Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userWhy the Co-based 115 compounds are different?: The case study of GdMIn$_5$ (M=Co, Rh, Ir)
89
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
The discovery in 2001 of superconductivity in some heavy fermion compounds of the RMIn$_5$ (R=4f or 5f elements, M=Co, Rh, Ir) family, has triggered enormous amount of research pointing to understand the physical origin of superconductivity and its relation with magnetism. Although many properties have been clarified, there are still crutial questions that remain unanswered. One of these questions is the particular role of the transition metal in determining the value of critical superconducting temperature (Tc). In this work, we analyse an interesting regularity that is experimentally observed in this family of compounds, where the lowest Neel temperatures are obtained in the Co-based materials. We focus our analysis on the GdMIn$_5$ compounds and perform density-functional-theory based total-energy calculations to obtain the parameters for the exchange coupling interactions between the magnetic moments located at the Gd$^{3+}$ ions. Our calculations indicate that the ground state of the three compounds is a $C$-type antiferromagnet determined by the competition between the first- and second-neighbor exchange couplings inside GdIn$_3$ planes and stabilized by the couplings across MIn$_2$ planes. We then solve a model with these magnetic interactions using a mean-field approximation and Quantum Monte Carlo simulations. The results obtained for the calculated Neel and Curie-Weiss temperatures, the specific heat and the magnetic susceptibility are in very good agreement with the existent experimental data. Remarkably, we show that the first neighbor interplane exchange coupling in the Co-based material is much smaller than in the Rh and Ir analogues due to a more two dimensional behaviour in the former. This result explains the observed lower Neel temperature in Co-115 systems and may shed light on the fact that the Co-based 115 superconductors present the highest Tc.
rate research
Read More
The Ce(Co,Rh,Ir)In$_5$ family of ``Ce-115 materials hosts an abundance of correlated electron behavior, including heavy-fermion physics, magnetism, superconductivity and nematicity. The complicated behavior of these entangled phenomena leads to a variety of exotic physical properties, which, despite the seemingly simple crystal structure of these compounds, remain poorly understood. It is generally accepted that the interplay between the itinerant and local character of Ce-$4f$ electrons is the key to their exotic behavior. Here, we report theoretical evidence that the Ce-115 materials are also topological semi-metals, with Dirac fermions around well-separated nodes. Dirac nodes in each compound are present on the $Gamma-Z$ plane close to the Fermi level. As the Dirac bands are derived from In-orbitals, they occur in all family members irrespective of the transition metal (Co,Rh,Ir). We present the expected Fermi-arc surface state patterns and show the close proximity of a topological Lifshitz transition, which possibly explains the high field physics of Ce-115 materials. Experimentally, we highlight the surprising similarity of Ce(Co,Rh,Ir)In$_5$ in high magnetic fields, despite the distinctly different states of the Ce-$4f$ electrons. These results raise questions about the role Dirac fermions play in exotic transport behavior, and we propose this class of materials as a prime candidate for unconventional topological superconductivity.
We report the synthesis, crystal structure and characterization by means of single crystal x-ray diffraction, neutron powder diffraction, magnetic, thermal and transport measurements of the new heavy fermion compounds Ce$_{2}$MAl$_{7}$Ge$_{4}$ (M = Co, Ir, Ni, Pd). These compounds crystallize in a noncentrosymmetic tetragonal space group P={4}2$_{1}$m, consisting of layers of square nets of Ce atoms separated by Ge-Al and M-Al-Ge blocks. Ce$_{2}$CoAl$_{7}$Ge$_{4}$, Ce$_{2}$IrAl$_{7}$Ge$_{4}$ and Ce$_{2}$NiAl$_{7}$Ge$_{4}$ order magnetically behavior below $T_{M}=$ 1.8, 1.6, and 0.8 K, respectively. There is no evidence of magnetic ordering in Ce$_{2}$PdAl$_{7}$Ge$_{4}$ down to 0.4 K. The small amount of entropy released in the magnetic state of Ce$_{2}$MAl$_{7}$Ge$_{4}$ (M = Co, Ir, Ni) and the reduced specific heat jump at $T_M$ suggest a strong Kondo interaction in these materials. Ce$_{2}$PdAl$_{7}$Ge$_{4}$ shows non-Fermi liquid behavior, possibly due to the presence of a nearby quantum critical point.
