Pac studies of spin deviations,pressure induced hyperfine field shifts,and temperature variation of supertransferred hyperfine fields

A PAC study of¹¹¹Cd substiuted antiferromagnetic transition metal salts is reported. Supertransferred hyperfine fields at¹¹¹Cd nuclei were used for the first time to observe three effects: zero-point spin deviations, temperature variation, and pressure shift of the hyperfine field. Comparison of KNiF₃ and RbMnF₃ with their corresponding quadraticlayer fluorides K₂NiF₄ and Rb₂MnF₄ yields an estimate for the magnitude of the zeropoint spin deviation in doped antiferromagnets. The temperature dependences of the Cd hyperfine fields in RbMnF₃/Cd and MnF₂/Cd have been determined. The shift in hyperfine field observed for -MnS/Cd under external pressure further supports our model for the origin of the supertransferred hyperfine fields.This work was supported by the US Energy Research and Development Administration.     

The magnetic hyperfine field at140Ce in nickel

The hyperfine interaction of¹⁴⁰Ce in nickel has been investigated by the time-differential perturbed-angular-correlation technique (TDPAC). The probe was produced by isotope separator implantation of the fission product¹⁴⁰Xe, the ^- decay chain of which finally populates excited states of¹⁴⁰Ce.Different spin rotation spectra were observed before and after an 8 h annealing at 415°C. The analysis of the spectra led to the conclusion that the Ce ions were in the diamagnetic 4⁺ state. The dominant contributions to the hyperfine interaction are two different magnetic hyperfine fields: |H _hf ¹|=385±7 kOe and |H _hf ²|=276±12 kOe.H _hf ¹ disappears after annealing. The fraction of nuclei which observeH _hf ² is increased by the annealing procedure from 16% to 75%. It is assumed thatH _hf ¹ is the hyperfine field of CeNi in an unperturbed substitutional site andH _hf ² is attributed to Ce ions which have trapped a single vacancy.     

The magnetic hyperfine field at Hg impurities in ferromagnetic Gd

The magnetic hyperfine field at dilute Hg impurities in Gd has been investigated by the conversion electron (e ^–)--time differential perturbed angular correlation (TDPAC) technique. The radioactivities^197m Hg and¹⁹⁹Tl were implanted into Gd foils by means of an isotope separator. TDPAC measurements were performed with the 165 keV-L-conversion electron—134 keV--cascade of¹⁹⁷Hg at different temperatures and with the 334 keV--158 keV-K-conversion electron cascade of¹⁹⁹Hg at 200 K.The regular site occupation probabilities were found to be 15(3)% for an annealed^197m HgGd sample and 29(5)% in unannealed¹⁹⁹TlGd samples.From the magnetic hyperfine interaction frequencies measured for the regular sites at 200 K the magnetic hyperfine fields |H _hf(¹⁹⁷HgGd; 200 K)|=256(13) kG and |H _hf(¹⁹⁹HgGd; 200 K)|=267(7) kG were deduced.On leave from the University of Lisboa, Portugal     

The hyperfine magnetic field in Fe-Hf amorphous alloys at low temperatures

The time-differential perturbed angular correlation (TDPAC) technique was applied to study the hyperfine magnetic field in amorphous Fe-Hf alloys with different Hf contents at low temperatures. The Hf content was changed from 20 to 40 at% andthe TDPAC measurements were carried out in the temperature range from room temperature down to 18 K. Very strong perturbations were observed for the specimen of low Hf content at low temperatures due to a strong hyperfine magnetic field. The characteristic feature observed by the present study is that the temperature dependence of the perturbation for the Fe-30 at% Hf source is quite different from that for other sources, indicating a maximum around 80 K. Discussions have been given on the explanation of the experimental results in the light of magnetic properties of these alloys.     

