Magnetic hyperfine field at caesium in iron

We report temperature dependence of nuclear orientation (NO), and the first observation of NMR/ON on Cs in iron.^{132, 136}Cs were implanted at room temperature into polycrystalline and single crystal iron. NO values for the (average) magnetic hyperfine field B_hf (CsFe) are close to 34T, intermediate between the value of 40.7T found in on-line samples made at mK temperatures and the NMR/ON value of 27.8 (2)T. The latter studies. The site/field distribution is briefly discussed. ISOLDE Collaboration, CERN     

Magnetic hyperfine field of arsenic in nickel by NMR/ON of71,72As

The magnetic hyperfine splitting frequencies of⁷¹AsNi and⁷²AsNi in a 0.11 Tesla external magnetic field have been determined by NMR/ON method as 66.00(6) MHz and 106.17(13) MHz respectively. Using the known magnetic moments of μ(⁷¹As)=1.6735(18) and μ(⁷²As)=−2.1566(3), the hyperfine fields were deduced asB _hf(⁷¹AsNi)=12.824(19) Tesla andB _hf(⁷²AsNi)=12.807(16) Tesla.     

Nuclear orientation and NMR/ON on implanted114mIn in Fe and Co

Nuclear orientation and NMR/ON of^114mIn implanted into Fe at an energy of 80 keV and dose of 3–5×10¹⁴ cm^–2 is reported. The zero applied field resonance frequencyv ₀=203.65(6) MHz is combined with the recently determinedB _hf(InFe) of 286.8(3) kG to yield (^114mIn)=+4.658(14) nm. The nuclear spin-lattice relaxation time for^114mIn in iron is measured to be 88(18) s at 18 mK and the applied field dependence of the NMR/ON resonance frequency gives the Knight shift for the system as –2.4(6)%. The absence of measurable nuclear orientation in similarly prepared^114mInCo sources is discussed.     

Magnetic hyperfine fields of Nb andMo in nickel by NMR-ON of90Nb and93mMo

The magnetic hyperfine splitting frequencies of⁹⁰NbNi and^93mMoNi in an external magnetic field of 0.2 T have been determined by the NMR-ON method to be 18.52(7) and23.73(10) MHz, respectively. With the assumption of Knight shift factorK=0 and with the knowng-factors, the hyperfine fields of⁹⁰NbNi and^93mMoNi were deduced asB _HF(⁹⁰NbNi)=-4.118(16) T andB _HF(^93mMoNi)=-3.491(33) T. The rather long spin-lattice relaxation time of 32(5) min was observed for⁹⁰NbNi at an external magnetic field of 0.2T and8 mK.     

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.     

Study of short-lived bromine isotopes

First experiments in the systematic study of the structure of ground states and isomeric states of Br isotopes as function of neutron number at ISOLDE, CERN are reported. The isotopes^{74g.74m,77,78,84g,84m}Br have been implanted into iron and studied with the techniques of low temperature nuclear orientation and nuclear magnetic resonance of oriented nuclei (NMR/ON). The experiments were performed with the NICOLE on-line nuclear orientation set-up using the isotope separator ISOLDE-3. NMR/ON experiments were successful for^74mBr with continuous on-line implantation and for⁷⁷Br. Using as value of the hyperfine field B_hf(BrFe)=+81.3S (3) T we obtain |g (^74mBr)|=0.455 (3) and |g (⁷⁷Br)|=0.6492 (3). Static nuclear orientation data have been measured for all above mentioned isotopes. From these data we derive |μ(⁷⁸Br, I=1)|=0.13 (3) and |μ(^84gBr, I=2)|=1.9 (7). The results are discussed within the systematics of the bromine isotopes.     

Nuclear resonance studies of95NbFe

Dilute alloys of 35-day⁹⁵Nb in polycrystalline iron have been studied by nuclear magnetic resonance on oriented nuclei (NMR/ON) using frequency modulation and fast passage techniques. Comparison of resonance frequencies with nuclear orientation results confirms the spin 9/2 for the⁹⁵Nb ground state. The zero-field resonance frequency is 275.29(9) MHz, leading to ag-factor of 1.3653(25) if the hyperfine field from spin-echo measurements on⁹³NbFe is used. Relaxation times, line shapes, and the frequencyversus field behavior are discussed. A summary of data for CoFe alloys, used here for calibration purposes, is also given.A preliminary report of this work was given at the International Conference on Low Temperature Physics (LT 14), Helsinki, 1975. The work was supported in part by the Deutsche Forschungsgemeinschaft (SFB 161).     

