Magnetic properties of Single Crystal GaFeO3

MRS Advances ◽  
2019 ◽  
Vol 4 (1) ◽  
pp. 61-66 ◽  
Author(s):  
Koki Tachiyama ◽  
Shintaro Yasui ◽  
Badari Narayana Aroor Rao ◽  
Takuro Dazai ◽  
Takamasa Usami ◽  
...  

Abstractκ-Al2O3-type GaFeO3 is a promising multiferroic material due to the coexistence of a large spontaneous magnetization and polarization near room temperature. In the current study, we present the magnetic properties of single crystalline GaFeO3 and compare it with that of ε-Fe2O3. Magnetic measurements revealed that spontaneous magnetization appears below 540 K in two steps, similar to that reported for ε−Fe2O3. Partial magnetic ordering takes place at 540 K (TN1), with Fe3+ ions in two distorted octahedral sites ordering antiparallel to one another. Upon further cooling at 200 K (TN2), the remaining Fe3+ ions in regular octahedra and tetrahedra order antiparallel to one another. Substitution of Ga for Fe in ε-Fe2O3 leads to a decrease in TN1 and TN2 from 850 to 540 K and from 480 to 200 K, respectively, caused by a dilution of magnetic Fe by nonmagnetic Ga and preferential site occupation of Ga.

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.


2014 ◽  
Vol 789 ◽  
pp. 415-418
Author(s):  
Cheng Long Lei ◽  
Qing Lin ◽  
Hai Fu Huang ◽  
Yun He ◽  
Rui Jun Wang

The cyano-bridged complex Co [Fe (CN)5NO]·5H2O has been synthesized. According to the reaction of cyanide-based unsaturated ligand precursor (molecular fragments)[BLy(CN)x]n-with the metal ions or complex unsaturated ligand, it is easy to control the structure of molecular magnets and tune up the magnetic properties. Hetero binuclear complex Co [Fe (CN)5NO]∙5H2O was prepared through [Fe (CN)5NO]2- ion. The room temperature Mossbauer spectrum revealed a doublet with the isomer shift parameter (-0.44(7) mm/s) and quadrupole splitting (QS = 1.91(3) mm / s) characteristic for low-spin Fe (III) ions. The low-spin (S = 1/2) of the Fe (III) ion of valence electrons on the electric field gradient (EFG) was caused by non-zero contribution. DC and AC magnetic measurements showed that the complexes belonged to the anti-ferromagnetic material, with a magnetic phase transition temperature below 2K.


2020 ◽  
Vol 6 (1) ◽  
pp. 12
Author(s):  
Bárbara Rodríguez-García ◽  
Jose Ramon Galan-Mascaros

The incorporation of the natural amino acid L-proline in the synthesis to vanadium-chromium Prussian blue derivatives results in materials exhibiting magnetic ordering including chiral magnetic centers. Although the amorphous nature of these materials makes difficult to assess the structural features of these proline-containing compounds, magnetic and spectroscopic data confirms their multifunctionality. They exhibit high-temperature magnetic ordering (Tc < 255 K) and a circular dichroic signal, representing the molecule-based chiral magnets with the highest ordering temperatures reported to date. In addition, the presence of chiral L-proline (or D-proline) has additional benefits, including higher redox stability and the appearance of magnetic hysteresis. The latter was not observed in the parent compounds, the series of room temperature molecule-based magnets V[Cr(CN)6]x.


2012 ◽  
Vol 545 ◽  
pp. 269-274
Author(s):  
Nor Hayati Alias ◽  
Abdul Halim Shaari ◽  
Wan Mohamad Daud Wan Yusoff ◽  
Che Seman Mahmood

A new perovskite based titano-manganite (La0.5-xPrxBa0.5)(Mn0.5Ti0.5)O3 at x concentration 0, 0.01, 0.03, 0.05, 0.07 and 0.09 has been successfully prepared by ceramic solid-state technique at sintering temperature of 1300 °C. Dielectric electrical properties of the synthesized materials at frequency ranging from 5 Hz to 1 MHz and magnetic properties have been studied at room temperature. Analyses have been carried out to determine the structural, magnetic and dielectric properties of the synthesized material as a candidate of multiferroic material.


