ZnO nanorod top plane shape.     

Hydrothermal growth of symmetrical ZnO nanorod arrays on nanosheets for gas sensing applications

The hierarchical ZnO nanostructures with 2-fold symmetrical nanorod arrays on zinc aluminum carbonate (ZnAl-CO₃) nanosheets have been successfully synthesized through a two-step hydrothermal process. The primary nanosheets, which serve as the lattice-matched substrate for the self-assembly nanorod arrays at the second-step of the hydrothermal route, have been synthesized by using a template of anodic aluminum oxide (AAO). The as-prepared samples were characterized by XRD, FESEM, TEM and SAED. The nanorods have a diameter of about 100 nm and a length of about 2 μm. A growth mechanism was proposed according to the experimental results. The gas sensor fabricated from ZnO nanorod arrays showed a high sensitivity to ethanol at 230°C. In addition, the response mechanism of the sensors has also been discussed according to the transient response of the gas sensors.     

Morphology-tuned growth of ZnO microstructures

Morphology-tuned ZnO microcrystals can be prepared by oxidizing zinc metal substrates in aqueous solution using hydrothermal technique. Some typical ZnO growth morphologies such as nanorod superstructures, nanorod arrays, microspheres, hierarchical nanostructures, and split crystals have been chemically fabricated. These microscopic shapes can be finely controlled by selecting Zn(NO₃)₂ concentration and solvent. A conceptual model was proposed to explain the formation of the as-prepared ZnO structures by selecting proper kinetic environments. This one-step, wet-chemical approach is controllable and reproducible, which can be conveniently transferred to industrial applications.     

Chemical vapor deposition-based growth of aligned ZnO nanowires on polycrystalline Zn<Subscript>2</Subscript>GeO<Subscript>4</Subscript>:Mn substrates

ZnO nanowires have been grown on polycrystalline Zn₂GeO₄:Mn substrates for the first time using a chemical vapor deposition method. Both Zn and ZnO sources were used to supply Zn vapor in the growth process of ZnO nanowires. The Zn₂GeO₄:Mn substrates were prepared using solid-state ceramic synthesis methods, and average grain sizes of ~1 μm were achieved. The nanowires of diameters in the range of 100–200 nm and length of ~30 μm were observed. In addition to nanowires, other morphologies of ZnO nanostructures, such as ZnO tetrapods, were observed when Zn powder was used as the source for the CVD growth. The results reveal that polycrystalline substrates are also promising as novel alternative substrates for growth of ZnO nanostructures. The as-synthesized ZnO nanowire/Zn₂GeO₄:Mn composites are being developed for future electroluminescent devices.     

Synthetics of ZnO nanostructures by thermal oxidation in water vapor containing environments

Metallic Zn films deposited on glass were wet or dry oxidized at 390 °C in pure N₂ or O₂ to understand the effects of water vapor in different oxygen partial pressure on growth of ZnO nanostructure during thermal oxidation. As-prepared ZnO oxides were characterized by a scanning electron microscope (SEM), an X-ray diffractometer (XRD), and a transmission electron microscope (TEM). Optical and electric properties of these ZnO films were characterized by photoluminescence (PL) and resistance measurements, respectively. It was found that the oxygen partial pressure and water vapor of environment significantly affect the morphologies of ZnO nanostructures. Decreasing oxygen partial pressure in dry oxidation can enhance a green light peak at 500 nm on PL spectra arising from defect-related emission and reduce the resistivity of the oxide films. High H₂O^(g)/O₂ ratio in wet oxidation will significantly increase the intensity of a green light peak and reduce the resistivity of the oxide films. The effect of oxygen partial pressure and H₂O^(g)/O₂ ratio on the PL spectra and resistivity of ZnO films are explained by the theory of defects equilibrium during oxidation.     

In situ calorimetric investigation of ZnO transformation from flower-like nanostructures to microrod

The evolution of Zn₄₍OH₎²⁻$\text{Zn}{{(\text{OH})}_4}^{2-}$ solution during hydrothermal processing was studied using in situ calorimetry and the solid products were characterized by X-ray diffraction, scanning electron microscopy. It was shown that the formation of flower-like ZnO nanostructures exhibited first endothermic and then exothermic processes, of which the associated heat effect was measured as being −50.45 ± 0.01 J mol⁻¹. Flower-like ZnO nanostructures and ZnO microrod may be selectively formed simply based on the hydrothermal reaction temperatures. The mechanism for the flower-like ZnO nanostructures and ZnO microrod has been suggested.     

