scholarly journals Structural and electrical properties of CuLayFe2-yO4 ferrites

2019 ◽  
Vol 11 (22) ◽  
pp. 102-109
Author(s):  
Muthafar F. Al- Hilli
Keyword(s):  
Dielectric Loss ◽  
Lattice Parameter ◽  
Secondary Phases ◽  
X Ray ◽  
Force Microscopy ◽  
Low Dielectric ◽  
Average Grain Size ◽  
La Addition ◽  
Diffraction Patterns ◽  
P Type

        Ferrite with the general formula CuLayFe2-yO4 (where y=0.02, 0.04, 0.06, 0.08 and 0.1), were prepared by standard ceramic technique. The main cubic spinel structure phase for all samples was confirmed by x-ray diffraction patterns with the appearance of small amount of secondary phases. The lattice parameter results were 8.285-8.348 Å. X-ray density increased with La addition and showed values between 5.5826 – 5.7461gm/cm3. The Atomic Force Microscopy (AFM) showed that the average grain size was decreasing with the increase in La concentration. The Hall coefficient was found to be positive. It demonstrates that the majority of charge carriers of p-type, suggesting that the mechanism of conduction is predominantly caused by hopping of holes. The resistivity was noticed to increase with the increase in La substitution. The activation energy Eav decreased with the frequency increase. The AC conductivity was found to increase with the frequency and La addition. Dielectric constant was noticed to decrease with frequency and La addition. The dielectric loss factor decreased with La content because rare earths are known as low dielectric loss materials.

scholarly journals A study of the structural and electrical properties of Ni1-x Cox Fe2O4 ferrites

2019 ◽  
Vol 12 (25) ◽  
pp. 69-79
Author(s):  
Hind Mohammed Hasan
Keyword(s):  
Lattice Parameter ◽  
Dielectric Constants ◽  
X Ray ◽  
Force Microscopy ◽  
Average Grain Size ◽  
Structural And Electrical Properties ◽  
Ray Density ◽  
Diffraction Patterns ◽  
Co Addition ◽  
P Type

Ferrite with general formula Ni1-x Cox Fe2O4(where x=0.0.1,0.3,0.5,0.7, and 0.9), were prepared by standard ceramic technique. The main cubic spinel structure phase for all samples was confirmed by x-ray diffraction patterns. The lattice parameter results were (8.256-8.299 °A). Generally, x -ray density increased with the addition of Cobalt and showed value between (5.452-5.538gm/cm3). Atomic Force Microscopy (AFM) showed that the average grain size and surface roughness was decreasing with the increasing cobalt concentration. Scanning Electron Microscopy images show that grains had an irregular distribution and irregular shape. The A.C conductivity was found to increase with the frequency and the addition of Cobalt, D.C conductivity was found to increase with temperature due to decreases in resistivity. Dielectric constants were noticed to decrease with frequency and Co addition. The Hall coefficient was found to be positive. This demonstrates that the majority of charge carriers are p-type, suggesting that the mechanism of conduction is predominantly caused by hopping of holes.

Structure and Magnetocaloric Effect of B-Doped Mn-Fe-P-Si Compounds

2021 ◽  
Vol 323 ◽  
pp. 152-158
Author(s):  
Shou Yuan Xing ◽  
Song Lin ◽  
Zhi Qiang Song ◽  
Zhi Qiang Ou
Keyword(s):  
Crystal Structure ◽  
Curie Temperature ◽  
Lattice Parameter ◽  
Magnetic Entropy ◽  
Field Change ◽  
X Ray Diffraction ◽  
X Ray ◽  
Diffraction Patterns ◽  
P Type ◽  
Type Crystal

We reported the structural, magnetic and magenetocaloric properties of Mn1.25Fe0.75P0. 50Si0.50Bx(x = 0.01, 0.02 and 0.04) X-ray diffraction patterns show that all compounds crystallize in the hexagonal Fe2P-type crystal structure. Lattice parameter a increases while c decreases with increasing B contents. The Curie temperature of the compounds have been determined, the values are 219, 268 and 323.2 K for x = 0.01, 0.02, 0.04, respectively. The maximum magnetic entropy changes in a field change of 0~1.5 T are 6.1, 5.3 and 3.5J/kg·K for x = 0.01, 0.02 and 0.04, respectively.

