The role of ammonia hydroxide in the formation of ZnO hexagonal nanodisks using sol–gel technique and their photocatalytic study

ZnO nanomaterials with large surface area are desired particularly for the gas sensor, biosensor and photocatalyst applications. In this study, ZnO hexagonal nanodisks with thickness to diagonal aspect ratio (～1/80) were successfully synthesised via sol–gel approach. By using aluminium sulphate as a complexing agent and carefully controlling the amount of ammonia hydroxide, zinc oxide hexagonal nanodisks were produced. The ZnO nanodisks had perfect hexagonal shape with about 4 μm in diagonal and 50 nm in thickness. The growth of the nanodisks was favoured along the six symmetric directions of ±[1ī00], ±[01ī0] and ±[10ī0]. The growth mechanism of ZnO hexagonal nanodisks is proposed as follows. The formation of ZnO hexagonal nanodisks was mediated by the adsorption of aluminate ions, Al(OH)₄^?, on the polar surface of ZnO. The Al(OH)₄^? ions were produced as a result of reaction between Al₂(SO₄)₃ and NH₄OH. The Al(OH)₄^? ions were bonded to the positively charged Zn²⁺-terminated (0001) polar surface of ZnO. This suppressed the preferential growth of ZnO along [0001] direction but allowed the lateral growth of ZnO in <01ī0>. Eventually, ZnO hexagonal nanodisks with ±(0001) top/bottom surfaces and {1ī00} side surfaces were formed. The size of the ZnO hexagonal nanodisks could be adjusted via the synthesis duration and the amount of ammonia hydroxide. The photocatalytic study indicates that ZnO hexagonal nanodisks were a good photocatalyst for the degradation of Rhodamine B under ultraviolet light irradiation with a rate constant of 0.036 min^?1.     

Acalypha indica–mediated green synthesis of ZnO nanostructures under differential thermal treatment: Effect on textile coating,hydrophobicity, UV resistance,and antibacterial activity

In this study, ZnO nanoparticles were green-synthesized from Acalypha indica leaf extract using zinc acetate as a precursor. The prepared ZnO nanoparticles were calcined at three different temperatures, namely 100, 300, and 600?°C. The structure/morphology of the green-synthesized ZnO nanoparticles was ascertained through X-ray diffraction, particle size analysis, scanning electron microscopy, transmission electron microscopy, and surface area analysis techniques. It was observed from the physico-chemical and biological characterization studies that ZnO nanoparticles calcined at high temperature (600?°C) exhibit high surface area (230?m²?g^?1) and small particle size (20?nm) with good antibacterial activity against Escherichia coli (22.89?±?0.06?mm) and Staphylococcus aureus (24.62?±?0.08?mm). In addition, cotton fabrics coated with these nanoparticles showed higher UV-protection (87.8?UPF), hydrophobicity (155°), and maximum zone of bacterial inhibition against E. coli and S. aureus (25.13?±?0.05 mm and 30.17?±?0.03?mm) than those coated with particles calcined at 100?°C and 300?°C. High temperature calcination has a vital role in the crystallization of the particles towards nanoscale with increased resistivity to UV exposure, washing treatments, and microbial infection in fabrics. Thus, the cost-effective ZnO nanoparticles obtained through green synthesis method proves their potential applications in the field of biomedical, textile, and cosmetic applications.     

Green synthesis of ZnO and Mg doped ZnO nanoparticles,and its optical properties

The Zinc oxide nanoparticles (ZnO NPs) and Magnesium doped ZnO nanoparticles (Mg doped ZnO NPs) are synthesized by Psidium guajava leaf extract. X-ray diffraction studies confirmed that, synthesized nanoparticles were retained the wurtzite hexagonal structure. In FESEM and HRTEM image analysis, ZnO and Mg doped ZnO NPs morphology were trigonal and spherical shape. Elemental compositions were identified by EDAX analysis. From FTIR result, the Zn–O stretching was observed at 453 and 448 cm^?1 for both ZnO samples. In Raman spectra, the high intensive E₂ ^high mode observed for 438 cm^?1 for ZnO NPs. But Mg doped ZnO NPs intensity of E₂ ^high mode decreased as compared to the pure ZnO NPs, it is due to the Mg²⁺ ion in to ZnO lattice site. The photoluminescence measurements revealed that the broad emission was composed of seven different bands due to zinc vacancies, oxygen vacancies and surface defects.     

