Shell Nanowires Research Articles

Fabrication of CuO (p)–ZnO (n) Core–Shell Nanowires and Their H2-Sensing Properties

Unlike the conventional one-dimensional (1D) core–shell nanowires (NWs) composed of p-type shells and n-type cores, in this work, an inverse design is proposed by depositing n-type ZnO (shell) layers on the surface of p-type CuO (core) NWs, to have a comprehensive understanding of their conductometric gas-sensing kinetics. The surface morphologies of bare and core–shell NWs were investigated by field emission scanning electron microscope (FE-SEM). The ZnO shell layer was presented by overlay images taken by electron dispersive X-ray spectroscopy (EDX) and high-resolution transmission electron microscopy (HRTEM). The pronounced crystalline plane peaks of ZnO were recorded in the compared glancing incident X-ray diffraction (GI-XRD) spectra of CuO and CuO–ZnO core–shell NWs. The ZnO shell layers broaden the absorption curve of CuO NWs in the UV-vis absorption spectra. As a result of the heterostructure formation, the intrinsic p-type sensing behavior of CuO NWs towards 250 and 500 ppm of hydrogen (H2) switched to n-type due to the deposition of ZnO shell layers, at 400 °C in dry airflow.

Silver nanoparticles decorated ZnO–CuO core–shell nanowire arrays with low water adhesion and high antibacterial activity

Nanostructured surfaces based on silver nanoparticles decorated ZnO–CuO core–shell nanowire arrays, which can assure protection against various environmental factors such as water and bacteria were developed by combining dry preparation techniques namely thermal oxidation in air, radio frequency (RF) magnetron sputtering and thermal vacuum evaporation. Thus, high-aspect-ratio ZnO nanowire arrays were grown directly on zinc foils by thermal oxidation in air. Further ZnO nanowires were coated with a CuO layer by RF magnetron sputtering, the obtained ZnO–CuO core–shell nanowires being decorated with Ag nanoparticles by thermal vacuum evaporation. The prepared samples were comprehensively assessed from morphological, compositional, structural, optical, surface chemistry, wetting and antibacterial activity point of view. The wettability studies show that native Zn foil and ZnO nanowire arrays grown on it are featured by a high water droplet adhesion while ZnO–CuO core–shell nanowire arrays (before and after decoration with Ag nanoparticles) reveal a low water droplet adhesion. The antibacterial tests carried on Escherichia coli (a Gram-negative bacterium) and Staphylococcus aureus (a Gram-positive bacterium) emphasize that the nanostructured surfaces based on nanowire arrays present excellent antibacterial activity against both type of bacteria. This study proves that functional surfaces obtained by relatively simple and highly reproducible preparation techniques that can be easily scaled to large area are very attractive in the field of water repellent coatings with enhanced antibacterial function.

Construction of pH-universal hydrogen evolution freeway in MoO3-MoNi4@Cu core–shell nanowires via synergetic electronic and geometric effect

Construction of pH-universal hydrogen evolution freeway in MoO3-MoNi4@Cu core–shell nanowires via synergetic electronic and geometric effect

Ultrahigh-Temperature-Tolerant NiO@Ag NW-Based Transparent Heater with High Stability, Durability, Ultraflexibility, and Quick Thermal Response

High-performance electrical heaters with high transmittance, fast response speed, superior heat resistance, ultraflexibility, high working temperature, and sufficient stabilities are highly desirable for application in heating systems in areas such as healthcare and aerospace. Herein, we demonstrate an ultrahigh-temperature-tolerant flexible transparent heater (FTH) consisting of a NiO@Ag core–shell nanowire (NiO@Ag NW) network and a colorless polyimide (cPI) film. NiO nanoshells are formed uniformly on the surface of Ag NWs through the solution process, which enhances the stability of Ag NWs. The heating behaviors and transmittance can be controlled by the NiO@Ag NW spin-coating cycle. The NiO@Ag NW-based FTHs show a fast thermal response of ∼15 s, a high transmittance of 86.2% in the visible region, and a large thermal figure of merit of 30.7 m2·°C/W under optimal preparation conditions. The saturation temperature of FTHs has barely changed after 20 taping tests and 1000 bending cycles at a bending radius of 0.5 mm. Particularly, the heating temperature of FTHs can reach 266 °C in the air under an applied voltage of 9 V. Moreover, the FTHs possess sufficient heating reliability, stability, and repeatability during the long-term and repeated heating cycles. In addition, the FTHs are resistant to a number of harsh environments.

