scholarly journals Hydrothermal Preparation of Ag/Ag1.69Sb2.27O6.25 Sesame-Hollow-Ball-Type Nanocomposites: The Formation Mechanism of Metallic Ag in the Ag-H2O System at 400 K

2020 ◽  
Vol 2020 ◽  
pp. 1-8
Author(s):  
Haomei Liu ◽  
Xihai Hao ◽  
Yuejun Liu ◽  
Aiguo Yan
Keyword(s):  
Electron Microscopy ◽  
Bet Surface Area ◽  
X Ray Diffraction ◽  
Hydrothermal Preparation ◽  
Transmission Electron ◽  
Ag Particles ◽  
Mean Size ◽  
One Step ◽  
Chemical States ◽  
Hollow Ball

Ag/Ag1.69Sb2.27O6.25 sesame-hollow-ball-type nanocomposites were prepared via a facile one-step hydrothermal method at 400 K. Power X-ray diffraction analysis shows that all diffraction peaks were well consistent with JCPDS card no: 89-6552 of Ag1.69Sb2.27O6.25. Scanning electron microscopy and high-resolution transmission electron microscopy images of the composites indicate that some smaller metallic Ag particles with size∼18.3 nm uniformly dense on the surface of Ag1.69Sb2.27O6.25 hollow nanospheres with a mean size of about 170 nm, producing Ag/Ag1.69Sb2.27O6.25 hollow-sesame-ball nanocomposites. The surface chemical state of Ag/Ag1.69Sb2.27O6.25 is investigated by XPS, and all peaks of Ag 3d, O 1s, and Sb 3d show their different chemical states. The BET surface area of the sample is 7.268 m2/g, and the pore sizes of nanocomposites are more than 5 nm. The light absorption property of as-prepared materials is studied by UV-vis/DRS, and the adsorption band is located at 445 nm, and the estimated energy band gap (Eg) is 2.55 eV. The calculated partial φ-pH diagrams in the Ag-H2O system at 400 K predict that the Ag+ ion can react with H2 to form metallic Ag.

Microwave-Assisted Hydrothermal Preparation of SnO2/MoS2 Composites and their Electrochemical Performance

NANO ◽  
2016 ◽  
Vol 11 (02) ◽  
pp. 1650023 ◽  
Author(s):  
Lin Ma ◽  
Xiaoping Zhou ◽  
Limei Xu ◽  
Xuyao Xu ◽  
Lingling Zhang
Keyword(s):  
Electron Microscopy ◽  
Synergetic Effect ◽  
Electrochemical Performances ◽  
Microwave Method ◽  
X Ray Diffraction ◽  
Hydrothermal Preparation ◽  
X Ray ◽  
Microwave Assisted ◽  
Transmission Electron ◽  
Mean Size

We introduce a two-step hydrothermal and microwave method to prepare novel SnO2/MoS2 composites. The as-prepared samples are well characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and high resolution transmission electron microscopy (HRTEM). The experimental results indicate that the SnO2/MoS2 composites are composed of MoS2 nanosheets and ultrafine SnO2 nanoparticles with mean size of 3–4[Formula: see text]nm which are well-distributed and anchored on the surface of MoS2 nanosheets. The resultant composites demonstrate prominently improved electrochemical performances, which could be attributed to the unique and robust microstructures and synergetic effect between MoS2 and SnO2.

scholarly journals Microwave-assisted preparation of ZnS and ZnSe nanocrystals with different morphologies for photodegradation process of organic dyes

2019 ◽  
Author(s):  
Katarzyna Matras-Postolek ◽  
A. Zaba ◽  
S. Sovinska ◽  
D. Bogdal
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Organic Dyes ◽  
Zinc Sulphide ◽  
Conventional Heating ◽  
Bet Surface Area ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Vis Spectroscopy

