Study of the Structure, Magnetic, Thermal and Electrical Characterisation of ZnCr2Se4: Ta Single Crystals Obtained by Chemical Vapour Transport

The new series of single-crystalline chromium selenides, Ta-doped ZnCr2Se4, was synthesised by a chemical vapour transport method to determine the impact of a dopant on the structural and thermodynamic properties of the parent compound. We present comprehensive investigations of structural, electrical transport, magnetic, and specific heat properties. It was expected that a partial replacement of Cr ions by a more significant Ta one would lead to a change in direct magnetic interactions between Cr magnetic moments and result in a change in the magnetic ground state and electric transport properties of the ZnCr2−xTaxSe4 (x = 0.05, 0.06, 0.07, 0.08, 0.1, 0.12) system. We found that all the elements of the cubic system had a cubic spinel structure; however, the doping gain linearly increased the ZnCr2−xTaxSe4 unit cell volume. Doping with tantalum did not significantly change the semiconductor and magnetic properties of ZnCr2Se4. For all studied samples (0 ≤ x ≤ 0.12), an antiferromagnetic order (AFM) below TN~22 K was observed. However, a small amount of Ta significantly reduced the second critical field (Hc2) from 65 kOe for x = 0.0 (ZnCr2Se4 matrix) up to 42.2 kOe for x = 0.12, above which the spin helical system changed to ferromagnetic (FM). The Hc2 reduction can lead to strong competition among AFM and FM interactions and spin frustration, as the specific heat under magnetic fields H < Hc2 shows a strong field decrease in TN.


Introduction
Single crystals are required in many fields of modern technology and the electronic industry. They are used for lasers, as an optical component for spectroscopy, in oscillators, in light-emitting diodes and in innumerable other devices. Among seleno-spinel crystals such as AB 2 Se 4 matrices, where A and B are the metallic ions occupying tetra-and octahedral sites, respectively, and matrices diluted with non-magnetic ions, due to the large cubic unit cell (about 10 Å), the effects of site disorder, lattice frustration and random distribution of spin interactions [1][2][3][4][5] create new potential applications.
The ZnCr 2 Se 4 belongs to the group of seleno-spinels and crystallises in a cubic system (SG: Fd3m, No. 27), a = 10.4891 Å [6]. This compound is a p-type semiconductor with a helical magnetic structure. Magnetic interactions are the result of the existence of exchangeable Cr-Cr interactions competing with each other. The Cr-Se-Cr interaction causes the ferromagnetic (FM) ordering of the magnetic moments of chromium ions. In contrast, the

Materials and Methods
Commercially available high-purity elements Zn, Ta, Cr, Se (5N, Sigma Aldrich, Poznań, Poland) and anhydrous CrCl 3 (Sigma Aldrich, Poznań, Poland) were used in the present study. Synthesis of ZnCr 2 Se 4 : Ta single crystals was carried out using a chemical transport reaction method. Chemical vapour transport is a method in which a solid substance is transferred using the reversible gaseous reaction from the T 1 temperature (dissolution zone) to the T 2 temperature (crystallisation zone). The partial equilibrium pressures of the components p i depend on the value of the equilibrium constant K a of the reaction, which can occur at a given temperature. The most significant changes in p i occur when K a reaches a value close to 1 (logK a ≈ 0).
For this purpose, a thermodynamic model of ZnCr 2 Se 4 : Ta single-crystal growth was prepared. To determine the ability and conditions of transport reaction, a set of all the hypothetical reactions that may appear in the ZnSe-Ta-Se-CrCl 3 system was created. These reactions, which were used to determine the dependence of logK a values on the temperature, were calculated using the HSC Chemistry computer programme (HSC Chemistry ver. 6.01, Release 2009, Metso Outotec Corporation, Helsinki, Finland) [22]. In this case, the modified chemical vapour transport method was used. The single crystals of ZnCr 2 Se 4 : Ta were grown from the binary selenide ZnSe, pure Ta and Se, and with CrCl 3 as a transport carrier. Therefore, the hypothetical reaction set included the reactions of binary ZnSe, pure tantalum and selenium with CrCl 3 and the dissociation products of CrCl 3 (CrCl 4 and Cl 2 ). The ZnSe was obtained by the ceramic method [14,18]. Mixtures of the ZnSe, Ta, Se and CrCl 3 were placed in quartz ampoules (length-200 mm, inner diameter-20 mm) evacuated to 10 −5 mbarr. The ampoules were placed in a two-zone tubular furnace. The furnace was cooled for 24 h, after around 500 h of heating. The chemical composition of the obtained single crystals and their surfaces were studied by scanning electron microscopy (SEM) Jeol 6480 (JEOL USA, INC., Peabody, MA, USA), with a propertied energy-dispersive X-ray spectrometer (SEM/EDS). Four single crystals with differing tantalum content were chosen for X-ray diffraction (XRD) measurements (Table 1). The structural parameters were determined using a SuperNova X-ray diffractometer (Agilent, Oxfordshire, UK). The technical details and the computer programmes used are described in [21,23]. Table 1. Conditions of growth and chemical composition of ZnCr 2 Se 4 : Ta single crystals. T d is the temperature of the dissolution zone, T c is the temperature of the crystallisation zone and ∆T is the difference in temperature between the dissolution and the crystallisation zones.

