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1.
Quadrupole interactions at111Cd in various rare-earth intermetallics have been investigated. The enhancement in the efg due to the electronic configurations is found to be small in contrast to pure metals.The authors thank K. Raghunathan for helpful discussions.  相似文献   

2.
The hyperfine interaction is studied in two different crystal lografic forms of Mn. In the -Mn no magnetic, but a distinct electric quadrupole interaction is found. Effects of heat treatment are discussed. For the -Mn two magnetic field sites are found. Their temperature dependence and dependence on the In concentration are discussed.  相似文献   

3.
The quadrupole interaction at111Cd in RRh3B2 compounds studied by the TDPAC technique supports the prediction that Ce in CeRh3B2 is not trivalent. The highly anisotropic EFG indicates that111Cd in GdRh3B2 cannot occupy the rare earth site. The transferred magnetic hyperfine field at111Cd is nearly zero which supports the conjecture that the impurity probe nuclei are at the 3g(Rh) site.  相似文献   

4.
The quandrupole interaction at181Ta in tellurium measured at various temperatures revealed two unique sites with an axially symmetric electric field gradient. These are interpreted as a near substitutional site with almost octahedral symmetry and a pure interstitial site in the tellurium lattice. The temperature dependence observed for QI frequencies corresponding to these sites supports this conclusion.  相似文献   

5.
The nuclear quadrupole interaction of Ta-181 in selenium was measured using perturbed angular correlation technique. The electric field gradient at room temperature is 4.56(32) × 1017 V/cm2. The temperature dependence of EFG follows the usual T3/2 behaviour.  相似文献   

6.
Tulapurkar  A.A.  Mishra  S.N. 《Hyperfine Interactions》1999,120(1-8):247-251
The temperature dependence of the electric quadrupole interaction and the magnetic hyperfine field at 111Cd probe sites in RMn2 (R=Gd, Tb) has been studied by TDPAC method. In the paramagnetic region the quadrupole interaction frequency νQ in both compounds varies linearly with temperature. Below the Neel temperature, we find an abrupt decrease in the magnitude of νQ which is consistent with an expansion of the unit cell. As an important feature, the data near TN shows the coexistence of localized and itinerant magnetism of Mn atoms. This revised version was published online in August 2006 with corrections to the Cover Date.  相似文献   

7.
The temperature dependence of the hyperfine field of substitutional111Cd in antiferromagnetic CoO has been measured by means of the perturbed angular correlation technique. The Larmor frequency ωL is found to obey a power law ωL(t0 t β) up tot max=0.4 wheret=1−T/T N is the reduced temperature withT N=291.2(3) K and β=0.393 (5) the critical exponent. The results are discussed and compared with PAC experiments on111Cd in NiO and Ni and with results obtained by other methods.  相似文献   

8.
Perturbed - angular correlation (PAC) spectroscopy was applied to study the hyperfine parameters for111In probes in In-Pd intermetallic compounds. The PAC spectra measured in In3Pd, In3Pd2 and InPd2 compounds reflect the number, population and symmetry of nonequivalent indium probe sites predicted by the crystallographic data. The temperature dependence of the observed electric field gradients was measured in the temperature range 80–873 K.  相似文献   

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The nuclear quadrupole interaction at57Fe nuclei in hcp -zirconium metal is measured in the temperature range 4.2 to 560 K using Mössbauer spectroscopy of57Fe. The quadrupole splitting at room temperature is measured to be 0.660(8) mm/sec which corresponds to an electric field gradient of |eq|=3.17×1017 V/cm2 at the57Fe nucleus in a -Zr host. As has been observed in many other systems, the results show significant electronic contributions. The temperature variation of the quadrupole interaction is much stronger than is expected from the lattice contributions and is found to follow theT 3/2 dependence approximately.57FeZr does not follow the universal correlation betweeneq ion andeq el observed in most of the normal metal hosts but follows the trends recently observed by Krusch and Forker for the transition metal hosts. Our results are compared with the predictions of the conduction electron charge shift model recently proposed by Bodenstedt and Perscheid.  相似文献   