Zinc sulphide (ZnS) and zinc selenide (ZnSe) and manganese-doped and un-doped with different morphologies from 1D do 3D microflowers were successfully fabricated in only a few minutes by solvothermal reactions under microwave irradiation. In order to compare the effect of microwave heating on the properties of obtained  nanocrystals, additionally the synthesis under conventional heating was conducted additionally in similar conditions. The obtained nanocrystals were systematically characterized in terms of structural and optical properties using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), diffuse reflectance UV-Vis spectroscopy (DR UV-Vis), Fourier-transform infrared spectroscopy (FT-IR), photoluminescence spectroscopy (PL), X-ray photoelectron spectroscopy (XPS) and Brunauer-Emmett-Teller (BET) surface area analysis. The photocatalytic activity of ZnSe, ZnS, ZnS:Mn and ZnSe:Mn nanocrystals with different morphologies was evaluated by the degradation of methyl orange (MO) and Rhodamine 6G (R6G), respectively. The results show that Mn doped NCs samples had higher coefficient of degradation of organic dyes under ultraviolet irradiation (UV).

The Influence of Introduction of Polyethylene Glycol on Synthesis of Bimodal Mesoporous γ-Al2O3

2013 ◽  
Vol 709 ◽  
pp. 89-92
Author(s):  
Xiang Li ◽  
Xin Mei Liu ◽  
Zi Feng Yan
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Polyethylene Glycol ◽  
Bet Surface Area ◽  
X Ray Diffraction ◽  
Relative Crystallinity ◽  
X Ray ◽  
Transmission Electron ◽  
Increasing Trend ◽  
Opposite Tendency

In the presence of polyethylene glycol (PEG2W),bimodal mesoporous γ-Al2O3 was successfully synthesized via hydrothermal method. The samples were respectively characterized by X-ray diffraction (XRD), N2 physisorption, transmission electron microscopy (TEM), thermogravimetric and differential scanning calorimeter (TG-DSC). Introduction of PEG2W can increase the relative crystallinity of AACH and γ-Al2O3. The BET surface area and pore volume of alumina shows an increasing trend with increasing of PEG2W content, while the pore size shows an opposite tendency. The PEG2W also plays an important role in inducing the formation of the nanorod-like alumina.

scholarly journals Cypermethrin elimination using Fe-TiO2 nanoparticles supported on coconut palm spathe in a solar flat plate photoreactor

2020 ◽  
Vol 29 ◽  
pp. 2633366X2090616
Author(s):  
Ricardo Andrés Solano Pizarro ◽  
Adriana Patricia Herrera Barros
Keyword(s):  
Electron Microscopy ◽  
Flat Plate ◽  
Diffuse Reflectance Spectroscopy ◽  
Cocos Nucifera ◽  
Operating Costs ◽  
Bet Surface Area ◽  
Gas Chromatography Mass Spectrometry ◽  
X Ray Diffraction ◽  
Molar Ratios ◽  
Transmission Electron

In this research, the photocatalytic degradation of cypermethrin using iron-titanium dioxide (Fe-TiO2) nanoparticles supported in a biomaterial was evaluated. The nanoparticles of TiO2 were synthesized by the green chemistry method assisted by ultrasound and doped by chemical impregnation using Fe+3:Ti molar ratios of 0, 0.05, 0.075 and 0.1 to make efficient use of direct sunlight ( λ > 310 nm). All nanoparticles were immobilized on the surface of coconut spathe ( Cocos nucifera). The degradation was carried out at room temperature and natural pH in a flat plate solar reactor, on which the composite material was subjected. The concentration of cypermethrin was determined after 12,000 J m−2 of accumulated radiation from gas chromatography–mass spectrometry and the resulting material was characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, Fourier-transform infrared spectroscopy, ultraviolet–visible diffuse reflectance spectroscopy, and Brunauer-Emmett-Teller (BET) surface area. The best results were achieved with the use of Evonik TiO2 P-25, Fe:Ti = 0 and Fe:Ti = 0.05 in suspension, with percentages of degradation of cypermethrin of 99.84%, 99.62%, and 100%, respectively. However, the materials supported on the biomaterial of coconut allowed to reach degradation percentages higher than 80%, with the advantage that it minimizes operating costs, as they are not necessarily filtering or centrifuging processes to separate the catalyst.