No.
Nominal Formula The electrical resistivity ρ(T) was measured by the four-point DC method with an accuracy of around ±0.6% using a KEITHLEY 6517B Electrometer/High Resistance Meter (Keithley Instruments, LLC, Solon, OH, USA) in the temperature range of 77-400 K. A Quantum Design SQUID-based MPMSXL-5-type magnetometer (Quantum Design, San Diego, CA, USA) to determine the specific heat and magnetic parameters in the temperature range 10-300 K was used. Measurements were carried out at a magnetic field of 100 Oe for both in the ZFC (zero-field cooling) and FC (field cooling) mode. The Néel temperature and the critical fields were determined as the temperature corresponding to dχ/dT vs. T and dM/dH vs. H. The effective magnetic moment was determined using the following equation [24,25]: where k B is the Boltzmann constant, N A is the Avogadro number, µ B is the Bohr magneton, and C is the molar Curie constant. The magnetic superexchange integrals for the first two coordination spheres J 1 and J 2 were calculated using the Holland and Brown equations [26].
The methods used to determine the electrical properties and specific heat are described in detail in [17,18,20]. Thermogravimetry and differential scanning calorimetry (TG/DSC) were carried out using a Labsys Evo system, with a heating rate of 5 • C/min and in an inert gas atmosphere (Ar).
We synthesised the samples with an amount of Ta ions higher than 0.3. For the samples with y = 0.4, 0.5, we did not observe single crystals in ampoules. One of the main reasons is that one end member of the Zn x Ta y Cr 2 Se 4 series, i.e., TaCr 2 Se 4, does not exist. Based on the reactions presented in Figure 1, it can be assumed that volatile zinc and selenium compounds are formed in the ZnSe-Ta-Se-CrCl 3 system, e.g., ZnCl 2 , Zn 2 Cl 4 , SeCl 2 , SeCl 4 and Se 2 . Thermodynamic calculations showed that in the ZnSe-Ta-Se-CrCl 3 system, ZnSe and Se are mainly transported by gaseous CrCl 3 and CrCl 4 (values of logK a are close to zero in the selected temperature range: 1000-1400 K; Figures 1 and 2).
The transport reactions presented in Figure 2 show that volatile tantalum compounds can be formed in the ZnSe-Ta-Se-CrCl 3 system, e.g., TaCl, TaCl 2 , TaCl 3 , TaCl 4 and TaCl 5 . For CrCl 4 , logK a reaches values close to zero at lower temperatures than for CrCl 3 . It can therefore be assumed that the chemical transport for Ta occurs mainly with CrCl 4 . The logK a of the transport reactions with CrCl 3 and CrCl 4 for tantalum has values and shapes similar to the corresponding Zn and Se transport reactions ( Figure 1). Thus, the conditions for the simultaneous transport of ZnSe, Ta and Se, and spinel crystallisation, are met. Calculated logK a values for transport reactions with chlorine are close to zero at higher temperatures. This indicates that chlorine is not involved in the transport process in the selected temperature range. Based on these calculations, the reaction conditions were chosen (temperatures of the dissolution and crystallisation zones and their difference). The crystallisation zone temperature was between 1070 and 1180 K. The melting zone temperature was in the range 1175-1233 K. Their difference was 50-70 K. Smaller differences in temperature (∆T) are more favourable for the crystallisation process. The choice of reaction conditions was based on our experience with the growth of ZnCr 2 Se 4 single crystals. The best results have been achieved using temperatures of the dissolution zone in the range 1123-1223 K. The choice of the reaction temperature is also limited by the thermal endurance of silica glass (~1500 K). These reaction conditions allowed us to obtain single crystals of good quality ( Figure 3). The transport reactions presented in Figure 2 show that volatile tantalum compounds can be formed in the ZnSe-Ta-Se-CrCl3 system, e.g., TaCl, TaCl2, TaCl3, TaCl4 and TaCl5. For CrCl4, logKa reaches values close to zero at lower temperatures than for CrCl3. It can therefore be assumed that the chemical transport for Ta occurs mainly with CrCl4. The logKa of the transport reactions with CrCl3 and CrCl4 for tantalum has values and shapes similar to the corresponding Zn and Se transport reactions ( Figure 1). Thus, the conditions for the simultaneous transport of ZnSe, Ta and Se, and spinel crystallisation, are met. Calculated logKa values for transport reactions with chlorine are close to zero at higher temperatures. This indicates that chlorine is not involved in the transport process in the selected temperature range. Based on these calculations, the reaction conditions were chosen (temperatures of the dissolution and crystallisation zones and their difference). The crystallisation zone temperature was between 1070 and 1180 K. The melting zone temperature was in the range 1175-1233 K. Their difference was 50-70 K. Smaller differences in temperature (ΔT) are more favourable for the crystallisation process. The choice of reaction conditions was based on our experience with the growth of ZnCr2Se4 single crystals. The best results have been achieved using temperatures of the dissolution zone in the range 1123-1223 K. The choice of the reaction temperature is also limited by the thermal endurance of silica glass (~1500 K). These reaction conditions allowed us to obtain single crystals of good quality ( Figure 3). Ta + CrCl 3(g) = TaCl (g) + CrCl 2(g) Ta + 2CrCl 3(g) = TaCl 2(g) + 2CrCl 2(g) Ta + 3CrCl 3(g) = TaCl 3(g) + 3CrCl 2(g) Ta + 4CrCl 3(g) = TaCl 4(g) + 4CrCl 2(g) Ta + 5CrCl 3(g) = TaCl 5(g) + 5CrCl 2(g)
As shown in Table 1, the determined real chemical composition showed a lower To determine the average chemical composition, measurements were carried out at 20 different locations of the single crystal. Each of the measuring areas was approximately 50 × 30 µm. Then, the average chemical composition was calculated. The error bar  Table 1.
As shown in Table 1, the determined real chemical composition showed a lower amount of incorporated tantalum than the nominal composition. On the one hand, this may be due to the lower amount of tantalum transported to the crystallisation zone. On the other hand, the separation of tantalum from the system during the dissolution and crystallisation processes is likely.