The hyperfine magnetic field of172Yb in Fe and Ni

Time-differential perturbed angular correlation measurements have been performed on the 91–1095 keV -ray cascade emitted by¹⁷²Yb nuclei in the capture decay of¹⁷²Lu, using implanted sources of¹⁷²Lu in Fe and Ni. From these measurements hyperfine field valuesB(YbFe)=–1253±83 kG andB(YbNi)=–143±12 kG follow at room temperature. From the modulation amplitude of the spectra it follows that only about 20% of the ytterbium nuclei participate in the precession.     

The magnetic hyperfine field of bromine in iron by NMR/ON

Nuclear magnetic resonance of⁸²Br oriented at low temperature in iron has been observed with a sample prepared by ion implantation atT<0.2 K. The asymmetric resonance signal can be decomposed in a broad background signal and a narrow line of FWHM=1.8 (4) MHz which can be attributed to⁸²Br in undisturbed substitutional sites of Fe. From the center frequency of this narrow line (B _ext=0)=201.86(13) MHz we derive the magnetic hyperfine field asB _hf(BrFe)=81.38(6) T. This value is considerably larger than the result of theoretical calculations.     

The magnetic hyperfine field of lutetium in iron by NMR/ON

Nuclear magnetic resonance of oriented¹⁷⁷Lu in iron has been found with a sample prepared by on-line implantation of¹⁷⁷Lu in iron at T<0.2 K. The broad resonance, FWHM=20.5 (1.3) MHz, has a centre frequency of _L=355.06 (51) MHz at zero external field. With the g-factor of¹⁷⁷Lu g=0.637 (3) from literature the magnetic hyperfine field of Lu in Fe is derived as B_hf=–73.12(36) T. Static nuclear orientation data are not compatible with a two site model where the nuclei which are oriented experience the hyperfine interaction found in NMR/ON. A fraction with a lower hyperfine field is necessary to explain the data.     

The temperature dependence of the magnetic hyperfine field of tantalum in dysprosium

The temperature dependence of the magnetic and electric hyperfine interactions at the site of ¹⁸¹Ta impurities in polycrystalline Dy has been measured between 4.2 and 178 K using the time differential perturbed angular correlation technique. The value of the magnetic hyperfine field at 4.2 K is: |H_hf(TaDy)| = 212(9) kG The temperature dependence of the magnetic hyperfine field follows closely the prediction of the molecular field model.     

First-principles studies of the magnetic hyperfine field in Fe multilayers

A detailed theoretical study of the magnetic moments and magnetic hyperfine fields in several Fe multilayers (Fe fcc(001)/5X fcc(001), X=Cu and Ag, and Fe bcc(001)/5X fcc(001), X=Ag and Au) as well as in bulk Fe is presented. The calculations have been performed using the spin-polarized, relativistic linear muffin-tin orbital (SPR-LMTO) method of band structure calculation. Therefore, not only the contribution to the hyperfine fields due to the conventional Fermi contact interaction but also due to the spin dipolar and orbital contributions induced by the crystal field and by spin-orbit coupling are accounted for. To decompose the hyperfine field of non-s-electrons into these contributions it has been assumed that they are proportional to the corresponding so-called magnetic dipole moment and the orbital magnetic moment, respectively. In contrast to previous results for pure metals and alloys not only the orbital but also the spin dipolar hyperfine field was found to be non-negligible. The anisotropy of the hyperfine field determined by calculations for in-plane and perpendicular orientation of the magnetisation was found to be very pronounced and closely connected with the corresponding anisotropy of the magnetic dipole moment and the orbital moment.     

On the effective magnetic hyperfine field in naturally occuring goethite

The asymmetric broadening of the Mössbauer absorption lines frequently observed in goethite is shown to be due to relaxation effects in the surface layers rather than being an intrinsic property of this material. The particle size determines entirely the shape of the observed M-spectrum at room temperature which can vary from a magnetically ordered spectrum to a pure paramagnetic one.     

