Doped Nanostructured Manganese Ferrites: Synthesis, Characterization, and Magnetic Properties

Nanocrystalline aluminum-doped manganese ferrite was synthesized by facile thermal treatment method. Nanostructure-doped ferrite with crystalline size that ranged between 3.71 and 6.35 nm was characterized via X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and vibrating-sample magnetometry (VSM). The Scherrer and Williamson-Hall hypothesis techniques were utilized to determine lattice constants and strain. Various types of structural properties including octahedral and tetrahedral site radius, bond lengths and angles, hopping parameter, oxygen positional parameters, site bonds, and edge lengths were determined from XRD spectrum analysis. Discrepancy in the hypothetically expected angle indicates improvement of A-B superexchange intercommunication. Furthermore, magnetic-hysteresis (M-H) and XPS analysis support the claim of enhancement. The presence of the ionic nature of iron and manganese in ferrite is FeII, FeIII, MnII, and MnIV as revealed by the results of XPS. Moreover, XPS assists in an excellent way to understand the properties such as configuration, chemical nature, and average inversion degree of doped ferrite samples. The spin noncollinearity and exquisite interaction amid the sublattice are responsible for the decrease in the saturation and remnant magnetization determined from the hysteresis loop at ambient temperature with maximum magnetic field of 1.8 T.

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Superparamagnetic Behavior of Granular Co-C Films Consisting of Nanocrystalline Cobalt Encapsulated in Carbon

MRS Proceedings ◽

10.1557/proc-614-f2.7.1 ◽

2000 ◽

Vol 614 ◽

Cited By ~ 2

Author(s):

Hao Wang ◽

S.P. Wong ◽

W.Y. Cheung ◽

N. Ke ◽

M.F. Chiah ◽

...

Keyword(s):

Photoelectron Spectroscopy ◽

Rutherford Backscattering Spectrometry ◽

Magnetic Measurements ◽

Magnetic Hysteresis ◽

Blocking Temperature ◽

Vacuum Arc ◽

Zero Field ◽

X Ray Diffraction ◽

X Ray ◽

Force Microscopy

ABSTRACTNanocomposite Co-C thin films of about 15 nm thick were prepared by pulsed filtered vacuum arc deposition. The films were characterized by x-ray photoelectron spectroscopy, non-Rutherford backscattering spectrometry, x-ray diffraction, magnetic force microscopy and magnetic measurements. The as-deposited films were amorphous. After annealing at 350°C for one hour in vacuum (< 10−3 Pa), the films were found to consist of nanocrystalline Co grains encapsulated in carbon. The superparamagnetism of the annealed Co36C64 film was demonstrated by the measurement of DC susceptibility and magnetic hysteresis using a SQUID magnetometer. The superparamagnetic relaxation blocking temperature was marked to be about 12K by the peak of the zero-field-cooled magnetization under a field of 100 Oe. The magnetic properties of these annealed granular Co-C films transform from superparamagnetism to ferromagnetism when the Co concentration increases.

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Morphological and magnetic features of columnar nanostructures CuO

Journal of Physics Conference Series ◽

10.1088/1742-6596/2094/2/022002 ◽

2021 ◽

Vol 2094 (2) ◽

pp. 022002

Author(s):

A V Ushakov ◽

I V Karpov ◽

L Yu Fedorov ◽

V G Demin

Keyword(s):

