Fiber optic magnetic field sensor using Co doped ZnO nanorods as cladding

A fiber optic magnetic field sensor is proposed and experimentally demonstrated. Pristine and Co doped ZnO nanorods of different Co concentrations (5, 10, 15 and 20 at%) were synthesized using a hydrothermal method. The synthesized nanorods were subjected to various characterization methods like X-ray diffraction (XRD), optical absorption, scanning electron microscopy, energy dispersive X-ray spectroscopy, Fourier transform infrared spectroscopy, vibrating sample magnetometry and X-ray photoelectron spectroscopy (XPS). XRD and XPS analysis confirms that the Co ions were successfully incorporated into the Zn site of the wurtzite ZnO lattice without altering the structure. The pristine and Co doped ZnO nanorods showed remarkable changes in the M–H loop where the diamagnetic behavior of ZnO changes to paramagnetic when doped with Co. The sensor structure is composed of cladding modified fiber coated with Co doped ZnO nanorods as a sensing material. The modified cladding is proportionally sensitive to the ambient magnetic field because of the magneto-optic effect. Experimental results revealed that the sensor has an operating magnetic field range from 17 mT to 180 mT and shows a maximum sensitivity of ∼18% for 15 at% Co doped ZnO nanorods. The proposed magnetic field sensor would be attractive due to its low cost fabrication, simplicity of the sensor head preparation, high sensitivity and reproducibility.

A fiber optic magnetic field sensor based on Co doped ZnO nanorods is proposed and demonstrated. The sensor has an operating magnetic field range of 17 mT to 180 mT and shows a maximum sensitivity of ∼18% for 15 at% Co doped ZnO nanorods.     

Unraveling the effect of Gd doping on the structural,optical, and magnetic properties of ZnO based diluted magnetic semiconductor nanorods

The structural, magnetic, and optical properties of the pristine and Gd-doped ZnO nanorods (NRs), prepared by facile thermal decomposition, have been studied using a combination of experimental and density functional theory (DFT) with Hubbard U correction approaches. The XRD patterns demonstrate the single-phase wurtzite structure of the pristine and doped ZnO. The rod-like shape of the nanoparticles has been examined by FESEM and TEM techniques. Elemental compositions of the pure and doped samples were identified by EDX measurement. Due to the Burstein–Moss shift, the optical band gaps of the doped samples have been widened compared to pristine ZnO. The PL spectra show the presence of complex defects. Room temperature magnetic properties have been measured using VSM and revealed the coexistence of paramagnetic and weak ferromagnetic ordering in Gd³⁺ doped ZnO-NRs. The magnetic moment was increased upon addition of more Gd ions into the ZnO host lattice. The DFT+U calculations confirm that the presence of vacancy-complexes has a significant effect on the structural, electronic, and magnetic properties of a pristine ZnO system.

Gd doped ZnO nanorods.     

Optimization of 3D ZnO brush-like nanorods for dye-sensitized solar cells

In a dye-sensitized solar cell (DSSC) the amount of adsorbed dye on the photoanode surface is a key factor that must be maximized in order to obtain enhanced DSSC performance. In this study 3D ZnO nanostructures, named brush-like, are demonstrated as alternative photoanodes. In these structures, long ZnO nanorods are covered with a metal–organic precursor, known as a layered-hydroxide zinc salt (LHZS), which is subsequently converted to crystalline ZnO using two-step annealing. The LHZS is able to easily grow on any surface, such as the ZnO nanorod surface, without needing the assistance of a seed-layer. Brush-like structures synthesized using different citrate concentrations in the growth solutions and different annealing conditions are characterized and tested as DSSC photoanodes. The best-performing structure reported in this study was obtained using the highest citrate concentration (1.808 mM) and the lowest temperature annealing condition in an oxidative environment. Conversion efficiency as high as 1.95% was obtained when these brush-like structures were employed as DSSC photoanodes. These results are extremely promising for the implementation of these innovative structures in enhanced DSSCs, as well as in other applications that require the maximization of surface area exposed by ZnO or similar semiconductors, such as gas- or bio-sensing or photocatalysis.