1970 ◽  
Vol 14 ◽  
pp. 433-440
Author(s):  
W. S. McCain ◽  
D. L. Albright ◽  
W. O. J. Boo

AbstractLattice constants were measured as a function of temperature by single crystal diffracrometry in the temperature range which includes the Néel temperature of VF2(TN= 7°K). The lattice constants of VF2(D4h14=P42m n m) were measured from room temperature down to 4.2°K. In this range rhe tetragonal c-axis contracts 0.58% from 3.2359 Å (RT) to 3.2170 Å (4.2°K). On the other hand, the a-axes show a net expansion of 0.18% from 4.8023 Å (RT) to 4.8110 Å at 4.2°K. The temperature dependence of the lattice constants can be correlated with anisotropy of exchange forces. Vanadium Ions occupy the center and corner positions of the unit cell. Strong magnetic interactions are directed parallel to the c-axis >001< with considerably weaker interactions parallel to the body diagonals >111< The relative strengths of the two exchange integrals are J >001< = 50 J >111<. As a consequence the magnetic ordering is one-dîmensional along the c-axis and the associated distortions arise from the strong magnetic interactions along this axis.


2013 ◽  
Vol 821-822 ◽  
pp. 1358-1361 ◽  
Author(s):  
Fan Zhang ◽  
Rui Liang Su ◽  
Li Zhi Shi ◽  
Yang Liu ◽  
Yan Na Chen ◽  
...  

CoFe2O4 (CFO) nanoparticles was synthesized by a simple hydrothermal method using NaOH solution as a mineralizer at 200 °C for 4 h. It was found that CFO particle sizes decreased firstly and then increased with the increasing of NaOH concentration, and had a minumum value about 10-20 nm when selected 4 mol/L NaOH solution, indicating the NaOH concentration played an important role in controlling the particle size of CFO powders. The room temperature magnetic measurements showed that the saturation magnetization value was 48 emu/g, which is less than the bulk value. The synthesis method is possible to be a general approach for the preparation of other spinel ferrite nanoparticles.


2005 ◽  
Vol 3 (3-4) ◽  
pp. 271-288 ◽  
Author(s):  
Ram K. Agarwal ◽  
Surendra Prasad

We describe the synthesis and characterization of cobalt(II) and nickel(II) coordination compounds of 4[N-(furan-2’-aldimine)amino]antipyrine thiosemicarbazone (FFAAPTS) and 4[N-(4'-nitrobenzalidene) amino]antipyrine thiosemicarbazone (4'-NO2BAAPTS). All the isolated compounds have the general composition MX2(L)(H2O) (M = Co2+or Ni2+; X = Cl, Br, NO3, NCS or CH3COO; L = FFAAPTS or 4'-NO2BAAPTS) and M(ClO4)2(L)2(M = Co2+or Ni2+; L = FFAAPTS or 4'-NO2BAAPTS). Infrared spectral studies indicate that both the thiosemicarbazones coordinate in their neutral form and they act as {N,N,S} tridentate chelating ligands. Room temperature magnetic measurements and electronic spectral studies suggest the distorted octahedral geometries of the prepared complexes. Thermogravimetric studies are also reported and the possible structures of the complexes are proposed. Antibacterial and antifungal properties of these metal-coordination compounds have also been studied.


2019 ◽  
Vol 21 (23) ◽  
pp. 12697-12703 ◽  
Author(s):  
Rostislav Langer ◽  
Piotr Błoński ◽  
Michal Otyepka

The recent discovery of hydroxofluorographene G(OH)F, a graphene derivative showing room temperature antiferromagnetic ordering, suggests that there may be other sp-materials based on sp3-functionalized graphene that exhibit magnetic ordering and whose properties can be controlled by selecting suitable functional groups.


