scholarly journals Preparation and Characterization of Paramagnetic Bis (8-Hydroxyquinoline) Manganese Crystals

Materials ◽  
2020 ◽  
Vol 13 (10) ◽  
pp. 2379
Author(s):  
Feng Jiang ◽  
Jiawen Song ◽  
Mengqi Dong ◽  
Yinong Wang
Keyword(s):  
Magnetic Properties ◽  
Dft Calculations ◽  
Photoelectron Spectroscopy ◽  
Quantum Interference ◽  
Physical Vapor Deposition ◽  
Density Functional ◽  
Magnetic Measurement ◽  
Energy Dispersive Spectrometer ◽  
Paramagnetic Property ◽  
X Ray

The magnetic properties of π-conjugated bis (8-hydroxyquinoline) manganese (Mnq2) crystals are investigated. Rod-shaped Mnq2 crystals are prepared by using the physical vapor deposition method. Field emission scanning electronic microscopy spectra show that the Mnq2 nanorods have perfect plane quadrangular ends. Energy dispersive spectrometer and X-ray photoelectron spectroscopy analysis demonstrates that the powders and nanorods are the same compound with a high purity. X-ray diffraction analysis shows the high crystal quality of the prepared Mnq2 nanorods. The magnetic measurement, using alternating gradient magnetometer and magnetic property measurement system superconducting quantum interference device vibrating sample magnetometer, indicates that the prepared Mnq2 nanorods show a paramagnetic property at room temperature. First-principles density functional theory (DFT) calculations are used to study the electronic structure and magnetic properties of the prepared Mnq2 crystals. DFT calculations show that the magnetic moment of the Mnq2 isolated molecule is 5 μB, which mainly comes from the localized Mn 3d orbital. The energy difference between the antiferromagnetic and ferromagnetic states of the Mnq2 monoclinic cell is only 0.1 meV, which may explain the paramagnetic property observed in the prepared Mnq2 nanorods and also indicates the difficulty of preparing intrinsic ferromagnetic Mnq2 crystals.

Study of Structural and Magnetic Properties of Spinel Zn Doped Cobalt Ferrites

2020 ◽  
Vol 310 ◽  
pp. 124-133
Author(s):  
B. Chun Feng ◽  
Ojiyed Tegus ◽  
T. Ochirkhyag ◽  
Dorj Odkhuu ◽  
Namsrai Tsogbadrakh ◽  
...  
Keyword(s):  
Magnetic Properties ◽  
Curie Temperature ◽  
Photoelectron Spectroscopy ◽  
Density Functional ◽  
Solid State Reaction Method ◽  
Element Analysis ◽  
X Ray ◽  
Cobalt Ferrites ◽  
Zn Concentration ◽  
Powder Samples

Herein, the spinel Co1-xZnxFe2O4 (x = 0.0, 0.2, 0.4 and 0.6) powder samples have been prepared by the solid-state reaction method. We have carried out the measurements of crystal structure, element analysis, material characterization, magnetic property and Curie temperature using the X-ray diffraction (XRD), Energy-dispersive X-ray spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS) and vibrating sample magnetometer, and the first-principles calculations within the framework of the density functional theory (DFT). The EDS measurement indicates that the Co1-xZnxFe2O4 powder samples have been successfully synthesized and exhibited the cubic spinel structures. Both the lattice constant and crystallite size increase with the Zn concentration due to the larger ionic radius of Zn2+ ion than the Co2+ ion. The concentration ratio of the Co2+ and Co3+ ions can be predicted by the distribution of cations between the A and B sites by the XPS measurement. For the magnetic properties, the residual magnetization, coercivity and Curie temperature decrease monotonically as the Zn concentration increases, while the saturation magnetization initially increases and then decreases at the room temperature. For the Co0.8Zn0.2Fe2O4 sample, the magnetic saturation reaches the maximum value of 62.98 Am2kg-1, due to a large amount of the Co3+ ions. The adequate replacement of Zn ion for the Co site can improve the magnetic properties of spinel Co1-xZnxFe2O4 powders, and effectively regulates the Curie temperature.

