Abnormal Diamagnetic Respond in Co0.2Mn1.7Sn Compound

2013 ◽  
Vol 650 ◽  
pp. 264-267 ◽  
Author(s):  
Wen Jiang Feng ◽  
Hao Hua Zhang ◽  
Yan He

The Co-doped Co0.2Mn1.7Sn compound was prepared by melting appropriate metals with purity higher than 99.9% in a magneto-controlled arc furnace. The compound shows single-phase characteristics. Magnetic measurements show that, the abnormal negative magnetization, i.e. diamagnetism occurs at low temperature. Moreover, it displays the common weak ferromagnetism, together with some spin-glass-like behavior. Besides, we conjure that abnormal negative magnetization should be from the magnetized sample when cooling the compound in the so-called zero field (in fact it is about 2.5×10-5 T).

2021 ◽  
Author(s):  
Andrei Kosterov ◽  
Leonid Surovitskii ◽  
Valerii Maksimochkin ◽  
Svetlana Yanson ◽  
Aleksey Smirnov

<p>Ti-rich titanomagnetite is a primary magnetic mineral in submarine basalts, as well as in some terrestrial volcanic rocks. On geological timescale, it undergoes a slow oxidation forming titanomaghemites. This natural process may be modeled to some extent by a prolonged annealing at moderately elevated temperatures. We test this by treating at 355°C for 4, 40, 110, and 375 hours a sample of submarine basalt containing titanomagnetite of approximate TM46 composition with Curie temperature of 205°C. To characterize the oxidation products emerged during annealing, we have carried out magnetic measurements between at cryogenic temperatures between 1.8 K and 300 K and at high temperatures up to 700°C.</p><p>Temperature dependences of magnetic susceptibility measured in an argon atmosphere reveal that annealing for 4 hours already leads to the formation of new magnetic phases (Phases 1 and 2 thereafter) with Curie temperatures of 420°C and 590°C, respectively. At the same time, a phase close to the initial titanomagnetite still remains in a noticeable amount, although its Curie point also shifts towards higher temperatures. Upon further annealing, the initial titanomagnetite completely disappears, the Curie temperature of Phase 1 increases, reaching 500°C after 375 hours, and the Curie temperature of Phase 2 remains practically unchanged. Phase 1 appears unstable to heating to 700°C in argon atmosphere. In samples annealed for up to 110 hours, Phase 1 disappears on cooling, and a phase with the same Curie temperature as the initial titanomagnetite reemerges. In the sample annealed for 375 hours, traces of Phase 1 are still visible in the cooling branch of the susceptibility vs. temperature curve, and the Curie temperature of the reemerged initial-like phase is 250°C. The newly formed Phase 2 remains stable when heated to 700°C in argon.</p><p>Effect of prolonged annealings is clearly seen in low-temperature magnetic properties. In the fresh sample, about one quarter of magnetization acquired at 1.8 K is demagnetized by 5 K. This feature holds for the annealed samples as well. The titanomagnetite phase in the fresh sample manifests itself in a magnetic transition at 58 K. Below this temperature, the FC and ZFC curves sharply diverge, as previously observed for titanomagnetites of intermediate composition. For the annealed samples, the shape of ZFC and FC curves and the ratio between them remain generally similar to those observed for the fresh sample, but there are also several differences. The magnetic transition temperature shifts to ~45 K, while the curves’ shape above the transition changes from concave-up to concave-down. RT-SIRM cycle to 1.8 K in zero field for the fresh sample has a characteristic convex shape and is almost reversible. Magnetization at 1.8 K is about 20% higher than the initial value at 300 K, and magnetization loss after the cycle is only 2-3%. The shape of RT-SIRM cycles changes progressively with increasing annealing time, the degree of irreversibility increasing to ~30% for the sample annealed for 375 hours. </p><p>This study is supported by Russian Foundation of the Basic Research, grants 19-05-00471 and 20-05-00573.</p>


NANO ◽  
2010 ◽  
Vol 05 (06) ◽  
pp. 349-355 ◽  
Author(s):  
SHALENDRA KUMAR ◽  
B. H. KOO ◽  
S. K. SHARMA ◽  
M. KNOBEL ◽  
C. G. LEE

We have used the co-precipitation technique to synthesize nanocrystalline Co -doped CeO2 dilute magnetic semiconductors with Co concentrations ranging from 0.0–0.07. X-ray diffraction patterns (XRD) demonstrate that all the samples display single phase cubic structure without any impurity phase. Average particle sizes calculated from XRD and transmission electron microscopy (TEM) studies showed a gradual decrease with increase in Co ions concentration. UV–visible optical spectroscopy measurements reflect an energy band gap, which decreases with the increasing concentration of dopant (x ≤ 0.03). Raman spectra show an intensity loss of classical CeO2 vibration modes, which is an indication of considerable structural modifications and disorder in CeO2 lattice. Magnetic measurements revealed that all the samples exhibit a weak ferromagnetism at room temperature.


