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At least 325 records · Page 18

Structural transformation in nickel doped zinc oxide nanostructures

Graphical abstract: Display Omitted Highlights: ► A systematic study of 1–10% Ni doped ZnO nanostructures (Ni:ZnO NS). ► Effect of Ni concentration on properties of Ni:ZnO NS was intensively investigated. ► Structural transformation in Ni:ZnO NS demonstrated through characterizations. ► Alteration in vibrational modes of Ni:ZnO NS were meticulously analyzed. ► Intricacies of structural evolution, from particles to rods, were comprehended. -- Abstract: In this article, structural transformation in nickel doped zinc oxide nanostructures is reported. The ZnO nanostructures are synthesized with 1–10% of nickel doping through a chemical precipitation method. The undoped and doped nanostructures were systematically investigated employing X-ray diffraction (XRD), transmission and scanning electron microscopy (TEM/SEM), Fourier transform infrared (FTIR) and micro-Raman spectroscopy (μRS). The wurtzite phase of the material and associated lattice parameters were ascertained through XRD analysis. TEM/SEM images reveal the structural transformation of ZnO nanostructures with variation in nickel doping. The study of vibrational modes of nanostructures at different stages of structural transformation, as performed through FTIR and Raman spectroscopy, assist in deciphering the pivotal role of doping concentration in gradual evolution of nickel doped ZnO structure from nanoparticles to nanorods.

36 MATERIALS SCIENCE↗

Silver chromate and silver dichromate nanostructures: Sonochemical synthesis, characterization, and photocatalytic properties

Graphical abstract: In this work, Ag{sub 2}CrO{sub 4} and Ag{sub 2}Cr{sub 2}O{sub 7} nanostructures have been sonochemically prepared using silver salicylate. The effect of preparation parameters on the morphology of the products was investigated by SEM images. Highlights: ► Herein, Ag{sub 2}CrO{sub 4} and Ag{sub 2}Cr{sub 2}O{sub 7} nanostructures have been sonochemically prepared. ► The effect of preparation parameters on the morphology of the products was investigated. ► The photocatalytic activity of the as-prepared Ag{sub 2}CrO{sub 4} nanoparticles was tested. ► XPS spectra indicated the high purity of Ag{sub 2}Cr{sub 2}O{sub 7} nanostructures obtained. - Abstract: In this work, Ag{sub 2}CrO{sub 4} and Ag{sub 2}Cr{sub 2}O{sub 7} nanostructures have been produced via a sonochemical method using silver salicylate as precursor. Besides silver salicylate, Na{sub 2}CrO{sub 4} and (NH{sub 4}){sub 2}Cr{sub 2}O{sub 7} as starting reagents were applied. To investigate the effect of preparation parameters on the morphology and particle size of Ag{sub 2}CrO{sub 4} and Ag{sub 2}Cr{sub 2}O{sub 7}, sonication time, type of surfactant and its concentration were changed. The as-produced nanostructures were characterized by techniques like powder X-ray diffraction, scanning electron microscopy, and X-ray photoelectron spectroscopy. The scanning electron micrographs showed that particle-like and rod-like nanostructures of Ag{sub 2}CrO{sub 4} and Ag{sub 2}Cr{sub 2}O{sub 7} were produced using different surfactants. To investigate the catalytic properties of Ag{sub 2}CrO{sub 4} nanoparticles, photooxidation of methyl orange (MO) was performed. According to the obtained results, it was found that the methyl orange degradation was about 87.3% after 280 min irradiation of visible light.

