ترغب بنشر مسار تعليمي؟ اضغط هنا

Fragile balance of the exchange interactions in Mn$_{1-x}$Co$_{x}$Ge compounds

70   0   0.0 ( 0 )
 نشر من قبل Sven-Arne Siegfried
 تاريخ النشر 2017
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

The magnetic system of the pseudobinary compound Mn$_{1-x}$Co$_{x}$Ge has been studied using small-angle neutron scattering and SQUID-measurements. It is found that Mn$_{1-x}$Co$_{x}$Ge orders magnetically at low temperatures in the whole concentration range of $x in [0 div 0.9]$. Three different states of the magnetic structure have been found: a short-periodic helical state at $x leq 0.45$, a long-periodic helical state at $0.45 < x leq 0.8$, and a ferromagnetic state at $x sim 0.9$. Taking into account that the relatively large helical wavevector $k gg 1$ nm$^{-1}$ is characteristic for systems with mainly Ruderman-Kittel-Kasuya-Yoshida (RKKY) interaction, we suggest that the short-periodic helical structure at $x leq 0.45$ is based on an effective RKKY interaction. Also the decay of $k$ with increasing $x$ is ascribed to a reduction of the interaction between second nearest neighbors and, therefore, to an increase of the influence of the Dzyaloshinskiy-Moriya interaction (DMI). As a result of the competition between these two interactions the quantum phase transition from a long-range ordered (LRO) to a short-range ordered (SRO) helical structure has been observed upon increase of the Co-concentration at $x_{c1} sim 0.25$. Further increase of $x$ leads to the appearance of a double peak in the scattering profile at $0.45 < x < 0.7$. The transition from a helical structure to a ferromagnetic state found at $x = 0.9$ is caused by the weakening of DMI as compared to the cubic anisotropy. In summary, the evolution of the magnetic structure of Mn$_{1-x}$Co$_{x}$Ge with increasing $x$ is an example of a continuous transition from a helical structure based on the effective RKKY interaction to a ferromagnetic structure passing through a helical structure based on DMI.



قيم البحث

اقرأ أيضاً

170 - S Chadov , G.H. Fecher , C. Felser 2008
This study presents the effect of local electronic correlations on the Heusler compounds Co$_2$Mn$_{1-x}$Fe$_x$Si as a function of the concentration $x$. The analysis has been performed by means of first-principles band-structure calculations based o n the local approximation to spin-density functional theory (LSDA). Correlation effects are treated in terms of the Dynamical Mean-Field Theory (DMFT) and the LSDA+U approach. The formalism is implemented within the Korringa-Kohn-Rostoker (KKR) Greens function method. In good agreement with the available experimental data the magnetic and spectroscopic properties of the compound are explained in terms of strong electronic correlations. In addition the correlation effects have been analysed separately with respect to their static or dynamical origin. To achieve a quantitative description of the electronic structure of Co$_2$Mn$_{1-x}$Fe$_x$Si both static and dynamic correlations must be treated on equal footing.
Magnetic and transport properties of Ge(1-x-y)Mn(x)Eu(y)Te crystals with chemical compositions 0.041 < x < 0.092 and 0.010 < y < 0.043 are studied. Ferromagnetic order is observed at 150 < T < 160 K. Aggregation of magnetic ions into clusters is foun d to be the source of almost constant, composition independent Curie temperatures in our samples. Magnetotransport studies show the presence of both negative (at T < 25 K) and linear positive (for 25<T <200 K) magnetoresistance effects (with amplitudes not exceeding 2%) in the studied alloy. Negative magnetoresistance detected at T < 25 K is found to be due to a tunneling of spin-polarized electrons between ferromagnetic clusters. A linear positive magnetoresistance is identified to be geometrical effect related with the presence of ferromagnetic clusters inside semiconductor matrix. The product of the polarization constant and the inter-grain exchange constant, J_P, varies between about 0.13 meV and 0.99 meV. Strong anomalous Hall effect (AHE) is observed for T < T_C with coefficients R_S independent of temperature. The scaling analysis of the AHE leads to a conclusion that this effect is due to a skew scattering mechanism.
The search and exploration of new materials not found in nature is one of modern trends in pure and applied chemistry. In the present work, we report on experimental and textit{ab initio} density-functional study of the high-pressure-synthesized seri es of compounds Mn$_{1-x}$(Co,Rh)$_x$Ge. These high-pressure phases remain metastable at normal conditions, therewith they preserve their inherent noncentrosymmetric B20-type structure and chiral magnetism. Of particular interest in these two isovalent systems is the comparative analysis of the effect of $3d$ (Co) and $4d$ (Rh) substitution for Mn, since the $3d$ orbitals are characterized by higher localization and electron interaction than the $4d$ orbitals. The behavior of Mn$_{1-x}$(Co,Rh)$_x$Ge systems is traced as the concentration changes in the range $0 leq x leq 1$. We applied a sensitive experimental and theoretical technique which allowed to refine the shape of the temperature dependencies of magnetic susceptibility $chi(T)$ and thereby provide a new and detailed magnetic phase diagram of Mn$_{1-x}$Co$_x$Ge. It is shown that both systems exhibit a helical magnetic ordering that very strongly depends on the composition $x$. However, the phase diagram of Mn$_{1-x}$Co$_x$Ge differs from that of Mn$_{1-x}$Rh$_x$Ge in that it is characterized by coexistence of two helices in particular regions of concentrations and temperatures.
X-ray absorption (XAS) and x-ray magnetic circular dichroism (XMCD) spectra at the L$_{2,3}$ edges of Mn in (Ge,Mn) compounds have been measured and are compared to the results of first principles calculation. Early textit{ab initio} studies show tha t the Density Functional Theory (DFT) can very well describe the valence band electronic properties but fails to reproduce a characteristic change of sign in the L$_{3}$ XMCD spectrum of Mn in Ge$_3$Mn$_5$, which is observed in experiments. In this work we demonstrate that this disagreement is partially related to an underestimation of the exchange splitting of Mn 2$p$ core states within the local density approximation. It is shown that the change in sign experimentally observed is reproduced if the exchange splitting is accurately calculated within the Hartree-Fock approximation, while the final states can be still described by the DFT. This approach is further used to calculate the XMCD in different (Ge,Mn) compounds. It demonstrates that the agreement between experimental and theoretical spectra can be improved by combining state of the art calculations for the core and valence states respectively.
The correlation between magnetic properties and microscopic structural aspects in the diluted magnetic semiconductor Ge$_{1-x}$Mn$_{x}$Te is investigated by x-ray diffraction and magnetization as a function of the Mn concentration $x$. The occurrence of high ferromagnetic-transition temperatures in the rhombohedrally distorted phase of slowly-cooled Ge$_{1-x}$Mn$_{x}$Te is shown to be directly correlated with the formation and coexistence of strongly-distorted Mn-poor and weakly-distorted Mn-rich regions. It is demonstrated that the weakly-distorted phase fraction is responsible for the occurrence of high-transition temperatures in Ge$_{1-x}$Mn$_{x}$Te. When the Mn concentration becomes larger, the Mn-rich regions start to switch into the undistorted cubic structure, and the transition temperature is suppressed concurrently. By identifying suitable annealing conditions, we successfully increased the transition temperature to above 200 K for Mn concentrations close to the cubic phase. Structural data indicate that the weakly-distorted phase fraction can be restored at the expense of the cubic regions upon the enhancement of the transition temperature, clearly establishing the direct link between high-transition temperatures and the weakly-distorted Mn-rich phase fraction.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا