Characterisation of Nanostructured Co3O4 Synthesised by the Thermal Decomposition of an Inorganic Precursor

2014 ◽  
Vol 67 (11) ◽  
pp. 1671 ◽  
Author(s):  
K. Kalpanadevi ◽  
C. R. Sinduja ◽  
R. Manimekalai
Keyword(s):  
Electron Microscopy ◽  
Thermal Decomposition ◽  
Cobalt Oxide Nanoparticles ◽  
Inorganic Precursor ◽  
Annealing Conditions ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Infrared Spectral ◽  
Average Size ◽  
Microscopy Techniques

Nanocrystalline Co3O4 has been synthesised using an inorganic precursor via thermal decomposition. The prepared inorganic precursor Co(cinnamate)2(N2H4)2 was characterised by hydrazine and metal analyses, infrared spectral analysis, and thermogravimetric analysis. Using appropriate annealing conditions, cobalt oxide nanoparticles of average size ~11 nm were synthesised by thermal treatment of the precursor. The nanoparticles’ size and structure were characterised using X-ray diffraction, high-resolution transmission electron microscopy, selected-area electron diffraction, and scanning electron microscopy techniques.

scholarly journals Characterisation of Zinc Oxide and Cadmium Oxide Nanostructures Obtained from the Low Temperature Thermal Decomposition of Inorganic Precursors

2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
K. Kalpanadevi ◽  
C. R. Sinduja ◽  
R. Manimekalai
Keyword(s):  
Electron Microscopy ◽  
Thermal Decomposition ◽  
Zinc Oxide ◽  
Low Temperature ◽  
Cadmium Oxide ◽  
Oxide Nanoparticles ◽  
Average Particle ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Infrared Spectral

Low temperature syntheses of zinc oxide and cadmium oxide nanoparticles are reported in this paper. The inorganic precursor complexes were prepared and characterised by hydrazine and metal analyses, infrared spectral analysis, and thermal analysis. Using appropriate annealing conditions, zinc oxide and cadmium oxide nanoparticles of average particle sizes around 13 nm and 30 nm were synthesised from the precursors by a simple thermal decomposition route. The synthesised nanoparticles were characterised for their size and structure using X-Ray diffraction (XRD), high resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED), and scanning electron microscopy (SEM) techniques.

Solid State Synthesis and Characterization of NiTe Nanocrystals

2014 ◽  
Vol 29 ◽  
pp. 35-39 ◽  
Author(s):  
C.E.M. Campos
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Solid State ◽  
Processing Time ◽  
Ferromagnetic Behavior ◽  
X Ray Diffraction ◽  
Selected Area Electron Diffraction ◽  
Nickel Powders ◽  
Transmission Electron ◽  
Average Size

NiTe nanocrystals were prepared through facile and fast solid state reaction (mechanical alloying) of pure elemental tellurium and nickel powders in an argon atmosphere. The samples processed for 3 h, 5 h and 10 h were characterized by X-ray diffraction, transmission electron microscopy, magnetization and Raman spectroscopy. Hexagonal NiTe crystals with an average size of 30 nm can be obtained after only 3 h of processing time. Transmission electron microscopy images showed a broad crystalline size distribution in the agglomerated particles and selected area electron diffraction revealed its crystalline character. NiTe ferromagnetic behavior was confirmed and magnetic parameters were dependent on processing time. Raman spectra showed no unreacted Te or tellurium oxides, but it also showed that laser induced phases transitions (including Te re-crystallization) can be observed for modest laser power (<3 mW).

Controlled Synthesis of Hierarchical Flower-Like CuS Spheres by a Facile Microwave Hydrothermal Method

2012 ◽  
Vol 512-515 ◽  
pp. 265-268 ◽  
Author(s):  
Hui Qi ◽  
Jian Feng Huang ◽  
Li Yun Cao ◽  
Jian Peng Wu
Keyword(s):  
Electron Microscopy ◽  
Cetyltrimethylammonium Bromide ◽  
Controlled Synthesis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Microwave Hydrothermal ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Average Size ◽  
20 Nm

–Hierarchical flower–like CuS spheres have been synthesized by a facile microwave hydrothermal (MH) method using cetyltrimethylammonium bromide (CTAB) as the surfactant. The as–prepared CuS crystallites under different CTAB contents were characterized by X–ray diffraction (XRD), field–emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), and selected area electron diffraction (SAED). Results show that the CTAB–assisted CuS particles have hierarchical flower–like microstructures that were assembled by thin nanoflakes with thickness of 10~20 nm. The corresponding HRTEM images reveal that these nanoflakes are composed of many nanoparticles with average size of about 7 nm. Moreover, when increasing the CTAB contents from 0 g⁄mL to 0.02 g⁄mL, the as–prepared CuS particles were found to have better dispersion stability with decreased average sizes of the hierarchical flower–like spheres. Comparing with the bulk CuS particles, the related UV–vis absorption spectrum of the as–prepared crystallites exhibits an obvious red shift with the absorption peak at 739 nm.

