Nuclear magnetic resonance on oriented194Ir (T 1/2=19.4 h) in Fe and Ni

The hyperfine interaction of¹⁹⁴Ir (j ^π =1^?;T _1/2=19.4 h) in Fe and Ni has been investigated with the technique of nuclear magnetic resonance on oriented nuclei. For both systems the electronic-orbital-momentum induced electric quadrupole splitting could be resolved. The magnetic and electric hyperfine splitting frequencies,v _M =¦gμ _N ^B _HF/h¦ andv _Q =e ² qQ/h, respectively, were measured as:¹⁹⁴IrFe:v _m =408.54 (23) MHz;v _q =?2.47(20) MHz;¹⁹⁴IrNi:v _M =135.24(5) MHz;v _q =?1.23 (3) MHz. Taking into account a 3% uncertainty arising from hyperfine anomalies theg-factor is deduced as ¦g¦=0.39 (1). The electric quadrupole moment,Q=+0.352 (18)b, is slightly smaller than expected from the known systematics of deformation parameters in this mass region.     

Nuclear magnetic resonance on oriented76,77,82Br in Fe

Nuclear magnetic resonance on oriented^76,77,82BrFe has been measured using recoil-implanted samples. The magnetic hyperfine splitting frequency of⁸²BrFe in a zero external magnetic field has been determined to be 201.90(3) MHz. The resonances of⁷⁶BrFe and⁷⁷BrFe were also observed in an external magnetic field of 0.2 T asv(⁷⁶BrFe)=340.9(3) MHz andv(⁷⁷BrFe)=403.5(2) MHz. With the known values of theg-factors, the hyperfine fields have been deduced:B _HF(⁸²BrFe)=81.397(27) T,B _HF(⁷⁶BrFe)=81.38(7) T. Theg-factor of⁷⁷Br was determined to be |0.6487(4)|.     

Nuclear magnetic resonance of brute force oriented110mAgAg

NMR on brute force oriented nuclei (NMRON/BF) has been observed for^110mAg in elemental silver. Resonances have been measured at approximately 7 T and 8 T with the resulting gradient of 4.583(5) MHzT⁻¹ which produces a value for the^110mAg moment of μ=3.589(4) nm (uncorrected). Factors pertinent to successful NMRON/BF in systems such as^110mAgAg, with a complex decay scheme and modestg-factor, are also discussed.     

Nuclear magnetic resonance on oriented192Ir in Fe and Ni

The hyperfine interaction of¹⁹²Ir nuclei as dilute impurities in Fe and Ni has been investigated with NMR on oriented nuclei. With the use of highly dilute and pure alloys the line widths could be reduced so far that the quadrupole splitting of¹⁹²IrFe and¹⁹²IrNi could be resolved. Taking hyperfine anomalies into account the ground state nuclear moments of¹⁹²Ir are deduced as |μ|=1.924(10)μ _N andQ=2.36(ll) b. The hyperfine field of IrNi was investigated as a function of the Ir concentrationc between 0.01 at % and 5 at %. The dependence ofH _HF onc was found to be significantly smaller than that reported from Mössbauer effect measurements. Forc=0.01 at %H _HF=?454.7(2.3)kG is deduced. The resonance shift with an external magnetic field has been studied precisely, yieldingK=0.012(23) andK=0.026(12) for the Knight-shift of¹⁹²Ir in Fe and Ni, respectively.     

Nuclear magnetic resonance on oriented 11/2− 129mXe and131mXe in Fe

The magnetic hyperfine splitting frequenciesν _M=¦gμ _NB_HF/h.¦ of the 11/2^? isomeric states^129m Xe (T_1/2=8.9d) and^131mXe (T_1/2=11.8d) in Fe were measured with nuclear magnetic resonance on oriented nuclei at temperatures of 10–15 mK as 188.0(1) MHz and 209.8(1) MHz, respectively, the samples being prepared with the technique of recoil implantation after (α, x n) reactions. The magnetic moments of^129m Xe and^131m Xe are deduced to be (?)0.8914(6)μ _N and (?)0.9943(6)μ _N, respectively. The missing γ-anisotropies for allγ-transitions following the decay of 36.4d ¹²⁷Xe indicateI=1/2 for the ground state spin of¹²⁷Xe.     