12.
BaHfO3 is prepared by sintering a mixture of BaCO3 and HfO2 giving the same heat treatments as for YBa2Cu3O7– (YBCO). X-ray diffraction analysis confirms the formation of cubic BaHfO3 along with some unreacted HfO2. A181Ta TDPAC study of the sample, prepared using neutron-irradiated HfO2 and BaCO3, shows a relaxation process to be present in the sample. The value of the relaxation constant0.26 ns is unusually large and temperature independent.  相似文献   

13.
The perturbed angular correlation technique and Mössbauer spectroscopy were applied to study the electric field gradient on 111Cd and 119Sn probe atoms in isostructural NiIn and CoSn compounds. The 111Cd PAC measurements performed in the temperature range 80--1100 K demonstrated the existence of two axially symmetric EFG's in each of the investigated compounds, related to the 2(d) and 1(a) probe sites in the B35 structure. A 1(a)-site preference for Cd probes in CoSn compound was observed. The temperature dependence of the quadrupole frequencies for 111Cd in both compounds, interpreted in terms of the empirical model proposed by Christiansen et al.[1], follows a T3/2 relation with different slope parameters for each of the observed frequencies. These results are combined with the data from the Mössbauer experiment. The 119Sn Mössbauer spectra taken at liquid nitrogen and at room temperatures showed two quadrupole split doublets with the intensity ratio 2:1 for CoSn and 8:1 for NiIn0.99Sn0.01sample, giving an evidence of 2(d)-site preference for tin atoms in NiIn. The EFG values measured on 119Sn are 2.5 to 4 times larger than those on 111Cd nuclei, while the ratio of the respective Sternheimer antishielding factors is equal to 0.77. Within the limits of errors no differences were observed in the magnitude and temperature dependence of Debye--Waller factors for 2(d) and 1(a) 119Sn positions in CoSn and NiIn lattices.  相似文献   

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15.
Pal  G.  Sebastian  K. C.  Somayajulu  D. R. S. 《Hyperfine Interactions》2001,136(3-8):613-617
TDPAC study of InBi1−x Te x with x=0.0, 0.01, 0.05, 0.1 and 0.2 as a function of temperature is done. Both pure and Te-doped samples show a semi-metallic character up to around room temperature. Above room temperature a steep transition to semiconducting state was observed, which is independent of the doping concentrations. Hence Te may be in the interstitial sites. Conductivity measurement of the above samples showed the same trend as observed in the EFG studies. Thus the importance of the conduction electron density is prominently seen in these systems. This revised version was published online in September 2006 with corrections to the Cover Date.  相似文献   

16.
Quadrupole interaction data recorded by Triplett et al for the C1hTm site in TmF3 are analysed via semi-empirical procedures, one of which employs rank 2 CF parameters derived from the155Gd: GdF3 Mössbauer results of Katila et al. The fitted crystal field interactions are compared with available optical spectroscopy results.  相似文献   

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18.
Quadrupole interaction at111Cd probe has been studied in the nearly heavy fermion system USn3– using the TDPAC method. We observe a large quadrupole interaction frequency withv Q =89.9(10) MHz at 300 K which is much higher than the earlier reported result. The observed frequency shows a linear temperature dependence in the range 25–300 K.  相似文献   

19.
111Cd–PAC measurements have been made using the high specific activity of 111In in the methanol–water mixtures of various concentrations at the room temperature. These experiments revealed that the perturbation factors 〈A 2 G 2〉 (integrated over two mean lives τN) do not follow the dependence of the macroscopic viscosity η. The observed dynamic character of the PAC spectra in ice is explained by the mobility of orientational and ionic defects. The activation energy for the diffusion process was determined to be E a =0.35(1) eV. This revised version was published online in September 2006 with corrections to the Cover Date.  相似文献   

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