EFFECTS OF A PARTIAL SUBSTITUTION OF Cu ELEMENTS BY Nb ELEMENTS IN YBaCuO SYSTEM

1990 ◽  
Vol 04 (12) ◽  
pp. 823-830 ◽  
Author(s):  
S. HIGO ◽  
Y. HAKURAKU ◽  
T. OGUSHI ◽  
I. KAWANO ◽  
Y. ISHIKAWA
Keyword(s):  
Solid State Reaction Method ◽  
Lattice Parameter ◽  
Partial Substitution ◽  
Maximum Temperature ◽  
X Ray ◽  
Cubic Lattice ◽  
Nb Content ◽  
Molecular Ratios ◽  
Diffraction Patterns ◽  
Two Phases

Samples of the YBaCuNbO system with different molecular ratios of YBa 2 NbO y to YBa 2 Cu 3 O 7−d, were prepared in air by the solid-state reaction method. The X-ray powder diffraction patterns showed that the sample was composed of two phases, one corresponding to the YBa 2 Cu 3 O 7−d phase and the other to the YBa 2 NbO y phase with a cubic lattice parameter of 8.425 Å to 8.436 Å depending on the Nb content. The superconducting zero resistivity temperature, T c 0, of the YBaCuNbO system increased with the increase of the molecular ratios, from 91.2 K up to a maximum temperature of 92.8 K, and then, by a further increase in the molecular ratio, the T c 0 was drastically reduced with a gradient of −1.94 K /%x.

Synchrotron X-ray studies of metal-organic framework M2(2,5-dihydroxyterephthalate), M = (Mn, Co, Ni, Zn) (MOF74)

2012 ◽  
Vol 27 (4) ◽  
pp. 256-262 ◽  
Author(s):  
W. Wong-Ng ◽  
J. A. Kaduk ◽  
H. Wu ◽  
M. Suchomel
Keyword(s):  
Powder Diffraction ◽  
Metal Organic Framework ◽  
National Laboratory ◽  
Argonne National Laboratory ◽  
Lattice Parameter ◽  
X Ray ◽  
Metal Organic ◽  
Sorbent Materials ◽  
Diffraction Patterns ◽  
Unsaturated Metal Sites

M2(dhtp)·nH2O (M = Mn, Co, Ni, Zn; dhtp = 2,5-dihydroxyterephthalate), known as MOF74, is a family of excellent sorbent materials for CO2 that contains coordinatively unsaturated metal sites and a honeycomb-like structure featuring a broad one-dimensional channel. This paper describes the structural feature and provides reference X-ray powder diffraction patterns of these four isostructural compounds. The structures were determined using synchrotron diffraction data obtained at beam line 11-BM at the Advanced Photon Source (APS) in the Argonne National Laboratory. The samples were confirmed to be hexagonal R 3 (No. 148). From M = Mn, Co, Ni, to Zn, the lattice parameter a of MOF74 ranges from 26.131 73(4) Å to 26.5738(2) Å, c from 6.651 97(5) to 6.808 83(8) Å, and V ranges from 3948.08 Å3 to 4163.99 Å3, respectively. The four reference X-ray powder diffraction patterns have been submitted for inclusion in the Powder Diffraction File (PDF).

Growth and Characterization of bulk GaN by Ga Vapor Transport

2004 ◽  
Vol 831 ◽  
Author(s):  
Phanikumar Konkapaka ◽  
Huaqiang Wu ◽  
Yuri Makarov ◽  
Michael G. Spencer
Keyword(s):  
Growth Rates ◽  
Vapor Transport ◽  
Spiral Growth ◽  
X Ray Diffraction ◽  
X Ray ◽  
Force Microscopy ◽  
Atomic Force ◽  
Bulk Gan ◽  
Diffraction Patterns