Nuclear magnetic resonance on oriented189,191 Pt in iron

Nuclear magnetic resonance measurements have been performed for¹⁸⁹Pt and¹⁹¹Pt oriented at 7 and 15 mk in iron host. The magnetic hyperfine splitting frequencies, ν=¦μB_HF/Ih¦, of the¹⁸⁹Pt and¹⁹¹Pt ground states were determined to be 277.61(5) and 319.88(3) MHz. With the hyperfine field of B_HF=-1280(26) kG the nuclear magnetic moments were deduced to be: ¦μ(¹⁸⁹Pt;3/2^?)¦=0.427(9) μ^N; ¦μ(¹⁹¹Pt,3/2^?) ¦=0.492(10) μ_N. The effective spinlattice relaxation time for¹⁹¹PtFe at 7 mK in a polarizing magnetic field of 2 kG has been found to be 30(2) s using a single-exponential fit.     

In-plane magnetic surface anisotropies in Fe(110)

In-plane magnetic surface anisotropies have been detected for Fe(110) on W(110) using in situ Conversion Electron Mössbauer Spectroscopy (CEMS). The phenomenon used for the determination of this anisotropy was a switching of the spontaneous magnetizationJ _s from [001] to [1¯10] with decreasing thickness. Analysis of the data is performed using a homogeneous magnetization approximation for competing surface and bulk anisotropies, which is justified by a micromagnetic analysis and established experimentally by CEMS. In-plane surface anisotropy constants for the clean Fe(110) surface, the Fe metal-interface and the FeGaAs interface are determined toK _s,p ^FeUHV =0.065 erg·cm^–2,K _s,p ^FeMetal =0.040 erg ·cm^–2, andK _s,p ^FeGaAs =0.047 erg ·cm^–2, all with an estimated accuracy of the order of 10%.     

Nuclear magnetic resonance of 131I and 132I oriented in Fe

Nuclear magnetic resonance has been applied to radioactive I nuclei oriented in Fe. By field shifting the ¹³¹I resonance the hyperfine field is determined as positive. The ¹³¹I resonance at 683.3 ± 1.0 MHz and the ¹³²I resonance at 674.0 ± 0.5 MHz give H_int = 1144.0 ± 1.5 kOe.     

Nuclear magnetic resonance study of HfV2Hx and ZrV2Hx (0 ⩽ x ⩽ 4.2) hydrides

A proton NMR spin echo study of the system HfV₂H_x and ZrV₂H_x (0 ? x ? 4.5) hydrides are reported. The T₁ spin lattice relaxation rate enables us to extract the activation energy for diffusion, E_a, as well as the attempt frequency v₀; both depend strongly on the hydrogen concentration. The existence of a correlation between E_a and v₀ in these and other hydride systems yield the temperature dependence of the activation energy.     

The ferromagnetic monolayer Fe(110) on W(110)

Ferromagnetic order in the pseudomorphic monolayer Fe(110) on W(110) was analyzed experimentally using Conversion Electron Mössbauer Spectroscopy (CEMS) and Torsion Oscillation Magnetometry (TOM). The monolayer is thermodynamically stable, crystallizes to large monolayer patches at elevated temperatures and therefore forms an excellent approximation to the ideal monolayer structure. It is ferromagnetic below a Curie-temperatureT _c,mono, which is given by (282±3) K for the Ag-coated layer, (290±10) K for coating by Cu, Ag or Au and ≈210 K for the free monolayer. For the Ag-coated monolayer, ground state hyperfine fieldB _hf (0)=(11.9±0.3) T and magnetic moment per atom μ=2.53 μ_B could be determined, in fair agreement with theoretical predictions. Unusual properties of the phase transition are detected by the combination of both experimental techniques. Strong magnetic anisotropies, which are essential for ferromagnetic order, are determined by CEMS.     

