scholarly journals Template-Free Synthesis of Porous Cu2O Nanospheres at Room Temperature and Investigation on Their Adsorption Property

2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
Ying Zhang ◽  
Dong Wang ◽  
Xu Zhang ◽  
Fengyu Qu

Porous cuprous oxide (Cu2O) nanospheres composed of small nanoparticles with diameters at 10~20 nm were successfully synthesized without surfactant at room temperature within 5 min. The products were characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), high resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED), N2adsorption-desorption, and Fourier transform infrared (FT-IR) spectrum. The adsorption ability of the as-prepared products towards methyl orange (MO) as the pollutant was investigated and FT-IR spectrum was employed to identify the adsorbed species. In addition, the reusability of the as-prepared products was studied as well.

2010 ◽  
Vol 97-101 ◽  
pp. 4213-4216
Author(s):  
Jian Xiong Liu ◽  
Zheng Yu Wu ◽  
Guo Wen Meng ◽  
Zhao Lin Zhan

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.


2015 ◽  
Vol 2015 ◽  
pp. 1-9 ◽  
Author(s):  
Yong-Fang Li ◽  
Ming Zhang ◽  
Qi-Jing Yang ◽  
Feng-Xian Zhang ◽  
Mei-Qi Zheng ◽  
...  

A simple and facile approach was developed in the solvothermal synthesis of hierarchical PbS microstars with multidendritic arms, which were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared (FT-IR) and photoluminescence (PL) spectroscopy. The morphologies of PbS products were strongly determined by the reaction time and temperature, the ratios of the precursors, and the mixed solvent with various components, and thereby their possible formation mechanism was discussed in some detail. The as-prepared PbS crystals displayed a sharp and strong photoluminescent peak at 437 nm at room temperature. It has potential and practical applications in photoluminescence, photovoltaics, IR photodetectors, electroluminescence, and solar absorbers.


2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
G. Sathiyadevi ◽  
B. Loganathan ◽  
B. Karthikeyan

The solvent-mediated eco-friendly monodispersed Ag/Pd bimetallic nanocomposites (BNCs) having thick core and thin shell have been prepared through novel green chemical solvent reduction method. Reducing solvent, dimethyl formamide (DMF) is employed for the controlled green synthesis. Characterization of the synthesized Ag/Pd BNCs has been done by x-ray diffraction (XRD) studies, high-resolution scanning electron microscopy (HR-SEM), energy-dispersive X-ray analysis (EDX), and high-resolution transmission electron microscopy (HR-TEM) with selected area electron diffraction (SAED) pattern. The nature of the interaction of L-cysteine with Ag/Pd BNCs has been studied by using surface plasmon spectroscopy, Fourier transform-infrared spectroscopy (FT-IR), cyclic voltammetry (CV), and theoretical methods.


2013 ◽  
Vol 27 (29) ◽  
pp. 1350211 ◽  
Author(s):  
ARBAB MOHAMMAD TOUFIQ ◽  
FENGPING WANG ◽  
QURAT-UL-AIN JAVED ◽  
QUANSHUI LI ◽  
YAN LI

In this paper, single crystalline tetragonal MnO 2 nanorods have been synthesized by a simple hydrothermal method using MnSO 4⋅ H 2 O and Na 2 S 2 O 8 as precursors. The crystalline phase, morphology, particle sizes and component of the as-prepared nanomaterial were characterized by employing X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED) and energy-dispersive X-ray spectroscopy (EDS). The photoluminescence (PL) emission spectrum of MnO 2 nanorods at room temperature exhibited a strong ultraviolet (UV) emission band at 380 nm, a prominent blue emission peak at 453 nm as well as a weak defect related green emission at 553 nm. Magnetization (M) as a function of applied magnetic field (H) curve showed that MnO 2 nanowires exhibited a superparamagnetic behavior at room temperature which shows the promise of synthesized MnO 2 nanorods for applications in ferrofluids and the contrast agents for magnetic resonance imaging. The magnetization versus temperature curve of the as-obtained MnO 2 nanorods shows that the Néel transition temperature is 94 K.


2013 ◽  
Vol 341-342 ◽  
pp. 13-17
Author(s):  
Xiao Yun Zhang ◽  
Hong Yan Qin ◽  
Xiu Xin Zheng ◽  
Shi Hu Yu ◽  
Wei Wu

CO2solid adsorbent was prepared through impregnating acrylonitrile (AN) modified monoethanolamine (MEA) into structurally disordered mesoporous silica (M) pore channel. Its structure was characterized by X-ray diffraction characterization (XRD), N2adsorption-desorption tests (BET), Transmission electron microscopy (TEM) and Fourier transform infrared (FT-IR). The capacity of CO2adsorption and desorption were measured and evaluated by comparison with MEA-impregnated material. The results showed that the capacity of M-MN-50 reached up to 125.8 mg·g-1and could desorb completely at the temperature of 40 °C by vacuum with 2.6 KPa. The hybrid material exhibited satisfactory performance during 10 turnovers.


2009 ◽  
Vol 7 (2) ◽  
pp. 259-266 ◽  
Author(s):  
Vendula Houšková ◽  
Václav Štengl ◽  
Snejana Bakardjieva ◽  
Nataliya Murafa ◽  
Václav Tyrpekl

AbstractNanocrystalline titania particles doped with ruthenium oxide have been prepared by the homogenous hydrolysis of TiOSO4 in aqueous solutions in the presence of urea. The synthesized particles were characterized by X-ray diffraction (XRD), Scanning Electron Microscopy (SEM), High Resolution Transmission Electron Microscopy (HRTEM), Selected Area Electron Diffraction (SAED) and Nitrogen adsorption-desorption was used for surface area (BET) and porosity determination (BJH). The photocatalytic activity of the Ru-doped titania samples were determined by photocatalytic decomposition of Orange II dye in an aqueous slurry during irradiation at 365 nm and 400 nm wavelengths.


