Crystallization of heavy fermions via epitaxial strain in spinel LiV 2 O 4 thin film

Author:

Niemann Ulrike12,Wu Yu-Mi1ORCID,Oka Ryosuke12,Hirai Daigorou2,Wang Yi1,Suyolcu Y. Eren1,Kim Minu1ORCID,van Aken Peter A.1ORCID,Takagi Hidenori123

Affiliation:

1. Max Planck Institute for Solid State Research, 70569 Stuttgart, Germany

2. Department of Physics, University of Tokyo, Tokyo 113-0033, Japan

3. Institute for Functional Matter and Quantum Technologies, University of Stuttgart, 70550 Stuttgart, Germany

Abstract

The mixed-valent spinel LiV 2 O 4 is known as the first oxide heavy-fermion system. There is a general consensus that a subtle interplay of charge, spin, and orbital degrees of freedom of correlated electrons plays a crucial role in the enhancement of quasi-particle mass, but the specific mechanism has remained yet elusive. A charge-ordering (CO) instability of V 3+ and V 4+ ions that is geometrically frustrated by the V pyrochlore sublattice from forming a long-range CO down to T = 0 K has been proposed as a prime candidate for the mechanism. Here, we uncover the hidden CO instability by applying epitaxial strain on single-crystalline LiV 2 O 4 thin films. We find a crystallization of heavy fermions in a LiV 2 O 4 film on MgO, where a charge-ordered insulator comprising of a stack of V 3+ and V 4+ layers along [001], the historical Verwey-type ordering, is stabilized by the in-plane tensile and out-of-plane compressive strains from the substrate. Our discovery of the [001] Verwey-type CO, together with previous realizations of a distinct [111] CO, evidence the close proximity of the heavy-fermion state to degenerate CO states mirroring the geometrical frustration of the V pyrochlore lattice, which supports the CO instability scenario for the mechanism behind the heavy-fermion formation.

Funder

KAKENHI, Ministry of education, sports, and culture

European Union's Horizon 2020 research and innovation programme

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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