Pd@PtRuNi core–shell nanowires as oxygen reduction electrocatalysts

Fuel cells, as the alternative to fossil energy, have engaged widespread attention by reason of the high conversion efficiency from the chemical energy to the electric energy combined with low pollution emissions. The cathodic ORR catalysts with excellent performance and cost-effectiveness are the dominant point towards the massive development of fuel cells. Here, our group select the Pd NWs as the template and construct the Pd@PtRuNi core–shell bilayer nanostructure to expand platinum atom utilization. Pd@PtRuNi bilayer core–shell NWs unfold elevated mass activity of at 0.9 V versus RHE in alkaline media, 2.03- and 6.23-fold of pristine Pd NWs and benchmark commercial Pt/C, respectively. Meanwhile, the cyclic stability tests reveal the excellent durability of Pd@PtRuNi NWs, whose mass activity is only 13.58% degradation after accelerated durability tests. The catalytic activity and durability towards ORR are better than the U.S. 2025 DOE target ( and less than 40% activity attenuation at 0.9 V after 30 000 potential cycles). The elevated catalytic properties can be traceable to the synergism between the ligand effect of Ni and Ru and one-dimensional structure superiority, which optimizes the electronic structure of active sites, promotes the charge transfer and restrains the agglomeration and detachment.

Multilayer Graphene-Coated Silicon Carbide Nanowire Formation Under Defocused Laser Irradiation

Graphene-coated silicon carbide (SiC@C) core–shell nanostructures have attracted attention in the fields of energy storage and nanoelectronics. In this study, multilayer graphene-coated silicon carbide (SiC) nanowires were obtained through the laser irradiation of a mixture target of graphite powder and silicon (Si) grinding sludge discharged from Si wafer manufacturing. Laser irradiation was performed using an ytterbium (Yb) fiber pulsed laser with a pulse width of 10 ms and a wavelength of 1070 nm with various defocus distances. The effect of laser defocusing on the morphology of the generated nanostructures was investigated. Results showed that nanowires were produced under the defocused conditions, and nanoparticles were observed at the on-focus position. The products obtained under all defocused conditions showed a core–shell structure, and the SiC nanowires were covered by graphene layers. The aspect ratio of the nanowires increased with the defocus distance. Observation of the laser-induced plume using a high-speed camera showed that when the laser was defocused, the plume propagation speed slowed down, and the shape of the plume changed to a swirling vortex. The nanowire formation was closely related to the propagation speed and shape variation of the plume. This successful production of SiC@C core–shell nanowires from Si waste opens up the possibility of the sustainable development of new materials for energy storage and nanoelectronics.

Comparison of two methods for one-dimensional Ga2O3-ZnGa2O4 core–shell heterostructure synthesis

While gallium oxide Ga2O3 has recently shown promise as a new ultra-wide bandgap semiconductor in the form of thin films and nanowires (NWs), its widespread applicability is limited due to lack of native p-type conductivity, thus requiring fabrication of heterojunctions. A potential matching material is spinel zinc gallate ZnGa2O4. In this work we demonstrated and compared two novel approaches of one-dimensional Ga2O3-ZnGa2O4 core–shell NW heterostructure preparation: (a) a direct deposition of a ZnGa2O4 coating using a reactive magnetron co-sputtering; (b) annealing of a sacrificial few-nm-thick ZnO coating, deposited via atomic layer deposition, at high temperature to enable solid state reaction between ZnO and Ga2O3. The as-grown nanostructures were characterized via scanning and transmission electron microscopies, X-ray diffraction and X-ray photoelectron spectroscopy. Room temperature optical features were disclosed using photoluminescence and optical absorption. While both methods are viable for production of the heterostructures, smoother and more uniform ZnGa2O4 coating around Ga2O3 NWs was obtained via sacrificial layer conversion in comparison to the sputter-deposited one. These heterostructures could potentially be used for photocatalysis and nanoscale ultra-wide bandgap electronics.

Achieving the high-energy-density asymmetric supercapacitor by hierarchical molybdenum-vanadium-sulphide@covalt sulphide core–shell nanoporous hybrid as cathode and iron oxide@carbon-nanofibers/nitrogen-doped reduced graphene oxide aerogel as anode

