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Submitted on 1 Jan 1971
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THE MAGNETIC FORM FACTOR OF TERBIUM
T. Brun, G. Lander
To cite this version:
T. Brun, G. Lander. THE MAGNETIC FORM FACTOR OF TERBIUM. Journal de Physique Colloques, 1971, 32 (C1), pp.C1-571-C1-572. �10.1051/jphyscol:19711196�. �jpa-00214020�
DENSITES DE MOMENTS ET NEUTRONS POLAR~SES
THE MAGNETIC FORM FACTOR OF TERBIUM (*) T. 0. BRUN
Ames Laboratory, Iowa State University, Ames, Iowa G. H. LANDER
Ames Laboratory and Argonne National Laboratory, Argonne, Illinois
R6sumB.
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Le facteur de forme magnktique du Terbium a kt6 mesurk avec des neutrons polarisks sur des mono- cristaux dans un champ magnktique applique de 24 kOe A la tempkrature ambiante. Except6 pour les rtflex~ons aux petits angles, les points exptrimentaux se placent sur une courbe r&guli&re a environ 14 % en dessous des valeurs du facteur de forme thkorique. Ces rksultats suggerent que les fonctions cl'onde de Hartree-Fock des electrons 4 f sont aussicontractks dans I'espace rkl.Abstract.
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The magnetic form factor of terbium has been measured with polarized neutrons using single crystals held in an applied magnetic field of 24 kOe at room temperature. Except for the low angle reflections the experimental points lie on a smooth curve approximately 14 % below the theoretical form factor. These results suggest that the Hartree- Fock 4 f-electron wavefunctions are too contracted in real space.I. Introduction. - The magnetic form factor of terbium in the ordered magnetic state at 4.2 OK has been measured with polarized neutrons [I]. The magnetic scattering length p is defined as
p = 0.27 x ,u x f (3) x 10-l2 c m ,
where p is the ordered moment in Bohr magnetons, and f (3 is the form factor. For terbium in the ordered state the moment is 9 p, so that at low scattering angles p is larger than the nuclear scattering length, b. Under these conditions the experimental difficulties asso- ciated with extinction become severe, and, in [I], no accurate values were reported for the low angle reflections. At high angles the experimental form factor for terbium was found to be essentially a smooth curve, but the latter was at least 10-15 % below the theoretical curve.
In view of the results obtained in a polarized- neutron study of thulium 121, we have remeasured the terbium form factor under different experimental conditions so as to obtain accurate values o f f ( K )
at low angles. By examining different orientations in the paramagnetic state we confirm that the crystal field interactions are isotropic within the basal plane.
11. Rexults. - The single crystals for these studies were kindly provided by Professor F. H. Spedding.
The crystals were cut in the shape of parallelopipeds and the field was applied along the long axes, either
<
10.0> or<
11.0>. Two crystals of each orientation, b and a, respectively, were studied. In order to mini- mize extinction the neutron wavelength was 0.85a,
and the neutron path lengths never exceeded 1.5 mm.
The crystals were also mechanically worked to increase the mosaic spread. The applied magnetic fields varied between 21 and 26 kOe, depending on the length
(*) Work performed under the auspices of the U. S . Atomic Energy Commission.
of the sample (6 to 9 mm). In each case the field was homogeneous, and the absolute field strength was measured with an accuracy of 1.5 %. The experiments were performed a t room temperature. A coherent scattering length of 0.76 x 10-l2 cm was used to normalize the magnetic scattering amplitudes.
For these values of the field and temperature the magnetization measurements [3] indicate that the Curie-Weiss law is obeyed, and the value of the induced moment is
-
0.88 ,uB, depending on the exact value of H. The magnetic form factor is calculated by taking account of the population of the various M, states.The calculation reduces to a very simple form if the Curie-Weiss law is strictly valid 143. For terbium the form factor associated with the induced moment in the paramagnetic state is given by
The functions
<
jo>
and<
j,>
are directly related to the radial wavefunction of the 4 f electrons, and have been tabulated by Blume, et. al. [5].The experimental points for both the a and b-axes crystals are shown in figure 1, together with the theo- retical form factor.
111. Discussion. - Within experimental error the points for the a and b orientations fall on the same smooth curve, indicating that the crystal field is iso- tropic within the basal plane. At high values of sin 8/1 the points lie on a smooth curve given by
0.86 ftheory ,
in agreement with the previous results for terbium [I].
At low angles the discrepancy between theory and experiment is much less, and this result is very similar to that found in thulium [2]. Since the normalization, i. e. f (0) = 1, depends on the nuclear scattering length and the magnetic field, this factor could be wrong by possibly 3-4 %. However, independently of the norma-
Article published online by EDP Sciences and available at http://dx.doi.org/10.1051/jphyscol:19711196
C 1
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572 T. 0. BRUN, G . H. LANDER0
0 0.2 0.4 0.6 0.8
SIN 8 a- 1
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XFIG. 1. - The experimental (points) and theoretical (solid line) magnetic form factors for terbium in the paramagnetic state.
The broken line is a smooth curve drawn through the expe- rimental points.
lization, the experimental points clearly cannot be scaled to fit the theoretical curve. A similar discrepancy in thulium was explained by postulating that a large 5 d conduction-electron polarization contributes to the magnetization density. The magnetization data for terbium [3] show that the effective moment is very close to that expected from the unpaired 4 f electrons.
Therefore the discrepancy between the experimental and theoretical magnetic form factors for terbium probably cannot be explained in terms of a large 5 d conduction-electron contribution to the magnetization density. A more likely interpretation of the discrepan- cies for both terbium and thulium is that the theoretical 4 f wavefunctions are too contracted. Of course, this interpretation is not incompatible with an effective contribution from the 5 d shell, since these electrons are more extended than those in the 4 f shell.
A comparison between the calculated and experi- mental values for the
<
r n>
crystal-field integrals for the heavy rare-earth metals [6] also provides further evidence that the theoretical wavefunctions are too contracted. The wavefunctions used in these compari- sons, and also in calculating the<
ji>
integrals for the magnetic form factor, are those given by Freeman and Watson [7]. In an attempt to resolve the discre- pancies between theory and experiment we have exa- mined more recent 4 f wavefunctions [8, 91, but they differ very little from those in [7], suggesting that the Hartree-Fock wavefunctions for the tripositive ions are a poor approximation to the metallic state.References
[I] STEINSVOLL (O.), SHIRANE (G.), NATHANS (R.), BLUME [5] BLUME (M.), FREEMAN (A. J.) and WATSON (R. E.) (M.), ALPERIN (H. A.) and PICKART (S. J.), Phys. J. Chem. Phys., 1962, 37, 1245.
Rev., 1967, 161, 499. [6] KASUYA (T.), in Magnetism IIB, ed. G . T. Rado and [2] BRUN (T. O.), and LANDER (G. H.), Phys. Rev. Letters, H. Suhl (Academic Press, New York, 1966).
1969, 23, 1295. [7] FREEMAN (A. J.) and WATSON (R. E.), Phys. Rev., 1962, 127, 2058.
i31 HEGLAND Phys. Rev., 1963, 131, 158. (D. E.), LEGVOLD and S ~ ~ D D I N ~ (F. He), [8] SYNEK 185, 38. (M.) and TIMMONS (W.), Phys. Rev., 1969, [4] LANDER (G. H.) and BRUN (T. O.), J. Chem. Phys. 191 RUEDENBERG (K.), Iowa State University, private
1970, 53, 1387. communication, 1970.