36 MATERIALS SCIENCE↗

Synthesis, morphology, optical and photocatalytic performance of nanostructured β-Ga{sub 2}O{sub 3}

Highlights: ► Nanostructures of β-Ga{sub 2}O{sub 3} were prepared using facile reflux condensation process. ► The pH of the reaction mixture shows evident influence on the size and shape of the nanostructures formed. ► The nanostructures exhibited good photocatalytic activity toward Rhodamine B and was found to be superior for higher pH value. - Abstract: Fine powders of β-Ga{sub 2}O{sub 3} nanostructures were prepared via low temperature reflux condensation method by varying the pH value without using any surfactant. The pH value of reaction mixture had great influence on the morphology of final products. High crystalline single phase β-Ga{sub 2}O{sub 3} nanostructures were obtained by thermal treatment at 900 °C which was confirmed by X-ray diffraction and Raman spectroscopy. The morphological analysis revealed rod like nanostructures at lower and higher pH values of 6 and 10, while spindle like structures were obtained at pH = 8. The phase purity and presence of vibrational bands were identified using Fourier transform infrared spectroscopy. The optical absorbance spectrum showed intense absorption features in the UV spectral region. A broad blue emission peak centered at 441 nm due to donor–acceptor gallium–oxygen vacancy pair recombination appeared. The photocatalytic activity toward Rhodamine B under visible light irradiation was higher for nanorods at pH 10.

36 MATERIALS SCIENCE↗

Controlled synthesis of snowflake-like self-assemblies palladium nanostructures under microwave irradiation

Graphical abstract: - Highlights: • We demonstrated the synthesis of snowflake-like palladium nanostructures for the first time. • We discussed the influencing factors on the synthesis of snowflake-like Pd nanostructures. • The molar ratio of H{sub 2}Pd{sub 4} to PVP at 5 is the optimal selection. • The growth process was discussed. - Abstract: Self-assembly snowflake-like palladium nanostructures were synthesized under microwave irradiation using H{sub 2}PdCl{sub 4} as precursor, benzyl alcohol as both solvent and reducing agent, and PVP as stabilizer. The Pd snowflake-like nanostructures were formed and then characterized by transmission electron microscopy (TEM) and X-ray powder diffraction. The TEM images showed that the Pd nano-snowflakes were self-assemblies organized by hundreds of small spherical nanoparticles. Pd snowflake-like nanostructures with well-defined shape and uniform size can be obtained by tuning the concentration of palladium precursor, the molar ratio of H{sub 2}PdCl{sub 4}/PVP, as well as the heating time by microwave irradiation. The possible growing process of the snowflake-like Pd structures was also proposed on the basis of investigating the properties of as-synthesized Pd nanostructures under different conditions.

36 MATERIALS SCIENCE↗

Sonochemical and hydrothermal synthesis of PbTe nanostructures with the aid of a novel capping agent

Graphical abstract: - Highlights: • PbTe nanostructures were prepared with the aid of Schiff-base compound. • Sonochemical and hydrothermal methods were employed to fabricate PbTe nanostrucrues. • The effect of preparation parameters on the morphology of PbTe was investigated. - Abstract: In this work, a new Schiff-base compound derived from 1,8-diamino-3,6-dioxaoctane and 2-hydroxy-1-naphthaldehyde marked as (2-HyNa)-(DaDo) was synthesized, characterized, and then used as capping agent for the preparation of PbTe nanostructures. To fabricate PbTe nanostructures, two different synthesis methods; hydrothermal and sonochemical routes, were applied. To further investigate, the effect of preparation parameters like reaction time and temperature in hydrothermal synthesis and sonication time in the presence of ultrasound irradiation on the morphology and purity of the final products was tested. The products were analyzed with the aid of SEM, TEM, XRD, FT-IR, and EDS. Based on the obtained results, it was found that pure cubic phased PbTe nanostructures have been obtained by hydrothermal and sonochemical approaches. Besides, SEM images showed that cubic-like and rod-like PbTe nanostructures have been formed by hydrothermal and sonochemical methods, respectively. Sonochemical synthesis of PbTe nanostructures was favorable, because the synthesis time of sonochemical method was shorter than that of hydrothermal method.