ABSTRACTBulk GaN crystals of dimensions 8.5 mm × 8.5 mm were grown at growth rates greater than 200μm/hr using Gallium Vapor Transport technique. GaN powder and Ammonia were used as the precursors for growing bulk GaN. Nitrogen is used as the carrier gas to transport the Ga vapor that was obtained from the decomposition of GaN powder. During the process, the source GaN powder was kept at 1155°C and the seed at 1180°C. Using this process, it was possible to achieve growth rates of above 200 microns/hr. The GaN layers thus obtained were characterized using X-Ray diffraction [XRD], scanning electron microscopy [SEM], and atomic force microscopy [AFM]. X-ray diffraction patterns showed that the grown GaN layers are single crystals oriented along c direction. AFM studies indicated that the dominant growth mode was dislocation mediated spiral growth. Electrical and Optical characterization were also performed on these samples. Hall mobility measurements indicated a mobility of 550 cm2/V.s and a carrier concentration of 6.67 × 1018/cm3

Structural and optical properties of Ba(Co1−xZnx)SiO4 (x = 0.2, 0.4, 0.6, 0.8)

2019 ◽  
Vol 34 (3) ◽  
pp. 242-250 ◽  
Author(s):  
J. Anike ◽  
R. Derbeshi ◽  
W. Wong-Ng ◽  
W. Liu ◽  
D. Windover ◽  
...  
Keyword(s):  
Lattice Parameter ◽  
X Ray Diffraction ◽  
Powder Diffraction File ◽  
Visible Absorption ◽  
X Ray ◽  
Lattice Volume ◽  
Uv Visible ◽  
Diffraction Patterns ◽  
Pattern Determination ◽  
Bright Blue

Structural characterization and X-ray reference powder pattern determination have been conducted for the Co- and Zn-containing tridymite derivatives Ba(Co1−xZnx)SiO4 (x = 0.2, 0.4, 0.6, 0.8). The bright blue series of Ba(Co1−xZnx)SiO4 crystallized in the hexagonal P63 space group (No. 173), with Z = 6. While the lattice parameter “a” decreases from 9.126 (2) Å to 9.10374(6) Å from x = 0.2 to 0.8, the lattice parameter “c” increases from 8.69477(12) Å to 8.72200(10) Å, respectively. Apparently, despite the similarity of ionic sizes of Zn2+ and Co2+, these opposing trends are due to the framework tetrahedral tilting of (ZnCo)O4. The lattice volume, V, remains comparable between 626.27 Å3 and 626.017 (7) Å3 from x = 0 to x = 0.8. UV-visible absorption spectrum measurements indicate the band gap of these two materials to be ≈3.3 and ≈3.5 eV, respectively, therefore potential UV photocatalytic materials. Reference powder X-ray diffraction patterns of these compounds have been submitted to be included in the Powder Diffraction File (PDF).

In situ coupling of atomic force microscopy and sub-micrometer focused X-ray techniques

2014 ◽  
Vol 1712 ◽  
Author(s):  
Thomas W. Cornelius ◽  
Zhe Ren ◽  
Francesca Mastropietro ◽  
Simon Langlais ◽  
Anton Davydok ◽  
...  
Keyword(s):  
Mechanical Response ◽  
Elemental Distribution ◽  
X Ray Diffraction ◽  
X Ray ◽  
Cu Nanowires ◽  
Force Microscopy ◽  
Indentation Tests ◽  
Scanning Force ◽  
Diffraction Patterns

ABSTRACTA scanning force microscope for in situ nanofocused X-ray studies (SFINX) has been developed which can be installed on diffractometers at synchrotron beamlines allowing for the combination with various techniques such as coherent X-ray diffraction and fluorescence. The capabilities of this device are demonstrated on Cu nanowires and on Au islands grown on sapphire (0001). The sample topography, crystallinity, and elemental distribution of the same area are investigated by recording simultaneously an AFM image, a scanning X-ray diffraction map, and a fluorescence map. Additionally, the mechanical response of Au islands is studied by in situ indentation tests employing the AFM-tip and recording 2D X-ray diffraction patterns during mechanical loading.