2020 ◽  
Author(s):  
Barbara Lesniak ◽  
Michalis Charilaou ◽  
Andreas Gehring

&lt;p&gt;Greigite (Fe&lt;sub&gt;3&lt;/sub&gt;S&lt;sub&gt;4&lt;/sub&gt;) is a ferrimagnetic mineral widespread in sedimentary environments, commonly found in lacustrine and marine sediments that records ancient geomagnetic field variations and environmental processes. However, its magnetic properties are not yet well understood due to the lack of a single crystal greigite suitable for magnetic measurements. In particular, the dependency of its magnetic properties with respect to structural and morphological properties remains uncertain.&lt;/p&gt;&lt;p&gt;In the present study, we analyzed the structural and magnetic properties of synthetic, polycrystalline greigite formed by controlled colloidal synthesis [Rhodes et al. 2017]. X-ray diffractometry and transition electron microscopy reveal that greigite forms flakes of about 100 nm that consist of epitaxial intergrown nanoparticles with a mean coherence length of 19 nm. Therefore, our synthetic greigite can be considered as polycrystalline flakes with a nanotexture.&lt;/p&gt;&lt;p&gt;The saturation magnetization (M&lt;sub&gt;s&lt;/sub&gt;) of the nanotextured greigite is 32.7 Am&lt;sup&gt;2&lt;/sup&gt;kg&lt;sup&gt;-1 &lt;/sup&gt;and the coercivity is B&lt;sub&gt;c&lt;/sub&gt; = 41 mT. The M&lt;sub&gt;s&lt;/sub&gt; is about 45% below the value for relatively large, synthetic crystal and this in turn is probably caused by the nanotexture, e.g., interfaces between nanocrystallites. The ratios M&lt;sub&gt;r.&lt;/sub&gt;/M&lt;sub&gt;S&lt;/sub&gt; = 0.54 and B&lt;sub&gt;ar&lt;/sub&gt;/B&lt;sub&gt;Sc&lt;/sub&gt; = 1.33 indicate single-domain (SD) particles with pre-dominant uniaxial anisotropy [Roberts 1995]. The FORC diagram at room temperature shows an oval contour plot supporting that the flakes are nanotextured with interacting SD particles. The hysteresis parameters B&lt;sub&gt;c&lt;/sub&gt; and M&lt;sub&gt;S&lt;/sub&gt; continuously increase upon cooling to 10 K.&lt;/p&gt;&lt;p&gt;Low-temperature cycling of the magnetization between 300 and 10 K in fields between 10 mT and 1000 mT shows the expected behavior for ferrimagnets with the superposition of the cooling and warming curves at fields B &amp;#179; 500 mT. At weaker fields a slight magnetic induction upon warming is found and the relative increase in magnetization is field dependent. This irreversibility most likely stems from the magnetization of the nanoparticle interfaces and their interactions in the flakes.&lt;/p&gt;&lt;p&gt;Ferromagnetic resonance spectroscopy (FMR) at room temperature shows a resonance field B&lt;sub&gt;res&lt;/sub&gt;= 213 mT and linewidth DB = 160 mT. Upon cooling the B&lt;sub&gt;res&lt;/sub&gt; decreases continuously down to 50 K followed by a pronounced shift to lower values down to 10 K. The shift goes along with markedly linewidth broadening. The discontinuity of the spectral parameters at T &lt; 50 K points to a change in the effective anisotropy of the flakes most likely due to changes of the magnetocrystalline and the interaction anisotropies in the nanotexture, because the shape anisotropy of the polycrystalline flakes undergoes no significant change.&amp;#160;&lt;/p&gt;&lt;p&gt;In summary, the magnetic properties of greigite can be critically affected by the nanotexture. The response of the nanotexture to the magnetization and anisotropy properties can be taken to identify and characterize greigite nanoparticles in natural environments and to critically evaluate their use for paleomagnetic studies.&lt;/p&gt;&lt;p&gt;Rhodes, Jordan M., et al. &quot;Phase-controlled colloidal syntheses of iron sulfide nanocrystals via sulfur precursor reactivity and direct pyrite precipitation.&quot;&amp;#160;Chemistry of Materials&amp;#160;29.19 (2017): 8521-8530.&lt;/p&gt;&lt;p&gt;Roberts, Andrew P. &quot;Magnetic properties of sedimentary greigite (Fe3S4).&quot;&amp;#160;Earth and Planetary Science Letters&amp;#160;134.3-4 (1995): 227-236.&lt;/p&gt;


2016 ◽  
Vol 843 ◽  
pp. 155-160 ◽  
Author(s):  
D.A. Vinnik ◽  
I.A. Zakharchuk ◽  
Erkki Lähderanta

This paper presents magnetic properties of manganese substituted barium hexaferrite BaFe12-xMnxO19 single crystals. Crystals of BaFe12–xMnxO19 with x up to 1.5 and sizes up to 8 mm were observed. The influence of Fe substitution by Mn on the magnetic properties was investigated. For the BaFe10.5Mn1.5O19 single crystal samples saturation magnetization reduced from 72 to 63.5 emu/g at room temperature, and Curie temperature decreased from 455 to 380 °C.


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