scholarly journals Hydrothermal Synthesis and Mechanism of Unusual Zigzag Ag2Te and Ag2Te/C Core-Shell Nanostructures

2014 ◽  
Vol 2014 ◽  
pp. 1-5
Author(s):  
Saima Manzoor ◽  
Yumin Liu ◽  
Zhongyuan Yu ◽  
Xiuli Fu ◽  
Guijun Ban
Keyword(s):  
Electron Microscopy ◽  
Single Step ◽  
Reducing Agent ◽  
Synthesis Process ◽  
Core Shell ◽  
Hydrothermal Route ◽  
Shell Nanostructures ◽  
Transmission Electron ◽  
Sodium Tellurite ◽  
Compositional Properties

A single step surfactant-assisted hydrothermal route has been developed for the synthesis of zigzag silver telluride nanowires with diameter of 50–60 nm and length of several tens of micrometers. Silver nitrate (AgNO3) and sodium tellurite (Na2TeO3), are the precursors and polyvinylpyrrolidone (PVP) is used as surfactant in the presence of the reducing agent, that is, hydrazine hydrate (N2H4·H2O). In addition to the zigzag nanowires a facile hydrothermal reduction-carbonization route is proposed for the preparation of uniform core-shell Ag2Te/C nanowires. In case of Ag2Te/C synthesis process the same precursors are employed for Ag and Te along with the ethylene glycol used as reducing agent and glucose as the carbonizing agent. Morphological and compositional properties of the prepared products are analyzed with the help of scanning electron microscopy, transmission electron microscopy, and energy dispersive X-ray spectroscopy, respectively. The detailed formation mechanism of the zigzag morphology and reduction-carbonization growth mechanism for core-shell nanowires are illustrated on the bases of experimental results.

Formation of bismuth iron oxide based core–shell structures and their dielectric, ferroelectric and magnetic properties

2019 ◽  
Vol 7 (5) ◽  
pp. 1280-1291 ◽  
Author(s):  
Alaka Panda ◽  
R. Govindaraj ◽  
R. Mythili ◽  
G. Amarendra
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Magnetic Properties ◽  
Iron Oxide ◽  
Shell Structures ◽  
Core Shell ◽  
Bismuth Iron Oxide ◽  
The Core ◽  
Shell Nanostructures ◽  
Transmission Electron

Bismuth and iron oxides subjected to ball milling followed by controlled annealing treatments showed the formation of core–shell nanostructures with Bi2Fe4O9 as the core and a shell of BiFeO3 and Bi25FeO40 phases as deduced based on the analysis of transmission electron microscopy results.

Synthesis of Trilaminar Core–Shell Au/α-Fe2O3@SnO2Nanocomposites and their Application for Nonenzymatic Dopamine Electrochemical Sensing

NANO ◽  
2019 ◽  
Vol 14 (11) ◽  
pp. 1950138 ◽  
Author(s):  
Sai Zhang ◽  
Shijun Yue ◽  
Jiajia Li ◽  
Jianbin Zheng ◽  
Guojie Gao
Keyword(s):  
Electron Microscopy ◽  
High Sensitivity ◽  
Electrochemical Sensing ◽  
Synthesis Process ◽  
Core Shell ◽  
X Ray Diffraction ◽  
X Ray ◽  
Long Term Stability ◽  
Transmission Electron

Au nanoparticles anchored on core–shell [Formula: see text]-Fe2O3@SnO2 nanospindles were successfully constructed through hydrothermal synthesis process and used for fabricating a novel nonenzymatic dopamine (DA) sensor. The structure and morphology of the Au/[Formula: see text]-Fe2O3@SnO2 trilaminar nanohybrid film were characterized by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM) and X-ray diffraction (XRD). The electrochemical properties of the sensor were investigated by cyclic voltammetry and amperometry. The experimental results suggest that the composites have excellent catalytic property toward DA with a wide linear range from 0.5[Formula: see text][Formula: see text]M to 0.47[Formula: see text]mM, a low detection limit of 0.17[Formula: see text][Formula: see text]M (S/[Formula: see text]) and high sensitivity of 397.1[Formula: see text][Formula: see text]A[Formula: see text]mM[Formula: see text][Formula: see text]cm[Formula: see text]. In addition, the sensor exhibits long-term stability, good reproducibility and anti-interference.

