Structural and magnetic properties of pure and cobalt doped Gallium Nitride nanocrystals

2010 ◽  
Vol 1257 ◽  
Author(s):  
Vottikondala Ganesh ◽  
Suresh Sundaram ◽  
Krishnan Baskar

AbstractIn the present study pure and doped gallium nitride (GaN) nanocrystals were synthesized using gallium trichloride (GaCl3), ethylene diamine tetra acetic acid (EDTA) and cobalt chloride as raw materials at a temperature of 900 °C in ammonia (NH3) atmosphere. The XRD spectrum for pure and cobalt doped GaN nanocrystals shows the formation of single phase wurtzite structure. No impurity phases were observed in the X-ray diffraction pattern for 5% Co doped sample whereas secondary phases were observed when the doping concentration exceeds 5 %. Shift in X-ray diffraction peaks were observed in Co doped samples towards lower angle side compared to pure GaN, it confirms that the Co atoms introduces in to the GaN lattice. Transmission electron microscopy images were taken for pure and Co doped GaN. Hexagonal morphology was observed in pure GaN samples. The average size of the particle was found to be ˜20 nm for pure and Co doped GaN. The magnetic measurements were carried out for the Co (5% & 10%) doped samples both at 10K and 300K. Clear hysteresis loop in the magnetization curve suggest the presence of ferromagnetic behavior in cobalt doped GaN. Temperature dependent magnetization (M-T) measurements were also carried out for doped samples using Super Conducting Quantum Interface Device (SQUID) from 10K to 300K The results have been discussed and correlated to structural and magnetic properties of the materials.

2012 ◽  
Vol 531-532 ◽  
pp. 299-302
Author(s):  
Ping Cao ◽  
Yue Bai

In this study, Zn0.99Co0.01Al0.015O thin film has been prepared by sol-gel method. The structural and magnetic properties of the sample were investigated. X-ray diffraction spectroscopy analyses indicate that the Co and Al codoping can not disturb the structure of ZnO. No additional peaks are observed in the Zn0.99Co0.01AlxO and Al3+ and Co2+ substitute for Zn2+ without changing the wurtzite structure. The resistance measurements confirm that Al ions increase the free carriers concentration. Based on the above experiments we think the ferromagnetic behavior of the sample could not originate from Co nanoclusters. The presence of free carriers and localized d spins is a prerequisite for the appearance of ferromagnetism. As the result, the carriers generated by Al doping is considered a main factor to induce the ferromagnetic phenomenon.


2020 ◽  
Vol 16 (4) ◽  
pp. 655-666
Author(s):  
Mona Rekaby

Objective: The influence of Manganese (Mn2+) and Cobalt (Co2+) ions doping on the optical and magnetic properties of ZnO nanoparticles was studied. Methods: Nanoparticle samples of type ZnO, Zn0.97Mn0.03O, Zn0.96Mn0.03Co0.01O, Zn0.95Mn0.03 Co0.02O, Zn0.93Mn0.03Co0.04O, and Zn0.91Mn0.03Co0.06O were synthesized using the wet chemical coprecipitation method. Results: X-ray powder diffraction (XRD) patterns revealed that the prepared samples exhibited a single phase of hexagonal wurtzite structure without any existence of secondary phases. Transmission electron microscope (TEM) images clarified that Co doping at high concentrations has the ability to alter the morphologies of the samples from spherical shaped nanoparticles (NPS) to nanorods (NRs) shaped particles. The different vibrational modes of the prepared samples were analyzed through Fourier transform infrared (FTIR) measurements. The optical characteristics and structural defects of the samples were studied through Photoluminescence (PL) spectroscopy. PL results clarified that Mn2+ and Co2+ doping quenched the recombination of electron-hole pairs and enhanced the number of point defects relative to the undoped ZnO sample. Magnetic measurements were carried out at room temperature using a vibrating sample magnetometer (VSM). (Mn, Co) co-doped ZnO samples exhibited a ferromagnetic behavior coupled with paramagnetic and weak diamagnetic contributions. Conclusion: Mn2+ and Co2+ doping enhanced the room temperature Ferromagnetic (RTFM) behavior of ZnO. In addition, the signature for antiferromagnetic ordering between the Co ions was revealed. Moreover, a strong correlation between the magnetic and optical behavior of the (Mn, Co) co-doped ZnO was analyzed.


2010 ◽  
Vol 25 (S1) ◽  
pp. S31-S35
Author(s):  
W. H. Zhang ◽  
J. Q. Li ◽  
Y. J. Yu ◽  
F. S. Liu ◽  
W. Q. Ao ◽  
...  

The structural and magnetic properties of the DyCo4−xFexGa compounds with x=0, 0.5, 1, and 1.5 have been investigated by X-ray diffraction and magnetic measurements. Powder X-ray diffraction analysis reveals that each of the DyCo4−xFexGa compounds has a hexagonal CaCu5-type structure (space group P6/mmm). The Fe solubility limit in DyCo4−xFexGa is x<1.5. The higher the value of x, the larger the unit-cell parameters a, c, V, and the 3d-sublattice moment but the smaller the 3d uniaxial anisotropy. Magnetic measurements show that the Curie temperature of DyCo4−xFexGa increases from 498 K for x=0 to 530 K for x=1.5, the compensation temperature Tcomp decreases from 286 K for x=0 to 238 K for x=1.5, and the spin-reorientation transition temperature increases from 403 K for x=0 to 530 K for x=0.5. No spin-reorientation transition was found in the samples with x=1.0 and 1.5. The saturation magnetization of DyCo4−xFexGa measured at 173 K increases but the magnetization measured at 300 K decreases with increasing Fe content x.