In recent decades, supercapacitors have attracted much research as low-cost, reliable, and environment-friendly energy storage devices. However, the low energy density and low operating voltage limit its wide applications. Herein, a novel 1D–2D constructed 3D multicomponent Mox:Vy–S@Co9S8 core–shell nanowires array is designed and fabricated as the cathode material through a simple and economical two-step hydrothermal reaction and electrodeposition process. The constructed 3D Mo0.5V0.5–S@Co9S8 electrode exhibits excellent charge storage capability; an area capacity of 0.91 mA h cm−2 with a corresponding specific capacity of 480.9 mA h g−1 at 2 mA cm−2. Moreover, a solid-state ASC (SS–ASC) is assembled with the as-obtained Fe2O3@CNFs/N–rGO aerogel as the anode, the constructed 3D Mox:Vy–S@Co9S8 NWAs as cathode, and KOH–PVA–gel as a gel electrolyte. As proof of concept, the assembled SS–ASC display an excellent operating voltage window of ~1.7 V and an outstanding energy density of ~108.47 W h kg−1 at ~520.65 W kg−1 power density. Also, when connected in series, the two SS–ASC devices can run an electronic clock for 30 min, demonstrating the practicability of the constructed 3D Mox:Vy–S@Co9S8 NWAs as a promising electrode material for the development of the high energy density ASC.

Flux-periodic oscillations in proximitized core–shell nanowires

Flux-periodic oscillations of the superconducting gap in proximitized core–shell nanowires are explored. Periodicity of oscillations in the energy spectrum of a cylindrical nanowire is compared with nanowires having hexagonal and square cross-section geometry, along with the effects of Zeeman and Rashba spin–orbit interaction. A transition between h/e and h/2e periodicity is found and shown to be dependent on the chemical potential, with correspondence to degeneracy points of the angular momentum quantum number. For a thin shell of a square nanowire, solely h/e periodicity is found in the infinite wire spectrum and shown to result from energy separation between the lowest groups of excited states.

From UV to Vis Broadband Photodetectors Based on ZnO/CuO/NiO Core–Shell–Shell Heterojunction Nanostructures

In recent years, with the development of wearable electronics, the demands for high-performance photodetectors with smaller size, lower power consumption, and higher sensitivity have increased remarkably. Photodetectors based on one-dimensional (1D) zinc oxide (ZnO) nanowires (NWs) have been intensively investigated owing to their geometrical nanostructure possessing a large surface-to-volume ratio, high carrier mobility, and adjustable optical absorption. However, ZnO NW photodetectors usually can only detect ultraviolet (UV) light, limiting their application in the field of photodetection. In this paper, a heterojunction photodetector (HPD) based on ZnO/CuO/NiO (ZCN) core–shell–shell NWs is reported. The nanoscale copper oxide (CuO) film is deposited on hydrothermally grown ZnO NWs as the visible light absorber. The nanoscale nickel oxide (NiO) shell layer is uniformly coated on the surface of ZnO/CuO NWs by spin coating, which improves the detection capability of the photodetector in the range of UV-to-visible (UV–vis) significantly. Benefited from the large light absorption area provided by the 1D nanostructure and the type II band alignment, the ZCN NW HPD shows a fast response (rise/decay 0.12/0.22 s) and a large sensitivity of 18.65 mA/W under UV irradiation at a 0 V bias. Experimental and simulation results show the key role of NiO shell layer in ZCN NW HPD. Our results suggest core–shell–shell heterojunction nanostructures to develop high-performance photodetectors for next-generation UV–vis broadband photosensing applications.

Shape and Composition Evolution in an Alloy Core-Shell Nanowire Heterostructure Induced by Adatom Diffusion.

A core-shell nanowire heterostructure is an important building block for nanowire-based optoelectronic devices. In this paper, the shape and composition evolution induced by adatom diffusion is investigated by constructing a growth model for alloy core-shell nanowire heterostructures, taking diffusion, adsorption, desorption and incorporation of adatoms into consideration. With moving boundaries accounting for sidewall growth, the transient diffusion equations are numerically solved by the finite element method. The adatom diffusions introduce the position-dependent and time-dependent adatom concentrations of components A and B. The newly grown alloy nanowire shell depends on the incorporation rates, resulting in both shape and composition evolution during growth. The results show that the morphology of nanowire shell strongly depends on the flux impingement angle. With the increase in this impingement angle, the position of the largest shell thickness on sidewall moves down to the bottom of nanowire and meanwhile, the contact angle between shell and substrate increases to an obtuse angle. Coupled with the shell shapes, the composition profiles are shown as non-uniform along both the nanowire and the shell growth directions, which can be attributed to the adatom diffusion of components A and B. The impacts of parameters on the shape and composition evolution are systematically investigated, including diffusion length, adatom lifetime and corresponding ratios between components. This kinetic model is expected to interpret the contribution of adatom diffusion in growing alloy group-IV and group III-V core-shell nanowire heterostructures.

