Synthesis, characterization and photoluminescence properties of Ce3+-doped ZnO-nanophosphors

2014 ◽  
Vol 68 (2) ◽  
Author(s):  
Sudheesh Shukla ◽  
Eric Agorku ◽  
Hemant Mittal ◽  
Ajay Mishra

AbstractThe present study involves the synthesis of Ce3+ doped ZnO nanophosphors by the zinc nitrate and cerium nitrate co-precipitation method. The synthesized nanophosphors were characterized with respect to their crystal structure, crystal morphology, particle size and photoluminescence (PL) properties using X-ray diffraction (XRD), scanning electron microscopy (SEM)/energy dispersive X-ray (EDX), transmission electron microscopy (TEM)/Energy-dispersive X-ray spectroscopy (EDS) and PL-spectroscopy respectively. XRD results revealed that ZnO nanophosphors are single phase and cubic type structures. Further, PL spectra of ZnO:Ce3+ nanophosphors showed green emission because of the charge transfer at single occupied oxygen vacancies with ZnO holes and red emission due to the cerium ion transitions. Intensity and fine structure of the Ce3+ luminescence and its temperature dependence are strongly influenced by the doping conditions. The formation of ZnO:Ce3+ nanophosphors was confirmed by Fourier transform infrared (FTIR) and XRD spectra.

2010 ◽  
Vol 434-435 ◽  
pp. 646-648 ◽  
Author(s):  
Jenn Kai Tsai ◽  
Ju Yu Wei ◽  
Yi Chi Chen ◽  
You Cheng Jheng ◽  
Teen Hang Meen

In this study, well-aligned single-crystalline zinc oxide (ZnO) nanorods arrays were synthesized on Si substrate by simple hydrothermal process in dilute aqueous solution which consisting of zinc nitrate tetrahydrate (Zn(NO3)2•4H2O) and hexamethyltetramine (C6H12N4, HMT) at 90 °C, in the autoclave. ZnO thin film was pre-deposited on Si substrate by the sputter deposition to serve as the seed layer. Aluminum nitrite (Al(NO3)3) also has been mixed into reaction solution. Al doped ZnO nanorod arrays were fabricated successfully. ZnO nanorods were characterized by high resolution X-ray diffraction, field emission scanning electron microscopy, transmission electron microscopy, energy dispersive x-ray spectroscopy, and photoluminescence measurement.


2021 ◽  
Author(s):  
Waseem Raza ◽  
Ghulam Nabi ◽  
Asim Shahzad ◽  
Nafisa Malik ◽  
Nadeem Raza

Abstract Lanthanum cerium ferrite nanoparticles has been synthesized for the first time via hydrothermal and co-precipitation method. The structural and morphological study of the nanoparticles have been examined by using X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and energy dispersive x-ray spectroscopy (EDX). The electrochemical study of J1 and J2 electrodes have been examined using three electrode system in 6 M KOH electrolyte using cyclic voltammetry (CV), galvanostatic charging-discharging (GCD) and electrochemical impendence spectroscopy (EIS). The highest specific capacitance of 1195 F/g has been obtained at a scan rate of 10 mV/s from hydrothermal synthesis nanomaterial electrode (J2) and long cycling life 92.3% retention after 2000th cycles. Furthermore, the energy density and power density of the J2 electrode at a current density of 5 A/g was 59 Wh/kg and 9234 W/kg respectively. Hence, the fabricated J2 electrode is a favorable candidate for super-capacitor applications.


2007 ◽  
Vol 280-283 ◽  
pp. 521-524
Author(s):  
Li Qiong An ◽  
Jian Zhang ◽  
Min Liu ◽  
Sheng Wu Wang

Yb3+ and Ho3+ co-doped Lu2O3 nanocrystalline powders were synthesized by a reversestrike co-precipitation method. The as-prepared powders were examined by the X-ray diffraction and transmission electron microscopy. The phase composition of the powders was cubic and the particle size was in the range of 30~50 nm. Emission and excitation spectra of the powders were measured by a spectrofluorometer and the possible upconversion luminescence mechanism was also discussed.


2014 ◽  
Vol 879 ◽  
pp. 155-163 ◽  
Author(s):  
Rahizana Mohd Ibrahim ◽  
Markom Masturah ◽  
Huda Abdullah

Nanoparticles of Zn1-xFexS ( x=0.0,0.1,0.2 and 0.3) were prepared by chemical co-precipitation method from homogenous solution of zinc and ferum salt at room temperature with controlled parameter. These nanoparticles were sterically stabilized using Sodium Hexamethaphospate (SHMP). Here, a study of the effect of Fe doping on structure, morphological and optical properties of nanoparticles was undertaken. Elemental analysis, morphological and optical properties have been investigated by Fourier-Transform-Infrared spectroscopy (FT-IR), X-Ray Fluorescence (XRF), Field Emmision Scanning Electron Microscopy (FESEM), X-ray Diffraction (XRD), Transmission Electron Microscopy (TEM) and UV-Visible Spectroscopy. FTIR measurement confirmed the presence of SHMP in the nanoparticles structure with the FESEM images depicting considerable less agglomeration of particles with the presence of SHMP. While XRF results confirm the presence of Fe2+ ion as prepared in the experiment. The particles sizes of the nanoparticles lay in the range of 2-10 nm obtained from the TEM image were in agreement with the XRD results. The absorption edge shifted to lower wavelengths with an increase in Fe concentration shown in the UV-Vis spectroscopy. The band gap energy value was in the range of 4.95 5.15 eV. The blueshift is attributed to the quantum confinement effect.


