N-Doped Cu11O2 (VO4)6 Photocatalyst Prepared by Sol-Gel Method

2011 ◽  
Vol 393-395 ◽  
pp. 1287-1290
Author(s):  
Min Wang ◽  
Qiong Liu ◽  
Qi Xing

The N-doped Cu11O2 (VO4)6 photocatalyst was prepared using the sol-gel method. Techniques of X-ray diffraction (XRD), scanning electron microscope (SEM) have been employed to characterize the as-synthesized materials. During liquid phase photocatalytic degradation of Methy lorange(MO) under the UV-light, the as-prepared N-doped Cu11O2 (VO4)6 exhibits higher activity than the pure Cu11O2 (VO4)6 without doped N. It found that the N-doped Cu11O2 (VO4)6 prepared with the molar ratio of citric acid to metal inons be 2:1, N/Cu molar ratio of 12%, pH=7 and calcinated under 500°C for 4 hours was pure triclinic phase. In this conditions, the sample had highest photocatalytic activity with the photodegradation rate was about 94.42% or so in 60min under 20W ultraviolet lamp.

2011 ◽  
Vol 361-363 ◽  
pp. 1598-1601
Author(s):  
Min Wang ◽  
Qiong Liu ◽  
Hai Yan Luan

Cu11O2 (VO4)6 powders have been synthesized by complexing Sol-Gel method using citric acid as chelate, calcined at different temperature without using any template. Techniques of X-ray diffraction (XRD) and scanning electron microscope (SEM) have been employed to characterize the as-synthesized materials. The photocatalytic activity was evaluated by photocatalytic degradation of methyl orange (MO) solution under UV-light. It revealed that temperature values can influence significantly on the morphologies and structures of the products.It also found that the sample prepared with the molar ratio of citric acid to metal inons be 2:1, pH=7 and calcinated under 500°C for 4 hours was pure triclinic Cu11O2 (VO4)6 phase.In this conditions, the sample had highest photocatalytic activity with the photodegradation rate was about 78.9% or so in 60min under 20W ultraviolet lamp.


2011 ◽  
Vol 361-363 ◽  
pp. 1819-1822
Author(s):  
Min Wang ◽  
Qiong Liu ◽  
Hai Yan Luan

A La-doped Cu11O2 (VO4)6 photocatalyst with optimum La/Cu molar ratio of 4% was prepared by sol-gel method. XRD,SEM and EDX have been employed to characterize the as-synthesized materials. During liquid phase photocatalytic degradation of MO under the UV-light, the as-prepared La/ Cu11O2 (VO4)6 exhibits higher activity than the pure Cu11O2 (VO4)6. It found that the La/ Cu11O2 (VO4)6 prepared with the La/Cu molar ratio of 4% and calcinated under 500°C for 4 hours was pure triclinic phase. In this conditions, the sample had highest photocatalytic activity with the photodegradation rate was about 92.45% or so in 60min under 20W UV light.


2011 ◽  
Vol 393-395 ◽  
pp. 1181-1184
Author(s):  
Min Wang ◽  
Qiong Liu ◽  
Qi Xing

Nd-doped Cu11O2 (VO4)6 photocatalyst was synthesized by complexing Sol-gel method and characterized by X-ray diffraction (XRD), scanning electron microscope (SEM) and energy Dispersive X-Ray Spectroscopy(EDX). The photocatalytic activity of Nd-doped Cu11O2 (VO4)6 was evaluated by photocatalytic degradation of methyl orange (MO) solution under UV-light. It revealed that the Nd-doped Cu11O2 (VO4)6 prepared with the molar ratio of citric acid to metal inons be 2:1, Nd/Cu molar ratio of 2%, pH=7 and calcinated under 500°C for 4 hours was pure triclinic phase. In this conditions, the sample had highest photocatalytic activity with the photodegradation rate was about 95.73% or so in 60min under 20W ultraviolet lamp.


2011 ◽  
Vol 99-100 ◽  
pp. 1307-1311 ◽  
Author(s):  
Min Wang ◽  
Qiong Liu ◽  
Hai Yan Luan

Bismuth vanadate (BiVO4) powders were synthesized by complexing Sol-Gel method using citric acid as chelate,calcined at different temperature and characterized with X-ray diffraction (XRD), scanning electron microsoope(SEM)and specific surface area (BET). The photocatalytic activity was evaluated by photocatalytic degradation of methyl orange (MO) solution under visible light. It revealed that temperature values can influence significantly on the morphologies and structures of the products.It also found that the sample prepared with the molar ratio of citric acid to metal inons be 2:1, pH=7 and calcinated under 400°C for 5 hours was pure monoclinic BiVO4 phase.In this conditions, the sample had highest photocatalytic activity with the photodegradation rate was about 94% or so in 20min under 250W halogen lamp.