36 MATERIALS SCIENCE↗

Selected Area Deposition of PtC x Nanostructures: Implications for Functional Coatings of 3D Nanoarchitectures

Here, we report that selected area deposition of 3D nanostructures is induced via a pyrolytic laser chemical vapor deposition (CVD) process where selected area heating results from the unique photothermal transport regime that is intrinsic to 3D nanostructures. PtC x composite nanostructures were deposited by focused electron beam-induced deposition (FEBID) and used as 3D templates. Subsequent simultaneous localized delivery of an organometallic PtC x precursor and pulsed 915 nm laser irradiation to the pre-defined nanostructures results in selected area deposition on the FEBID features. Results indicate the ability to initiate the process on sub-diffraction-limit nanoscale features. To elucidate the mechanisms that are operative in the selected area deposition, we analyze the effects of the laser repetition rate, power, and pulse duration. Thermal simulations corroborate that the pseudo-1D thermal transport of the nanostructure geometry coupled with the optical and thermal properties of the nanostructure governs the CVD reaction. The results demonstrated here suggest that controlling the thermal transport in nanomaterial architectures could be a useful means to spatially control localized photothermally stimulated chemical reactions and induce selected area reactions.

36 MATERIALS SCIENCE↗

Enhanced room temperature ferromagnetism in electrodeposited Co-doped ZnO nanostructured thin films by controlling the oxygen vacancy defects

We report the growth of un-doped and cobalt doped ZnO nanostructures fabricated on FTO coated glass substrates using electrodeposition method. A detailed study on the effects of dopant concentration on morphology, structural, optical, and magnetic properties of the ZnO nanostructures has been carried out systematically by varying the Co concentration (c.{sub Co}) from 0.01 to 1 mM. For c.{sub Co }≤ 0.2 mM, h-wurtzite phase with no secondary phases of Co were present in the ZnO nanostructures. For c.{sub Co} ≤ 0.2 mM, the photoluminescence spectra exhibited a decrease in the intensity of ultraviolet emission as well as band-gap narrowing with an increase in dopant concentration. All the doped samples displayed a broad emission in the visible range and its intensity increased with an increase in Co concentration. It was found that the defect centers such as oxygen vacancies and zinc interstitials were the source of the visible emission. The X-ray photoelectron spectroscopy studies revealed, Co was primarily in the divalent state, replacing the Zn ion inside the tetrahedral crystal site of ZnO without forming any cluster or secondary phases of Co. The un-doped ZnO nanorods exhibited diamagnetic behavior and it remained up to a c.{sub Co} of 0.05 mM, while for c.{sub Co }> 0.05 mM, the ZnO nanostructures exhibited ferromagnetic behavior at room temperature. The coercivity increased to 695 G for 0.2 mM Co-doped sample and then it decreased for c.{sub Co }> 0.2 mM. Our results illustrate that up to a threshold concentration of 0.2 mM, the strong ferromagnetism is due to the oxygen vacancy defects centers, which exist in the Co-doped ZnO nanostructures. The origin of strong ferromagnetism at room temperature in Co-doped ZnO nanostructures is attributed to the s-d exchange interaction between the localized spin moments resulting from the oxygen vacancies and d electrons of Co{sup 2+} ions. Our findings provide a new insight for tuning the defect density by precisely controlling the dopant concentration in order to get the desired magnetic behavior at room temperature.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Correlation between surface modification and photoluminescence properties of β-Ga{sub 2}O{sub 3} nanostructures