Crystal structures and magnetic properties of Fe–N thin films deposited by dc magnetron sputtering

2004 ◽  
Vol 19 (4) ◽  
pp. 352-355 ◽  
Author(s):  
Wei Tao Zheng ◽  
Xin Wang ◽  
Xianggui Kong ◽  
Hongwei Tian ◽  
Shansheng Yu ◽  
...  
Keyword(s):  
Thin Films ◽  
Magnetic Properties ◽  
Magnetron Sputtering ◽  
Crystal Structures ◽  
Photoelectron Spectroscopy ◽  
Quantum Interference ◽  
Flow Ratio ◽  
Dc Magnetron Sputtering ◽  
X Ray ◽  
Glass Substrates

Fe–N thin films were deposited on glass substrates by dc magnetron sputtering under various Ar∕N2 discharge conditions. Crystal structures and elemental compositions of the films were characterized by X-ray diffraction and X-ray photoelectron spectroscopy. Magnetic properties of the films were measured using a superconducting quantum interference device magnetometer. Films deposited at different N2∕(Ar+N2) flow ratios were found to have different crystal structures and different nitrogen contents. When the flow ratios were 60%, 50%, and 30%, a nonmagnetic single-phase FeN was formed in the films. At the flow ratio of 10%, two crystal phases of γ′-Fe4N and ε-Fe3N were detected. When the flow ratio reduced to 5%, a mixture of α-Fe, ε-Fe3N, FeN0.056, and α″-Fe16N2 phases was obtained. The value of saturation magnetization for the mixture was found to be larger than that of pure Fe.

Effect of Sputtering Input Power of Co on Structure and Magnetic Properties of Fe-Co-N Thin Films

2009 ◽  
Vol 79-82 ◽  
pp. 635-638 ◽  
Author(s):  
Xin Wang ◽  
Hui Jia ◽  
Wei Tao Zheng ◽  
Wei Xu ◽  
Bei Hong Long
Keyword(s):  
Thin Films ◽  
Magnetic Properties ◽  
Photoelectron Spectroscopy ◽  
Quantum Interference ◽  
Input Power ◽  
Superconducting Quantum Interference Device ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Composition Structure

Fe-Co-N thin films with various Co content were synthesized on Si (111) substrate using facing-target magnetron sputtering by changing sputtering input power on Co target. During deposition, the input power on Fe target was kept at 160 W. The composition, structure, and magnetic properties were examined by X-ray photoelectron spectroscopy, X-ray diffraction (XRD), transmission electron microscopy (TEM), and superconducting quantum interference device. XRD and TEM investigations showed that at lower input power of 11.2 W on Co target, the phases in the film were -(Fe,Co)4N and Co3N. Increasing sputtering input power, the content of Co in the film increased. At input power of 14 W, film contained -(Fe,Co)8N phase was produced which exhibited higher saturation magnetization (252.85 Am2/kg) and lower value of coercivity (3.66 kAm-1), corresponded to the 12% content of Co in the film.

scholarly journals Cationic Ordering and Its Influence on the Magnetic Properties of Co-Rich Cobalt Ferrite Thin Films Prepared by Reactive Solid Phase Epitaxy on Nb-Doped SrTiO3(001)

Materials ◽  
2021 ◽  
Vol 15 (1) ◽  
pp. 46
Author(s):  
Jannis Thien ◽  
Jascha Bahlmann ◽  
Andreas Alexander ◽  
Kevin Ruwisch ◽  
Jari Rodewald ◽  
...  
Keyword(s):  
Magnetic Properties ◽  
Photoelectron Spectroscopy ◽  
Quantum Interference ◽  
Cobalt Ferrite ◽  
Solid Phase ◽  
Magnetic Circular Dichroism ◽  
Solid Phase Epitaxy ◽  
X Ray ◽  
Atomic Force ◽  
Ferrite Films

Here, we present the (element-specific) magnetic properties and cation ordering for ultrathin Co-rich cobalt ferrite films. Two Co-rich CoxFe3−xO4 films with different stoichiometry (x=1.1 and x=1.4) have been formed by reactive solid phase epitaxy due to post-deposition annealing from epitaxial CoO/Fe3O4 bilayers deposited before on Nb-doped SrTiO3(001). The electronic structure, stoichiometry and homogeneity of the cation distribution of the resulting cobalt ferrite films were verified by angle-resolved hard X-ray photoelectron spectroscopy. From X-ray magnetic circular dichroism measurements, the occupancies of the different sublattices were determined using charge-transfer multiplet calculations. For both ferrite films, a partially inverse spinel structure is found with increased amount of Co3+ cations in the low-spin state on octahedral sites for the Co1.4Fe1.6O4 film. These findings concur with the results obtained by superconducting quantum interference device measurements. Further, the latter measurements revealed the presence of an additional soft magnetic phase probably due to cobalt ferrite islands emerging from the surface, as suggested by atomic force microscope measurements.