2013 ◽  
Vol 320 ◽  
pp. 220-225 ◽  
Author(s):  
Xiao Ye Fu ◽  
Xiu Hong Liang

In this paper, we prepared a series of powders (pure TiO2 and Ce-doped TiO2) by sol-gel method and characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), infrared spectrometer (IR) and UV spectrophotometer. The results indicated that the doped Ce influence the crystal structure of TiO2 and improve the temperature of crystal transformation. In the degradation of MB experiment, after 5 hours, the degradation efficiency of them (pure TiO2 , Ce-doped TiO2 and P25) under UV light is about 99.1%, while under visible light,Ce-doped TiO2 is about 60% higher than pure TiO2 and P25, up to 73%. This illustrates that the doped Ce increase the absorption to visible light and improve the photocatalytic efficiency.Key Words: TiO2, Ce-doped TiO2, photocatalyst, sol-gel method, crystal form


2012 ◽  
Vol 545 ◽  
pp. 275-278 ◽  
Author(s):  
Lili Widarti Zainuddin ◽  
Norlida Kamarulzaman

A ceramics sample of LiTaO3 was prepared using a sol-gel method. The sample is annealed at 750 °C for 48 hours. X-ray diffraction analysis indicate the formation of single phase, rhombohedral structure. An ac impedance study was used to analyse the conductivity of LiTaO3 at room temperature and at various temperatures.


2011 ◽  
Vol 268-270 ◽  
pp. 356-359 ◽  
Author(s):  
Wen Song Lin ◽  
C. H. Wen ◽  
Liang He

Mn, Fe doped ZnO powders (Zn0.95-xMnxFe0.05O2, x≤0.05) were synthesized by an ameliorated sol-gel method, using Zn(CH3COO)2, Mn(CH3COO)2and FeCl2as the raw materials, with the addition of vitamin C as a kind of chemical reducer. The resulting powder was subsequently compacted under pressure of 10 MPa at the temperature of 873K in vacuum. The crystal structure and magnetic properties of Zn0.95-xMnxFe0.05O2powder and bulk samples have been investigated by X-ray diffraction (XRD) and vibrating sample magnetometer (VSM). X-ray photoelectron spectroscopy (XPS) was used to study chemical valence of manganese, iron and zinc in the samples. The x-ray diffraction (XRD) results showed that Zn0.95-xMnxFe0.05O (x≤0.05) samples were single phase with the ZnO-like wurtzite structure. No secondary phase was found in the XRD spectrum. X-ray photoelectron spectroscopy (XPS) showed that Fe and Mn existed in Zn0.95-xMnxFe0.05O2samples in Fe2+and Mn2+states. The results of VSM experiment proved the room temperature ferromagnetic properties (RTFP) of Mn, Fe co-doped ZnO samples.


Nanopages ◽  
2019 ◽  
pp. 1-11
Author(s):  
G. M. Taha ◽  
M. N. Rashed ◽  
M. S. El-Sadek ◽  
M. A. Moghazy

Abstract BiFeO3 (BFO) nanopowder was synthesized in a pure form via a sol- gel method based on glycol gel reaction. Effect of drying and preheating temperature on preventing other phases was studied. Many parameters were studied as calcination temperature and time & stirring temperature as well. The prepared powder was characterized by X-Ray Diffraction of powder (XRD) and Transmission Electron Microscope (TEM). High pure BiFeO3 was obtained by preheated process at 400 °C for 0.5 h and calcination at 600 °C for 0.5 h without any impurities compared to dry at110 °C.


2011 ◽  
Vol 399-401 ◽  
pp. 1447-1450
Author(s):  
Zhi Yong Yu ◽  
Han Xing Liu

The layered LiNi1/2Mn1/2O2 cathode materials were synthesized by a sol gel method. The effects of calcination temperature and time on the structural and electrochemical properties of the LiNi1/2Mn1/2O2 were investigated. The prepared samples were characterized by X-ray diffraction (XRD) and electrochemical analysis. The results revealed that the layered LiNi1/2Mn1/2O2 material could be optimal synthesized at temperature of 900°C for 10h. The sample prepared under the above conditions has the highest initial discharge capacity of 151 mAh/g and showed no dramatic capacity fading during 20 cycles between 2.5-4.5V at a current rate of 20mA/g.


2021 ◽  
Vol 2114 (1) ◽  
pp. 012004
Author(s):  
Duha S. Ahmed ◽  
Noor Q. Ali ◽  
Ali A. Taha

Abstract In this paper, we reported the synthesis of NiO NPs and Mg doped-NiO NPs using the facile sol-gel method. Besides, the influence of the variation of Mg dopant on the structural, morphological and optical properties of the prepared Mg-NiO NPs was studied. The synthesized Mg-NiO NPs nanoparticles were characterized by X-Ray Diffraction Analysis (XRD), Energy Dispersive X-ray Spectroscopy (EDS), Fourier-Transform Infrared Spectroscopy (FTIR), Field-Emission Scanning Electron Microscopy (FE-SEM), and UV-Vis spectrophotometer. The X-ray diffraction confirmed the formation of the cubic structure of Mg doped-NiO NPs after doping with the magnesium. The increase in the crystal size was observed with the increase in the concentration of the Mg dopant element. The FESEM images reveal the formation of nickel oxide through the appearance of spherical clusters, while the hybrids appear as wrinkled surface covered with spherical particles of magnesium. The UV-Vis spectrum showed a shift towards shorter wavelengths with an increase in the concentration of the Mg dopant element due to the quantum confinement effect. The hemolysis activity study showed that NiO NPs had a low hemolysis percentage of 1.47% and increased with increasing concentration. While, increasing of the RBC hemolysis (5.9%) after NiO doped with Mg. The antibacterial activity was studied against S. aureus and P. aeruginosa bacteria, and indicated the highest growth inhibition zones of Mg-doped NiO NPs as compared with NiO NPs against of Staphylococcus aureus and Pseudomonas aeruginosa, respectively.


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