2010 ◽  
Vol 1256 ◽  
Author(s):  
Kashif Nadeem ◽  
Heinz Krenn

AbstractWe prepared single-phase nickel ferrite nanoparticles separated by silicon dioxide using sol-gel method with tetraethyl orthosilicate (TEOS) as a precursor for SiO2. The magnetic properties are investigated by using SQUID-magnetometry over a broad temperature range (4.2 – 350 K), magnetic field (2–70,000 Oe) and frequency (0.1 – 1000 Hz) range. The particle size is in the range 8 – 12 nm. Exchange bias and spin disorder appear at the core-shell interface due to broken bonds on the surface. Disorder and core-shell interaction induces spin-glass freezing which is manifested by a low temperature peak in the AC susceptibility well separated from magnetic blocking peak. This low temperature peak is assigned to spin-glass freezing. The proof of spin-glass freezing is managed by zero field cooled/field cooled (ZFC/FC), frequency and DC field dependence of AC susceptibility, low temperature hysteresis loop and time dependent thermoremanent magnetization at different temperatures. All the measurements stated above signify blocking/unblocking at higher temperatures and surface spin-glass freezing at low temperatures. The aim of our work is to contribute to a better understanding of “spin-frozen” magnetic ferrite nanoparticles at diameters 8 – 12 nm which could be important in future for stabilizing the magnetic state of “core-shell”-structured nanomagnets.


2009 ◽  
Vol 87 (5) ◽  
pp. 57004 ◽  
Author(s):  
Javed Iqbal ◽  
Xiaofang Liu ◽  
Abdul Majid ◽  
Dapeng Yu ◽  
Ronghai Yu

2013 ◽  
Vol 2013 ◽  
pp. 1-6
Author(s):  
Rajneesh Mohan ◽  
Nupinderjeet Kaur ◽  
N. K. Gaur

The discovery of the coexistence of superconductivity and weak ferromagnetism in ruthenocuprates like (Ru, R-1222; R = Eu, Gd) and RuSr2GdCu2O8 (Ru-1212) has created a tremendous interest both experimentally as well as theoretically. Here, we have prepared polycrystalline samples of RuSr2R1.4Ce0.6Cu2O10 (R = Gd, Eu, and Sm) by the standard solid state reaction method. These samples were characterized by XRD, SEM, dc resistivity, and squid measurements. All the prepared samples were single phase without any trace of impurity. From the low-temperature resistivity measurement, the samples of (R = Eu and Gd) were found to be superconducting, while the samples of RuSr2Sm1.6Ce0.4Cu2O10 show semiconducting behavior. The magnetization (M) versus field (H) hysteresis at 5 K clearly shows the ferromagnetic behavior of the samples. The zero field cooled magnetization () and field cooled magnetization () diverge at 100 K.


2012 ◽  
Vol 557-559 ◽  
pp. 680-683
Author(s):  
Yi Yun Yang

The magnetization, ac susceptibility and magnetic relaxation of Nd0.90Sr0.10CoO3polycrystalline sample were systematically investigated in this paper. The experimental studies of susceptibility and magnetic relaxation evidence the existence of a low-temperature spin-glass. A dynamic analysis of ac susceptibility implies a spin-glass transition temperature TSG =12.17 K and the dynamical exponent zv=8. Moreover, low-temperature zero-field cooling and field cooling magnetic relaxation show perfectly mirror symmetry, and field cooling processes relaxation obeys a stretched exponential form. Therefore, our study confirms that the phase separation in Nd0.90Sr0.10CoO3originates from both the ferromagnetic clusters interaction and the spin glasslike phase at low temperature.


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.


2021 ◽  
Vol 763 ◽  
pp. 138243
Author(s):  
Priyanka Sehrawat ◽  
R.K. Malik ◽  
Priti Boora ◽  
Monika Punia ◽  
Monika Sheoran ◽  
...  
Keyword(s):  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Mily Kundu ◽  
Santanu Pakhira ◽  
Renu Choudhary ◽  
Durga Paudyal ◽  
N. Lakshminarasimhan ◽  
...  

AbstractTernary intermetallic compound $${\text {Pr}}_2 {\text {Co}}_{0.86} {\text {Si}}_{2.88}$$ Pr 2 Co 0.86 Si 2.88 has been synthesized in single phase and characterized by x-ray diffraction, scanning electron microscopy with energy dispersive x-ray spectroscopy (SEM-EDX) analysis, magnetization, heat capacity, neutron diffraction and muon spin rotation/relaxation ($$\mu$$ μ SR) measurements. The polycrystalline compound was synthesized in single phase by introducing necessary vacancies in Co/Si sites. Magnetic, heat capacity, and zero-field neutron diffraction studies reveal that the system undergoes magnetic transition below $$\sim$$ ∼ 4 K. Neutron diffraction measurement further reveals that the magnetic ordering is antiferromagnetic in nature with an weak ordered moment. The high temperature magnetic phase has been attributed to glassy in nature consisting of ferromagnetic clusters of itinerant (3d) Co moments as evident by the development of internal field in zero-field $$\mu$$ μ SR below 50 K. The density-functional theory (DFT) calculations suggest that the low temperature magnetic transition is associated with antiferromagnetic coupling between Pr 4f and Co 3d spins. Pr moments show spin fluctuation along with unconventional orbital moment quenching due to crystal field. The evolution of the symmetry and the crystalline electric field environment of Pr-ions are also studied and compared theoretically between the elemental Pr and when it is coupled with other elements such as Co. The localized moment of Pr 4f and itinerant moment of Co 3d compete with each other below $$\sim$$ ∼ 20 K resulting in an unusual temperature dependence of magnetic coercivity in the system.


Sign in / Sign up

Export Citation Format

Share Document