Surface coatings of zinc oxide–tantalum pentoxide on multicrystalline Si solar cell as effective light harvester

One of the key elements to enhance the performance of solar cells was antireflective surface coatings. It can be employed through different deposition techniques such as spin coating, dip coating, blade coating, etc., In this research work, the coating materials such as ZnO, Ta₂O₅ and ZnO–Ta₂O₅ blends were coated over silicon solar cells through electrospraying technique. The performance of coated solar cells were evaluated using different characterization techniques. At the coating time of 90 min and input voltage supply of 17 kV, almost uniform thin films were attained. This was confirmed through FESEM and AFM analysis. The transmittance and power output characteristics of coated glass slides and Si solar cells were examined through UV–Vis spectroscopy and I–V source meter. In comparison with other solar cells, the ZnO–Ta₂O₅ blend (H3) coated cell exhibit uniform layer deposition and minimal light reflectance of 5%. The maximum power conversion efficiency was achieved for H3 solar cell of 17.7% (direct sunlight) and 19.6% (neodymium light source), due to increased transmittance of photons reaching the depletion region. The electrical resistivity of H3 solar cell was noted as 3.57?×?10^?3 Ω cm using four probe method, which was lesser than other solar cells. From the obtained experimental outcomes, ZnO–Ta₂O₅ blend coated solar cell reveal the maximum performance than other coated and uncoated solar cells. Hence, ZnO–Ta₂O₅ blends were found to be better antireflective material for attaining maximum output performance of solar cell.

     

A Facile Strategy to Construct Silver‐Modified,ZnO‐Incorporated and Carbon‐Coated Silicon/Porous‐Carbon Nanofibers with Enhanced Lithium Storage

For Si anode materials used for lithium ion batteries (LIBs), developing an effective solution to overcome their drawbacks of large volume change and poor electronic conductivity is highly desirable. Here, the composites of ZnO‐incorporated and carbon‐coated silicon/porous‐carbon nanofibers (ZnO‐Si@C‐PCNFs) are designed and synthesized via a traditional electrospinning method. The prepared ZnO‐Si@C‐PCNFs can obviously overcome these two drawbacks and provide excellent LIB performance with excellent rate capability and stable long cycling life of 1000 cycles with reversible capacity of 1050 mA h g^?1 at 800 mA g^?1. Meanwhile, anodes of ZnO‐Si@C‐PCNFs attached with Ag particles display enhanced LIB performance, maintaining an average capacity of 920 mA h g^?1 at a large current of 1800 mA g^?1 even for 1000 cycles with negligible capacity loss and excellent reversibility. In addition, the assembling method with important practical significance for a simple pouch full cell is designed and used to evaluate the active materials. The Ag/ZnO‐Si@C‐PCNFs are prelithiated and assembled in full cells using LiNi_0.5Co_0.2Mn_0.3O₂(NCM523) as cathodes, exhibiting higher energy density (230 W h kg^?1) of 18% than that of 195 W h kg^?1 for commercial graphite//NCM523 full pouch cells. Importantly, the comprehensive mechanisms of enhanced electrochemical kinetics originating from ZnO‐incorporation and Ag‐attachment are revealed in detail.     

