Seminar: Bulk electronic structure of EuTGe3 (T=Co, Ni, Rh, Ir) studied by hard x-ray photoelectron spectroscopy Yuki Utsumi
Synchrotron SOLEIL, Gif sur Yvette, France
23.10.2017. u 15:00h
IF - predavaonica u zgradi Mladen Paić

Strongly correlated 4f-electron system has been a platform of various anomalous phenomena, such as valence fluctuation, unconventional superconductivity, heavy fermion behavior and spin/charge ordering [1]. The ground state property of these compounds is characterized by conflicting Kondo effect and Rudermann-Kittel-Kasuya-Yoshida (RKKY) interaction. Both interactions originate in the interplay of localized f electron and itinerant conduction electrons, though the former quenches the magnetic moments, while the latter leads to magnetic ordering in the ground state. The competition between Kondo effect and RKKY interactions in Ce and Yb-compounds are often discussed using a Doniach phase diagram [2], while Eu-compounds exhibit very different phase diagrams from them. Most of the reported Eu-compounds favor Eu2+ (4f 7J=7/2) valence state with an antiferromagnetic ground state. However, the energy difference between Eu2+ and non-magnetic Eu3+ (4f 6J=0) valence state is not so large and is reachable by applying external pressure or chemical substitution, that is accompanied by a first order phase transition. Due to the different ionic size between Eu2+ and Eu3+, the change of the Eu valence state is often assigned to the Kondo volume collapse effect.

Eu-based ternary germanide EuTGe3 (T= Co, Ni, Rh, Ir) possesses BaNiSn3-type crystal structure without inversion symmetry. The existence of the polycrystalline EuTGe3 has been known for decades, though a high quality single crystal becomes available only recently and its unique magnetic property is discovered [3]. The magnetic susceptibility measurement and Mössbauer spectroscopy report the presence of magnetic Eu2+ ions in all the compounds and localized Eu 4f moments order antiferromagnetically at similar temperature [3-6]. The magnetic moments order antiferromagnetically along the c-axis at TN=15.4, 13.5 and 12.3 K for EuCoGe3, EuNiGe3 and EuIrGe3, respectively. Conversely in EuRhGe3, the magnetic moments order perpendicular to the c-axis at ∼12 K. Despite the variation of transition metal substitution and the change in the unit cell volume, the Eu ions seem to have robust Eu2+ valence state with TN being barely affected. In order to study the effect of transition metal substitution on the electronic structure, a bulk sensitive hard x-ray photoelectron spectroscopy (HAXPES) was performed at GALAXIES beamline of SOLEIL synchrotron. In the seminar talk, I will present a detailed HAXPES result of EuTGe3.

[1] C. M. Varma, Rev. Mod. Phys. 48, 219 (1976).

[2] S. Doniach, Physica B 91, 231 (1977).

[3] O. Bednarchuk, et al., J. Alloys Comp. 622432-439 (2015): A. Phys. Pol. A 127, 418 (2015).

[4] A. Maurya, et al., J. Phys. : Condens. Matter 26216001 (2014).

[5] A. Maurya, et al., J. Mag. Mag. Mat. 401823-831 (2016).

[6] M. Kakihana, et al., J. Alloys Comp. 694439-451 (2017).


IF Ⓒ 2017 Ndoc Deda