Ga2O3@Al2O3 Core–Shell Nanowires for High-Performance Solar-Blind Photodetectors

High-performance solar-blind photodetectors (SBPDs) have been indispensable in both military and civilian applications. Herein, Ga2O3@Al2O3 core–shell nanowires (NWs) are synthesized by plasma-enhanced atomic layer deposition (PEALD) Al2O3 layer on the surface of Ga2O3 nanowires. The Ga2O3@Al2O3 NW has a length of tens of micrometers, and the thickness of Ga2O3 and Al2O3 layers in the NW is approximately 30 and 5 nm, respectively. The PEALD method passivates surface defects to improve the crystal quality of Ga2O3. The metal–semiconductor–metal (MSM) Ga2O3@Al2O3 NW-based SBPDs exhibit a superhigh sensitivity of 1.07 × 103 A/W and a high response speed of less than 83 ms at 5 V bias voltage under 254 nm irradiation. Additionally, the Ga2O3@Al2O3 NW PDs exhibit a superhigh specific detectivity of 3.38 × 1011 Jones, an external quantum efficiency (EQE) of 5.22 × 105%, and a high deep ultraviolet (DUV)/visible responsivity rejection ratio (R254/405) of 4.81 × 102. These results suggest that this method is an effective way to design and prepare high-performance photonic devices.

Nanograin network memory with reconfigurable percolation paths for synaptic interactions

The development of memory devices with functions that simultaneously process and store data is required for efficient computation. To achieve this, artificial synaptic devices have been proposed because they can construct hybrid networks with biological neurons and perform neuromorphic computation. However, irreversible aging of these electrical devices causes unavoidable performance degradation. Although several photonic approaches to controlling currents have been suggested, suppression of current levels and switching of analog conductance in a simple photonic manner remain challenging. Here, we demonstrated a nanograin network memory using reconfigurable percolation paths in a single Si nanowire with solid core/porous shell and pure solid core segments. The electrical and photonic control of current percolation paths enabled the analog and reversible adjustment of the persistent current level, exhibiting memory behavior and current suppression in this single nanowire device. In addition, the synaptic behaviors of memory and erasure were demonstrated through potentiation and habituation processes. Photonic habituation was achieved using laser illumination on the porous nanowire shell, with a linear decrease in the postsynaptic current. Furthermore, synaptic elimination was emulated using two adjacent devices interconnected on a single nanowire. Therefore, electrical and photonic reconfiguration of the conductive paths in Si nanograin networks will pave the way for next-generation nanodevice technologies.

Structural design of triangular core–shell nanowires for sensing polarized mid-infrared light

Manipulating and detecting polarization states of light plays an important role in developing technology in various fields, such as remote sensing, medical phototherapy, and quantum information. However, polarization control in mid-infrared (mid-IR) wavelengths, especially longer than 10 µm, is obstructed by the limitation of material properties. Searching for materials and designing structures that respond to polarized light in this spectral range is still challenging. In this work, triangular core–shell AlGaAs/GaAs nanowires are numerically studied using the finite difference method. The effects of the core shift and rotating angle on the absorption coefficients are concentrated. Highly anisotropic absorption of polarized light in the mid-IR range is found when the core shifts upward and downward. Our results show that this anisotropic property is influenced by the symmetries of electron quantum states confined in the system. Broadband absorption wavelengths from 9.7 to 17.5 µm are unexpectedly found in the structure with appropriate system size. Our finding indicates that triangular core–shell nanowires are a potential platform for next-generation photonic devices capable of manipulating polarized light in a wide range of mid-IR wavelengths.

Self-Organized Growth of Nanowires on a Graphene Film

The self-organized growth of nanowires (NWs) on a graphene film is realized through the van der Waals epitaxy mechanism by metalorganic chemical vapor deposition. It is a fundamental phenomenon which is qualitatively different from the known growth mechanisms, such as self- and metal-catalyzed NW growth. We present a theoretical model that explains the self-organized nucleation of InGaAs NWs on graphene, starting from the formation of InAs NW segments. Then, newly formed InAs NWs act just like seeds to initiate the subsequent growth of InAs/InxGa1–xAs core–shell NWs with spontaneous phase segregation. The model shows that due to the introduction of the graphene film, the nucleation speed of InAs and InGaAs nanoislands in the horizontal direction far exceeds that of the vertical direction. It also elucidates why the radius of the InAs core is two times larger than the InGaAs shell thickness by considering the adatom collection ability of the InAs core and InGaAs shell, respectively, during the transformative process. Thus, the theoretical analysis of the self-organized NW growth on a graphene film is of vital importance for further optimizing the fabrication procedures of two-dimensional material-based NWs.