Facile hydrothermal synthesis and optical properties of flower-like CeO<Subscript>2</Subscript> composed of numerous porous nanorods

Flower-like CeO₂ hierarchical structures have been successfully synthesized by a facile template-free hydrothermal method using ethanol/water mixtures as solvent. X-ray diffraction shown that the synthesized flower-like CeO₂ nanostructures exhibited a fluorite cubic structure. It was found that the flower-like CeO₂ hierarchical structures with a diameter of 2–5 µm are composed of numerous porous nanorods as the petals with an average diameter of about 15 nm, which connect at one end and diverge at the other end to form an open hierarchical architecture. The synthesized CeO₂ samples show excellent room temperature optical properties, which is likely associated with Ce³⁺ ions and oxygen vacancies in the samples as supported by the XPS and Raman scattering data.     

Shape and size-controlled fabrication of ZnO nanostructures using novel templates

A simple wet chemical method was developed to control the size and shape of the Zinc oxide (ZnO) nanostructures in the presence of new, efficient, and low-cost templates like ameline, sorbitol, and polyethylene glycol (PEG, M_w = 200) at low temperature within a few minutes. Nanorods and nanoparticles have been achieved through applying these templates and tuning other growth parameters. The products were characterised by X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The effect of the growth parameters such as template, Zn²⁺ source/Template ratio, pH, reaction time, and temperature on the growth and morphology of ZnO nanostructures have been investigated in detail. The results revealed that template has an important effect on the morphology and size of the ZnO nanostructures. Also, reaction time is believed to be a key factor because it can change the quality of nano ZnO produced by this method. By tuning these parameters nanorods, nano particle/rod, nano porous structures have been achieved.     

ZnO nanostructured microspheres and grown structures by thermal treatment

Synthesis of flower-shaped ZnO nanostructures composed of ZnO nanosticks was achieved by the solution process using zinc acetate dihydrate, sodium hydroxide and polyethylene glycol-20000 (PEG-20000) at 180°C for 4 h. The diameter of individual nanosticks was about 100 nm. Detailed structure characterizations demonstrate that the synthesized products are wurtzite hexagonal phase, grown along the [001] direction. The infrared (IR) spectrum shows the standard peak of zinc oxide at 571 cm⁻¹. Raman scattering exhibits a sharp and strong E ₂ mode at 441 cm⁻¹ which further confirms the good crystal and wurtzite hexagonal phase of the grown nanostructures.     

Hierarchical α‐MnO2 Nanowires@Ni1‐xMnxOy Nanoflakes Core–Shell Nanostructures for Supercapacitors

A facile two‐step solution‐phase method has been developed for the preparation of hierarchical α‐MnO₂ nanowires@Ni_1‐xMn_xO_y nanoflakes core–shell nanostructures. Ultralong α‐MnO₂ nanowires were synthesized by a hydrothermal method in the first step. Subsequently, Ni_1‐xMn_xO_y nanoflakes were grown on α‐MnO₂ nanowires to form core–shell nanostructures using chemical bath deposition followed by thermal annealing. Both solution‐phase methods can be easily scaled up for mass production. We have evaluated their application in supercapacitors. The ultralong one‐dimensional (1D) α‐MnO₂ nanowires in hierarchical core–shell nanostructures offer a stable and efficient backbone for charge transport; while the two‐dimensional (2D) Ni_1‐xMn_xO_y nanoflakes on α‐MnO₂ nanowires provide high accessible surface to ions in the electrolyte. These beneficial features enable the electrode with high capacitance and reliable stability. The capacitance of the core–shell α‐MnO₂@Ni_1‐xMn_xO_y nanostructures (x = 0.75) is as high as 657 F g^?1 at a current density of 250 mA g^?1, and stable charging‐discharging cycling over 1000 times at a current density of 2000 mA g^?1 has been realized.