NMR-ON measurements of187WFe,182,183,186ReNi,186ReFe and203PbFe

The magnetic hyperfine splitting frequencies of¹⁸⁷WFe,¹⁸²Re(j ^π=2⁺)Ni,¹⁸³ReNi,¹⁸⁶ReNi,¹⁸⁶ReFe and²⁰³PbFe in a zero external magnetic field have been determined by the NMR-ON method at about 7 mK as 225.56(6), 130.9(1), 98.17(4), 136.6(4), 1007.0(3) and 58.43(3) MHz, respectively. With the knowng-factors ofg(¹⁸⁶Re, 1⁻)=1.739(3) andg(²⁰³Pb, 5/2⁻)=0.27456(20), the following hyperfine fields were deduced:B _HF(¹⁸⁶ReNi)=−103.05(35) kG;B _HF(¹⁸⁶ReFe)=−759.7(13) kG;B _HF(²⁰³PbFe)=+279.18(25) kG. Taking hyperfine anomalies into account, theg-factor of¹⁸³Re was deduced as |g(¹⁸³Re, 5/2⁺)|=1.267(6). With the assumption of Knight shift factorK=0, theg-factors of¹⁸²Re and¹⁸⁷W and the hyperfine field of¹⁸⁷WFe were determined as |g(¹⁸²Re, 2⁺)|=1.63(5), |g(¹⁸⁷W, 3/2⁻)|=0.414(10) andB _HF(¹⁸⁷WFe) =−714(18) kG. The large hyperfine anomaly was deduced to be¹⁸³W Δ¹⁸⁷W =−0.124(22).     

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.     

Hyperfine interaction of13O and23Mg implanted in Pt

The spin relaxation timeT ₁ for short-lived beta emitters¹³O and²³Mg implanted in Pt have been measured for the first time;T ₁T¹³O) = 2.90 ±0.65 Ks andT ₁ T(²³Mg) = 1665 ±140 Ks. The Knight shift for¹³O in Pt was measured at 300 K to beK(¹³O) = +(4.23 ±0.14) × 10^–3. In the case of¹³O, the Knight shift is unusually large and the relaxation time is unusually fast compared with other interstitial impurities in Pt. A KKR band-structure calculation reproduces the present large Knight shift fairly well.     

Anomalous anisotropies and field dependencies of the muon Knight shift and the relaxation rate in monocrystalline Bi

The angular dependence of the muon Knight shift,K _μ, and the muon relaxation rate in Bi at 11 K were measured in external magnetic fields up to 1 T. BothK _μ and the second moment,M ₂, are field dependent and involveP ₄ ⁰(cos θ) andP ₄ ³(cos θ) terms in the angular dependence. The Knight shift behaviour is discussed in terms of the dipole-dipole interaction and the de Haas-van Alphen effect, a consistent interpretation was not achieved in either case. The field dependence ofM ₂ is in complete contrast to the second moment calculations and points to a field dependent redistribution of the charge distribution around the interstitial site.     

μ+knight shifts and trapping in diluteSbSn alloys

Giant μ⁺ Knight shifts K_μ have been studied previously in Sb andSbBi alloys. Here we report μ⁺SR measurements on Sb with dilute heterovalent Sn impurities. A dramatic concentration dependence is observed: K_μ is increased slightly (relative to the value in pure Sb) by Sn concentrations of <0.1%, whereas larger concentrations cause a drastic reduction of K_μ. One concern could be that K_μ values in the alloy might reflect local band structure in trap sites near Sn impurities rather than the bulk “host” band structure of the alloy. This is indeed the case in bothSbSn (0.03%) andSbSn (0.06%), where a second, lower frequency TF-μSR signal begins to appear for T>60K. The amplitude of the low K_μ signal grows with increasing T at the expense of the amplitude of the high-K_μ, low-T signal, suggesting that the μ⁺ migrates through the host lattice to trap sites. A simple trapping model correctly describes the observed T-dependence of the amplitudes, phases and relaxation rates of the two signals. We conclude that the low-T Knight shift is truly characteristic of the host band structure while the much lower K_μ value of the high-T site is characteristic of a specific trap site, presumably adjacent to a Sn impurity.     

μ+ shift study inCdMgx (x=1%, 2%, 2.5%)shift study inCdMgx (x=1%, 2%, 2.5%)

In continuation of our earlier studies of the anomalous temperature dependence of the μ⁺ Knight shift K_μ in Cd,CdHg (1.2 at %) andCdMg (3.38 at %) — interpreted as due to Van Hove-type singularities in the local density of electron states /1/ — we have studied the temperature dependence of the μ⁺ Knight shift in polycrystallineCdMg (1.04 at %, 2.05 at %) and in a single crystal ofCdMg (2.5 at %). In contrast to pure Cd no anisotropies in K_μ could be detected. The temperature dependence of K_μ in aCdMg (2.05 at %) sample and in the monocrystallineCdMg (2.5 at %) sample essentially reproduces the one previously observed in polycrystallineCdMg (3.38 at %), showing a steplike discontinuity and a logarithmic singularity. A complete different behaviour is observed inCdMg (1.04 at %), where no logarithmic singularity seems to show up and where a steplike discontinuity of opposite sign at around 90 K is clearly seen. If these singularities are still to be interpreted in terms of Van Hove singularities, the question arises why there is such a nonlinear dependence on the Mg concentration.     