2016 ◽  
Vol 34 (3) ◽  
pp. 529-533 ◽  
Author(s):  
Anukorn Phuruangrat ◽  
Budsabong Kuntalue ◽  
Surachai Artkla ◽  
Surin Promnopas ◽  
Wonchai Promnopas ◽  
...  

AbstractPbMoO4 and PbWO4 were successfully synthesized by microwave radiation using different lead salts (acetate, chloride, nitrate and sulfate) and Na2MO4 (M = Mo, W) in propylene glycol. The products were characterized by X-ray diffraction (XRD), scanning and transmission electron microscopy (SEM, TEM), Fourier transform infrared (FT-IR), Raman spectroscopy and photoluminescence (PL) spectroscopy. In this research, morphologies, crystallization and photoluminescence of the products were influenced by the kinetics of anions, including the detection of M–O (M = Mo, W) stretching modes in the (MO4)2− tetrahedrons. Photoluminescence of PbMoO4 synthesized from Pb(NO3)2 and of PbWO4 synthesized from PbCl2 showed the strongest blue emission due to the electronic diffusion in tetrahedrons at room temperature.


NANO ◽  
2015 ◽  
Vol 10 (05) ◽  
pp. 1550076 ◽  
Author(s):  
Tianjiao Bi ◽  
Jiafeng Wan ◽  
Shilin Yang ◽  
Xiujuan Yu ◽  
Fangwei Ma

Nitrogen-doped mesoporous carbon spheres (NMCSs) supporting anatase TiO 2 ( NMCSs – TiO 2) were prepared by a simple two-step solvothermal approach. The characterizations for the physicochemical properties of prepared samples under different solvothermal temperatures were carried out by X-ray diffraction (XRD) analyses, scanning electron microscopy (SEM), transmission electron microscopy (TEM), N 2 adsorption–desorption (Brunauer–Emmett–Teller (BET) measurements), Fourier transform infrared (FT-IR) spectroscopy, Raman scattering and UV-Vis diffuse reflectance spectra, were combined in order to determine the crystal phase and grain size, shape, degree of mesoporous carbon incorporation, and nature of the resultant oxycarbide chemical bonding on the surface and in the bulk. The high relative photocatalytic activity of NMCSs – TiO 2 nanoparticle was evaluated through a study of the decomposition of phenol under visible-light excitation.


2019 ◽  
Vol 21 (4) ◽  
pp. 98-105 ◽  
Author(s):  
Ishaq F. E. Ahmed ◽  
Ahmed I. El-Shenawy ◽  
Moamen S. Refat

Abstract Herein, the photocatalytic degradation of the Congo Red (CR) and Crystal Violet (CV) dyes in an aqueous solution were discussed in the presence of an indium(III) oxide (In2O3) as optical catalyst efficiency. The caproate bidentate indium(III) precursor complex has been synthesized and well interpreted by elemental analysis, molar conductivity, Fourier transform infrared (FT-IR), UV-Vis, and thermogravimetric (TGA) with its differential thermogravimetric (DTG) studies. The microanalytical and spectroscopic assignments suggested that the associated of mononuclear complex with 1:3 molar ratio (M3+:ligand). Octahedral structure is speculated for this parent complex of the caproate anion, CH3(CH2)4COO− ligand. The In2O3 NPs with nanoscale range within 10–20 nm was synthesized by a simple, low cost and eco-friendly method using indium(III) caproate complex. Indium oxide nanoparticles were formed after calcination of precursor in static air at 600°C for 3 hrs. The structural, grain size, morphological and decolorization efficiency of the synthesized NPs were characterized using the FT-IR, X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX) and transmission electron microscopy (TEM) analyses. It was worthy mentioned that the prepared In2O3 NPs showed a good photodegradation properties against CR and CV organic dyes during 90 min.


2021 ◽  
pp. 096739112110365
Author(s):  
Mohd Urooj Shariq ◽  
Ahmad Husain ◽  
Mahfoozurrahman Khan ◽  
Anees Ahmad

In this study, polypyrrole (PPy) and polypyrrole/molybdenum oxide composite (PPy/MoO3) were synthesized by the chemical oxidative method in an aqueous medium, using anhydrous ferric chloride (FeCl3) as an oxidant. The successful preparation of materials was confirmed by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmittance electron microscopy (TEM). PPy and PPy/MoO3 were converted into pellets which were used as the sensor. A four-in-line probe device was used for studying DC electrical conductivity–based ammonia vapour–sensing properties at three different ammonia concentrations, that is, 1 M, 0.5 M and 0.1 M. The PPy/MoO3 sensor showed much-improved sensing performance than the PPy sensor in terms of % sensing response and reversibility. PPy/MoO3 sensor showed excellent selectivity for ammonia vapours against various VOCs. The % sensing response of PPy/MoO3 sensor towards ammonia was found to be 2.19, 2.50, 3.16, 3.87, 4.1, 5.15, 6.19, 6.55 and 7.77 times greater than ethanol, methanol, acetone, acetaldehyde, formaldehyde, toluene, benzene, chloroform and n-hexane, respectively. In the end, a sensing mechanism was also proposed, which is based on rapid adsorption–desorption of ammonia molecules on the PPy/MoO3 sensor’s surface.


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