2
6
N. Suzuki et al. / Journal of Alloys and Compounds 290 (1999) 25–29
diagram of CrTe12xSb (0.0#x#1.0) by magnetic mea-
x
surements.
2
. Experiments
Polycrystalline samples of CrTe12xSbx (0.0#x#1.0)
were prepared from powders of Cr (99.9%), Te
99.9999%) and Sb (99.99%). They were mixed in the
(
desired proportion, sealed in evacuated silica tubes and
heated at 9008C for 7 days and then quenched in water.
The reaction products were pulverized, mixed and heated
at 9008C for 7 days and then quenched.
The X-ray diffraction lines of the prepared samples were
indexed with the hexagonal NiAs-type structure. The
˚
lattice parameters were found to be a53.999 A, c56.240
˚
˚
˚
A for CrTe and a54.129 A, c55.470 A for CrSb. These
results are consistent with those previously reported by
Takei et al. [7], Grazhdankina and Bersenev [3], Ido et al.
Fig. 3. The unit-cell volume V and the axial ratio c/a versus con-
centration x at room temperature for CrTe12xSb . The closed circles show
x
unit-cell volume V and the open circles axial ratio c/a.
[1], Lotgering and Gorter [15] and Nagasaki et al. [16].
The concentration dependence of the lattice parameters
a and c at room temperature for CrTe12xSb is shown in
temperature dependence of the magnetization s of the
x
Fig. 2. The open circles show the lattice parameter a and
the closed circles the lattice parameter c. The lattice
parameter a increases with increasing Sb concentration. On
the other hand, the lattice parameter c decreases with
increasing x. The unit-cell volume V and the axial ratio c/a
CrTe12xSb powdered samples were measured at 10 kOe
x
by a pendulum type magnetometer and vibrating sample
magnetometer (VSM) in the temperature range from 4.2 K
to 800 K. The measurements of high field magnetization at
4.2 K were carried out by an induction method in pulsed
magnetic fields up to 300 kOe.
of CrTe12xSb are shown as function of concentration x in
x
Fig. 3. The closed circles show the unit-cell volume V and
the open circles show the axial ratio c/a. As shown in the
figure, the unit cell volume V and the axial ratio c/a
decrease with increasing x.
3. Results and discussions
The magnetic transition temperatures were determined
by measuring the temperature dependence of the AC initial
permeability m using an AC transformer method. The
Fig. 4(a) and (b) show the temperature dependence of
the initial permeability m for CrTe and CrTe0.6Sb0.4
,
respectively. As seen in the figure, the initial permeability
of CrTe decreases sharply with temperature around 330 K.
The Curie temperature was defined as the intersection
point of the two lines, as shown by an arrow in the figure.
The Curie temperature is found to be 343 K. This value is
in good agreement with 342 K given by Grazhdankina and
Zainullina [14] but somewhat smaller than 350 K reported
Ohta et al. [6]. The m 2 T curve of CrTe0.6Sb0.4 has an
anomaly around 125 K below the Curie temperature T 5
C
2
50 K. The temperature of the anomaly Tt1 corresponds to
the canted-ferromagnetic transition as mentioned below. A
similar anomaly is also observed around 110 K for CrTe0.7
Sb0.3
.
Fig. 5(a) and (b) show the high field magnetization
curves of CrTe12xSb with 0.0#x#0.2 and 0.3#x#0.9 at
x
4
.2 K in magnetic fields up to 300 kOe, respectively. As
seen in Fig. 5(a), the magnetization of samples with x5
.0, 0.1 and 0.2 is saturated at about 30 kOe. The
0
magnetization of samples with 0.3#x#0.9 is not saturated
in the magnetic fields up to 300 kOe, and the mag-
netization decreases rapidly with increasing x. The samples
Fig. 2. Lattice parameters a and c versus concentration x at room
temperature for CrTe12xSb . The open circles show lattice parameter a
x
and the closed circles lattice parameter c.