Low temperature nuclear orientation of a dilute RhCr alloy

A dilute^101mRhCr alloy has been investigated by means of low temperature nuclear orientation in the temperature range of 6–60 mK. The magnetic hyperfine field has been found proportional to the macroscopic chromium magnetization and follows even at these low temperatures an Overhauser distribution. The maximum hyperfine field value is B_o (T=6 mK)=7.0(5) T. A Knight shift of –16% affects the external magnetic field at the nuclear site.     

The183Re ground state dipole moment and nuclear spin-lattice relaxation of Re in Fe

The hyperfine interaction of the system¹⁸³Re(70d)Fe has been investigated with the NMR/ON technique. With the hyperfine field valueB _hf(ReFe)=–76.0(1.5) T the ground state magnetic moment was determined as: (5/2⁺,¹⁸³Re)=+3.12(6) _N. The field dependent nuclear spin-lattice relaxation time has been measured. The result for the high-field relaxation rateR _exp=1.65(5)·10^–15 T ²s K^–1 is explained in terms of indirect spin-wave interaction.     

On-line nuclear orientation and relaxation studies of Cs isotopes

The hyperfine field of CsFe has been measured to be (+)40.8(0.7)T, using the technique of on-line low temperature nuclear orientation. The time dependent relaxation of¹²¹Cs^m Fe has also been investigated using a new technique, giving a Korringa constant C_k of 0.059 (15) sK. From this, an effective relaxation time of 3.0 (0.8)s can be deduced for the short lived¹¹⁸Cs^m(T_1/2=17s). This value has then been used to extract the magnetic moment of¹¹⁸Cs^m to be |μ|=5.4 (1.1) nm.     

NMR-ON on196,197m,198,198m,200mAu in Fe and Ni

The zero-field hyperfine splitting frequencies of a series of Au isotopes in Fe and Ni have been determined with nuclear magnetic resonance on oriented nuclei. The results are:. For¹⁹⁸Au(2^–) in Fe the quadrupole splitting could be resolved. The results are ¦g_NB_HF/h|=259.48 (3) MHz and e²qp/h=–2.08(4) MHz. Our measurements show that most hyperfine splittings published on these isotopes have been incorrect. The quadrupole splitting of¹⁹⁸AuFe disagrees in magnitudeand sign from the value reported by single-passage NMR on oriented nuclei. The following nuclear quantities are deduced: (^197mAu,11/2^–)=5.98(9) _N; (^198mAu, 12^–)=5.85(9) _N; (^200mAu, 12^–)=5.90(9) _N; Q(¹⁹⁸Au,2^–)/Q(¹⁹⁹Au, 3/2⁺)=1.37(3). Our measurements show further that the non-contact hyperfine field for Au in Ni is smaller than assumed previously, and that the magnetic hyperfine splitting frequency of¹⁹⁷AuFe known from NMR is inconsistent with the magnetic hyperfine splitting frequencies of^{198, 199}AuFe.     

NMR/ON of206Bi implanted at T < 0.2 K and at room temperature into nickel

NMR/ON has been observed for²⁰⁶BiNi with samples prepared by implantation at T<0.2 K and at room temperature. The integrated destruction of anisotropy for the sample implanted at 290 K is only about half of that for the on-line implanted sample but the resonance line is less broad and has a narrow component with centre frequency _L= 223.62(10) MHz for zero external field. With the known g-factor of²⁰⁶Bi we derive from this frequency the hyperfine field of BiNi as B_hf=38.3(4) T.     