MOF-derived carbon coating on self-supported ZnCo<Subscript>2</Subscript>O<Subscript>4</Subscript>–ZnO nanorod arrays as high-performance anode for lithium-ion batteries

The C–ZnCo₂O₄–ZnO nanorod arrays (NRAs), which consist of MOF-derived carbon coating on ZnCo₂O₄–ZnO NRAs, are rational designed and synthesized via a facile template-based solution route on Ti foil and used as high-performance anode for lithium-ion batteries (LIBs). The uniform coated MOF-derived carbon layers on the ZnCo₂O₄–ZnO nanorods surface can serve as a conductive substrate as well as buffer layer to restrain volume expansion during charge–discharge process. When tested as anodes for LIBs, the C–ZnCo₂O₄–ZnO NRAs show high reversible capacity of 1318 mA h g^?1 at 0.2 A g^?1 after 150 charge–discharge cycles. Furthermore, C–ZnCo₂O₄–ZnO NRAs also exhibit brilliant rate performance of 886.2, 812.8, 732.2 and 580.6 mA h g^?1 at 0.5, 1, 2 and 5 A g^?1, respectively. The outstanding lithium storage performance of C–ZnCo₂O₄–ZnO NRAs could be ascribed to the stimulated kinetics of ion diffusion and electron transport originated from the shortened lithium-ion diffusion pathway and improved electronic conductivity benefit from uniformly coating MOF-derived carbon.     

Spin coating of transparent zinc oxide films using novel precursor

The coating of transparent ZnO films using zinc 2-ethylhexanoate [Zn(OOCH(C₂H₅)C₄H₉)₂] as a novel metal organic monomer is reported. Zinc 2-ethylhexanoate is liquid at room temperature and can be spin-coated on a flat substrate without precipitation of ZnO under ambient condition. The spin-coated films were heated at different temperatures to remove unwanted organic materials from the surface. It was found that transparent ZnO films could be produced on glass substrates at low heating temperature (~400 °C). The ZnO films produced using the new monomer were free of cracks and defects. Also the ZnO films produced using the new monomer have excellent optical transmittance, mechanical properties and small surface roughness. The surface morphology and degree of crystallinity of the films coated by the new monomer were compared with these properties of ZnO films produced using zinc acetate-based sol–gels. The results clearly indicate that the novel monomer is a potential precursor for coating transparent ZnO films at low temperatures.     

Effect of zinc addition and vacuum annealing time on the properties of spin-coated low-cost transparent conducting 1 at% Ga–ZnO thin films

Abstract

Pure and 1 at% gallium (Ga)-doped zinc oxide (ZnO) thin films have been prepared with a low-cost spin coating technique on quartz substrates and annealed at 500 °C in vacuum ～10^?3 mbar to create anion vacancies and generate charge carriers for photovoltaic application. Also, 0.5–1.5 at% extra zinc species were added in the precursor sol to investigate changes in film growth, morphology, optical absorption, electrical properties and photoluminescence. It is shown that 1 at% Ga–ZnO thin films with 0.5 at% extra zinc content after vacuum annealing for 60 min correspond to wurtzite-type hexagonal structure with (0001) preferred orientation, electrical resistivity of ～9 × 10^?3 Ω cm and optical transparency of ～65–90% in the visible range. Evidence has been advanced for the presence of defect levels within bandgap such as zinc vacancy (V_Zn), zinc interstitial (Zn_i), oxygen vacancy (V_o) and oxygen interstitial (O_i). Further, variation in ZnO optical bandgap occurring with Ga doping and insertion of additional zinc species has been explained by invoking two competing phenomena, namely bandgap widening and renormalization, usually observed in semiconductors with increasing carrier concentration.     