In this work three different growth methods have been used to grow β-Ga{sub 2}O{sub 3} nanostructures. The nanostructures were characterized by Grazing Incident X-Ray Diffraction, Scanning Electron Microscopy, Transmission Electron Microscopy and Photoluminescence Spectroscopy. Photoluminescence spectra for all the samples of β-Ga{sub 2}O{sub 3} nanostructures exhibit an UV and blue emission band. The relative intensity of UV and blue luminescence is strongly affected by the surface defects present on the nanostructures. Our study shows that Photoluminescence intensity of UV and blue luminescence can be reliably used to determine the quality of β-Ga{sub 2}O{sub 3} nanostructures. Further the work opens up the possibility of using UV excitation and subsequent Photoluminescence analysis as a possible means for oxygen sensing. The Photoluminescence mechanism in β-Ga{sub 2}O{sub 3} nanostructures is also discussed.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Fabrication of field-effect transistors with transfer-free nanostructured carbon as semiconducting channel material

Carbon nanostructures as active channel material in field effect transistors (FETs) are appealing in microelectronics for their improved performance such as high speed and low energy dissipation. However, these devices require the incorporation of nanostructure transfer steps in the fabrication process flow, which makes difficult its application in large scale integration circuits. Here we present a novel method for the fabrication of FETs with nanostructured carbon in the channel with p-type semiconducting properties and intermediate drain-source current (IDS) on/off ratio. The method is based on the use of Ni nanoparticles in the source-drain gap region as seed material for the formation of carbon nanostructures in the FET channel. FETs without Ni nanoparticles in the channel showed no modulation of IDS as a function of gate voltage. The device fabrication process does not require any carbon nanostructure transfer steps since it directly forms carbon nanostructures electrically connected to the device's source and drain electrodes via electron-beam evaporation of carbon and conventional lithographic processes. Since all device fabrication steps are compatible with Si technology processes, they are capable of being further optimized following process development protocols practiced by the semiconductor industry.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Toward white light emission from plasmonic-luminescent hybrid nanostructures

We study the light emission of plasmonic-luminescent hybrid nanostructures consisting of Ag nanoparticles (NPs) embedded in europium oxide (EuO X ). The Ag NPs present a bidimensional organization in the nanostructures and they optically behave as oblate spheroids. The photoluminescence (PL) spectral response of the nanostructures evolves from a narrow red emission characteristic of Eu 3+ ions in absence of Ag NPs to a broad blue-green emission band associated with Eu 2+ ions when the layer of Ag NPs is present. This behavior is not related to a change in the Eu 2+ /Eu 3+ ratio, which is verified by compositional analysis. Instead, a detailed investigation of the PL emission of the nanostructures suggests that the coupling of the Ag NPs to the Eu 2+ ions present in the EuO X layer, which manifests itself in an efficient sensitization of these ions, enhances their broad visible emission. In particular, the longitudinal mode of the Ag NPs surface plasmon is considered to be responsible for the efficient energy transfer for the non-normal incidence excitation PL configuration used. Finally, the use of a capping amorphous Al 2 O 3 layer allows improving the robustness of hybrid nanostructures and further enhances their PL emission. These findings provide a new path to actively control the selective excitation of Eu 2+ and Eu 3+ ions via a controlled coupling with the surface plasmon resonance modes of the Ag NPs and points to these nanostructures as promising building blocks for the development of integrable white light sources.

36 MATERIALS SCIENCE↗

Nanostructures for Electrical Energy Storage (NEES) (2020 Final Technical Report)

