Electronic correlations and spin frustration in the molecular conductors $\kappa$-(BEDT-TTF)$_2$X probed by magnetic quantum oscillations

TL;DR

This study uses magnetic quantum oscillations to investigate how physical and chemical pressure influence electronic correlations and spin frustration in $ppa$-(BEDT-TTF)$_2$X molecular conductors, revealing pressure-dependent changes in electronic structure and magnetic properties.

Contribution

It provides detailed insights into how pressure and anion substitution affect the electronic correlation and spin frustration ratios in $ppa$-(BEDT-TTF)$_2$X, advancing understanding of Mott physics in these materials.

Findings

Pressure reduces electronic correlation strength and magnetic ordering.

Anion substitution increases spin frustration without affecting correlation strength.

Electronic structure and magnetic properties are tunable via pressure and chemical modifications.

Abstract

The layered molecular conductors $\kappa$-(BEDT-TTF)$_2$X are a perfect experimental platform for studying the physics of the Mott transition and related exotic electronic states. In these materials, the subtle balance between various instabilities of the normal metallic state can be efficiently changed by applying a very moderate external pressure or by subtle chemical modifications, e.g. by a replacement of the insulating anion X$^{-}$, frequently referred to as ``chemical pressure''. A crucially important but still unsettled issue is an exact understanding of the influence of physical and chemical pressure on the electronic structure. Here, we use magnetic quantum oscillations to explore in a broad pressure range the behavior of the key parameters governing the Mott physics, the electronic correlation strength ratio $U/t$ and the spin frustration ratio $t'/t$ in two $\kappa$ salts, the ambient-pressure antiferromagnetic insulator with X = Cu[N(CN)$_2$]Cl and the ambient-pressure superconductor with X = Cu(NCS)$_2$. Our analysis shows that pressure effectively changes not only the conduction bandwidth but also the degree of spin frustration, thus weakening both the electronic correlation strength and the magnetic ordering instability. At the same time, we find that the replacement of the anion Cu[N(CN)$_2$]Cl$^-$ by Cu(NCS)$_2^-$ results in a significant increase of the frustration parameter $t'/t$, leaving the correlation strength essentially unchanged.