Optimized 3D ZnO brush-like nanorods showing large surface area are presented as the photoanode in enhanced high-current-density DSSCs.     

l-Alanine capping of ZnO nanorods: increased carrier concentration in ZnO/CuI heterojunction diode

ZnO nanorods were capped with a simple amino acid, viz., l-alanine to increase the carrier concentration and improve the performance of ZnO/CuI heterojunction diodes. The effect of l-alanine capping on the morphology, structural, optical, electrochemical and electrical properties of ZnO nanorods had been studied in detail. The stable structure with two equally strong Zn–O coordinate bonds predicted by density functional theory was in agreement with the experimental results of FTIR spectroscopy. Due to the presence of electron-releasing (+I effect) moieties in l-Alanine, the carrier concentration of capped ZnO nanorods was two orders of magnitude higher and the ZnO/CuI heterojunction device showed more than a two-fold increase in the photovoltaic power conversion efficiency.

ZnO nanorods were capped with a simple amino acid, viz., l-Alanine to increase the carrier concentration and improve the performance of ZnO/CuI heterojunction diodes.     

Growth and properties of ZnO nanorods by RF-sputtering for detection of toxic gases

There is a strong demand for nanostructured materials prepared by an industrially-scalable technique. The current work is devoted to the preparation of ZnO polycrystalline nanorods using RF sputtering at 400 °C and Sn droplets as a catalyzer layer, for highly sensitive gas sensors. Nanorods with diameters ranging from 100 to 200 nm can be tailored by changing the RF power and the deposition time. Raman and PL spectroscopy indicate that the material obtained is ZnO, with a characteristic emission spectrum in the UV region and in the visible. The functional properties of the ZnO nanorods were investigated by studying the response to CBRN (acetonitrile and DMMP), explosive (H₂), and pollutant gases (H₂S, acetone, and NO₂) in the temperature range 200–500 °C. The sensors showed good response to reducing gases at higher temperatures (500 °C) and to NO₂ at lower temperature (200 °C).

ZnO polycrystalline nanorods were easily prepared via RF sputtering and proved excellent sensors for H₂S and other toxic/explosive gases.     

Insights into non-noble metal based nanophotonics: exploration of Cr-coated ZnO nanorods for optoelectronic applications

Herein, the room temperature photoluminescence and Raman spectra of hydrothermally grown ZnO nanorods coated with Cr are investigated for optoelectronic applications. A thorough examination of the photoluminescence spectra of Cr coated ZnO nanorods showed the suppression of deep level emissions by more than twenty five times with Cr coating compared to that of pristine ZnO nanorods. Moreover, the underlying mechanism was proposed and can be attributed to the formation of Schottky contacts between Cr and ZnO resulting in defect passivation, weak exciton–plasmon coupling, enhanced electric field effect and formation of hot carriers due to interband transitions. Interestingly, with the increase in sputtering time, the ratio of the intensities corresponding to the band gap emission and deep level emission was observed to increase from 6.2 to 42.7, suggesting its application for UV only emission. Further, a planar photodetector was fabricated (Ag–ZnO–Ag planar configuration) and it was observed that the dark current value got reduced by more than ten times with Cr coating, thereby opening up its potential for transistor applications. Finally, Cr coated ZnO nanorods were employed for green light sensing. Our results demonstrated that ZnO nanorods decorated with Cr shed light on developing stable and high-efficiency non-noble metal based nanoplasmonic devices such as photodetectors, phototransistors and solar cells.

Herein, the room temperature photoluminescence and Raman spectra of hydrothermally grown ZnO nanorods coated with Cr are investigated for optoelectronic applications.     