Structural,optical, photocurrent and mechanism-induced photocatalytic properties of surface-modified ZnS thin films by chemical bath deposition

ZnS thin films were prepared by chemical bath codeposition using ZnSO₄–ZnCl₂ or Zn(CH₃COO)₂–ZnCl₂ as zinc ion sources. The presence of SO₄ ^2? favors the heterogeneous growth of ZnS thin film. The coexistence of two zinc salts impedes the formation of homogeneous precipitation and improves the growth rate of ZnS film. XRD and HRTEM results show that all the samples exhibit the cubic structure. EDS analysis shows that Zn/S atom ratios from the codeposition are closer to 1:1 than those deposited from a single zinc salt, and ZnS thin films of S3 and S7 are very uniform without stirring. FTIR reveals that –NH₂ group as a surface modifier is adsorbed on the surface of ZnS nanoparticles. Raman spectra further reveal that S3, S4 and S7 form the ZnS films, and ZnO phase is present in short or middle range of the S6 nanocrystal, indicating that different amounts of zinc salts affect the structure of ZnS films significantly after three 2.5 h deposition cycles. The grain sizes determined by FESEM are inversely proportional to RMS determined by AFM. The band gap values of ZnS thin films agree well with the results of HRTEM. The photocurrent responses of different samples are similar, indicating that different amounts of zinc salts have little effect on the photocurrent of ZnS films. The photocatalytic performance of S6 and S8 is much better than that of S1–S5. S6 decomposes 65 % of methyl orange within 3 h, and its K value is 4.78 × 10^?1 h^?1. The photocatalytic performance is induced by the growth mechanism, which determines the grain size of ZnS thin film. The tendency of grain sizes of ZnS films agrees well with that of photocatalytic performance, especially under the clusters by clusters deposition.     

Structural and morphological studies of zinc oxide incorporating single-walled carbon nanotubes as a nanocomposite thin film

Pure zinc-oxide and a composition of zinc oxide-single walled carbon nanotubes (ZnO-SWCNTs) thin films were prepared by using a sol–gel doctor blade technique. A precursor of zinc acetate dehydrate (Zn(CH₃COO)₂·2H₂O), absolute ethanol (C₂H₅OH) and triethanolamine were mixed in one solution. Non-acid treatment SWCNTs were doped in the prepared solution. Structural and morphological properties of ZnO and ZnO-SWCNTs thin films were studied by means of X-ray diffractometer (XRD), field-emission scanning electron microscopy (FESEM), atomic force microscopy (AFM) and transmission electron microscopy (TEM). XRD measurements indicated that the crystallite size of ZnO was bigger than the crystallite size of ZnO-SWCNTs; 0.4331 and 0.3386 nm, respectively. The FESEM images showed the hexagonal and nanorod structures of ZnO thin film and a broccoli-like ZnO nanostructures coated with CNTs for ZnO-SWCNTs thin film. The AFM analysis revealed smoother surface morphology of ZnO-SWCNTs thin film compared to the surface of pure ZnO thin film. TEM results captured the inner structures of ZnO and ZnO-SWCNTs. Inner and outer diameter of non-acid treatment SWCNTs were recorded about 5.09 and 14.95 nm, respectively. Photovoltaic performance of ZnO-SWCNTs based dye-sensitized solar cell (DSSC) showed high power conversion efficiency of 0.102 % compared to ZnO based DSSC (0.019 %). This study suggests that SWCNTs should be acid-treated to produce highly porous structure and greater surface area for better photovoltaic performance of the DSSCs.     

Novel synthesis and electrochemical investigations of ZnO/C composites for lithium-ion batteries

For the first time, ZnO/C composites were synthesized using zinc glycerolate as a precursor through one-step calcination under a nitrogen atmosphere. The effect of the heat treatment conditions on the structure, composition, morphology as well as on the electrochemical properties regarding application in lithium-ion batteries are investigated. The products obtained by calcination of the precursor in nitrogen at 400—800 °C consist of zinc oxide nanoparticles and amorphous carbon that is in-situ generated from organic components of the glycerolate precursor. When used as anode material for lithium-ion batteries, the as-prepared ZnO/C composite synthesized at a calcination temperature of 700 °C delivers initial discharge and charge capacities of 1061 and 671 mAh g^?1 at a current rate of 100 mA g^?1 and hence 1.5 times more than bare ZnO, which reaches only 749/439 mAh g^?1. The native carbon improves the conductivity, allowing efficient electronic conductivity and Li-ion diffusion. By means of ex-situ XRD studies a two-step storage mechanism is proven.