Characterisation of 3D-GaN/InGaN core-shell nanostructures by transmission electron microscopy

2014 ◽  
Vol 11 (3-4) ◽  
pp. 425-427 ◽  
Author(s):  
Ian Griffiths ◽  
David Cherns ◽  
Xue Wang ◽  
Hergo-Heinrich Wehman ◽  
Martin Mandl ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Core Shell ◽  
Shell Nanostructures ◽  
Transmission Electron

scholarly journals Towards Iron-Titanium Oxide Nanostructures from Ecuadorian Black Mineral Sands

Minerals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 122
Author(s):  
Karina J. Lagos ◽  
Bojan A. Marinkovic ◽  
Alexis Debut ◽  
Karla Vizuete ◽  
Víctor H. Guerrero ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Titanium Oxide ◽  
Low Cost ◽  
Mineral Resources ◽  
Added Value ◽  
Secondary Phases ◽  
Hydrothermal Route ◽  
Oxide Nanostructures ◽  
Transmission Electron ◽  
Pre Treatment

Ecuadorian black mineral sands were used as starting material for the production of iron-titanium oxide nanostructures. For this purpose, two types of mineral processing were carried out, one incorporating a pre-treatment before conducting an alkaline hydrothermal synthesis (NaOH 10 M at 180 °C for 72 h), and the other prescinding this first step. Nanosheet-assembled flowers and nanoparticle agglomerates were obtained from the procedure including the pre-treatment. Conversely, nanobelts and plate-like particles were prepared by the single hydrothermal route. The nanoscale features of the product morphologies were observed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analyses. The ilmenite and hematite molar fractions, within the ilmenite-hematite solid solution, in the as-synthetized samples were estimated by Brown’s approach using the computed values of unit-cell volumes from Le Bail adjustments of X-ray powder diffraction (XRPD) patterns. The resulting materials were mainly composed of Fe-rich ilmenite-hematite solid solutions (hematite molar contents ≥0.6). Secondary phases, which possibly belong to lepidocrocite-like or corrugated titanate structures, were also identified. The current study demonstrated the feasibility of employing Ecuadorian mineral resources as low-cost precursors to synthesize high-added-value nanostructures with promising applications in several fields.

scholarly journals Epitaxial Growth of Ordered In-Plane Si and Ge Nanowires on Si (001)

Nanomaterials ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 788
Author(s):  
Jian-Huan Wang ◽  
Ting Wang ◽  
Jian-Jun Zhang
Keyword(s):  
Electron Microscopy ◽  
Epitaxial Growth ◽  
Molecular Beam ◽  
Core Shell ◽  
High Quality ◽  
Quantum Devices ◽  
Wafer Scale ◽  
Transmission Electron ◽  
Controllable Growth

Controllable growth of wafer-scale in-plane nanowires (NWs) is a prerequisite for achieving addressable and scalable NW-based quantum devices. Here, by introducing molecular beam epitaxy on patterned Si structures, we demonstrate the wafer-scale epitaxial growth of site-controlled in-plane Si, SiGe, and Ge/Si core/shell NW arrays on Si (001) substrate. The epitaxially grown Si, SiGe, and Ge/Si core/shell NW are highly homogeneous with well-defined facets. Suspended Si NWs with four {111} facets and a side width of about 25 nm are observed. Characterizations including high resolution transmission electron microscopy (HRTEM) confirm the high quality of these epitaxial NWs.

scholarly journals Study on Structure, Thermal Behavior, and Viscoelastic Properties of Nanodiamond-Reinforced Poly (vinyl alcohol) Nanocomposites