Transparent and flexible ZnO nanorods induced by thermal dissipation annealing without polymer substrate deformation for next-generation wearable devices

The fabrication of a transparent and flexible ultraviolet photodetector based on hydrothermally grown ZnO nanorods requires an annealing step to render the sol–gel spin-coated ZnO seed layer crystalline. As high-temperature annealing deforms low-melting-point polymer substrates, we herein devised a thermal dissipation annealing (TDA) method in which heat transfer to ZnO thin films is synchronized with heat release from the polymer substrate to crystallize the ZnO seed layer without polymer substrate deformation and melting. ZnO nanorods (NRs) were hydrothermally grown on non-annealed and annealed ZnO seed layers, and NR density and diameter were shown to be higher in the latter case, as the crystallized ZnO seed layer provided heterogeneous nucleation sites for NR growth. In addition, the larger density and diameter of ZnO NRs grown on the annealed ZnO seed layer were confirmed by analysis of O 1s signal intensities. A transparent and flexible UV photodetector based on ZnO NRs grown on the annealed ZnO seed layer exhibited a higher photocurrent/dark current ratio, photosensitivity, and photoresponsivity than that fabricated using a non-annealed seed layer. Taken together, the above results suggest that the TDA method is an effective way of fabricating transparent and flexible UV photodetectors with high photosensitivity, photoresponsivity, and photocurrent stability and it means that the next generation wearable devices can be easily realized by using the TDA method.

A transparent and flexible ultraviolet (UV) photodetector based on ZnO nanorods grown onto the thermal dissipation annealed ZnO seed layer exhibited high photosensitivity, photoresponsivity, and photocurrent stability without substrate deformation.     

Synthesis of Ni–Ag–ZnO solid solution nanoparticles for photoreduction and antimicrobial applications

ZnO is one of the most promising and efficient semiconductor materials for various light-harvesting applications. Herein, we reported the tuning of optical properties of ZnO nanoparticles (NPs) by co-incorporation of Ni and Ag ions in the ZnO lattice. A sonochemical approach was used to synthesize pure ZnO NPs, Ni–ZnO, Ag–ZnO and Ag/Ni–ZnO with different concentrations of Ni and Ag (0.5%, 2%, 4%, 8%, and 15%) and Ni doped Ag–ZnO solid solutions with 0.25%, 0.5%, and 5% Ni ions. The as-synthesized Ni–Ag–ZnO solid solution NPs were characterized by powdered X-ray diffraction (pXRD), FT-IR spectroscopy, scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), UV-vis (UV) spectroscopy, and photoluminescence (PL) spectroscopy. Ni–Ag co-incorporation into a ZnO lattice reduces charge recombination by inducing charge trap states between the valence and conduction bands of ZnO and interfacial transfer of electrons. The Ni doped Ag–ZnO solid solution NPs have shown superior 4-nitrophenol reduction compared to pure ZnO NPs which do not show this reaction. Furthermore, a methylene blue (MB) clock reaction was also performed. Antibacterial activity against E. coli and S. aureus has inhibited the growth pattern of both strains depending on the concentration of catalysts.

The synergic effect of Ni and Ag in Ni–Ag–ZnO solid solutions has tuned the optoelectronic properties of ZnO for photoreduction reactions.     

Template-free synthesis and lithium-ion storage performance of multiple ZnO nanoparticles encapsulated in hollow amorphous carbon shells

Due to the limited utilization of electrode materials, the rational design and facile synthesis of composite structures are still challenging issues for lithium-ion batteries (LIBs). Herein, a simple approach has been developed to prepare multiple core–shell structures of ZnO nanoparticles (NPs) encapsulated in hollow amorphous carbon (AC) shells. The as-synthesized ZnO@AC composites showed a uniform dispersion of ZnO NPs, compliant buffer AC shells, and nanoscale void spaces between the ZnO NP cores and AC shells. As a result of their structural merits, the ZnO@AC composites were evaluated as anode materials for LIBs and delivered enhanced coulombic efficiency, high reversible capacity, high rate capability, and improved cycling stability.

Core–shell structure of ZnO@amorphous carbon shell was synthesized using a simple and effective method, and exhibited excellent electrochemical performance as anode of lithium-ion batteries.     