Nanostructures for Electrical Energy Storage (NEES, www.efrc.umd.edu) was an Energy Frontier Research Center supported by the DOE Office of Science, Basic Energy Sciences, from 8/1/2009 to 7/31/2020. Led by the University of Maryland, NEES enjoyed extensive collaborations with its funded partners, including two DOE Laboratories and six universities. The NEES vision has been to reveal a set of scientific insights and design principles that can underpin a next-generation electrical energy storage approach, building on advances in nanoscale science and technology to achieve simultaneous high power and high energy over extended charge/discharge cycling. The vision is motivated by the recognition that scaling into the nano regime opens the door to new physical phenomena and that the tools enlisted in nanoscale research provide major new opportunities for the synthesis not only of materials at molecular scale but for structures at nano scale and above. NEES has translated this vision into its research program based on two observations. First, while the behavior of ions and electrons in electrolytes and in electrode materials is crucial to electrical energy storage (or more appropriately electrochemical energy storage), it is the transport of ion and electron charge between different structural components of a storage device that ultimately determine its performance. With it well recognized that the choice of electrode materials typically constrain ion transport kinetics as well as maximum ion concentration, the search for better electrode materials has been a primary driver of battery research. At the same time the synthesis of electrodes is typically based on aggregation of particles with varying size, shape, and orientation in the electrode. Together with the presence of additional materials to impart electrical conductivity and cohesion to the composite electrode, change in electrode materials is necessarily accompanied by structural changes at the nano/micro scale that are difficult to categorize and manage. From the beginning, NEES’ vision has been to create and study simpler, highly controlled spatial arrangements of known materials as battery components (electrodes, current collectors, and electrolyte) and to understand how design and structure above the molecular scale determines the energy storage performance available from known materials. Second, advances in nanoscience dramatically expanded the portfolio of synthesis methods, structural motifs, and new phenomena available for research. Some of these gave rapid access to new building blocks at the deep nanoscale (e.g., carbon nanotubes grown by self-assembly, nanoscale arrays formed by electrochemical self-alignment, monolayer films controlled by self-limiting reaction). Such advances served as the enabler for the NEES vision to be pursued experimentally through study of 3D structures created and controlled at the nano, micro, and meso scales. Here, we use meso as in the BES MESO Report, implying not only intermediate or varying length scales, but very much the way behavior is influenced by other factors including aggregation of nanocomponents at different densities and spatial configurations, statistical variations in the aggregates, hierarchical architectures in which they can be assembled, or local 3D configurations that result from the architectures. Over its life cycle, NEES has pursued two overarching goals: (1) to understand the scientific fundamentals of electrochemical storage from the nanoscale to the mesoscale; and (2) to create and learn from innovative, controlled, heterogeneous nanostructures, where such nanostructures can enable the first goal and serve as models for future paradigms in energy storage. Specific goals have included: Synthesize heterogeneous nanostructures comprised of multiple materials arranged in controlled fashion and characterize their behavior; Demonstrate and elucidate design principles for achieving simultaneous high power and high energy; Develop materials processes which enable precision control of thin layers and 3D structures; Investigate the impact of artificial interphases on electrode stability during ion insertion/deinsertion; Create dense arrays of nanostructures to understand how the architecture of these assemblies, along with nanostructure design, influences energy storage behavior at the mesoscale; Identify and understand the consequences of nanoconfinement and local inhomogeneities in 3D mesoscale arrays; Develop and apply computational models to stimulate, guide and interpret experiments.

25 ENERGY STORAGE↗

Capillary Rise of Nanostructured Microwicks

Capillarity refers to the driving force to propel liquid through small gaps in the absence of external forces, and hence enhanced capillary force has been pursued for various applications. In this study, flower like ZnO nanostructures are successfully deposited to enhance capillarity of microwick structures that are specially designed to augment boiling heat transfer performance. Microreactor-assisted nanomaterial deposition, MAND TM , is employed with a flow cell to deposit the ZnO nanostructures on a large sized microwick (4.3 cm × 10.7 cm) with dual-channel configuration. A capillary rise experiment based on the mass gain method is first performed using water and ethanol (EtOH) as the working liquids to demonstrate the enhanced capillary force induced by the ZnO nanostructure on the microwick structure. It is found that the coating of ZnO nanostructure effectively propels the working fluids through the nano- or micro pores created from the ZnO nanostructure and consequently improves the capillary force. In order to investigate the wicking mechanism of the ZnO coated microwick structure, the capillary rise result based on height measurement was compared with analytical models. It is found that the gravity effect and viscous force play an important role in wicking rise of the coated wick structure. This study aims at demonstrating the capability of the integrated MAND process with a flow cell for producing a large scaled nanostructured surface, which eventually has a great potential for enhanced boiling heat transfer.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Probing electronic transport of individual nanostructures with atomic precision

