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Register a new userKondo Effect and Spin Glass Behavior of Dilute Iron Clusters in Silver Studied by M{o}ssbauer Spectroscopy and Resistivity
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Added by
Wiliam Herrera Trujillo
Publication date
2008
fields
Physics
and research's language is
English
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Thin films of silver containing 0.3 - 1.5 at % Fe have been prepared by vapor co-deposition. Depending on substrate temperature and iron concentration we could systematically follow the formation of nanometer size clusters of iron from initially dilute iron monomers. samples were characterized via X-ray diffraction, resistivity and M{o}ssbauer spectroscopic measurements. The magnetic behavior derived from M{o}ssbauer data can be best described with an ensemble of ferromagnetic mono-domain particles. The magnetic freezing observed at low temperatures, is controlled via the inter-particle interactions mediated via conduction electron polarization, i.e. RKKY interaction. The interaction of the cluster magnetic moments with the conduction electron sea is best quantified by the electrical resistivity data. For all studied concentrations we find a non-monotonic variation with temperature which can be understood by competing shielding of the cluster moments by conduction electron spin scattering due to Kondo effect and the magnetic coupling.
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We exploit the decoherence of electrons due to magnetic impurities, studied via weak localization, to resolve a longstanding question concerning the classic Kondo systems of Fe impurities in the noble metals gold and silver: which Kondo-type model yields a realistic description of the relevant multiple bands, spin and orbital degrees of freedom? Previous studies suggest a fully screened spin $S$ Kondo model, but the value of $S$ remained ambiguous. We perform density functional theory calculations that suggest $S = 3/2$. We also compare previous and new measurements of both the resistivity and decoherence rate in quasi 1-dimensional wires to numerical renormalization group predictions for $S=1/2,1$ and 3/2, finding excellent agreement for $S=3/2$.
The compound EuFe(2-x)Co(x)As2 was investigated by means of the 57Fe and 151Eu Moessbauer spectroscopy versus temperature (4.2 - 300 K) for x=0 (parent), x=0.34 - 0.39 (superconductor) and x=0.58 (overdoped). It was found that spin density wave (SDW) is suppressed by Co-substitution, however it survives in the region of superconductivity, but iron spectra exhibit some non-magnetic component in the superconducting region. Europium orders anti-ferromagnetically regardless of the Co concentration with the spin re-orientation from the a-axis in the parent compound toward c-axis with the increasing replacement of iron by cobalt. The re-orientation takes place close to the a-c plane. Some trivalent europium appears in EuFe(2-x)Co(x)As2 versus substitution due to the chemical pressure induced by Co-atoms and it experiences some transferred hyperfine field from Eu2+. Iron experiences some transferred field due to the europium ordering for substituted samples in the SDW and non-magnetic state both, while the transferred field is undetectable in the parent compound. Superconductivity coexists with the 4f-europium magnetic order within the same volume. It seems that superconductivity has some filamentary character in EuFe(2-x)Co(x)As2 and it is confined to the non-magnetic component seen by the iron Moessbauer spectroscopy.
We have measured the electrical resistivity of cerium monochalcogenices, CeS, CeSe, and CeTe, under high pressures up to 8 GPa. Pressure dependences of the antiferromagnetic ordering temperature $T_{N}$, crystal field splitting, and the $ln T$ anomaly of the Kondo effect have been studied to cover the whole region from the magnetic ordering regime at low pressure to the Fermi liquid regime at high pressure. $T_{N}$ initially increases with increasing pressure, and starts to decrease at high pressure as expected from the Doniachs diagram. Simultaneously, the $ln T$ behavior in the resistivity is enhanced, indicating the enhancement of the Kondo effect by pressure. It is also characteristic in CeX$_{c}$ that the crystal field splitting rapidly decreases at a common rate of $-12.2$ K/GPa. This leads to the increase in the degeneracy of the $f$ state and further enhancement of the Kondo effect. It is shown that the pressure dependent degeneracy of the $f$ state is a key factor to understand the pressure dependence of $T_{N}$, Kondo effect, magnetoresistance, and the peak structure in the temperature dependence of resistivity.
We report the coexistence of the Kondo effect and spin glass behavior in Fe-doped NbS$_2$ single crystals. The Fe$_x$NbS$_2$ shows the resistance minimum and negative magnetoresistance due to the Kondo effect, and exhibits no superconducting behavior at low temperatures. The resistance curve follows a numerical renormalization-group theory using the Kondo temperature $T_K =12.3$~K for $x=0.01$ as evidence of Kondo effect. Scanning tunneling microscope/spectroscopy (STM/STS) revealed the presence of Fe atoms near sulfur atoms and asymmetric spectra. The magnetic susceptibility exhibits a feature of spin glass. The static critical exponents determined by the universal scaling of the nonlinear part of the susceptibility suggest a three-dimensional Heisenberg spin glass. The doped-Fe atoms in the intra- and inter-layers revealed by the X-ray result can realize the coexistence of the Kondo effect and spin glass.
The origin of the interfacial perpendicular magnetic anisotropy (PMA) induced in the ultrathin Fe layer on the Au(111) surface was examined using synchrotron-radiation-based M{o}ssbauer spectroscopy (MS), X-ray magnetic circular dichroism (XMCD), and angle-resolved photoemission spectroscopy (ARPES). To probe the detailed interfacial electronic structure of orbital hybridization between the Fe 3$d$ and Au 6$p$ bands, we detected the interfacial proximity effect, which modulates the valence-band electronic structure of Fe, resulting in PMA. MS and XMCD measurements were used to detect the interfacial magnetic structure and anisotropy in orbital magnetic moments, respectively. $In$-$situ$ ARPES also confirms the initial growth of Fe on large spin-orbit coupled surface Shockley states under Au(111) modulated electronic states in the vicinity of the Fermi level. This suggests that PMA in the Fe/Au(111) interface originates from the cooperation effects among the spin, orbital magnetic moments in Fe, and large spin-orbit coupling in Au. These findings pave the way to develop interfacial PMA using $p$-$d$ hybridization with a large spin-orbit interaction.
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