High aspect ZnO nanorod growth over electrodeposited tubes for photocatalytic degradation of EtBr dye

In this work, vertically grown rod type ZnO nanostructures have been synthesized on metallic nickel tube films fabricated through the cost-effective process of electroforming. The use of tubular metal substrates for the growth of ZnO nanorods has been found to be advantageous for the photocatalytic degradation of EtBr dye because of their high surface area-to-volume ratio. The nickel tubes with ZnO nanorods were characterized using X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM). The developed system was utilized for the photocatalytic degradation of EtBr dye and its efficacy was revealed through the comprehensive mineralization of the dye within 150 min. The mechanism of the degradation process has been revealed through total organic carbon (TOC), chemical oxygen demand (COD) and high-performance liquid chromatography (HPLC) studies. A substantially lower amount of the photocatalyst has been used because of the homogeneously distributed growth of nanorods on the substrate. Density functional theory-based analysis has also been performed to study the photocatalytic degradation and adsorption properties of EtBr on ZnO nanorods. Using first principles DFT theory, geometry optimizations and vibrational analysis are performed which show a negative charge transfer from the substrate to the photocatalyst. For the first time this article reports the use of DFT analysis for investigating the adsorption of EtBr on ZnO nanorods, and the experimental growth of nanorods over electroformed Ni tubes.

In this work, vertically grown rod type ZnO nanostructures have been synthesized on metallic nickel tube films fabricated through the cost-effective process of electroforming..     

Fragmented lignin-assisted synthesis of a hierarchical ZnO nanostructure for ammonia gas sensing

In the present study, we demonstrated the use of fragmented lignin in the synthesis of a hierarchical-type structure of ZnO nanorods. Lignin was isolated from bagasse by the microwave assisted method and its fragmentation was achieved in alkaline conditions along with hydrogen peroxide. Lignin and fragmented lignin were purified by crystallisation followed by column chromatography and characterized by UV-visible spectroscopy, Frontier infra-red spectroscopy (FTIR), ¹H-NMR and high resolution mass spectroscopy (HRMS). Fragmented lignin was utilized as a template for the synthesis of ZnO nanorods, which were characterized by powder XRD, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and UV-DRS for the determination of crystal structure, particle morphology and band gap. XRD of the ZnO samples revealed a hexagonal wurtzite structure. The morphology of ZnO without fragmented lignin showed agglomerated nanoparticles and with fragmented lignin, a self-assembled hierarchical nanostructure due to nanorods of 30 nm diameter and 200–500 nm length was observed. The fragmented lignin showed a pronounced effect on the particle size and morphology of ZnO nanoparticles. We measured the response of the hierarchical ZnO nanostructure (50 ppm) for sensing NH₃ in terms of change in voltage across known resistance. We observed the response and recovery upon introduction of the analyte ammonia gas at 175 °C.

Flow sheet for isolation of fragmented lignin.     

Dye wastewater treatment enabled by piezo-enhanced photocatalysis of single-component ZnO nanoparticles

Conventionally, composite materials are usually employed as a catalyst in piezo-photocatalytic dye wastewater treatment. Here, we report the synthesis of ZnO nanoparticles, as a single-component catalyst, by surfactant-assisted precipitation in which the size of ZnO nanoparticles (20–100 nm) can be simply controlled by the use of Tween80 as a surfactant. Although, ZnO nanoparticles exhibited appreciable photocatalytic activities for the degradation of methylene blue (MB) dye, upon the addition of a mechanical force, the photocatalytic dye degradation efficiency was substantially improved. Furthermore, we postulated that the surface properties of ZnO play an important role in charge transfer phenomena based on photoluminescence results together with functional groups on the surface of ZnO. In addition, application of single-component ZnO in piezo-promoted photocatalytic degradation of cationic and anionic dyes was accomplished. Our results regarding the behaviour of single-component ZnO nanoparticles under vibrational energy in addition to their conventional solar harvesting can provide a promising strategy for developing photocatalysts for practical wastewater treatment.

Single-component ZnO nanoparticles, synthesized by a simple synthetic method, exhibit appreciable piezo-enhanced photocatalytic activities, representing an alternative to other complex systems.     