Structural Study
The origin of the unit cell is agreed with the point 3m of the space group Fd3m (No. 227). In a normal spinel, the Zn 2+ ions occupy the tetrahedral position 8a: 1/8, 1/8, 1/8 (A site), and the Cr 3+ ions occupy the position 16d: 1 2 , 1 2 , 1 2 (B site). To determine the cation distribution, two models were taken into account for each composition.
The first model of the structure refinement was considering the Ta ions' presence in the A sites (tetrahedral) with coupled site occupancy factors (SOF) and constrained atomic displacements. Due to the strong correlation, the SOFs for Zn and Ta were refined separately in alternative calculations. The convergence caused the rejection of Ta ions from the tetrahedral sites.
The same procedure was applied to Ta ions occupied by the B sites (octahedral). This approach led to acceptable atomic displacement parameters and SOFs, which allowed for description of the general chemical formula for obtained single crystals as presented in Tables 2 and 3. On the other hand, a slightly increased thermal shift at the B site may indicate a static disturbance in the position of the Cr 3+ /Ta 3+ pseudoion, which is mainly caused by the difference in ionic charges and in ionic and covalent radii (r i (Zn 2+ ) = 0.60 Å, r i (Cr 3+ ) = 0.62 Å, r i (Ta 3+ ) = 0.72 Å and R c (Zn 2+ ) = 0.74 Å, R c (Cr 3+ ) = 0.76 Å, R c (Ta 3+ ) = 0.86 Å, respectively) [27]. Based on the structural study, the formula describing cation distribution in the system is: ZnCr 2-x Ta x Se 4 , where x = 0.05, 0.06, 0.07, 0.08, 0.10 and 0.12, which is shown in Tables 2 and 3. In these chemical compositions, the region of the solubility limit of tantalum in the ZnCr 2-x Ta x Se 4 system was found to be equal to 0.12. The structural study showed the obtained ZnCr 2-x Ta x Se 4 single crystals crystallise in a cubic system with space group Fd3m (No.227, Z = 8). The lattice parameters of the obtained single crystals were larger than the lattice parameter of non-substituted ZnCr 2 Se 4 (a = 10.489 Å) and increased with the rising amount of tantalum (Table 2). Tantalum ions accommodated the octahedral sites, substituting Cr 3+ ions. The enhancement of the lattice parameters was linear ( Figure 4) and confirmed the presence of tantalum ions as Ta 3+ in the crystal lattice of ZnCr 2 Se 4 . This phenomenon is consistent with the differences between the ionic radii of Zn 2+ , Ta 3+ (in octahedral coordination) and Cr 3+ . The positional parameter of Se (u), which is a measure of the anion sublattice distortion from the cubic close packing, did not change significantly from the ideal value of x = 0.250. The tantalum amount did not influence the u parameter. The slight differences between the tested single crystals were in the range of the standard deviation ( Table 3). The same was observed in the metal-metal and metal-selenium distances (Table 4), where the differences were insignificant. The structure refinement parameters are presented in Table 3, while the selected bond distances and angles are shown in Table 4. Tantalum ions accommodated the octahedral sites, substituting Cr 3+ ions. The enhancement of the lattice parameters was linear ( Figure 4) and confirmed the presence of tantalum ions as Ta 3+ in the crystal lattice of ZnCr2Se4. This phenomenon is consistent with the differences between the ionic radii of Zn 2+ , Ta 3+ (in octahedral coordination) and Cr 3+ . The positional parameter of Se (u), which is a measure of the anion sublattice distortion from the cubic close packing, did not change significantly from the ideal value of x = 0.250. The tantalum amount did not influence the u parameter. The slight differences between the tested single crystals were in the range of the standard deviation (Table 3). The same was observed in the metal-metal and metal-selenium distances (Table 4), where the differences were insignificant. The structure refinement parameters are presented in Table 3, while the selected bond distances and angles are shown in Table 4.