     

Enhancement of green luminescence of ZnO powders by annealing with carbon black

This paper reports the characterization of nanocrystalline ZnO powders synthesized by a precipitation method and annealed with carbon black. The X-ray diffraction (XRD) and Fourier Transformed Infrared (FT-IR) results revealed that the synthesized ZnO powder has the wurtzite structure with absorbed CO₃^? species on the surface of the ZnO particles. Singly ionized oxygen vacancy (V_O⁺) and CO₃^? species were also perceived from electron paramagnetic resonance (EPR) analysis. The intensity of the EPR signals of CO₃^? species increased as the amount of carbon increased whereas that of V_O⁺ did not vary significantly. A green emission at 528 nm for the powders annealed with carbon was observed and a good correlation between the intensity of green emission and the intensity of EPR signals of CO₃^? was obtained Experimental results suggest that the formation of the free carriers has significant effect on the intensity of the green emission. The mechanism responsible for the green emission enhancement based on the relevance of the observations is discussed.     

Optical and electrical properties of Bi doped ZnO thin films deposited by ultrasonic spray pyrolysis

Undoped Zinc oxide (ZnO) and Bismuth doped zinc oxide (ZBO) thin films have been prepared by a simple and inexpensive technique namely ultrasonic spray pyrolysis. Films were prepared from an aqueous solution of zinc acetate on glass and silicon substrates at temperature of 350 °C. Doping is achieved by adding a small amount of Bi(NO₃), H₂O salt to the starting solution which is mixed thoroughly prior to spraying. The goal of this work is to study the influence of doping (Bi) with different concentrations on the structural, optical, and electrical properties of Bi doped ZnO films. Structural analysis shows that the ZBO layers are polycrystalline with a wurtzite structure and (100) preferential orientation which disappears gradually with increasing doping concentration. The optical transmittance average of all films, regardless the doping concentration, was higher than 80% in the visible range. The obtained films gaps values vary in the range from 3.19 to 3.24 eV and the Urbach energy lies in the range 11 to 530 meV. The measured conductivity, in dark and at room temperature, varies with four order of decade level (from 10^?3 to 10⁺¹ (??cm)^?1)with increasing Bi doping level.     

Self‐Assembled Ordered Three‐Phase Au–BaTiO3–ZnO Vertically Aligned Nanocomposites Achieved by a Templating Method

Complex multiphase nanocomposite designs present enormous opportunities for developing next‐generation integrated photonic and electronic devices. Here, a unique three‐phase nanostructure combining a ferroelectric BaTiO₃, a wide‐bandgap semiconductor of ZnO, and a plasmonic metal of Au toward multifunctionalities is demonstrated. By a novel two‐step templated growth, a highly ordered Au–BaTiO₃–ZnO nanocomposite in a unique “nanoman”‐like form, i.e., self‐assembled ZnO nanopillars and Au nanopillars in a BaTiO₃ matrix, is realized, and is very different from the random three‐phase ones with randomly arranged Au nanoparticles and ZnO nanopillars in the BaTiO₃ matrix. The ordered three‐phase “nanoman”‐like structure provides unique functionalities such as obvious hyperbolic dispersion in the visible and near‐infrared regime enabled by the highly anisotropic nanostructures compared to other random structures. Such a self‐assembled and ordered three‐phase nanocomposite is obtained through a combination of vapor–liquid–solid (VLS) and two‐phase epitaxy growth mechanisms. The study opens up new possibilities in the design, growth, and application of multiphase structures and provides a new approach to engineer the ordering of complex nanocomposite systems with unprecedented control over electron–light–matter interactions at the nanoscale.     