scholarly journals A facile synthesis of a carbon-encapsulated Fe3O4 nanocomposite and its performance as anode in lithium-ion batteries

2013 ◽  
Vol 4 ◽  
pp. 699-704 ◽  
Author(s):  
Raju Prakash ◽  
Katharina Fanselau ◽  
Shuhua Ren ◽  
Tapan Kumar Mandal ◽  
Christian Kübel ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Lithium Ion ◽  
Iron Pentacarbonyl ◽  
X Ray Diffraction ◽  
Facile Synthesis ◽  
X Ray ◽  
Transmission Electron ◽  
Lithium Ion Cell ◽  
Carbon Framework ◽  
One Step

A carbon-encapsulated Fe3O4 nanocomposite was prepared by a simple one-step pyrolysis of iron pentacarbonyl without using any templates, solvents or surfactants. The structure and morphology of the nanocomposite was investigated by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, Brunauer–Emmett–Teller analysis and Raman spectroscopy. Fe3O4 nanoparticles are dispersed intimately in a carbon framework. The nanocomposite exhibits well constructed core–shell and nanotube structures, with Fe3O4 cores and graphitic shells/tubes. The as-synthesized material could be used directly as anode in a lithium-ion cell and demonstrated a stable capacity, and good cyclic and rate performances.

Activation of persulfate by heterogeneous catalyst ZnCo2O4–RGO for efficient degradation of bisphenol A

2020 ◽  
Vol 98 (12) ◽  
pp. 771-778
Author(s):  
Xin Chang ◽  
Xiangyang Xu ◽  
Zhifeng Gao ◽  
Yingrui Tao ◽  
Yixuan Yin ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Bisphenol A ◽  
Photoelectron Spectroscopy ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
X Ray ◽  
Transmission Electron ◽  
Nucleation Sites ◽  
One Step ◽  
Application Potential

A nanocomposite, reduced graphene oxide (RGO) modified ZnCo2O4 (ZnCo2O4–RGO) was synthesized via one-step solvothermal method for activating persulfate (PS) to degrade bisphenol A (BPA). The morphology and structure of the nanocomposite were identified by X-ray diffraction, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy, and transmission electron microscopy. RGO provides nucleation sites for ZnCo2O4 to grow and inhibits the agglomeration of the nanoparticles. The influence of different reaction conditions on the oxidation of BPA catalyzed by ZnCo2O4–RGO was investigated, including the content of RGO, the dosage of catalyst, the concentration of humic acid (HA), anions in the environment, the reaction temperature, and pH. BPA can be totally degraded within 20 min under optimized reaction conditions. The presence of HA, Cl−, and NO3− only has a slight effect on the oxidation of BPA, whereas the presence of either H2PO4− or HCO3− can greatly inhibit the reaction. ZnCo2O4–RGO shows good cycling stability and practical application potential. A reaction mechanism of the degradation of BPA was also explored.

scholarly journals Visible-light-driven photocatalytic degradation of rhodamine B in water by BiOClxI1−x solid solutions

2020 ◽  
Vol 81 (5) ◽  
pp. 1080-1089
Author(s):  
Huan-Yan Xu ◽  
Dan Lu ◽  
Qu Tan ◽  
Xiu-Lan He ◽  
Shu-Yan Qi
Keyword(s):  
Electron Microscopy ◽  
Solid Solutions ◽  
Rhodamine B ◽  
Diffuse Reflectance Spectroscopy ◽  
Bet Surface Area ◽  
Order Kinetic ◽  
X Ray Diffraction ◽  
Sunlight Irradiation ◽  
Transmission Electron ◽  
Visible Light Driven