Electrical and Magnetic Properties
The electrical measurements of ZnCr 2-x Ta x Se 4 (x = 0.5, 0.6, 0.7, 0.8, 0.10 and 0.12) showed the semiconducting properties and thermally activated conduction in the intrinsic region (200-400 K) with the activation energy of E a~0 .22 eV. In the extrinsic region (77-125 K), the activation of electrical conductivity was not observed ( Figure 5). The influence of anisotropy on the value of electrical resistivity in the studied spinel single crystals was not observed, as in the CuCr 1.6 V 0. 4

Electrical and Magnetic Properties
The electrical measurements of ZnCr2-xTaxSe4 (x = 0.5, 0.6, 0.7, 0.8, 0.10 and 0.12) showed the semiconducting properties and thermally activated conduction in the intrinsic region (200-400 K) with the activation energy of Ea∼0.22 eV. In the extrinsic region (77-125 K), the activation of electrical conductivity was not observed ( Figure 5). The influence of anisotropy on the value of electrical resistivity in the studied spinel single crystals was not observed, as in the CuCr1.6V0.4Se4 spinel single crystal, in which the resistance was measured in the direction of [001] and [111] [28]. A similar dependence of electrical resistance ρ(T) on temperature was observed by Watanabe [29] in ZnCr2Se4 single crystals measured in different crystallographic directions. No significant influence of the crystallographic orientation on the value of the specific electrical resistance was observed. This may have been because the spinel structure A similar dependence of electrical resistance ρ(T) on temperature was observed by Watanabe [29] in ZnCr 2 Se 4 single crystals measured in different crystallographic directions. No significant influence of the crystallographic orientation on the value of the specific electrical resistance was observed. This may have been because the spinel structure had a high cubic symmetry. The SANS measurements also confirmed the isotropic phase transitions with respect to the field direction in the monocrystalline ZnCr 2 Se 4 spinel [11]. The observed ρ(T) dependence in Figure 5 means that doping of the ZnCr 2 Se 4 single crystals under study with tantalum did not affect the thermal activation of electrical conductivity.
The results of magnetic measurements of ZnCr 2-x Ta x Se 4 spinels are shown in Figures 6-8 and Table 5. The dependence of the dc (in both ZFC and FC mode) showed an AFM order below the Néel temperature T N~2 2 K and FM short-range interactions, evidenced by the positive Curie-Weiss temperature θ CW < 100 K. The T N temperature essentially does not depend on the concentration of Ta ion. On the other hand, these ions strongly influence the short-range magnetic interactions visible for different values of θ CW ( Table 5).
The results mentioned above were confirmed by the negative values of the superexchange integral for the first coordination sphere (J 1 ) and the positive values of the superexchange integral for the second coordination sphere (J 2 ) ( Table 5). The effective magnetic moment calculated from the magnetic susceptibility expansion at high temperature corresponded to the effective number of Bohr magnetons estimated for the corresponding content of x chromium ions, as the tantalum ion was in the +III oxidation state of the octahedral site in the spinel structure. However, an additional magnetic ion may appear when tantalum is in the +II or +IV oxidation state. Then, its magnetic susceptibility is in the order of 154 × 10 −6 emu/mol at 293 K. No split of the ZFC-FC susceptibility was observed, which suggests a lack of spin frustration in the studied single crystals (Figure 6).