Polymers ◽  
2021 ◽  
Vol 13 (9) ◽  
pp. 1426
Author(s):  
Tomáš Remiš ◽  
Petr Bělský ◽  
Tomáš Kovářík ◽  
Jaroslav Kadlec ◽  
Mina Ghafouri Azar ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Mechanical Analysis ◽  
Single Step ◽  
Poly Vinyl Alcohol ◽  
Scanning Calorimetry ◽  
X Ray Scattering ◽  
Transmission Electron ◽  
Primary Particles ◽  
Solution Casting Method ◽  
Average Size

In this work, advanced polymer nanocomposites comprising of polyvinyl alcohol (PVA) and nanodiamonds (NDs) were developed using a single-step solution-casting method. The properties of the prepared PVA/NDs nanocomposites were investigated using Raman spectroscopy, small- and wide-angle X-ray scattering (SAXS/WAXS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and dynamic mechanical analysis (DMA). It was revealed that the tensile strength improved dramatically with increasing ND content in the PVA matrix, suggesting a strong interaction between the NDs and the PVA. SEM, TEM, and SAXS showed that NDs were present in the form of agglomerates with an average size of ~60 nm with primary particles of diameter ~5 nm. These results showed that NDs could act as a good nanofiller for PVA in terms of improving its stability and mechanical properties.

Effect of hydrothermal dwell time on the diameter-controlled synthesis and magnetic property of MnO2 nanorods

2014 ◽  
Vol 28 (06) ◽  
pp. 1450045 ◽  
Author(s):  
Arbab Mohammad Toufiq ◽  
Fengping Wang ◽  
Qurat-ul-Ain Javed ◽  
Yan Li
Keyword(s):  
Electron Microscopy ◽  
Reaction Time ◽  
Dwell Time ◽  
Hydrothermal Reaction ◽  
Ferromagnetic Behavior ◽  
X Ray Diffraction ◽  
Hydrothermal Route ◽  
Transmission Electron ◽  
Facile Hydrothermal Route ◽  
Hydrothermal Reaction Time

In this paper, single crystalline 1D tetragonal MnO 2 pen-type nanorods were synthesized by varying the dwell time through a facile hydrothermal route at a reaction temperature of 250°C. X-ray diffraction (XRD) and transmission electron microscopy (TEM) studies showed that the diameter of MnO 2 nanorods decreases from 460 nm to 250 nm with the increase in hydrothermal reaction time from 5 h to 15 h. Field-emission scanning electron microscopy (FESEM) and TEM studies revealed the evolution of improved surface morphology of MnO 2 nanorods that are prepared with longer hydrothermal reaction time. The magnetic properties of the products were evaluated using vibrating sample magnetometer (VSM) at room temperature, which showed that the as-prepared samples exhibit weak ferromagnetic behavior. The effect of diameter on the magnetization values was observed and discussed in detail.

scholarly journals Effects of Different Surfactant Charges on the Formation of Gold Nanoparticles by the LASiS Method

Materials ◽  
2021 ◽  
Vol 14 (11) ◽  
pp. 2937
Author(s):  
Muhammad Zulfajri ◽  
Wei-Jie Huang ◽  
Genin-Gary Huang ◽  
Hui-Fen Chen
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Gold Nanoparticles ◽  
Laser System ◽  
Synthesis Process ◽  
Au Nps ◽  
Laser Fluences ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
532 Nm

The laser ablation synthesis in solution (LASiS) method has been widely utilized due to its significant prospects in laser microprocessing of nanomaterials. In this study, the LASiS method with the addition of different surfactant charges (cationic CTAB, nonionic TX-100, and anionic SDS) was used to produce Au NPs. An Nd:YAG laser system at 532 nm excitation with some synthetic parameters, including different laser fluences, ablation times, and surfactant concentrations was performed. The obtained Au NPs were characterized by UV-Vis spectroscopy, transmission electron microscopy, and zeta potential analyzer. The Au NPs exhibited the maximum absorption peak at around 520 nm for all samples. The color of Au NPs was changed from red to reddish by increasing the laser fluence. The surfactant charges also played different roles in the Au NPs’ growth during the synthesis process. The average sizes of Au NPs were found to be 8.5 nm, 5.5 nm, and 15.5 nm with the medium containing CTAB, TX-100, and SDS, respectively. Besides, the different surfactant charges induced different performances to protect Au NPs from agglomeration. Overall, the SDS and CTAB surfactants exhibited higher stability of the Au NPs compared to the Au NPs with TX-100 surfactant.