Secondary Phases Present in Spray Formed Al-10.5Zn-2.0Mg-1.5Cu Alloy

2010 ◽  
Vol 97-101 ◽  
pp. 1073-1076
Author(s):  
Shu Guo ◽  
Zhi Liang Ning ◽  
Fu Yang Cao ◽  
Jian Fei Sun
Keyword(s):  
Electron Microscopy ◽  
Spray Forming ◽  
Crystallographic Structure ◽  
Secondary Phases ◽  
Eutectic Liquid ◽  
Large Area ◽  
Intergranular Phase ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Average Size

Al-10.5Zn-2.0Mg-1.5Cu alloy was produced by spray forming (SF) technique. The initial microstructure, particularly secondary phases, present in the as-SFed alloy was examined by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) with attached energy dispersive X-ray spectroscopy (EDS). The results indicated that the equiaxed α-Al grains have an average size of about 18-20 μm in diameter. The intergranular phase was identified as MgZn2 by selected area electron diffraction (SAED) pattern, which was also distributed in the grain interior as well as Al2Mg3Zn3. A needle-like Al23Cu(FeCrMn)4 precipitate was detected. The combined analysis of morphology and crystallographic structure suggested that the Al23Cu(FeCrMn)4 grew along its long axis of <001> orientation. The refinement of the intergranular phases occurred, which is probably due to a decreased amount of eutectic liquid phase finally solidifying on a large area of grain boundaries.

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.

Synthesis and Photoluminescence Properties of Novel SnO2 Zigzag Nanoribbons

2010 ◽  
Vol 97-101 ◽  
pp. 4213-4216
Author(s):  
Jian Xiong Liu ◽  
Zheng Yu Wu ◽  
Guo Wen Meng ◽  
Zhao Lin Zhan
Keyword(s):  
Electron Microscopy ◽  
Room Temperature ◽  
Vapour Deposition ◽  
Chemical Vapour ◽  
Photoluminescence Properties ◽  
X Ray Diffraction ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Ceramic Boat

Novel single-crystalline SnO2 zigzag nanoribbons have been successfully synthesized by chemical vapour deposition. Sn powder in a ceramic boat covered with Si plates was heated at 1100°C in a flowing argon atmosphere to get deposits on a Si wafers. The main part of deposits is SnO2 zigzag nanoribbons. They were characterized by means of X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM) and selected-area electron diffraction (SAED). SEM observations reveal that the SnO2 zigzag nanoribbons are almost uniform, with lengths near to several hundred micrometers and have a good periodically tuned microstructure as the same zigzag angle and growth directions. Possible growth mechanism of these zigzag nanoribbons was discussed. A room temperature PL spectrum of the zigzag nanoribbons shows three peaks at 373nm, 421nm and 477nm.The novel zigzag microstructures will provide a new candidate for potential application.

A novel additive-free oxides–hydrothermal approach for monazite-type LaPO4nanomaterials with controllable morphologies

2010 ◽  
Vol 43 (5) ◽  
pp. 990-997 ◽  
Author(s):  
Jie Ma ◽  
Qingsheng Wu
Keyword(s):  
Electron Microscopy ◽  
Treatment Time ◽  
Synthesis Temperature ◽  
Molar Ratio ◽  
Hydrothermal Conditions ◽  
Typical Sample ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
High Resolution Tem ◽  
Hydrothermal Approach

A facile oxides–hydrothermal (O–HT) method is demonstrated to prepare high-purity monazite-type LaPO4nanomaterials. In this approach, La2O3and P2O5powder are first directly used as precursors under additive-free hydrothermal conditions. The as-prepared samples are characterized with X-ray diffraction, Fourier transform IR spectroscopy, thermogravimetry, scanning electron microscopy, transmission electron microscopy (high-resolution TEM, energy dispersive spectroscopy) and selected-area electron diffraction. The typical sample obtained at 433 K in 24 h comprises uniform single-crystal nanofibres with a diameter of ∼15–28 nm and an aspect ratio of 30–50. The influences of treatment time, synthesis temperature and P/La molar ratio are investigated. The phase transition from hexagonal hydrate to monoclinic anhydrous lanthanum phosphate and the growth process of nanofibres are revealed by the experimental results. The formation mechanism of the monoclinic LaPO4is discussed. The result indicates that the P/La ratio does not influence the composition and crystal phase but changes the morphology of the product in the O–HT system.

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