2011 ◽  
Vol 347-353 ◽  
pp. 1416-1419
Author(s):  
You Ning Xu ◽  
Hai Zhao ◽  
Duo Jiao Guan

Fe-Mn-Ce metal oxides nanosized particles have been prepared by co-precipitation approach using three kinds of precipitants NaOH, NH4OH and Na2CO3. The products were characterized by Powder X-ray Diffraction (XRD), Transmission Electron Microscopy (TEM) and BET study. It was found that the samples prepared with NH4OH as a precipitator show higher surface areas and larger sulfur capacity at low calcinations temperature. At high reaction temperatures, the samples prepared with Na2CO3 as precipitator exhibited much better activities for SCR of nitric oxide with ammonia than catalysts prepared with NH4OH and NaOH as the precipitants.


2012 ◽  
Vol 271-272 ◽  
pp. 320-323
Author(s):  
Xiao Chun Ma ◽  
Lei Hao Cui ◽  
Guang Fei Xu

In this paper, the Fe3O4 magnetic nanometer particle was prepared by co-precipitation method. At the same time, the samples were characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). The results show that the surface active agent (PEG4000) can be good for the dispersion performance of Fe3O4 magnetic nanometer particle; and the temperature of 80°C is the appropriate drying temperature to prepare the Fe3O4 magnetic nanometer particle.


Author(s):  
Fengfeng Li ◽  
Mingxi Zhang ◽  
Jin Wang ◽  
Yongfeng Cai ◽  
Dushao Zhao ◽  
...  

Abstract In this work, we fabricate a highly efficient photocatalytic AgBr/Ag2CO3 heterojunction through the co-precipitation method. The obtained samples were characterized by means of X-ray diffraction, scanning electron microscopy, transmission electron microscopy, ultraviolet-visible diffuse reflectance spectra and X-ray photoelectron spectroscopy. The photocatalytic activities of obtained samples can be assessed by visible light (λ ≥ 400 nm) degradation of rhodamine B solution. X-ray diffraction revealed that the crystallinity of the AgBr/Ag2CO3heterojunction was significantly higher than pure AgBr and Ag2CO3. Moreover, the AgBr/ Ag2CO3 heterojunction prepared at pH = 6 has the best photocatalytic performance, it can raise the degradation degree of rhodamine B over 95% at 20 min. Finally, a possible photocatalytic mechanism is discussed.


2008 ◽  
Vol 8 (3) ◽  
pp. 1211-1213 ◽  
Author(s):  
Luo Jun-Ming ◽  
Li Yong-Xiu ◽  
Deng Li-Ping ◽  
Yuan Yong-Rui ◽  
Chen Wei-Fan

Y2O3 nanoparticles doped with different concentrations of Er3+ were prepared by the co-precipitation method. X-ray diffraction and transmission electron microscopy results show that Er3+ dissolves completely in the Y2O3 cubic phase. The Er3+:Y2O3 nanoparticles are homogeneous in size and nearly spherical, and the average diameter of the particles after being calcined at 1,000 °C for 2 h is in the range of 40–60 nm. When Er3+:Y2O3 nanoparticles are excited under a 980 nm diode laser, there are two main emission bands: green emission centered at 562 nm corresponding to the 4S3/2/2H11/2 → 4I15/2 radiative transitions and red emission centered at 660 nm corresponding to the 4F9/2 ∼ 4I15/2 radiative transitions. By changing the doping concentration of Er3+ ions, the up-conversion luminescence can be gradually tuned from green to red.


2020 ◽  
Vol 81 (6) ◽  
pp. 1296-1307
Author(s):  
R. Jeyachitra ◽  
S. Kalpana ◽  
T. S. Senthil ◽  
Misook Kang

Abstract Methylene blue (MB) dye is the most common harmful, toxic, and non-biodegradable effluent produced by the textile industries. The present study investigates the effect of zinc oxide (ZnO) nanoparticles (NPs) and Ag–Ni doped ZnO NPs on the performance of photocatalytic degradation of MB dye. Pure ZnO and Ag–Ni doped ZnO NPs are synthesized using the co-precipitation method. The crystalline nature and surface morphology of the synthesized pure ZnO and Ag–Ni doped ZnO NPs was characterized by powder X-ray diffraction, scanning electron microscopy (SEM), and high resolution transmission electron microscopy (HRTEM) analysis. The presence of spherical-like morphologies was confirmed from SEM and HRTEM analysis. The presence of Ni–O and Zn–O bands in the synthesized materials was found by Fourier transform infrared (FTIR) spectroscopy analysis. The MB dye was degraded under UV-light exposure in various pH conditions. The Ag (0.02%)–Ni doped ZnO NPs exhibits highest photocatalytic activity of 77% under pH 4.


2015 ◽  
Vol 778 ◽  
pp. 183-186
Author(s):  
Yan Xia Han ◽  
Qian Nan Li ◽  
Hai Yun Shen ◽  
Qiu Hua Yang

Ce3+doped cubic KLaF4system was synthesized by co-precipitation method. The sample was characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), UV-Vis spectrophotometer and fluorescence spectrophotometer. The result indicated the nanoparticle diameter of KLaF4:Ce3+was 12.5 nm. The KLaF4:Ce3+had a stronger absorption at 250 nm, which could be explained by d elecronic transition of Ce3+. The maximum emission peak of KLaF4:Ce3+was 355 nm in its luminescent spectrum, and emission band of Ce3+also belonged to 5d→4f transition.


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