Abstract Bismuth oxyhalides (BiOXs, X = Cl, Br and I) are emerging photocatalytic materials with unique layered structure, flexible band structure and superior photocatalytic activity. The purpose of this study was to develop a facile alcoholysis route to prepare BiOClxI1−x nanosheet solid solutions at room temperature. X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), UV-vis diffuse reflectance spectroscopy (UV-vis DRS), photoluminescence emission spectroscopy (PL) and Brunauer–Emmett–Teller (BET) surface area analyzer were used to characterize the as-prepared photocatalysts. These results revealed that two-dimension BiOClxI1−x nanosheet solid solutions could be obtained with high percentage of {001} crystal facets exposed. Moreover, the formation of solid solution could regularly change the optical absorption thresholds and band gaps of BiOClxI1−x photocatalysts. The photocatalytic experiments indicated that BiOCl0.75I0.25 exhibited the highest photocatalytic performance for the degradation of Rhodamine B (RhB) under simulated sunlight irradiation and the photocatalytic process followed a pseudo-first-order kinetic equation. A possible mechanism of RhB photodegradation over BiOClxI1−x solid solutions was proposed based on the structural properties of BiOClxI1−x solid solutions and RhB photosensitization.

scholarly journals Hydrothermal Synthesis and Characterization of Single-Crystalline -Fe2O3Nanocubes

2011 ◽  
Vol 2011 ◽  
pp. 1-5 ◽  
Author(s):  
Wenqing Qin ◽  
Congren Yang ◽  
Ran Yi ◽  
Guanhua Gao
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Infrared Spectrometry ◽  
X Ray Diffraction ◽  
Single Crystalline ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Alkaline Agent ◽  
One Step

Single-crystalline - nanocubes were successfully obtained in large quantities through a facile one-step hydrothermal synthetic route under mild conditions. In this synthetic system, aqueous iron (III) nitrate () served as iron source and triethylamine served as precipitant and alkaline agent. By prolonging reaction time from 1 h to 24 h, the evolution process of -, from nanorhombohedra to nanohexahedron, and finally nanocube, was observed. The products were characterized by Powder X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), High-resolution Transmission Electron Microscopy (HRTEM), Selected-Area Electron Diffraction (SAED), and Fourier Transform Infrared Spectrometry (FTIR). The possible formation mechanism was discussed on basis of the experimental results.

Preparation and Characterization of Vanadium Pentoxide Hollow Microspheres with Tunable Sizes

2016 ◽  
Vol 697 ◽  
pp. 706-709
Author(s):  
Ming Gong ◽  
Chang An Wang
Keyword(s):  
Electron Microscopy ◽  
Solvothermal Method ◽  
Hollow Microspheres ◽  
Soft Template ◽  
X Ray Diffraction ◽  
X Ray ◽  
Molecular Weights ◽  
Transmission Electron ◽  
One Step

V2O5 hollow microspheres were synthesized by a one-step solvothermal method, with the assistance of PVP as the soft template, ethylene glycol (EG) as the solvent, and vanadium (iii) acetylacetonate (acac) as the metal-ions source. The samples were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), transmission electron microscopy (TEM). The size of V2O5 hollow microspheres, which can be easily tuned by using PVP of different molecular weights, was about 2.5μm, 4.5μm and 6μm when using PVP-K17, PVP-K30 and PVP-K60 as the template, respectively.

Solvothermal Synthesis and Electrochemical Properties of Hairball-Like Bismuth Trisulphide Microcrystallines

2011 ◽  
Vol 233-235 ◽  
pp. 2289-2293
Author(s):  
Pin Jiang Li ◽  
Wen Jun Fa ◽  
Yan Ge Zhang ◽  
Bao Jun Huang ◽  
Yi Dong Zhang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Solvothermal Synthesis ◽  
Growth Process ◽  
Solvothermal Process ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
One Step ◽  
Scanning Electron

Hairball-like bismuth trisulphide microcrystallines has been successfully prepared via one step solvothermal process and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and high-resolution transmission electron microscopy (HRTEM) techniques. The morphologies of the Bi2S3 microcrystallines were influenced by reaction time, temperature, the mole ratio of the reactants and concentration of starting materials, and the growth process has been proposed. The electrochemical behavior of Bi2S3 was investigated using the cyclic voltammetry.

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