The results of magnetic measurements of ZnCr2-xTaxSe4 spinels are shown in Figures  6-8 and Table 5. The dependence of the dc (in both ZFC and FC mode) showed an AFM order below the Néel temperature TN ∼22 K and FM short-range interactions, evidenced by the positive Curie-Weiss temperature θCW < 100 K. The TN temperature essentially does not depend on the concentration of Ta ion. On the other hand, these ions strongly influ ence the short-range magnetic interactions visible for different values of θCW (Table 5).        The magnetisation isotherms depicted in Figure 7 at 10, 20, 30, 40 and 60 K show characteristic behaviour for the AFM order of magnetic moments and a lack of saturation in the magnetic field of 70 kOe, below the Néel temperature. Magnetisation isotherms plotted at 10 K for all samples show two critical fields and an unexpected increase in the magnetic moment with the rise in the tantalum content ( Figure 8). Arrows indicate the metamagnetic transition at the first critical field H c1 , and the breakdown of the helical spin arrangement at the second critical field H c2 in Figure 8. The values of both critical fields weakly depend on the tantalum content in the sample. However, the tantalum ions strongly reduce the second critical field by approximately 20 kOe to that for the ZnCr 2 Se 4 matrix [30], without significantly affecting the content of the first critical field. The result is a lack of magnetisation saturation above the second critical field due to weaker short-range ferromagnetic interactions. is a lack of magnetisation saturation above the second critical field due to weaker short range ferromagnetic interactions. Figures 9 and 10 show the change in the temperature TN with the increasing magneti field B.  The specific heat experimental data obtained for the series of various Zn1Cr2-xTaxSe (x = 0.05 − 0.12) compounds show very similar behaviour in the CB(T) characteristics ob tained at different magnetic fields, which suggests that either the off-stoichiometry in Zn and/or Cr sites or Ta doping do not change the magnetic properties of the pristine ZnCr2Se4 compound. The magnetic field strongly decreases the temperature TN character istic of the magnetic transitions and decreases the intensity of the C peak at TN.  (x = 0.05 − 0.12) compounds show very similar behaviour in the CB(T) characteristics obtained at different magnetic fields, which suggests that either the off-stoichiometry in Zn and/or Cr sites or Ta doping do not change the magnetic properties of the pristine ZnCr2Se4 compound. The magnetic field strongly decreases the temperature TN characteristic of the magnetic transitions and decreases the intensity of the C peak at TN.    T dT calculated at the magnetic fields B = 0 and 5 T, respectively. For all investigated samples, the value of the magnetic and phonon contribution to the entropy at the ordering temperature T N and B = 0 is around 50% of the entropy expected, considering the magnetic contribution S m = R × ln(2S + 1) = 11.52 J/Kmol Cr . The field dependence of C shown in Figure 12 is associated with the metamagnetic transition at the first critical field H c1 . A very similar C B (T) behaviour was experimentally documented recently for a series of spinels, which did not show a change in the magnetic structure at H c2 . Figure 12 also indicates magnetic contribution ∆S(T) = S(T, B = 0) − S(T, B = 5T) for temperatures T > T N , which seems to be characteristic of the family of doped ZnCr 2 Se 4 and recently was discussed as an effect of spin fluctuations in the paramagnetic regime [14]. For all investigated samples, the value of the magnetic and phonon contribution to the entropy at the ordering temperature TN and B = 0 is around 50% of the entropy expected, considering the magnetic contribution Sm = R × ln(2S + 1) = 11.52 J/KmolCr. The field dependence of C shown in Figure 12 is associated with the metamagnetic transition at the first critical field Hc1. A very similar CB(T) behaviour was experimentally documented recently for a series of spinels, which did not show a change in the magnetic structure at Hc2. Figure 12 also indicates magnetic contribution ΔS(T) = S(T, B = 0) − S(T, B = 5T) for temperatures T > TN, which seems to be characteristic of the family of doped ZnCr2Se4 and recently was discussed as an effect of spin fluctuations in the paramagnetic regime [14].