scholarly journals Neutron and X-ray powder diffraction study of skutterudite thermoelectrics

2016 ◽  
Vol 31 (1) ◽  
pp. 16-22
Author(s):  
H. Wang ◽  
M. J. Kirkham ◽  
T. R. Watkins ◽  
E. A. Payzant ◽  
J. R. Salvador ◽  
...  
Keyword(s):  
Neutron Diffraction ◽  
Melt Spinning ◽  
Lattice Parameter ◽  
Type Material ◽  
General Motors ◽  
X Ray Diffraction ◽  
Filling Fraction ◽  
Cubic Symmetry ◽  
X Ray ◽  
P Type

N- and p-type filled-skutterudite materials prepared for thermoelectric power generation modules were analyzed by neutron diffraction at the POWGEN beam line of the Spallation Neutron Source (SNS) and X-ray diffraction (XRD). The skutterudite powders were processed by melt spinning, followed by ball milling and annealing. The n-type material consists of Ba–Yb–Co–Sb and the p-type material consists of Di–Fe–Ni–Sb or Di–Fe–Co–Sb (Di = didymium, an alloy of Pr and Nd). Powders for prototype module fabrication from General Motors and Marlow Industries were analyzed in this study. XRD and neutron diffraction studies confirm that both the n- and p-type materials have cubic symmetry. Structural Rietveld refinements determined the lattice parameters and atomic parameters of the framework and filler atoms. The cage filling fraction was found to depend linearly on the lattice parameter, which in turn depends on the average framework atom size. This knowledge may allow the filling fraction of these skutterudite materials to be purposefully adjusted, thereby tuning the thermoelectric properties.

scholarly journals High-performance colossal permittivity materials of (Nb + Er) co-doped TiO2 for large capacitors and high-energy-density storage devices

2016 ◽  
Vol 18 (35) ◽  
pp. 24270-24277 ◽  
Author(s):  
Mei-Yan Tse ◽  
Xianhua Wei ◽  
Jianhua Hao
Keyword(s):  
Dielectric Properties ◽  
Dielectric Loss ◽  
High Performance ◽  
High Energy ◽  
High Energy Density ◽  
Secondary Phases ◽  
Storage Devices ◽  
Low Dielectric ◽  
Colossal Permittivity ◽  
Co Doped

Our work shows contributions to the high-performance dielectric properties, including a CP of up to 104–105 and a low dielectric loss down to 0.03 in (Er0.5Nb0.5)xTi1−xO2 materials with secondary phases.

scholarly journals Effect of TeO2 addition on the dielectric properties of CaCu3Ti4O12 ceramics derived from the oxalate precursor route

2013 ◽  
Vol 03 (04) ◽  
pp. 1350028 ◽  
Author(s):  
P. Thomas ◽  
K. B. R. Varma
Keyword(s):  
Dielectric Properties ◽  
Dielectric Loss ◽  
Room Temperature ◽  
X Ray Diffraction ◽  
Oxalate Precursor ◽  
X Ray ◽  
Practical Applications ◽  
Low Dielectric ◽  
Precursor Route ◽  
Tan Δ

CaCu 3 Ti 4 O 12 (CCTO) ceramics which has perovskite structure gained considerable attention due to its giant permittivity. But it has high tan δ (0.1 at 1 kHz) at room temperature, which needs to be minimized to the level of practical applications. Hence, TeO 2 which is a good glass former has been deliberately added to CCTO nanoceramic (derived from the oxalate precursor route) to explore the possibility of reducing the dielectric loss while maintaining the high permittivity. The structural, morphological and dielectric properties of the pure CCTO and TeO 2 added ceramics were studied using X-ray diffraction, Scanning Electron Microscope along with Energy Dispersive X-ray Analysis (EDX), spectroscopy and Impedance analyzer. For the 2.0 wt.% TeO 2 added ceramics, there is a remarkable difference in the microstructural features as compared to that of pure CCTO ceramics. This sample exhibited permittivity values as high as 7387 at 10 KHz and low dielectric loss value of 0.037 at 10 kHz, which can be exploited for the high frequency capacitors application.

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