NMR properties of hcp Ru metal — first detection of the99Ru and101Ru NMR in a paramagnetic solid

Results of nuclear magnetic resonance (NMR) measurements on hexagonal close-packed Rumetal are presented. The field spectra of both isotopes, having a nuclear spinI of 5/2, show a shape characteristic for quadrupolar disturbed NMR. From a simulation of these spectra, the electric field gradientV _zz has been determined to be (37±0.5)×10^–13 esu/cm³ in agreement with recent band structure calculations. The Knight shift tensor elements deduced from the spectra areK _x =K _y =0.46±0.02% andK _z =0.56±0.02%. These rather high and positive shifts are completely in line with that of the neighboring elements in the periodic system and have primarily to be ascribed to the Van Vleck contribution. This part of the Knight shift is also responsible for the rather strong anisotropy, that has been found.     

Magnetic hyperfine fields of Zr in nickel and iron measured by the DPAD method

The magnetic hyperfine fields of Zr in nickel and iron were measured by the DPAD method. Using the 8⁺ isomeric states in⁹⁰Zr and⁸⁸Zr these fields were found to beH _hf(ZrNi)=–4.65(10) T andH _hf(ZrFe)=–27.4(4) T, respectively.     

NMR study of the magnetic properties and electronic structure of amorphous Ni−B−P alloys

The¹¹B and³¹P NMR Knight shift (K) and Korringa spin-lattice relaxation rate (1/T ₁ T) have been measured for amorphous Ni_81.5B_18.5−x P _x alloys with 0≤x≤18.5. In accordance with previous bulk measurements, the³¹P NMR parameters vary markedly with composition whereas the¹¹B NMR parameters remain almost constant except for small P-contents. It is suggested that the d-band contribution toK(³¹P) is positive and that toK(¹¹B) is negative. The data further support our previous conclusion that amorphous Ni_81.5B_18.5 is a Pauli paramagnet rather than a weak itinerant ferromagnet.     

Nuclear magnetic resonance in icosahedral Al-Pd-Mn alloys

²⁷Al and⁵⁵Mn nuclear magnetic resonance shift,K, and²⁷Al spin lattice relaxation time,T ₁, have been measured for the six-dimensional face-centered icosahedral quasicrystals, Al_75-x Pd₁₅Mn_10+x withx=0, 2 and7. The Al₇₅Pd₁₅Mn₁₀ quasicrystal exhibits a temperature independent Knight shiftK and(T ₁ T)^–1=0.022±0.002 (K s)^–1 in a temperature range from room temperature to 5 K because there exist no Mn atoms with local magnetic moment. The replacement of Al with Mn drastically decreases the²⁷AlK, the⁵⁵MnK andT ₁ of²⁷Al, andthe²⁷AlK becomes negative. There is an additional contribution to the spin lattice relaxation time independent of temperature. This is considered to be due to the presence of a localized magnetic moment in the replaced Mn atoms.     

Discrepancies in NMRON Knight Shifts of impurity nuclei in ferromagnets

Precision NMRON field shift studies have been carried out up to 8T on a⁵⁴MnNi single crystal along a hard [100] direction and on a¹²⁵SbFe single crystal along a hard [110] direction. For both systems, high field (B _app>-1T) and low field (0.3T<B _app<0.8T) data sets are obtained. The analysis reveals a significant discrepancy between the apparent Knight Shift dependent on whether the low field or high field data set is utilised. For both systems, consideration of the high field data sets yield a zero Knight Shift K(⁵⁴MnNi)=+0.0(0.2)% and K(¹²⁵SbFe)=+0.2(1.4)%, whereas the low field data sets yield K(⁵⁴MnNi)=+7.5(3.9)% and K(¹²⁵SbFe)=−5.4(3.3)% respectively. The field range dependence of K suggests that only Knight shifts measured in large fields (>-1T) are meaningful for establishing systematics. This casts some doubt on the greater bulk of the literature’s NMRON Knight shift studies, where predominantly low fields have been used to determine K.     

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)|.     

Radiative widths of neutral kaon excitations

We observe 147 events of the axial vector pairK ₁(1270)–K ₁(1400) produced in the Coulomb field of a Pb target and measure the radiative widths Γ(K ₁(1400)→K ⁰ + γ) = 280.8 ±23.2(stat.) ±40.4(syst.) keV and Γ(K ₁(1270) →K ⁰ + γ) = 73.2 ±6.1(stat.) ±28.3(syst.) keV. These first measurements are lower than the quark-model predictions. We also place upper limits on the radiative widths forK*(1410) andK ₂ ^* (1430) and find that the latter is very small in accord withSU(3)invariance in the naive quark model.     