The magnetic moments of (vg 9/2)-levels in odd Zn isotopes

^69m,71mZn have been implanted with an isotope separator on-line into a cold iron host matrix. Nuclear magnetic resonance of the low-temperature oriented isotopes has been observed. The resonance frequencies for zero external magnetic field are v_L(^69mZnFe@#@) =36.814(35) MHz andv _L (^71mZnFe)=33.47(19) MHz. From these the magnetic moments of the 9/2⁺ iosmeric states have been derived as μ(^69mZn)=(?)1.138(18) n.m. andμ(^71mZn)=(?)1.035(18) n.m. The experimentally known magnetic moments of (vg _9/2)-levels in odd zinc isotopes are compared to theoretical estimates.     

Anomalous temperature dependence of the magnetic hyperfine field of99Ru in gadolinium

The magnetic hyperfine field at dilute⁹⁹Ru impurities in ferromagnetic Gd has been investigated as a function of temperature by time differential perturbed angular correlation (TDPAC) measurements. The saturation field at 11 K is H_hf(Ru Gd)=51(2) KOe. This value fits well into the systematics of 4d impurity hyperfine fields in Gd. The magnetic hyperfine field of RuGd does not follow the magnetization of the host (T_c=290 K) but vanishes abruptly at about 70 K. A similar behaviour has previously been observed for the 5d impurity Os in Gd. From first TDPAC measurements of the hyperfine interactions in the intermetallic phases of the Ru-Sc system it can not be completely ruled out that the observed collapse of the hyperfine field at 70 K is due to the formation of the intermetallic compound RuGd₃.This work has been supported by the Minister für Wissenschaft und Forschung des Landes Nordrhein-Westfalen     

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     

Analysis of175Lu NMR data on dilute alloys of Lu in Tb and Dy

Results of Sano, Shimizu and Itoh on NMR frequencies of¹⁷⁵Lu in ferromagnetic Lu_0.02Tb_0.98 and Lu_0.02Dy_0.98 alloys are fitted by use of a model with five adjustable parameters. Two of these are related to the magnitude and asymmetry of the electric-field-gradient (EFG) tensor at a Lu nucleus, and three others specify the magnitude of the magnetic hyperfine field and its orientation with respect to the principal axes of the EFG tensor. For LuDy it is found that (i) the hyperfine field is tilted with respect to these axes, and (ii) the asymmetry of the EFG tensor differs in magnitude from published calculated values based on a point-change model. For LuTb at least one of these two statements is shown to be true. Tilting of the hyperfine field is consistent with inferences from neutron scattering data that the 4f moment is tipped away from the b axis in Tb metal.     

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)|.     

Magnetic hyperfine field for zinc in iron

The magnetic hyperfine field for zinc in iron has been measured by the DPAD method following the reaction ⁶⁴Ni(α, n)⁶⁷Zn^m. Measurements performed with a sandwich target and with ⁶⁴Ni($\text{Fe}$) alloy targets containing 3% and 6% nickel yielded similar results: H_hf(0) = -191 ± 3 kG.     

Nuclear magnetic moment of 12 d 11/2− 131mXe

NMR-ON measurements were performed on^131mXe (I=11/2^–; T_1/2=12.0 d) in Fe, the sample being prepared by recoil implantation after the¹³⁰Te(,3n)^131mXe compound reaction at E=40 Mev. The hyperfine splitting _NB_HF/h¦, extrapolated to zero external magnetic field, was found to be 209.9(1) MHz. Taking B_HF=+1523(8) kG for the hyperfine field of XeFe, the magnetic moment of^131mXe is deduced to be (–)0.994(5) _N. As a byproduct, the zero-field hyperfine splitting of^129mXe (I=11/2^–; T_1/2=8.9d) in Fe was measured as 188.1(1) MHz, with which a magnetic moment of (–)0.891(5) _N is deduced for^129mXe.     

The magnetic hyperfine field at181Ta impurities in the 4f-ferromagnets Ho and Er

The magnetic hyperfine fieldH _hf at¹⁸¹Ta impurities in the ferromagnetic Rare Earth metals Ho and Er has been determined by time differential perturbed angular correlation measurements at 4.2 K. The results |H _hf(TaHo)|=101(8)kG |H _hf(TaEr)|= 94(8)kG together with the previously determined values ofH _hf(TaGd) andH _hf(TaDy) show that the magnetic hyperfine field at Ta impurities in the Rare Earth metals is predominantly due to the conduction electron polarization of the hosts.