Magnetic Measurements ◽

Magnetic Hysteresis ◽

Coherent Scattering ◽

Magnetic Hysteresis Loop ◽

Ferromagnetic Behavior ◽

X Ray Diffraction ◽

Monoclinic Crystal ◽

X Ray ◽

Monoclinic Crystal Structure ◽

Ionic Nature

Abstract Columnar nanostructures (CNS) were grown by plasma chemical synthesis at a gas mixture pressure of 90% He + 10% O2 200 Pa and substrate temperatures of 340K (sample 1) and 370K (sample 2). The effect of substrate temperature on the morphological, crystalline, magnetic, and impedance properties of CNS was studied. Scanning microscopy (SEM) showed that the morphology of CNS varies significantly from dendritic to wire structure. Energy dispersive X-ray spectroscopy (EDS) showed a change in the stoichiometry of the deficiency samples (Cu52O48) to an excess of oxygen (Cu42O58). X-ray diffraction analysis (XRD) and Rietveld fitting showed that samples 1 and 2 have a monoclinic crystal structure with a large proportion of the amorphous phase, the size of coherent scattering regions (CSR) was 26 nm (sample 1). Magnetic measurements showed that sample 1 exhibits ferromagnetic behavior, and at 6 K a magnetic hysteresis loop appears. Sample 2 from 250 K to room temperature exhibits diamagnetic behavior. A connection was found between the appearance of diamagnetism and a jump in the dielectric constant of sample 2. An assumption was made about the electron-ionic nature of the diamagnetism of sample 2.

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STRUCTURAL, MAGNETIC AND DIELECTRIC PROPERTIES OF Fe-DOPED BaTiO3 SOLIDS

Modern Physics Letters B ◽

10.1142/s021798491250056x ◽

2012 ◽

Vol 26 (09) ◽

pp. 1250056 ◽

Cited By ~ 29

Author(s):

ZHENGANG GUO ◽

LIHONG YANG ◽

HONGMEI QIU ◽

XUEDAN ZHAN ◽

JINHUA YIN ◽

...

Keyword(s):

Dielectric Properties ◽

Photoelectron Spectroscopy ◽

Magnetic Hysteresis ◽

Hysteresis Loops ◽

Double Exchange ◽

Exchange Interactions ◽

Magnetic Element ◽

X Ray Diffraction ◽

X Ray ◽

Ferromagnetic Order

The structural, ferroelectric and magnetic properties of bulk perovskite Fe -doped BaTiO 3 (BFTO) prepared by standard solid-state reaction have been investigated. X-ray diffraction (XRD) identifies the tetragonal structure of BFTO samples. Rietveld refinements of XRD data indicates that the doping ions led to ab-plane expansion and out-of-ab-plane shrinkage of the BFTO phases. X-ray photoelectron spectroscopy (XPS) measurements for the prepared samples reveals that Fe 3+ and Fe 4+ ions replaces Ti 4+ ions in the crystal lattice to form single-phase BFTO solids. The results of the temperature-dependent dielectric properties and magnetic hysteresis loops for the BFTO solids show simultaneously the ferroelectric order and ferromagnetic order at room temperature. The doping of magnetic element Fe brings about ferromagnetic order for the samples, and the measured magnetic moment for each Fe atom increases from 0.70 μB to 1.55 μB in BFTO samples. The origin of ferromagnetism of the BFTO samples should be attributed to the double exchange interactions of Fe 3+– O 2– Fe 4+ ions.

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Investigation of the Effect of Uv-Assisted Oxidation and Nitridation of Hafnium Metal Films

MRS Proceedings ◽

10.1557/proc-780-y5.5 ◽

2003 ◽

Vol 780 ◽

Author(s):

C. Essary ◽

V. Craciun ◽

J. M. Howard ◽

R. K. Singh

Keyword(s):

Uv Radiation ◽

Photoelectron Spectroscopy ◽

Grazing Angle ◽

X Ray Diffraction ◽

Metal Thin Films ◽

X Ray ◽

Force Microscopy ◽

Si Substrates ◽

Atomic Force ◽

Silicon Interface

AbstractHf metal thin films were deposited on Si substrates using a pulsed laser deposition technique in vacuum and in ammonia ambients. The films were then oxidized at 400 °C in 300 Torr of O2. Half the samples were oxidized in the presence of ultraviolet (UV) radiation from a Hg lamp array. X-ray photoelectron spectroscopy, atomic force microscopy, and grazing angle X-ray diffraction were used to compare the crystallinity, roughness, and composition of the films. It has been found that UV radiation causes roughening of the films and also promotes crystallization at lower temperatures.Furthermore, increased silicon oxidation at the interface was noted with the UVirradiated samples and was shown to be in the form of a mixed layer using angle-resolved X-ray photoelectron spectroscopy. Incorporation of nitrogen into the film reduces the oxidation of the silicon interface.

