Unraveling 5f-6d hybridization in uranium compounds via spin-resolved L-edge spectroscopy

R. D. dos Reis (1, 2) , L. S. I. Veiga (1, 2) , C. A. A Escanhoela (1) , J. C. Lang (3) , Yves Joly (4) , F. G. Gandra (2) , D. Haskel (3) , N. M. Souza-Neto (1, 3)

1 LNLS - Laboratório Nacional de Luz Sìncrotron
2 UNICAMP - Universidade Estadual de Campinas = University of Campinas
3 APS - Advanced Photon Source [ANL]
4 NEEL - SIN - Surfaces, Interfaces et Nanostructures

The multifaceted character of 5f electrons in actinide materials, from localized to itinerant and in between, together with their complex interactions with 6d and other conduction electron states, has thwarted efforts for fully understanding this class of compounds. While theoretical efforts abound, direct experimental probes of relevant electronic states and their hybridiza-tion are limited. Here we exploit the presence of sizable quadrupolar and dipolar contributions in the uranium L 3-edge X-ray absorption cross section to provide unique information on the extent of spin-polarized hybridization between 5f and 6d electronic states by means of X-ray magnetic circular dichroism. As a result, we show how this 5f-6d hybridization regulates the magnetism of each sublattice in UCu 2 Si 2 and UMn 2 Si 2 compounds, demonstrating the potentiality of this methodology to investigate a plethora of magnetic actinide compounds.

Domaines: Science des matériaux [cond-mat.mtrl-sci]

R. D. dos Reis, L. S. I. Veiga, C. A. A Escanhoela, J. C. Lang, Yves Joly, et al.. Unraveling 5f-6d hybridization in uranium compounds via spin-resolved L-edge spectroscopy. Nature Communications, 2017, 8, pp.1203. ⟨10.1038/s41467-017-01524-1⟩. ⟨hal-01626956⟩