Accessing individual nanostructures with atomic precision is an important process in the bottom-up fabrication and characterization of electronic nanodevices. Local electrical contacts, namely nanoelectrodes, are often fabricated by using top-down lithography and chemical etching techniques. These processes however lack atomic precision and introduce the possibility of contamination. Here, we review recent reports on the application of a field-induced emission process in the fabrication of local contacts onto individual nanowires and nanotubes with atomic spatial precision. In this method, gold nanoislands are deposited onto nanostructures precisely by using a scanning tunneling microscope tip, which provides a clean and controllable process to ensure both electrically conductive and mechanically reliable contacts. The applicability of the technique has been demonstrated in a wide variety of nanostructures, including silicide atomic wires, carbon nanotubes, and copper nanowires. These local contacts bridge the nanostructures and the transport probes, allowing for the measurements of both electrical transport and scanning tunneling microscopy on the same nanostructures in situ. The direct correlation between electronic and transport properties and atomic structures can be explored on individual nanostructures at the unprecedented atomic level.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Self-Repair of Structure and Bioactivity in a Supramolecular Nanostructure

Supramolecular nanostructures formed through self-assembly can have energy landscapes, which determine their structures and functions depending on the pathways selected for their synthesis and processing and on the conditions they are exposed to after their initial formation. We report here on the structural damage that occurs in supramolecular peptide amphiphile nanostructures, during freezing in aqueous media, and the self-repair pathways that restore their functions. We found that freezing converts long supramolecular nanofibers into shorter ones, compromising their ability to support cell adhesion, but a single heating and cooling cycle reverses the damage and rescues their bioactivity. Thermal energy in this cycle enables noncovalent interactions to reconfigure the nanostructures into the thermodynamically preferred long nanofibers, a repair process that is impeded by kinetic traps. In addition, we found that nanofibers disrupted during freeze-drying also exhibit the ability to undergo thermal self-repair and recovery of their bioactivity, despite the extra disruption caused by the dehydration step. Following both freezing and freeze-drying, which shorten the 1D nanostructures, their self-repair capacity through thermally driven elongation is inhibited by kinetically trapped states, which contain highly stable noncovalent interactions that are difficult to rearrange. These states decrease the extent of thermal nanostructure repair, an observation we hypothesize applies to supramolecular systems in general and is mechanistically linked to suppressed molecular exchange dynamics.

36 MATERIALS SCIENCE↗

Design of Hollow Nanostructures for Energy Storage, Conversion and Production

Abstract Hollow nanostructures have shown great promise for energy storage, conversion, and production technologies. Significant efforts have been devoted to the design and synthesis of hollow nanostructures with diverse compositional and geometric characteristics in the past decade. However, the correlation between their structure and energy‐related performance has not been reviewed thoroughly in the literature. Here, some representative examples of designing hollow nanostructure to effectively solve the problems of energy‐related technologies are highlighted, such as lithium‐ion batteries, lithium‐metal anodes, lithium–sulfur batteries, supercapacitors, dye‐sensitized solar cells, electrocatalysis, and photoelectrochemical cells. The great effect of structure engineering on the performance is discussed in depth, which will benefit the better design of hollow nanostructures to fulfill the requirements of specific applications and simultaneously enrich the diversity of the hollow nanostructure family. Finally, future directions of hollow nanostructure design to solve emerging challenges and further improve the performance of energy‐related technologies are also provided.