Potassium adsorption on Fe(110)

LEED, AES, UPS and XPS were used to study submonolayer coverages of potassium on Fe(110). At room temperature the maximum potassium coverage is characterized by a LEED superstructure. This LEED pattern is interpreted as being due to a hexagonal close-packed K layer on Fe(110), resulting in a maximum atom density of 5.3 × 10¹⁴ cm^?2, i.e.θ k = 0.31. The work function change and the shift of the K(2p) and K(3p) core levels with potassium coverage indicate a charge transfer from potassium to iron at low potassium coverages.     

Effects of the magneto-crystalline anisotropy on the magnetic properties of Fe/Cr/Fe (110) trilayer

Using a variational procedure based on Lee-Low-Pines and Huybrechts canonical transformations, we study the stability region of two-dimensional bipolarons confined in a parabolic quantum dot, subject to a uniform magnetic field. In the framework of our approach, we calculate the ground-state energy for two-dimensional magnetobipolarons, together with the free polaron ground-state energy, by performing a self consistent calculation. We then obtain the binding energy for two-dimensional magnetobipolarons, in the usual way, to explore the properties of bipolaron formation in two-dimensional quantum dot structures. The stability region is found to be very sensitive to the confinement length of the parabolic potential and to the magnetic field strength, as well as to the material parameters and . The stability region is also found to be remarkably enhanced by increasing the degree of spatial confinement and magnetic field. Our results are both in qualitative and quantitative agreement with those found in the literature.Received: 11 December 2003, Published online: 9 April 2004PACS: 71.38.Fp Large or Fröhlich polarons - 63.20.Kr Phonon-electron and phonon-phonon interactions     

Energetics of Carbon deposition on Fe(100) and Fe(110) surfaces and subsurfaces

Spin-polarized density functional theory calculations have been performed to investigate carbon deposition and carbide formation on Fe(100) and Fe(110) at different carbon coverage. On Fe(100) with increasing carbon coverage, the most stable carbon adsorption configuration changes from surface carbon adsorption to surface carbon diffusion into subsurface, and surface carbon clustering is not favored thermodynamically. However, surface carbon clustering is more favored kinetically than carbon diffusion; and carbon diffusion into subsurface and surface carbon clustering become competitive. On Fe(110) with increasing surface carbon coverage, the most stable adsorption configuration changes from surface carbon adsorption to surface carbon diffusion into subsurface, and this process is favored both kinetically and thermodynamically, and surface carbon clustering is neither favored nor competitive. Surface carbon deposition might form on Fe(100), while carbide formation might be found on Fe(110).     

Nuclear magnetic resonance studies of CePd2In and LaPd2In at low temperatures

We report on In nuclear magnetic resonance (NMR) and nuclear quadrupolar resonance (NQR) measurements on the new heavy-electron compound CePdZIn over a wide temperature range, from 45 mK up to 30 K. CePd₂In undergoes an antiferromagnetic (AF) phase transition at T _N = 1.23 K involving small localised Ce moments of 0.11 μ_B. In zero field, the spin-lattice relaxation rate T ₁ ^?1 (T) shows remarkable changes in its temperature dependence. Above 3 K, T ₁ ^?1 is constant and 850 sec^?1. Between T _N and 2T _N, (T ₁ T)^?1 = 330 (Ksec)^?1, but rapidly decreases below T _N. A Korringatype relaxation, characteristic for simple metals at low temperatures, with (T ₂ T)^?1 = 17(Ksec)¹ is resumed below 0.6 K. This value is an order of magnitude larger than (T ₁ T)^?1 for LaPd₂In and therefore is associated with low-energy excitations of the itinerant charge carriers with 4f symmetry. The T ₁ ^?1 data at various non-zero magnetic fields fall on a single curve when plotted as a function of (T/H) if H exceeds 3.5 T. Thus the AF ordering, the 4f moment fluctuations and the Kondo screening are drastically suppressed by the application of fields H of the order of 3.5 T.