Collapse of the $Gd^{3+}$ ESR fine structure throughout the coherent temperature of the Gd-doped Kondo Semiconductor $CeFe_{4}P_{12}$

TL;DR

This study investigates the collapse of the Gd3+ ESR fine structure in Gd-doped CeFe4P12 across the insulator-metal transition, revealing the role of temperature-dependent hybridization and fluctuating valence in the electronic structure.

Contribution

It introduces a comprehensive explanation for the ESR spectral evolution in a Kondo semiconductor, emphasizing the importance of fluctuating valence alongside exchange narrowing.

Findings

ESR fine structure collapses at the insulator-metal transition around 160 K.

Temperature-dependent hybridization influences the ESR spectra.

Fluctuating valence of Ce ions is key to understanding the ESR behavior.

Abstract

Experiments on the $Gd^{3+}$ Electron Spin Resonance (ESR) in the filled skutterudite $Ce_{1-x}Gd_{x}Fe_{4}P_{12}$ ($x \approx 0.001$), at temperatures where the host resistivity manifests a smooth insulator-metal crossover, provides evidence of the underlying Kondo physics associated with this system. At low temperatures (below $T \approx K$), $Ce_{1-x}Gd_{x}Fe_{4}P_{12}$ behaves as a Kondo-insulator with a relatively large hybridization gap, and the $Gd^{3+}$ ESR spectra displays a fine structure with lorentzian line shape, typical of insulating media. The electronic gap is attributed to the large hybridization present in the coherent regime of a Kondo lattice, when Ce 4f-electrons cooperate with band properties at half-filling. Mean-field calculations suggest that the electron-phonon interaction is fundamental at explaining the strong 4f-electron hybridization in this filled skutterudite. The resulting electronic structure is strongly temperature dependent, and at about $T^{*} \approx 160 K$ the system undergoes an insulator-to-metal transition induced by the withdrawal of 4f-electrons from the Fermi volume, the system becoming metallic and non-magnetic. The $Gd^{3+}$ ESR fine structure coalesces into a single dysonian resonance, as in metals. Still, our simulations suggest that exchange-narrowing via the usual Korringa mechanism, alone, is not capable of describing the thermal behavior of the ESR spectra in the entire temperature region ($4.2$ - $300$ K). We propose that temperature activated fluctuating-valence of the Ce ions is the missing ingredient that, added to the usual exchange-narrowing mechanism, fully describes this unique temperature dependence of the $Gd^{3+}$ ESR fine structure observed in $Ce_{1-x}Gd_{x}Fe_{4}P_{12}$.