Difference in the deactivation of Au catalysts during ethanol transformation when supported on ZnO and on TiO2

Au nanoparticles of different sizes were supported by the deposition–precipitation method on two metal oxides: ZnO and TiO₂. The resulting catalysts were tested in the ethanol catalytic transformation reaction. Both metal oxide support materials exerted a different influence on the achieved Au particle size as well as on the behavior of the subsequent catalyst, with regard to their initial conversion values, product distribution and stability. While TiO₂ favors the formation of smaller nanoparticles, ZnO offers larger Au particle sizes when prepared under similar conditions. At the same time, TiO₂ produced catalysts which displayed higher initial conversions in comparison with AuZnO catalysts, even when observing catalysts of each series with similar particle sizes. At the same time, catalysts supported on ZnO exhibited higher resistance to deactivation caused by coke formation. These results were evidenced employing different characterization techniques on both used and fresh catalyst samples. The decline in deactivation was generally accompanied by an increase in the carbon content on the catalyst''s surface.

Au NPs of different sizes were supported on two metal oxides: ZnO and TiO₂. Differences in ethanol transformation for Au of similar particle size reveal that TiO₂ support induces condensation products while ZnO only gives place to dehydrogenation.     

Electrochemical synthesis of hydroxyl group-functionalized PProDOT/ZnO for an ultraviolet photodetector

Ultraviolet (UV) detectors based on zinc oxide (ZnO) nanorods (NRs) are ideal materials for UV radiation detection. However, owing to the surface effect of ZnO NRs, their speed of photoresponse and photosensitivity need to be improved. In this study, a UV photodetector was fabricated via electrochemical coating of poly(3,4-propylenedioxythiophene) grafted with functional groups (–OH) on a hydrothermally grown ZnO NRs. For comparison, poly(3,4-propylenedioxythiophene)/ZnO composites were synthesized using the same method. The structure of the composite film was characterized by Fourier transform infrared spectroscopy (FT-IR), UV-visible spectroscopy (UV-vis), X-ray diffraction (XRD), Raman spectroscopy (Raman), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and energy dispersive X-ray spectroscopy (EDS). The effect of the polymer structure on the UV sensing ability of ZnO NRs was evaluated by fabricating a UV detector with a composite material. The structural results indicated that the PProDOT-type conductive polymer and ZnO composites were successfully synthesized. The UV photodetection results showed that the presence of functional groups (–OH) in polymer chains could enhance the responsivity of the material. The response time of the ZnO/PProDOT–OH composite was 15 s shorter than that of the ZnO/PProDOT composite. A rise in photocurrent induced an increase from 2.5 A W⁻¹ to 34.75 A W⁻¹ in the UV photoresponsivity of the ZnO/PProDOT–OH composite, compared with that of the pure ZnO NRs. The external quantum efficiency and detectivity significantly improved, the increases of which were attributed to the coupling of the polymer and ZnO NRs.

Ultraviolet (UV) detectors based on zinc oxide (ZnO) nanorods (NRs) are ideal materials for UV radiation detection.     

Enhancing the mechanical performance of poly(ether ether ketone)/zinc oxide nanocomposites to provide promising biomaterials for trauma and orthopedic implants

Poly(ether ether ketone)/zinc oxide (PEEK/ZnO) composites were manufactured by using the injection molding technique. Before blending with the PEEK resin matrix, some ZnO nanoparticles were modified by γ-aminopropyltriethoxylsilane (APTES). The effect of surface modification of ZnO nanoparticles by amino groups and Si–O bonds was investigated. PEEK/ZnO composites were characterized by scanning electron microscopy (SEM), thermogravimetric analysis, and X-ray diffraction. The scanning electron micrographs showed that ZnO nanoparticles were encapsulated in the PEEK phase; within this phase, the nanoparticles were homogeneously dispersed. Mechanical and tribological properties were measured by tensile strength, flexural strength, coefficient of friction, and wear rate. It was shown that the interfacial compatibility between ZnO nanoparticles and PEEK matrix was significantly enhanced due to the amino and Si–O bonds decorated on the ZnO nanoparticles. More importantly, the thermal stability of PEEK improved upon the incorporation of ZnO nanoparticles into this matrix. Cell viability studies with mouse osteoblasts demonstrated that cell growth on PEEK and PEEK/ZnO was significantly enhanced. On the basis of the obtained results, PEEK/ZnO composites are recommended as promising candidates for orthopaedic materials and trauma implants.