scholarly journals Effects of Perpendicular Magnetic Field Annealing on the Structural and Magnetic Properties of [Co/Ni]2/PtMn Thin Films

2021 ◽  
Vol 7 (3) ◽  
pp. 38
Author(s):  
Roshni Yadav ◽  
Chun-Hsien Wu ◽  
I-Fen Huang ◽  
Xu Li ◽  
Te-Ho Wu ◽  
...  
Keyword(s):  
Magnetic Field ◽  
Thin Films ◽  
Magnetic Properties ◽  
Photoelectron Spectroscopy ◽  
Perpendicular Magnetic Field ◽  
Face Centered Cubic ◽  
Lattice Image ◽  
X Ray ◽  
Field Annealing ◽  
Face Centered

In this study, [Co/Ni]2/PtMn thin films with different PtMn thicknesses (2.7 to 32.4 nm) were prepared on Si/SiO2 substrates. The post-deposition perpendicular magnetic field annealing (MFA) processes were carried out to modify the structures and magnetic properties. The MFA process also induced strong interlayer diffusion, rendering a less sharp interface between Co and Ni and PtMn layers. The transmission electron microscopy (TEM) lattice image analysis has shown that the films consisted of face-centered tetragonal (fct) PtMn (ordered by MFA), body-centered cubic (bcc) NiMn (due to intermixing), in addition to face-centered cubic (fcc) Co, Ni, and PtMn phases. The peak shift (2-theta from 39.9° to 40.3°) in X-ray diffraction spectra also confirmed the structural transition from fcc PtMn to fct PtMn after MFA, in agreement with those obtained by lattice images in TEM. The interdiffusion induced by MFA was also evidenced by the depth profile of X-ray photoelectron spectroscopy (XPS). Further, the magnetic properties measured by vibrating sample magnetometry (VSM) have shown an increased coercivity in MFA-treated samples. This is attributed to the presence of ordered fct PtMn, and NiMn phases exchange coupled to the ferromagnetic [Co/Ni]2 layers. The vertical shift (Mshift = −0.03 memu) of the hysteresis loops is ascribed to the pinned spins resulting from perpendicular MFA processes.

Magnetic Properties of Bulk Zn0.95-XMnXFe0.05O2 Prepared by Sol-Gel Method and Subsequent Hot Pressing

2011 ◽  
Vol 268-270 ◽  
pp. 356-359 ◽  
Author(s):  
Wen Song Lin ◽  
C. H. Wen ◽  
Liang He
Keyword(s):  
Magnetic Properties ◽  
Photoelectron Spectroscopy ◽  
Raw Materials ◽  
Sol Gel ◽  
Secondary Phase ◽  
X Ray Diffraction ◽  
Gel Method ◽  
X Ray ◽  
Sol Gel Method ◽  
Doped Zno

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.

scholarly journals Magnetic assessment and modelling of the Aramis undulator beamline

2018 ◽  
Vol 25 (3) ◽  
pp. 686-705 ◽  
Author(s):  
M. Calvi ◽  
C. Camenzuli ◽  
R. Ganter ◽  
N. Sammut ◽  
Th. Schmidt
Keyword(s):  
Magnetic Properties ◽  
Magnetic Measurement ◽  
Hall Probe ◽  
Measurement Equipment ◽  
Series Production ◽  
Close Collaboration ◽  
X Ray ◽  
Short Period ◽  
Reduction Methods ◽  
Paul Scherrer