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Non-Thermal Plasma-Modified Ru-Sn-Ti Catalyst for Chlorinated Volatile Organic Compound Degradation

Catalysts ◽

10.3390/catal10121456 ◽

2020 ◽

Vol 10 (12) ◽

pp. 1456

Author(s):

Yujie Fu ◽

You Zhang ◽

Qi Xin ◽

Zhong Zheng ◽

Yu Zhang ◽

...

Keyword(s):

Plasma Treatment ◽

Photoelectron Spectroscopy ◽

High Surface ◽

High Surface Area ◽

Surface Oxidation ◽

Treatment Method ◽

X Ray ◽

Chlorinated Volatile Organic Compounds ◽

Volatile Organic ◽

Doped Titania

Chlorinated volatile organic compounds (CVOCs) are vital environmental concerns due to their low biodegradability and long-term persistence. Catalytic combustion technology is one of the more commonly used technologies for the treatment of CVOCs. Catalysts with high low-temperature activity, superior selectivity of non-toxic products, and resistance to chlorine poisoning are desirable. Here we adopted a plasma treatment method to synthesize a tin-doped titania loaded with ruthenium dioxide (RuO2) catalyst, possessing enhanced activity (T90%, the temperature at which 90% of dichloromethane (DCM) is decomposed, is 262 °C) compared to the catalyst prepared by the conventional calcination method. As revealed by transmission electron microscopy, X-ray diffraction, N2 adsorption, X-ray photoelectron spectroscopy, and hydrogen temperature-programmed reduction, the high surface area of the tin-doped titania catalyst and the enhanced dispersion and surface oxidation of RuO2 induced by plasma treatment were found to be the main factors determining excellent catalytic activities.

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α-Cellulose Fibers of Paper-Waste Origin Surface-Modified with Fe3O4 and Thiolated-Chitosan for Efficacious Immobilization of Laccase

Polymers ◽

10.3390/polym13040581 ◽

2021 ◽

Vol 13 (4) ◽

pp. 581

Author(s):

Gajanan S. Ghodake ◽

Surendra K. Shinde ◽

Ganesh D. Saratale ◽

Rijuta G. Saratale ◽

Min Kim ◽

...

Keyword(s):

Enzyme Immobilization ◽

Photoelectron Spectroscopy ◽

Cellulose Fibers ◽

Relative Activity ◽

Significant Activity ◽

X Ray Diffraction ◽

X Ray ◽

Transmission Electron ◽

Laccase Immobilization ◽

Surface Modified

The utilization of waste-paper-biomass for extraction of important α-cellulose biopolymer, and modification of extracted α-cellulose for application in enzyme immobilization can be extremely vital for green circular bio-economy. Thus, in this study, α-cellulose fibers were super-magnetized (Fe3O4), grafted with chitosan (CTNs), and thiol (-SH) modified for laccase immobilization. The developed material was characterized by high-resolution transmission electron microscopy (HR-TEM), HR-TEM energy dispersive X-ray spectroscopy (HR-TEM-EDS), X-ray diffraction (XRD), vibrating sample magnetometer (VSM), X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared spectroscopy (FT-IR) analyses. Laccase immobilized on α-Cellulose-Fe3O4-CTNs (α-Cellulose-Fe3O4-CTNs-Laccase) gave significant activity recovery (99.16%) and laccase loading potential (169.36 mg/g). The α-Cellulose-Fe3O4-CTNs-Laccase displayed excellent stabilities for temperature, pH, and storage time. The α-Cellulose-Fe3O4-CTNs-Laccase applied in repeated cycles shown remarkable consistency of activity retention for 10 cycles. After the 10th cycle, α-Cellulose-Fe3O4-CTNs possessed 80.65% relative activity. Furthermore, α-Cellulose-Fe3O4-CTNs-Laccase shown excellent degradation of pharmaceutical contaminant sulfamethoxazole (SMX). The SMX degradation by α-Cellulose-Fe3O4-CTNs-Laccase was found optimum at incubation time (20 h), pH (3), temperatures (30 °C), and shaking conditions (200 rpm). Finally, α-Cellulose-Fe3O4-CTNs-Laccase gave repeated degradation of SMX. Thus, this study presents a novel, waste-derived, highly capable, and super-magnetic nanocomposite for enzyme immobilization applications.