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.     

Isomeric transitions between shape coexisting states in iodine isotopes withA=115, 119 and 121

Applying delayed- r.f. coincidences and generalized centroid-shift analysis, nanosecond isomers in some odd-A iodine isotopes are studied in-beam. The reactions¹⁰⁶Cd(¹²C,p2n) and^116,118Sn(⁶Li,3n) have been used. The following half-lives were determined:T _1/2(565 keV)=0.50±0.10 ns andT _1/2(837 keV) =0.90±0.20 ns in¹¹⁵I,T _1/2(687 keV)=5.50±0.50 ns andT _1/2(2418 keV)=4.0±0.50 ns in¹¹⁹I as well asT _1/2(812 keV)=0.35±0.20 ns andT _1/2(445 keV)<0.10 ns=">¹²¹I. A systematics of the absolute probabilities for the transitions deexciting theg _9/2 9/2⁺ and _11/2 11/2 ₁ ^– band heads in^115–125I is presented and discussed.Partly supported by the Bulgarian National Research Foundation under contracts PH14, and PH31 and Kernforschungszentrum Karlsruhe, Stabsabteilung Internationale Beziehungen     

Lifetime measurements of the3 P 2 and4 P 5 2/0 states in He- and Li-like titanium and chromium

Ti and Cr ions at specific energies of 3.6 MeV/N and 5.0 MeV/N have been excited by passing them through thinC foils. The emission ofK-x rays andK-Auger electrons have been investigated using a flat crystal spectrometer and an electrostatic cyclindrical mirror analyzer. The lifetimes of the (1s2p)³ P ₂ and (1s2s2p)⁴ P _5/2 states have been determined by applying the time-of-flight technique. The experimental resultsτ(Ti²⁰⁺,³ P ₂)=(404±40)ps,τ(Cr²²⁺,³ P ₂)=(215±35)ps,τ(Ti¹⁹⁺,⁴ P _5/2)=(236±12)ps, andτ(Cr²¹⁺,⁴ P _5/2)=(140±8)ps are compared with calculated lifetimes.     

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.     

Nuclear spin lattice relaxation of191mIr in Fe

Thermal cycling of the lattice temperature was used to determine the nuclear spin lattice relaxation of^191m IrFe in polarizing fields of 0.05 to 1.3 T. At low temperatures, the relaxation time is not very much shorter than the lifetime of^191m Ir. In the first part of the paper, the master equation formalism is extended to include a finite lifetime. Our result for the reduced relaxation constant, ² C _K =(1.48±0.11)·10¹⁴ K s^–1 T^–2 (high field limit) is in serious disagreement with that of a spin echo measurement of¹⁹³IrFe, but fits much better into the general systematics. A comparison of relaxation rates for 3d-, 4d-, and 5d-impurities in Fe is given. As a by-product, a Kapitza conductivity constant ofl _K =1.5 mW cm^–2 K^–4±30% was found between Fe and dilute³He/⁴He.     

Rietveld refinements and vibrational spectroscopic studies of Na1−xKxPb4(PO4)3 lacunar apatites (0≤x≤1)

Synthesis of apatites, Na_1−xK_xPb₄(PO₄)₃ 0≤x≤1, with anion vacancy was carried out using solid state reactions. The solid solution of apatite-type structure crystallizes in the hexagonal system, space group P6₃/m (No 176). Rietveld refinements showed that 75% of Pb²⁺ cations are located in the (6h) sites; the ninefold coordination sites (4f) are equally occupied by the other 25% lead cations and the K⁺ and Na⁺ monovalent ions.The structure can be described as built up from [PO₄]³⁻ tetrahedra and Pb²⁺ of sixfold coordination cavities (6h positions), which delimit void hexagonal tunnels running along [0 0 1]. These tunnels are connected by cations of mixed sites (4f) half occupied by Pb²⁺ and half by Na⁺/K⁺ mixed cations. The assignment of the observed frequencies in the Raman and infrared spectra is discussed on the basis of a unit cell group analysis and by comparison with other apatites. The Raman modes of all the compositions show some linear shifts of the frequencies as a function of the composition toward lower values due the substitutions of Na⁺ by K⁺ with a larger radius.     

Muon knight shift in platinum and in β-PdHx (x=0.70, 0.75, 0.86)

The ⁺ Knight shift in Platinum has been measured between 20 K and 785 K. It shows a strong temperature dependence and scales with the magnetic bulk susceptibility. A temperature independent contribution of +53±15 ppm and a d-electron induced hyperfine field per unpaired d-electron per atom of B _hfd ^a =–5.03 kG(±8.5%) are obtained. The ⁺ Knight shift in PdH_0.70, PdH_0.75 and PdH_0.86 shows no dependence on temperature between 20 K and RT and increases from K=–(8±3) ppm for x=0.70 to K =+(6.5±3) ppm K=+(6.5±3) ppm for x=0.86, in good agreement with proton Knight shift measurements.