Wang, Jiangyan↗

Effects of laser fluence on the Cd(OH){sub 2}/CdO nanostructures produced by pulsed laser ablation method

In this experimental study, Cd (OH){sub 2}/CdO nanostructures were produced by pulsed laser ablation method. The beam of a Q-switched Nd:YAG laser with wavelength of 1064 nm at different fluences was employed to irradiate the cadmium target in distilled water. The obtained products at different fluences of laser pulse were characterized by UV–Vis-NIR spectroscopy, X-ray diffraction, scanning electron microscopy, and transmission electron microscopy. Results show that both morphology and chemical bonds of produced Cd nanostructures were changed by increasing the laser fluence. The absorption spectra shows that the Cd(OH){sub 2} nanostructures could be transformed into CdO nanostructures with increasing the laser fluence. XRD analysis showed the presence of crystalline γ-Cd(OH){sub 2}, Cd(OH){sub 2} and CdO phases, in the monoclinic, hexagonal and cubic structure, respectively. Results revealed that obtained nanostructures are particle in lowest fluence, while wire shaped nanostructures were formed with increasing the laser fluence. An increase of the laser fluence induced the synthesis of higher aspect ratio nanowires with a smaller tendency of adhesion.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Hydrothermal synthesis of urchin-like Co{sub 3}O{sub 4} nanostructures and their electrochemical sensing performance of H{sub 2}O{sub 2}

Nanostructured tricobalt tetraoxide, Co{sub 3}O{sub 4}, was hydrothermally synthesized starting from cobalt dichloride hexahydrate (CoCl{sub 2}·6H{sub 2}O) and urea (H{sub 2}NCONH{sub 2}) as precursor and polyethylene glycol-400 (PEG-400) as a structure-directing agent. Uniform urchin-like nanostructures were hydrothermally obtained at 150 °C for 16 h, and the Co{sub 3}O{sub 4} morphology did not collapse after a subsequent calcination at 300 °C for 2 h. XRD measurements indicated that the average sizes of Co{sub 3}O{sub 4} particles prior and after heating at 300 °C are 64 and 44 nm, respectively. This material has been successfully used for the nanostructuration of screen-printed carbon electrodes (SPCEs) which were used for the sensitive electrochemical detection of hydrogen peroxide (H{sub 2}O{sub 2}). The sensor is endowed with a large dynamic range (0.1 to 50 µM) and a limit of detection of 0.145 µM. The as obtained results show that the Co{sub 3}O{sub 4} nanomaterial could be a candidate to be used as sensors for the detection of analytes. - Graphical abstract: The nanowires appear to have a common center and grow to the outside along the radial direction. - Highlights: • Nanostructured was hydrothermally prepared using PEG-400. • Uniform urchin-like Co{sub 3}O{sub 4} nanostructures were hydrothermally obtained. • X-ray diffraction showed a cubic structure after calcinations process. • Nanostructured Co{sub 3}O{sub 4} was used for the sensitive electrochemical detection of H{sub 2}O{sub 2.} • The sensor is endowed with a large dynamic range 0.1 to 50 µM.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Fabrication, characterization, cathodoluminescence, and field-emission properties of silica (SiO{sub 2}) nanostructures

High-quality one dimensional amorphous SiO{sub 2} nanostructures with different morphologies (nanowires and starfish-like nanostructures) are synthesized through a simple catalysis-free approach and effective thermal evaporation process. The morphologies, microstructures, and compositions of the products are investigated by X-ray powder diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). A promising optical property (cathodoluminescence (CL) in a strong ultraviolet (UV) emission and a weak blue emission at room temperature) was detected in the as-synthesized nanostructures. Field-emission measurements show that the SiO{sub 2} nanostructures may also be a promising FE emitter candidate if we can improve the conductivity and decrease the density of the nanostructures. - Highlights: Black-Right-Pointing-Pointer A simple catalysis-free approach and effective thermal evaporation process Black-Right-Pointing-Pointer High-quality one dimensional amorphous SiO{sub 2} nanostructures Black-Right-Pointing-Pointer A strong ultraviolet (UV) emission and a weak blue emission at room temperature Black-Right-Pointing-Pointer A promising FE emitter's candidate.

36 MATERIALS SCIENCE↗