The synthesis, crystal structure, and physical properties studied by means of x-ray diffraction, magnetic, thermal and transport measurements of CeMAl$_{4}$Si$_{2}$ (M = Rh, Ir, Pt) are reported, along with the electronic structure calculations for LaMAl$_{4}$Si$_{2}$ (M = Rh, Ir, Pt). These materials adopt a tetragonal crystal structure (space group P4/mmm) comprised of BaAl$_4$ blocks, separated by MAl$_2$ units, stacked along the $c$-axis. Both CeRhAl$_{4}$Si$_{2}$ and CeIrAl$_{4}$Si$_{2}$ order antiferromagnetically below $T_{N1}$=14 and 16 K, respectively, and undergo a second antiferromagnetic transitition at lower temperature ($T_{N2}$=9 and 14 K, respectively). CePtAl$_{4}$Si$_{2}$ orders ferromagnetically below $T_C$ =3 K with an ordered moment of $mu_{sat}$=0.8 $mu_{B}$ for a magnetic field applied perpendicular to the $c$-axis. Electronic structure calculations reveal quasi-2D character of the Fermi surface.
We analyze theoretically a common experimental process used to obtain the magnetic contribution to the specific heat of a given magnetic material. In the procedure, the specific heat of a non-magnetic analog is measured and used to subtract the non-magnetic contributions, which are generally dominated by the lattice degrees of freedom in a wide range of temperatures. We calculate the lattice contribution to the specific heat for the magnetic compounds GdMIn$_5$ (M = Co, Rh) and for the non-magnetic YMIn$_5$ and LaMIn$_5$ (M = Co, Rh), using density functional theory based methods. We find that the best non-magnetic analog for the subtraction depends on the magnetic material and on the range of temperatures. While the phonon specific heat contribution of YRhIn$_5$ is an excellent approximation to the one of GdCoIn$_5$ in the full temperature range, for GdRhIn$_5$ we find a better agreement with LaCoIn$_5$, in both cases, as a result of an optimum compensation effect between masses and volumes. We present measurements of the specific heat of the compounds GdMIn$_5$ (M = Co, Rh) up to room temperature where it surpasses the value expected from the Dulong-Petit law. We obtain a good agreement between theory and experiment when we include anharmonic effects in the calculations.
Low temperature magnetic properties of Cd-doped Ce2MIn8 (M = Rh and Ir) single crystals are investigated. Experiments of temperature dependent magnetic susceptibility, heat capacity and electrical resistivity measurements revealed that Cd-doping enhances the antiferromagnetic (AFM) ordering temperature from TN = 2.8 K (x = 0) to TN = 4.8 K (x = 0.21) for Ce2RhIn8-xCdx and induces long range AFM ordering with TN = 3.8 K (x = 0.21) for Ce2IrIn8-xCdx. Additionally, X-ray and neutron magnetic scattering studies showed that Cd-doped samples present below TN a commensurate antiferromagnetic structure with a propagation vector (1/2,1/2,0). The resolved magnetic structures for both compounds indicate that the Cd-doping tends to rotate the direction of the ordered magnetic moments toward the ab-plane. This result suggests that the Cd-doping affects the Ce3+ ground state single ion anisotropy modifying the crystalline electrical field (CEF) parameters at the Ce3+ site. Indications of CEF evolution induced by Cd-doping were also found in the electrical resistivity measurements. Comparisons between our results and the general effects of Cd-doping on the related compounds CeMIn5 (M = Co, Rh and Ir) confirms the claims that the Cd-doping induced electronic tuning is the main effect favoring AFM ordering in these compounds.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