Poly(ether ether ketone)/zinc oxide (PEEK/ZnO) composites were manufactured by using the injection molding technique.     

Electrodeposited Pd/graphene/ZnO/nickel foam electrode for the hydrogen evolution reaction

Efficient electrocatalysts are crucial to water splitting for renewable energy generation. In this work, electrocatalytic hydrogen evolution from Pd nanoparticle-modified graphene nanosheets loaded on ZnO nanowires on nickel foam was studied in an alkaline electrolyte. The high electron mobility stems from the cylindrical ZnO nanowires and the rough surface on the graphene/ZnO nanowires increases the specific surface area and electrical conductivity. The catalytic activity arising from adsorption and desorption of intermediate hydrogen atoms by Pd nanoparticles improves the hydrogen evolution reaction efficiency. As a hydrogen evolution reaction (HER) catalyst, the Pd/graphene/ZnO/Ni foam (Pd/G/ZnO/NF) nanocomposite exhibits good stability and superior electrocatalytic activity. Linear sweep voltammetry (LSV) revealed an overpotential of −31 mV and Tafel slope of 46.5 mV dec⁻¹ in 1 M KOH. The economical, high-performance, and environmentally friendly materials have excellent prospects in hydrogen storage and hydrogen production.

Efficient electrocatalysts are crucial to water splitting for renewable energy generation.     

Enhanced moisture sensing properties of a nanostructured ZnO coated capacitive sensor

This work reports the enhancement in sensitivity of a simple and low-cost capacitive moisture sensor using a thin film of zinc oxide (ZnO) nanoparticles on electrodes. The ZnO nanoparticles are systematically characterized using X-ray diffraction, atomic force microscopy, transmission electron microscopy, BET surface area analysis, Fourier transform infrared spectroscopy, and UV-visible and photoluminescence (PL) spectroscopy. The average crystallite size of the ZnO nanoparticles is ∼16 nm with a surface roughness of ∼3 nm. Blue emission in the PL spectrum confirms the presence of oxygen vacancy dipoles, which are responsible for enhancing the dielectric properties of the ZnO nanoparticles. The effect of the ZnO nanoparticles on the sensitivity of a moisture sensor cell has been studied using wheat grains with a moisture content from 7% to 25%. An enhancement in sensitivity of 36.4% at 1 MHz and 97.4% at 500 Hz has been observed. A detailed sensing mechanism is proposed and the enhancement in sensing has been explained based on the interaction of ZnO with water vapor and the dielectric behavior of the nanostructured ZnO. The present results establish ZnO as a sensing material for improving the utility of moisture sensors.

This work reports the enhancement in sensitivity of a simple and low-cost capacitive moisture sensor using a thin film of zinc oxide (ZnO) nanoparticles on electrodes.     

Band gap engineered zinc oxide nanostructures via a sol–gel synthesis of solvent driven shape-controlled crystal growth

A reliable sol–gel approach, which combines the formation of ZnO nanocrystals and a solvent driven, shape-controlled, crystal-growth process to form well-organized ZnO nanostructures at low temperature is presented. The sol of ZnO nanocrystals showed shape-controlled crystal growth with respect to the solvent type, resulting in either nanorods, nanoparticles, or nanoslates. The solvothermal process, along with the solvent polarity facilitate the shape-controlled crystal growth process, augmenting the concept of a selective adhesion of solvents onto crystal facets and controlling the final shape of the nanostructures. The XRD traces and XPS spectra support the concept of selective adhesion of solvents onto crystal facets that leads to yield different ZnO morphologies. The shift in optical absorption maxima from 332 nm in initial precursor solution, to 347 nm for ZnO nanocrystals sol, and finally to 375 nm for ZnO nanorods, evidenced the gradual growth and ripening of nanocrystals to dimensional nanostructures. The engineered optical band gaps of ZnO nanostructures are found to be ranged from 3.10 eV to 3.37 eV with respect to the ZnO nanostructures formed in different solvent systems. The theoretical band gaps computed from the experimental XRD spectral traces lie within the range of the optical band gaps obtained from UV-visible spectra of ZnO nanostructures. The spin-casted thin film of ZnO nanorods prepared in DMF exhibits the electrical conductivity of 1.14 × 10⁻³ S cm⁻¹, which is nearly one order of magnitude higher than the electrical conductivity of ZnO nanoparticles formed in hydroquinone and ZnO sols. The possibility of engineering the band gap and electrical properties of ZnO at nanoscale utilizing an aqueous-based wet chemical synthesis process presented here is simple, versatile, and environmentally friendly, and thus may applicable for making other types of band-gap engineered metal oxide nanostructures with shape-controlled morphologies and optoelectrical properties.

