Concentration Dependence of Room Temperature Magnetic Ordering in Dilute Fe: Ge1 − x Te x Alloy

2005 ◽  
Vol 160 (1-4) ◽  
pp. 241-246 ◽  
Author(s):  
D. R. S. Somayajulu ◽  
Narendra Patel ◽  
Mukesh Chawda ◽  
Mitesh Sarkar ◽  
K. C. Sebastian
IWNMS 2004 ◽  
2006 ◽  
pp. 241-246
Author(s):  
D. R. S. Somayajulu ◽  
Narendra Patel ◽  
Mukesh Chawda ◽  
Mitesh Sarkar ◽  
K. C. Sebastian

MRS Bulletin ◽  
2000 ◽  
Vol 25 (11) ◽  
pp. 21-30 ◽  
Author(s):  
Joel S. Miller ◽  
Arthur J. Epstein

Molecule-based magnets are a broad, emerging class of magnetic materials that expand the materials properties typically associated with magnets to include low density, transparency, electrical insulation, and low-temperature fabrication, as well as combine magnetic ordering with other properties such as photoresponsiveness. Essentially all of the common magnetic phenomena associated with conventional transition-metal and rare-earth-based magnets can be found in molecule-based magnets. Although discovered less than two decades ago, magnets with ordering temperatures exceeding room temperature, very high (∼27.0 kOe or 2.16 MA/m) and very low (several Oe or less) coercivities, and substantial remanent and saturation magnetizations have been achieved. In addition, exotic phenomena including photoresponsiveness have been reported. The advent of molecule-based magnets offers new processing opportunities. For example, thin-film magnets can be prepared by means of low-temperature chemical vapor deposition and electrodeposition methods.


2011 ◽  
Vol 106 (8) ◽  
Author(s):  
Minoru Soda ◽  
Taishi Ishikura ◽  
Hiroyuki Nakamura ◽  
Yusuke Wakabayashi ◽  
Tsuyoshi Kimura

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.


1993 ◽  
Vol 46 (5) ◽  
pp. 679 ◽  
Author(s):  
JM Cadogan ◽  
SJ Campbell ◽  
XL Zhao ◽  
E Wu

Mossbauer spectra of YC012B6 and NdCo12B6 doped with enriched 57Fe have been obtained at various temperatures between 4�2 K and room temperature. The spectrum of YC012B6 at 4�2 K indicates that the Co sublattice orders in the crystallographic basal plane. NdCo12B6 orders along or close to the crystallographic c-axis at 4�2 K and undergoes a spin-reorientation with increasing temperature until at ~55 K the magnetisation lies in or near the basal plane.


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.


2020 ◽  
Vol 32 (9) ◽  
pp. 095701
Author(s):  
Jayaseelan Dhakshinamoorthy ◽  
Sachin Kumar Srivastava ◽  
Durgamadhab Mishra ◽  
Biji Pullithadathil

2011 ◽  
Vol 1307 ◽  
Author(s):  
Jing Liu ◽  
P. A. Dowben ◽  
Guangfu Luo ◽  
Wai-Ning Mei ◽  
Anil Kumar Rajapitamahuni ◽  
...  

ABSTRACTThe local spin configuration and band structure of chromium doped boron carbide calculated by density functional theory suggests local magnetic ordering. While the long range dopant position appears random in the boron carbide semiconductor, the local position and initial empirical/computational results suggest the promise of large magneto-resistive effects. The chromium doped boron carbide thin films, fabricated by boron carbide-chromium co-deposition, were studied by current-voltage (I-V) characteristics measurements. The results provide some reason to believe that magneto-resistive effects are indeed present at room temperature.


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