Thermal Analysis
For the thermal measurements, the single crystals with a more significant amount of Ta were chosen to show the changes in thermal properties under the influence of Ta. The thermogravimetric (TG) results and differential scanning calorimetry (DSC) measurements vs. temperature are shown in Figure 13 for the ZnCr1.90Ta0.10Se4 single crystals.

Thermal Analysis
For the thermal measurements, the single crystals with a more significant amount of Ta were chosen to show the changes in thermal properties under the influence of Ta. The thermogravimetric (TG) results and differential scanning calorimetry (DSC) measurements vs. temperature are shown in Figure 13 for the ZnCr 1.90 Ta 0.10 Se 4 single crystals.

Conclusions
In summary, we have presented new ZnCr2Se4 single crystals doped with tantalum. The single crystals ZnCr2-xTaxSe4 (where x = 0.05, 06, 07, 08, 010 and 0.12) were obtained by chemical vapour transport (CVT method), examined and analysed with XRD, SEM, DSC/TG, SQUID and QD-PPMS. Structural, electrical, magnetic, specific heat and thermal measurements showed the spinel structure with the presence of tantalum ions as Ta 3+ in the octahedral sites, semiconducting properties in the intrinsic region, AFM order below the Néel temperature of 22 K with the FM short-range interactions as well as a strong shift in the specific heat peak towards lower temperatures with an increase in the magnetic field and a weaker than expected magnetic and phonon contribution to entropy. Generally, the shift in the specific heat peak and the Néel temperature towards lower temperatures with increasing dc magnetic field is usually accompanied by a phase transition from a cubic to a tetragonal structure. In other words, a strong dc magnetic field broadens the temperature range of the paramagnetic state and the cubic structure of the spinel under study. The upper critical field indicates that the sample reached the state of FM order below the structural transition. The situation is similar in the case of the ZnCr2Se4 matrix. The greatest influence of tantalum was observed in the increase in magnetisation and reduction in the second critical field. The TG curve shows a mass loss of 34%. This is a similar value to the pure ZnCr 2 Se 4 ( Table 6). The differential scanning calorimetry (DSC) curve showed a small endothermic peak at 710 • C for ZnCr 1.90 Ta 0. 10 Se 4 , which confirmed that the melting effect occurs at a high temperature. These peaks indicate that, for the investigated crystals, the melting effect appears at high temperatures. However, a shift in the peak towards lower temperatures was observed. This was caused by additional cations (Ta 3+ ), which caused stiffening of the crystal lattice. On the one hand, this effect could be caused by an increase in covalent binding. On the other hand, the presence of Ta 3+ ions is a kind of "impurity", which induces a change in the endothermic peak position. Similar behaviour was observed in the (Zn 1-x Nd x ) Cr 2 Se 4 system [20].

Conclusions
In summary, we have presented new ZnCr 2 Se 4 single crystals doped with tantalum. The single crystals ZnCr 2-x Ta x Se 4 (where x = 0.05, 06, 07, 08, 010 and 0.12) were obtained by chemical vapour transport (CVT method), examined and analysed with XRD, SEM, DSC/TG, SQUID and QD-PPMS. Structural, electrical, magnetic, specific heat and thermal measurements showed the spinel structure with the presence of tantalum ions as Ta 3+ in the octahedral sites, semiconducting properties in the intrinsic region, AFM order below the Néel temperature of 22 K with the FM short-range interactions as well as a strong shift in the specific heat peak towards lower temperatures with an increase in the magnetic field and a weaker than expected magnetic and phonon contribution to entropy. Generally, the shift in the specific heat peak and the Néel temperature towards lower temperatures with increasing dc magnetic field is usually accompanied by a phase transition from a cubic to a tetragonal structure. In other words, a strong dc magnetic field broadens the temperature range of the paramagnetic state and the cubic structure of the spinel under study. The upper critical field indicates that the sample reached the state of FM order below the structural transition. The situation is similar in the case of the ZnCr 2 Se 4 matrix. The greatest influence of tantalum was observed in the increase in magnetisation and reduction in the second critical field.