Improving the intrinsic conductance of selective area grown in-plane InAs nanowires with a GaSb shell

The nanoscale intrinsic electrical properties of in-plane InAs nanowires grown by selective area epitaxy are investigated using a process-free method involving a multi-probe scanning tunneling microscope. The resistance of oxide-free InAs nanowires grown on an InP(111)B substrate and the resistance of InAs/GaSb core–shell nanowires grown on an InP(001) substrate are measured using a collinear four-point probe arrangement in ultrahigh vacuum. They are compared with the resistance of two-dimensional electron gas reference samples measured using the same method and with the Van der Pauw geometry for validation. A significant improvement of the conductance is achieved when the InAs nanowires are fully embedded in GaSb, exhibiting an intrinsic sheet conductance close to the one of the quantum well counterpart.

One Pot Self-Assembling Fe@PANI Core–Shell Nanowires for Radar Absorption Application

The one-pot process, which combines the polymerization of polyaniline (i.e., PANI) with subsequent reduction of iron nanowire (i.e., Fe NW) under a magnetic field, was developed to produce Fe@PANI core-shell nanowires. The synthesized nanowires with various PANI additions (0-30 wt.%) were characterized and used as microwave absorbers. Epoxy composites with 10 wt.% absorbers were prepared and examined using the coaxial method to reveal their microwave absorbing performance. Experimental results showed that the Fe NWs with PANI additions (0-30 wt.%) had average diameters ranging from 124.72 to 309.73 nm. As PANI addition increases, the α-Fe phase content and the grain size decrease, while the specific surface area increases. The nanowire-added composites exhibited superior microwave absorption performance with wide effective absorption bandwidths. Among them, Fe@PANI-90/10 exhibits the best overall microwave absorption performance. With a thickness of 2.3 mm, effective absorption bandwidth was the widest and reached 3.73 GHz, ranging from 9.73 to 13.46 GHz. Whereas with a thickness of 5.4 mm, Fe@PANI-90/10 reached the best reflection loss of -31.87 dB at 4.53 GHz.

Tunable Sulfur Incorporation into Atomic Layer Deposition Films Using Solution Anion Exchange

Metal sulfide and oxysulfide thin films deposited by atomic layer deposition (ALD) are important functional materials for a range of applications including solar cells, catalysts, and electronic devices. However, ALD of sulfur-containing films typically requires H2S, a toxic, corrosive, and flammable gas. To circumvent these challenges, we propose a method of tuning sulfur incorporation into ALD films by first growing a metal oxide, using CuOx as a model system, followed by a solution-phase sulfur anion-exchange process. By controlling the reaction time, solution molarity, and temperature, we demonstrate tunable sulfur incorporation into the films, which is described using a coupled reaction-diffusion model. The evolution of the film crystallinity, composition, and morphology was quantified as a function of the anion-exchange process parameters. Conformal anion exchange on a ZnO@TiO2@CuO core–shell–shell nanowire is shown, demonstrating the ability to maintain the conformality of the initial ALD process on high-aspect-ratio structures. Additionally, area-selective anion exchange was performed on micro-patterned substrates, illustrating a pathway toward device fabrication. Finally, the electrical properties of the converted films were evaluated, indicating a tunable reduction in sheet resistance of up to 4 orders of magnitude. In the future, the combination of ALD and anion-exchange chemistry can be used to incorporate sulfur without the need for H2S gas, while maintaining the atomically precise and conformal properties of the original ALD process.

Microstructures and Photovoltaic Properties of TiO2/BiFeO3 Core–Shell Nanowire Arrays

Microstructures and Photovoltaic Properties of TiO2/BiFeO3 Core–Shell Nanowire Arrays

Polarized emission from hexagonal-silicon–germanium nanowires

We present polarized emission from single hexagonal silicon–germanium (hex-SiGe) nanowires. To understand the nature of the band-to-band emission of hex-SiGe, we have performed photoluminescence spectroscopy to investigate the polarization properties of hex-SiGe core–shell nanowires. We observe a degree of polarization of 0.2 to 0.32 perpendicular to the nanowire c-axis. Finite-difference time-domain simulations were performed to investigate the influence of the dielectric contrast of nanowire structures. We find that the dielectric contrast significantly reduces the observable degree of polarization. Taking into account this reduction, the experimental data are in good agreement with polarized dipole emission perpendicular to the c-axis, as expected for the fundamental band-to-band transition, the lowest energy direct band-to-band transition in the hex-SiGe band structure.