Within the SwissFEL project at the Paul Scherrer Institute (PSI), the hard X-ray line (Aramis) has been equipped with short-period in-vacuum undulators, known as the U15 series. The undulator design has been developed within the institute itself, while the prototyping and the series production have been implemented through a close collaboration with a Swiss industrial partner, Max Daetwyler AG, and several subcontractors. The magnetic measurement system has been built at PSI, together with all the data analysis tools. The Hall probe has been designed for PSI by the Swiss company SENIS. In this paper the general concepts of both the mechanical and the magnetic properties of the U15 series of undulators are presented. A description of the magnetic measurement equipment is given and the results of the magnetic measurement campaign are reported. Lastly, the data reduction methods and the associated models are presented and their actual implementation in the control system is detailed.

scholarly journals Nano-PAA-CuCl2 Composite as Fenton-Like Reusable Catalyst to Enhanced Degrade Organic Pollutant MB/MO

Catalysts ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 10
Author(s):  
Yang Dang ◽  
Yu Cheng ◽  
Yukun Zhou ◽  
Yifei Huang ◽  
Kaige Wang
Keyword(s):  
Photoelectron Spectroscopy ◽  
Self Assembly ◽  
Organic Pollutant ◽  
Energy Dispersive Spectrometer ◽  
Chemical Properties ◽  
Anodic Alumina ◽  
Alumina Substrate ◽  
Reusable Catalyst ◽  
X Ray ◽  
Nanoporous Anodic Alumina

The treatment of organic dye contaminants in wastewaters has now becoming more imperative. Fenton-like degradation of methylene blue (MB) and methyl orange (MO) in aqueous solution was investigated by using a nanostructure that a layer of CuCl2 nanoflake film grown on the top surface of nanoporus anodic alumina substrate (nano-PAA-CuCl2) as catalyst. The new nano-PAA-CuCl2 composite was fabricated with self-assembly approach, that is, a network porous structure film composed of CuCl2 nanoflake grown on the upper surface of nanoporous anodic alumina substrate, and the physical and chemical properties are characterized systematically with the X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM), and high-resolution transmission electron microscopy (HRTEM), Energy Dispersive Spectrometer (EDS), X-ray photoelectron spectroscopy (XPS). The experimental results showed that the nano-PAA-CuCl2 catalyst presented excellent properties for the degradation of two typical organic pollutants such as MB and MO, which were almost completely degraded with 8 × 10−4mol/L nano-PAA-CuCl2 catalyst after 46 min and 60 min at reaction conditions of H2O2 18 mM and 23 mM, respectively. The effects of different reaction parameters such as initial pH, H2O2 concentration, catalyst morphology and temperature were attentively studied. And more, the stability and reusability of nano-PAA-CuCl2 were examined. Finally, the mechanism of MB and MO degradation by the nano-PAA-CuCl2/H2O2 system was proposed, based on the experimental data of the BCA and the temperature-programmed reduction (H2-TPR) and theoretical analysis, the reaction kinetics belonged to the pseudo-first-order equation. This new nanoporous composite material and preparation technology, as well as its application in Fenton-like reaction, provide an effective alternative method with practical application significance for wastewater treatment.

High Temperature Oxidation Behavior of SUS310S Austenitic Stainless Steel

2014 ◽  
Vol 941-944 ◽  
pp. 212-215
Author(s):  
Tao Zheng ◽  
Jing Tao Han
Keyword(s):  
Photoelectron Spectroscopy ◽  
Oxidation Behavior ◽  
Layer Structure ◽  
Energy Dispersive Spectrometer ◽  
Austenitic Stainless Steels ◽  
Temperature Oxidation ◽  
X Ray ◽  
High Temperature Oxidation Behavior ◽  
High Oxidation Resistance ◽  
Ray Diffusion

The oxidation behavior of SUS310S austenitic stainless steels was studied in isothermal conditions at different temperatures between 800oC and 1100oC for 96h in air. The oxidation kinetics was analyzed, the surface and cross-section of the oxide scale grown by oxidation were characterized by using scanning electron microscopy (SEM), energy dispersive spectrometer (EDS), X-ray diffusion (XRD) and X-ray photoelectron spectroscopy (XPS). The SUS310S steel has high oxidation resistance at 800oC and with the increase of the temperature, the parabolic rate constants is constantly increasing. Examination of the morphology and composition of oxide layers reveals a double-layer structure, The inner layer is mainly chromium oxide (Cr2O3) and is covered by an uneven thinness outer layer of manganese-chromium or iron-chromium spinel oxide.

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