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Photocatalytic Reduction of CO2 to Methanol Using a Copper-Zirconia Imidazolate Framework

Catalysts ◽

10.3390/catal11030346 ◽

2021 ◽

Vol 11 (3) ◽

pp. 346

Author(s):

Sonam Goyal ◽

Maizatul Shima Shaharun ◽

Ganaga Suriya Jayabal ◽

Chong Fai Kait ◽

Bawadi Abdullah ◽

...

Keyword(s):

Photoelectron Spectroscopy ◽

Catalyst Support ◽

Oxidation Potential ◽

Molar Ratio ◽

X Ray Diffraction ◽

X Ray ◽

Molar Ratios ◽

Optimum Parameters ◽

Reduction Of Co2 ◽

Enhanced Yield

A set of novel photocatalysts, i.e., copper-zirconia imidazolate (CuZrIm) frameworks, were synthesized using different zirconia molar ratios (i.e., 0.5, 1, and 1.5 mmol). The photoreduction process of CO2 to methanol in a continuous-flow stirred photoreactor at pressure and temperature of 1 atm and 25 °C, respectively, was studied. The physicochemical properties of the synthesized catalysts were studied using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and photoluminescence (PL) spectroscopy. The highest methanol activity of 818.59 µmol/L.g was recorded when the CuZrIm1 catalyst with Cu/Zr/Im/NH4OH molar ratio of 2:1:4:2 (mmol/mmol/mmol/M) was employed. The enhanced yield is attributed to the presence of Cu2+ oxidation state and the uniformly dispersed active metals. The response surface methodology (RSM) was used to optimize the reaction parameters. The predicted results agreed well with the experimental ones with the correlation coefficient (R2) of 0.99. The optimization results showed that the highest methanol activity of 1054 µmol/L.g was recorded when the optimum parameters were employed, i.e., stirring rate (540 rpm), intensity of light (275 W/m2) and photocatalyst loading (1.3 g/L). The redox potential value for the CuZrIm1 shows that the reduction potential is −1.70 V and the oxidation potential is +1.28 V for the photoreduction of CO2 to methanol. The current work has established the potential utilization of the imidazolate framework as catalyst support for the photoreduction of CO2 to methanol.

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Study on the Electrical, Structural, Chemical and Optical Properties of PVD Ta(N) Films Deposited with Different N2 Flow Rates

Coatings ◽

10.3390/coatings11080937 ◽

2021 ◽

Vol 11 (8) ◽

pp. 937

Author(s):

Yingying Hu ◽

Md Rasadujjaman ◽

Yanrong Wang ◽

Jing Zhang ◽

Jiang Yan ◽

...

Keyword(s):

Crystal Structure ◽

Optical Properties ◽

Photoelectron Spectroscopy ◽

Crystal Size ◽

Silicon Substrates ◽

X Ray Diffraction ◽

Dc Magnetron Sputtering ◽

Flow Rates ◽

X Ray ◽

N2 Flow Rate

By reactive DC magnetron sputtering from a pure Ta target onto silicon substrates, Ta(N) films were prepared with different N2 flow rates of 0, 12, 17, 25, 38, and 58 sccm. The effects of N2 flow rate on the electrical properties, crystal structure, elemental composition, and optical properties of Ta(N) were studied. These properties were characterized by the four-probe method, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and spectroscopic ellipsometry (SE). Results show that the deposition rate decreases with an increase of N2 flows. Furthermore, as resistivity increases, the crystal size decreases, the crystal structure transitions from β-Ta to TaN(111), and finally becomes the N-rich phase Ta3N5(130, 040). Studying the optical properties, it is found that there are differences in the refractive index (n) and extinction coefficient (k) of Ta(N) with different thicknesses and different N2 flow rates, depending on the crystal size and crystal phase structure.