Green Biosynthesis of Anisotropic Gold Nanoparticles Using Ampelopsis grossedentata Extract and their Shape-Controlled by Halogen

2016 ◽  
Vol 40 ◽  
pp. 128-135 ◽  
Author(s):  
Qing Quan Guo ◽  
Xin Fu Ma ◽  
Hai Xiang Ma ◽  
Yao Lu
Keyword(s):  
Electron Microscopy ◽  
Metallic Nanoparticles ◽  
Research Field ◽  
Synthesis Process ◽  
Halide Ions ◽  
Transmission Electron ◽  
Shape Controlled ◽  
Tea Extract ◽  
Ampelopsis Grossedentata ◽  
Anisotropic Gold Nanoparticles

The preparation of size- and shape- controlled metallic nanoparticles using biological methodologies is a noticeably stimulating research field due to their unique physicochemical properties. In this paper, biosynthesis of anisotropic AuNPs using Ampelopsis grossedentata extract and the effects of halide ions on the formation of AuNPs has been demonstrated. The sizes and morphologies of AuNPs were characterized by UV-vis-NIR spectrophotometer and Transmission Electron Microscopy (TEM). It showed that the shape, size and optical properties of AuNPs can be fine-tuned by varying the dosage of the vine tea extract. The presence of halogen ions has significantly influence the morphology of AuNPs during the synthesis process. Both of Br- and Cl- could produced nanoplates, whereas I- distorted the triangle nanoparticles to induce the formation of aggregated spherical ones.

scholarly journals Synthesis of Gold Nanoparticles Using p-Aminobenzoic Acid and p-Aminosalicylic Acid as Reducing Agent

2019 ◽  
Vol 19 (1) ◽  
pp. 68
Author(s):  
Abdul Aji ◽  
Eko Sri Kunarti ◽  
Sri Juari Santosa
Keyword(s):  
Gold Nanoparticles ◽  
Optimum Condition ◽  
Reducing Agents ◽  
Reducing Agent ◽  
Hydroxyl Group ◽  
Synthesis Process ◽  
Aminobenzoic Acid ◽  
Aminosalicylic Acid ◽  
Amino Groups ◽  
Transmission Electron

Synthesis of gold nanoparticles (AuNPs) by reduction of HAuCl4 with p-aminobenzoic acid and p-aminosalicylic acid as a reducing agent was investigated. This work was conducted in order to determine the optimum condition of AuNPs synthesis and examine the effect of the hydroxyl group in p-aminosalicylic acid towards the size, shape, and stability of the synthesized gold nanoparticles (AuNPs). The optimum condition of the gold nanoparticles synthesis was determined by UV/Vis spectrophotometer, the shape and size of gold nanoparticles were measured by Transmission Electron Microscope (TEM). The synthesis process was started by reacting HAuCl4 and the reducing agents in an aqueous solution at 86 ºC. The initial gold concentration, reducing agents concentration and pH were varied in order to obtain the optimum condition. In the optimum condition, the results showed that p-aminosalicylic acid containing both hydroxyl and amino groups performed higher reduction ability compared to p-aminobenzoic acid that only containing an amino group. Reducing agents which have a hydroxyl group (p-aminosalicylic acid) could produce AuNPs with a smaller concentration of HAuCl4 than p-aminobenzoic acid. Gold nanoparticles that were synthesized with p-aminosalicylic acid were more stable and had a smaller particle size compared to its counterpart that is synthesized with p-aminobenzoic acid.

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