Performance of Eu2O3 coated ZnO nanoparticles-based DSSC

To provide an inherent energy barrier between the electrode and electrolyte interface, the surface of the ZnO nanoparticles has been modified by Eu₂O₃ layer. The synthesis of ZnO, Eu₂O₃ coated ZnO nanoparticles have been carried out by chemical precipitation method and solvothermal treatment. The synthesized samples were characterized by XRD and the diffraction plane (222) of Eu₂O₃ detected, demonstrating the existence of Eu₂O₃ on the surface of ZnO, which is further verified using energy dispersive X-ray spectroscopy and Fourier transform infrared spectroscopy. The strong quenching in photoluminescence emission, in case of Eu₂O₃/ZnO nanoparticles, has been attributed to the decrease in recombination rate of photo-generated electron–hole pairs. Compared to ZnO electrodes, Eu₂O₃ coated ZnO electrodes adsorbed more dye. The photoelectrochemical properties of the Eu₂O₃/ZnO electrodes have been found to improve and the energy conversion efficiency increase from 0.44 to 1.45 % under the illumination of simulated light of 100 mW/cm².     

Preparation and properties of composite particles made by nano zinc oxide coated with titanium dioxide

In this paper, composite particles of nano zinc oxide coated with titanium dioxide were prepared and characterized by TEM, XRD, XPS and FT-IR, and the properties of the composite particles for photo catalysis and light absorption were studied. Tetrabutyl titanate (TBT) was hydrolyzed in an alcoholic suspension of nano zinc oxide with diethanolamine (DEA) as an additive, resulting in a film with a thickness of 20–30 nm being coated on the surface of nano zinc oxide, and the composite particles contained ZnTiO₃ after drying and calcination. Photocatalysis capabilities of the composite particles for the degradation of phenol in an aqueous solution were greatly improved as compared with nano zinc oxide particles before coating, with pure nano ZnO and nano TiO₂ with similar average sizes, or with the mixture of nano ZnO and TiO₂ with the similar composition as the composite particles. The light absorption scope of the composite particles was enlarged when compared to nano titanium dioxide with same average size.     

Preparation and characterization of copper nanoparticles/zinc oxide composite modified electrode and its application to glucose sensing

We report a new method for selective detection of d(+)-glucose using a copper nanoparticles (Cu-NPs) attached zinc oxide (ZnO) film coated electrode. The ZnO and Cu-NPs were electrochemically deposited onto indium tin oxide (ITO) coated glass electrode and glassy carbon electrode (GCE) by layer-by-layer. In result, Cu-NPs/ZnO composite film topography was characterized by scanning electron microscopy (SEM) and atomic force microscopy (AFM), respectively. SEM and AFM confirmed the presence of nanometer sized Cu-NPs/ZnO composite particles on the electrode surface. In addition, X-ray diffraction pattern revealed that Cu-NPs and ZnO films were attached onto the electrode surface. Indeed, the Cu-NPs/ZnO composite modified electrode showed excellent electrocatalytic activity for glucose oxidation in alkaline (0.1 M NaOH) solution. Further, we utilized the Cu-NPs/ZnO composite modified electrode as an electrochemical sensor for detection of glucose. This glucose sensor showed a linear relationship in the range from 1 × 10^? 6 M to 1.53 × 10^? 3 M and the detection limit (S/N = 3) was found to be 2 × 10^? 7 M. The Cu-NPs/ZnO composite as a non-enzymatic glucose sensor presents a number of attractive features such as high sensitivity, stability, reproducibility, selectivity and fast response. The applicability of the proposed method to the determination of glucose in human urine samples was demonstrated with satisfactory results.     