A reliable and simple sol–gel synthesis followed by a solvent-driven, shape controlled, crystal growth process to make ZnO nanostructures is demonstrated.     

Copper–zinc oxide heterojunction catalysts exhibiting enhanced photocatalytic activity prepared by a hybrid deposition method

Heterojunction copper–zinc oxide catalysts were prepared by a hybrid two-step methodology comprising hydrothermal growth of ZnO nanorods (ZnO-NR) followed by deposition of Cu₂O nanoparticles using an advanced gas deposition technique (AGD). The obtained bicatalysts were characterized by SEM, AFM, XRD, XPS, PL and spectrophotometry and revealed well-dispersed and crystalline Cu₂O nanoparticles attached to the ZnO-NR. The adsorption properties and photocatalytic degradation of Orange II dye in water solutions were measured. It was found that the bicatalysts exhibited a conversion rate and quantum yield that both were about 50% higher compared with ZnO-NR alone, which were attributed to the intrinsic electric field created at the p–n junction formed at the Cu₂O/ZnO interface facilitating charge separation of electron–hole pairs formed upon interband photon absorption. The interpretation was evidenced by efficient quenching of characteristic deep level ZnO photoluminescence bands and photoelectron core-level energy shifts. By comparisons with known energy levels in Cu₂O and ZnO, the effect was found to be most pronounced for the non-polar ZnO-NR side facets, which accounted for about 95% of the exposed surface area of the catalyst and hence the majority of dye adsorption. It was also found that the dye adsorption capacity of the ZnO nanorods increased considerably after Cu₂O deposition thereby facilitating the oxidation of the dye. The results imply the possibility of judiciously aligning band edges on structurally controlled and well-connected low-dimensional semiconductor nanostructures using combined two-step synthesis techniques, where in particular vacuum-based techniques such as AGD allow for growth of well-connected nanocrystals with well developed heterojunction interfaces.

Hybrid synthesis of Cu₂O/ZnO nanorod heterojunction exhibiting enhanced interfacial charge transfer and photocatalytic activity comprising hydrothermal synthesis step of ZnO nanorods followed by advanced gas deposition of Cu nanoparticles.     

Hierarchical assembly of ZnO nanowire trunks decorated with ZnO nanosheets for lithium ion battery anodes

Hierarchical architectures composed of nanomaterials in different forms are essential to improve the performance of lithium-ion battery (LIB) anodes. Here, we systematically studied the effects of hierarchical ZnO nanostructures on the electrochemical performance of LIBs. ZnO nanowire (NW) trunks were decorated with ZnO NWs or ZnO nanosheets (NSs) by successive hydrothermal synthesis to create hierarchical three-dimensional nanostructures. The branched ZnO NSs on the ZnO NW trunk exhibited a two-fold higher specific gravimetric capacity compared to ZnO NWs and branched ZnO NWs on ZnO NW trunks after 100 cycles of charging–discharging at 0.2C (197.4 mA g⁻¹). The improvement in battery anode performance is attributable to the increased interfacial area between the electrodes and electrolyte, and the void space of the branched NSs that facilitates lithium ion transport and volume changes during cycling.

Hierarchical architectures composed of nanomaterials in different forms are essential to improve the performance of lithium-ion battery (LIB) anodes.