External field influence on the magnetic hyperfine fields in alpha-manganese

We report a study on the magnetic nature of the two hyperfine fields observed in α-Mn by PAC. Both of the field sites behave completely differently under the influence of an external field ranging from zero to 4 Tesla. The so-called high field originates from the local moment antiferromagnetism of the matrix, while the low field should be associated with an itinerant magnetism.     

The temperature dependence of the57Fe hyperfine magnetic field distribution in Fe-Ni

The temperature dependence of the⁵⁷Fe hyperfine magnetic field (hmf) in Fe-Ni is stronger than the temperature dependence of the⁵⁷Fe hmf in pure Fe. By analyzing the shape of the⁵⁷Fe hmf distribution, and with the help of experiments with Si in Fe-Ni, we deduce that this anomalous temperature dependence originates from a large thermal sensitivity of the magnetic moments at those Fe atoms with more Ni nearest neighbors. A strong temperature dependence of the recoilfree fraction was also observed in Fe-Ni alloys. We suggest that a large mean square thermal displacement of Fe atoms in Fe-Ni is the cause of the anomalous temperature dependence.     

The splitting of hyperfine lines of57Fe nuclei in RF magnetic field

It is shown experimentally, that for Moessbauer nuclei affected by the radio-frequency (RF) magnetic field of sufficient intensity at frequencies corresponding to NMR, splitting of Zeeman sublevels of nuclei and changes in Moessbauer spectral structure occurs. Depending on the frequency of alternating field each spectral line is splitinto (2·Ig,e +1) comporients, Ig,e-being the nuclear spin of ground and excited state, respectively. The intensity of RF components and the energy gap between them are extremely sensitive to the frequency and the intensity of the RF magnetic field.     

The magnetic hyperfine field and the electric field gradient at181Ta impurities in Gd metal

The magnetic hyperfine fieldH _hf and the electric field gradientV _zz at¹⁸¹Ta impurties in metallic Gd were determined by time differential perturbed angular correlation measurements with the 133 keV K-conversion electron 482 keV -cascade of¹⁸¹Ta. The sources for these measurements were prepared by implantation of radioactive¹⁸¹Hf ions into Gd. The results are: |H _hf(TaGd; 77 K)|=285(14)kG, and |V _zz(TaGd; 330 K)|=5.32(15)·10¹⁷V/cm². The value ofH _hf fits well into the systematics for 5d impurities in Gd and indicates a positive core polarisation contribution, which is expected if the conduction electrons of Gd have to a large extent d-character. The electric field gradients of the 5d impurities in Gd are not consistent with a proportionality between the ionic and the electronic contribution.     

The magnetic hyperfine field of 111Cd in the light rare earth metal neodymium

The magnetic hyperfine field of the non-magnetic impurity ¹¹¹Cd in the light rare earth metal Nd has been determined by a perturbed angular correlation (TDPAC) measurement to be |H_hf| = 76.5 (1.5) kOe at 4.2 K. This value fits excellently into the linear relation between H_hf and the rare earth spin projection (g − 1)J observed for ¹¹¹Cd in the heavy rare earth series Gd to Tm. The data suggest a maximum of the s-f coupling constant J(0) for Sm.     

The hyperfine field of sodium in iron

The hyperfine field of NaFe has been measured using Low Temperature Nuclear Orientation of cold implanted²⁴Na. The combination of both the γ-and β-anisotropies yields information on the implantation fraction of Na in Fe. Furthermore, an, upper limit for the relaxation time of Na in Fe could be deduced.     

The hyperfine field on impurities in Gd

Predictions are given for the hyperfine fields on s-p impurities in Gd.     

The hyperfine field of oxygen in iron

From an on-line nuclear orientation measurement on¹⁵O implanted in iron, the hyperfine field of oxygen in iron was deduced as +12.2(16) T. This experiment, together with two measurements on¹⁷F, which was implanted in the same foil, also yielded information on the relaxation and implantation behaviour of light impurities when implanted at low dose and at low temperature.