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Optical, XPS and XRD Studies of Semiconducting Copper Sulfide Layers on a Polyamide Film

International Journal of Photoenergy ◽

10.1155/2009/304308 ◽

2009 ◽

Vol 2009 ◽

pp. 1-8 ◽

Cited By ~ 69

Author(s):

Valentina Krylova ◽

Mindaugas Andrulevičius

Keyword(s):

Photoelectron Spectroscopy ◽

Copper Sulfide ◽

Diffusion Method ◽

X Ray Diffraction ◽

Xps Spectra ◽

X Ray ◽

Xrd Studies ◽

Polyamide Film ◽

Indirect Band Gap ◽

Xrd Method

Copper sulfide layers were formed on polyamide PA 6 surface using the sorption-diffusion method. Polymer samples were immersed for 4 and 5 h in 0.15 mol⋅ solutions and acidified with HCl (0.1 mol⋅) at . After washing and drying, the samples were treated with Cu(I) salt solution. The samples were studied by UV/VIS, X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) methods. All methods confirmed that on the surface of the polyamide film a layer of copper sulfide was formed. The copper sulfide layers are indirect band-gap semiconductors. The values of are 1.25 and 1.3 eV for 4 h and 5 h sulfured PA 6 respectively. Copper XPS spectra analyses showed Cu(I) bonds only in deeper layers of the formed film, while in sulfur XPS S 2p spectra dominating sulfide bonds were found after cleaning the surface with ions. It has been established by the XRD method that, beside , the layer contains as well. For PA 6 initially sulfured 4 h, grain size forchalcocite, , was nm and fordjurleite, , it was 54.17 nm. The sheet resistance of the obtained layer varies from 6300 to 102 .

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Biodiesel Production on Monometallic Pt, Pd, Ru, and Ag Catalysts Supported on Natural Zeolite

Materials ◽

10.3390/ma14010048 ◽

2020 ◽

Vol 14 (1) ◽

pp. 48

Author(s):

Pawel Mierczynski ◽

Magdalena Mosińska ◽

Lukasz Szkudlarek ◽

Karolina Chalupka ◽

Misa Tatsuzawa ◽

...

Keyword(s):

Photoelectron Spectroscopy ◽

Natural Zeolite ◽

Noble Metals ◽

Methyl Esters ◽

Physicochemical Characteristics ◽

Biodiesel Production ◽

X Ray Diffraction ◽

X Ray ◽

Yield Values ◽

Temperature Programmed

Biodiesel production from rapeseed oil and methanol via transesterification reaction facilitated by various monometallic catalyst supported on natural zeolite (NZ) was investigated. The physicochemical characteristics of the synthesized catalysts were studied by X-ray diffraction (XRD), Brunauer–Emmett–Teller method (BET), temperature-programmed-reduction in hydrogen (H2-TPR), temperature-programmed-desorption of ammonia (NH3-TPD), Scanning Electron Microscope equipped with EDX detector (SEM-EDS), and X-ray photoelectron spectroscopy (XPS) methods. The highest activity and methyl ester yields were obtained for the Pt/NZ catalyst. This catalyst showed the highest triglycerides conversion of 98.9% and fatty acids methyl esters yields of 94.6%. The activity results also confirmed the high activity of the carrier material (NZ) itself in the investigated reaction. Support material exhibited 90.5% of TG conversion and the Fatty Acid Methyl Esters yield (FAME) of 67.2%. Introduction of noble metals improves the TG conversion and FAME yield values. Increasing of the metal loading from 0.5 to 2 wt.% improves the reactivity properties of the investigated catalysts.

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