2011 ◽  
Vol 10 (04n05) ◽  
pp. 967-971 ◽  
Author(s):  
U. K. GOUTAM ◽  
SHASHWATI SEN ◽  
JAGANNATH ◽  
A. K. SINGH ◽  
R. MUKUND ◽  
...  

Co -doped SnO2 nanowires were grown by thermal evaporation of a mixture of Tin metal powder and CoCl2 · 6H2O in a tubular furnace. The growth occurs by vapor–solid growth mechanism. Nanowires grew along the sidewall of the alumina boat placed in the tubular furnace and the diameter of these nanowires (as was evident from scanning electron microscopy), was found to be in the range of 50 nm to 200 nm. Co was successfully doped in SnO2 lattice as revealed by X-ray diffraction data and was found to be in Co2+ state in the nanowires as detected by X-ray Photoelectron Spectroscopy measurements. Room temperature magnetic measurements, carried out using Vibrating Sample Magnetometer, indicated ferromagnetic behavior of the nanowires indicating their potential for spintronics applications. With increasing Co doping (upto 1%), the lattice parameters of SnO2 decreased and the saturation magnetization increased, suggesting a strong structure-magnetic property relationship.


2010 ◽  
Vol 09 (06) ◽  
pp. 567-570
Author(s):  
AHMED M. AL-SAIE ◽  
ADNAN JAAFAR ◽  
MOHAMED BOUOUDINA

A mixture of Fe 2 O 3 and SnO oxides has been mechanically milled to form SnFe 2 O 4 spinel phase. X-ray diffraction pattern of the milled mixture shows that after milling, both peaks of Fe 2 O 3 and SnO remain with a drastic decrease of their intensities and broadening. The appearance of a broad halo around 2θ ~ 31° indicates the formation of an amorphous phase. After annealing at 750°C for 1 h, SnO peaks disappear completely and new diffraction peaks emerge indicating the formation of a new nanophase i.e. SnO 2. Magnetic measurements of the as-milled mixture show a ferromagnetic behavior with saturation magnetization Ms = 6.8 emu/g which drastically decreases after annealing to 0.6 emu/g.


2018 ◽  
Vol 54 (1A) ◽  
pp. 96
Author(s):  
Dao Viet Thang

Structural, optical and magnetic properties of polycrystalline BiFeO3 and Bi0.9RE0.1Fe0.95Ni0.05O3 (RE = Sm, Y, Nd) prepared by sol–gel method have been investigated. X-ray diffraction (XRD) patterns reveal that all samples crystalize in rhombohedrally distorted perovskite structure belonging to space group R3c. Analyzed results of both XRD and Raman scattering data show an increase of lattice distortion with co-replacing of rare earths and nickel atoms into Bi and Fe sites respectively. All samples exhibit a weak ferromagnetic behavior at room temperature with enhancement of the magnetization of RE and Ni co-doped samples.


1989 ◽  
Vol 169 ◽  
Author(s):  
Debra L. Kaiser ◽  
Frank W. Gayle ◽  
Lydon J. Swartzendruber ◽  
Winnie Wong-Ng ◽  
Steven F. Watkins ◽  
...  

AbstractWe have conducted structural and magnetic investigations on thermomechanically-detwinned YBa2Cu3O6+x single crystals. Single crystal x-ray diffraction studies on a fully untwinned crystal with a superconducting onset temperature of 54 K have revealed that oxygen atoms in the basal plane are offset from the crystallographic mirror plane in the a direction, leading to “zig-zag” Cu-O chains. Magnetic measurements on untwinned and twinned crystals at 77 K indicate low levels of flux pinning in both crystals, with a slightly larger amount of pinning in the twinned crystal.


2016 ◽  
Vol 2016 ◽  
pp. 1-13 ◽  
Author(s):  
V. G. Il’ves ◽  
S. Yu. Sokovnin ◽  
A. M. Murzakaev

The nanopowders (NPs) ZnO-Zn-Fe and ZnO-Fe with the various concentrations of Fe (xFe) (0≤xFe≤0.619mass.%) were prepared by the pulsed electron beam evaporation method. The influence of doping Fe on structural and magnetic properties of NPs was investigated. X-ray diffraction showed that powders contain fine-crystalline and coarse-crystalline ZnO fractions with wurtzite structure and an amorphous component. Secondary phases were not found. The magnetic measurements made at room temperature, using the vibration magnetometer and Faraday’s scales, showed ferromagnetic behavior for all powders. Magnetization growth of NPs ZnO-Zn and ZnO-Zn-Fe was detected after their short-term annealing on air at temperatures of 300–500°C. The growth of magnetization is connected with the increase in the concentration of the phase ZnO with a defective structure as the result of oxidation nanoparticles (NPles) of Zn. The scanning transmission electron microscopy (STEM) showed a lack of Fe clusters and uniform distribution of atoms dopant in the initial powder ZnO-Zn-Fe. A lack of logical correlation between magnetization and concentration of a magnetic dopant of Fe in powders is shown.


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.


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