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- Gupta, A., et al.
(författare)
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Synthetic magnetic opals
- 2002
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Ingår i: Pramana (Bangalore). - : Springer Science and Business Media LLC. - 0304-4289 .- 0973-7111. ; 58:06-maj, s. 1051-1059
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Tidskriftsartikel (refereegranskat)abstract
- We present studies of novel nanocomposites of BiNi impregnated into the structure of opals as well as inverse opals. Atomic force microscopy and high resolution elemental analyses show a highly ordered structure and uniform distribution of the BiNi filler in the matrix. These BiNi-based nanocomposites are found to exhibit distinct ferromagnetic-like ordering with transition temperature of about 675 K. As far as we know there exists no report in literature on any BiNi compound which is magnetic.
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- Sharma, P., et al.
(författare)
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Ferromagnetism above room temperature in bulk and transparent thin films of Mn-doped ZnO
- 2003
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Ingår i: Nature Materials. - : Springer Science and Business Media LLC. - 1476-1122 .- 1476-4660. ; 2:10, s. 673-677
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Tidskriftsartikel (refereegranskat)abstract
- The search for ferromagnetism above room temperature in dilute magnetic semiconductors has been intense in recent years. We report the first observations of ferromagnetism above room temperature for dilute (<4 at.%) Mn-doped ZnO. The Mn is found to carry an average magnetic moment of 0.16 μ(B) per ion. Our ab initio calculations find a valance state of Mn2+ and that the magnetic moments are ordered ferromagnetically, consistent with the experimental findings. We have obtained room-temperature ferromagnetic ordering in bulk pellets, in transparent films 2-3 μm thick, and in the powder form of the same material. The unique feature of our sample preparation was the low-temperature processing. When standard high-temperature (T>700degreesC) methods were used, samples were found to exhibit clustering and were not ferromagnetic at room temperature. This capability to fabricate ferromagnetic Mn-doped ZnO semiconductors promises new spintronic devices as well as magneto-optic components.
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- Sharma, L Ajitkumar, et al.
(författare)
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Molecular magnetic properties of two-copper(II) containing complexes [Cu(II) (1-phenylamidino-O-n-butylurea) en (H2O)(2)(2+) and [Cu(II) sulphato-mono (1-phenylamidino-O-methylurea)](2) - An EPR study
- 2004
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Ingår i: Spectrochimica Acta Part A - Molecular and Biomolecular Spectroscopy. - : Elsevier BV. - 1386-1425 .- 1873-3557. ; 60:7, s. 1593-1600
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Tidskriftsartikel (refereegranskat)abstract
- Electron paramagnetic resonance (EPR) investigations were conducted on [Cu(II) (1-phenylamidino-O-n-butylurea) en (H2O)12 21 (1) and [Cu(II) sulphato-mono (1-phenylamidino-O-methylurea)](2) (2) respectively, in the temperature range 300-77 K. Fine structure characteristics of S = 1 system, was observed in both complexes with zero field splitting of 0.0525 and 0.0225 cm(-1), respectively, suggesting the formation of dimeric complexes. The presence of the half-field signal (DeltaM(s)= +/-2), in the complex 1, further confirmed the formation of dimer. The temperature dependence of EPR signal intensity has given evidence for the ferromagnetic (FM) coupling between the two Cu2+ ions. The isotropic exchange interaction constants J, were evaluated from this and were found out to be similar to57 and similar to27 cm(-1), respectively, for the complexes I and 2. The photoacoustic spectra of these complexes had shown a band around 26,400 cm(-1) characteristic of metal-metal bonding giving an independent support for the existence of dimeric Cu2+ species. The high magnetic moment values at room temperature for complex I (2.68mu(B)) and complex 2 (2.00mu(B)), obtained from the magnetic susceptibility measurements, support the formation of ferromagnetically coupled Cu2+ dimers.
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- Iqbal, Z., et al.
(författare)
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Evidence for a solid phase of dodecahedral C-20
- 2003
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Ingår i: European Physical Journal B. - : Springer Science and Business Media LLC. - 1434-6028 .- 1434-6036. ; 31:4, s. 509-515
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Tidskriftsartikel (refereegranskat)abstract
- Evidence is presented for the formation of a solid phase based on the smallest fullerene, C-20, in thin diamond-like carbon films deposited by ultraviolet laser ablation from diamond onto nickel substrates at room temperature in the presence of 10(-4) torr of cyclohexane or benzene. Laser desorption mass spectrometry from the films shows the presence of C-20, C-21 and C-22 species, while micro-Raman spectroscopy and electron diffraction from selected particles together with first principle density-functional calculations, indicate a cubic solid with dodecahedral C-20 Cages as building blocks. Unlike solid C-60 and fully protonated C-20, which are bound by van der Waals forces, the proposed structure is stabilized by linking of the C-20 dodecahedra with bridging carbon atoms at interstitial tetrahedral sites to form a face-centered-cubic lattice with 22 carbon atoms per unit cell.
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