Formation of D–V<Subscript>Zn</Subscript> complex defects and possible p-type conductivity of ZnO nanoparticle via hydrogen adsorption

The hydrogen adsorption on surfaces and on defect sites of ZnO nanoparticles (NPs) has been studied by using Raman and Fourier transform infrared spectroscopic methods. The presence of hydrogen at defect sites bound to zinc vacancy with different coordinations has been confirmed. To further identify the existence of isolated V_Zn and H–V_Zn complexes in the ZnO NPs, coincidence Doppler broadening (CDB) spectroscopic studies have been performed with respect to the CDB spectra of a 99.9999% pure Al single crystal. The broad momentum dip ρ_L showed between 15–17?×?10^?3 m₀c suggests the trapping of positrons with the core electrons of 3p Zn. However, positron annihilation takes place between ρ_L 20–25?×?10^?3 m₀c and this may occur with an electron belonging to OH bonds (V_Zn–H_i–O). Here the lattice hydrogen H⁺ ion acts as a compensating centre, and it can bind with the V_Zn around the dislocation and stacking faults (SFs) core, which may produce the acceptor-type complex defect for p-type conductivity. Finally, the existence of SFs and dislocation defects, including edges and steps, was confirmed by transmission electron microscopy.     

Effects of ZnO nanowire synthesis parameters on the photovoltaic performance of dye-sensitized solar cells

Determination of the effects of ZnO nanowires on the efficiency of ZnO nanowire-based dye-sensitized solar cells (DSSCs) is important. In this study, we determined the effects of different OH^- precursors, concentrations, the ratio of zinc nitrate to hexamethylene tetramine (HMT), and the hydrothermal synthesis temperature on the physical, crystal, and optical properties of ZnO nanowires and investigated the performance of the resulting DSSCs. We observed that ZnO nanowires synthesized using an equimolar ratio of HMT to zinc nitrate yielded a DSSC with high incident photon-to-current efficiency (IPCE), cell efficiency, short circuit current density (J_sc), and fill factor (FF), and low ZnO-dye-electrolyte interface resistance due to an increased amount of dye and a decreased density of defects. Furthermore, ZnO nanowires made using optimal concentrations and ratios of zinc nitrate to HMT had a high surface area and low defect density. All the photovoltaic performance parameters of DSSCs assessed such as IPCE, cell efficiency, J_sc, open circuit potential (V_oc), and FF increased with synthesis temperature, which was related to a decrease in the resistance at the ZnO-dye-electrolyte interface. We attributed these results to an increased amount of dye facilitated by a large nanowire surface area and fast electron transfer because of the improved crystalline structure of the ZnO nanowires and their low defect density. By optimizing the ZnO nanowires, we increased DSSC efficiency to 0.26% using ZnO nanowires synthesized with 25 mM of both zinc nitrate and HMT at 90 °C, while only a 0.02% increase in efficiency was obtained when NH₄OH was used as OH⁻ precursor.     

Superior Functionality by Design: Selective Ozone Sensing Realized by Rationally Constructed High‐Index ZnO Surfaces

A new technique is reported for the transformation of smooth nonpolar ZnO nanowire surfaces to zigzagged high‐index polar surfaces using polycrystalline ZnO thin films deposited by atomic layer deposition (ALD). The c‐axis‐oriented ZnO nanowires with smooth nonpolar surfaces are fabricated using vapor deposition method and subsequently coated by ALD with a ZnO particulate thin film. The synthesized ZnO–ZnO core–shell nanostructures are annealed at 800 °C to transform the smooth ZnO nanowires to zigzagged nanowires with high‐index polar surfaces. Ozone sensing response is compared for all three types of fabricated nanowire morphologies, namely nanowires with smooth surfaces, ZnO–ZnO core–shell nanowires, and zigzagged ZnO nanowires to determine the role of crystallographic surface planes on gas response. While the smooth and core–shell nanowires are largely non‐responsive to varying O₃ concentrations in the experiments, zigzagged nanowires show a significantly higher sensitivity (ppb level) owing to inherent defect‐rich high‐index polar surfaces.