Geometrically frustrated lattices can display a range of correlated phenomena, ranging from spin frustration and charge order to dispersionless flat bands due to quantum interference. One particularly compelling family of such materials is the half-valence spinel LiB2O4 materials. On the B-site frustrated pyrochlore sublattice, the interplay of correlated metallic behavior and charge frustration leads to a superconducting state in LiTi2O4 and heavy fermion behavior in LiV2O4. To date, however, LiTi2O4 has primarily been understood as a conventional BCS superconductor despite a lattice structure that could host more exotic ground states. Here, we present a multimodal investigation of LiTi2O4, combining ARPES, RIXS, proximate magnetic probes, and ab-initio many-body theoretical calculations. Our data reveals a novel mobile polaronic ground state with spectroscopic signatures that underlie co-dominant electron-phonon coupling and electron-electron correlations also found in the lightly doped cuprates. The cooperation between the two interaction scales distinguishes LiTi2O4 from other superconducting titanates, suggesting an unconventional origin to superconductivity in LiTi2O4. Our work deepens our understanding of the rare interplay of electron-electron correlations and electron-phonon coupling in unconventional superconducting systems. In particular, our work identifies the geometrically frustrated, mixed-valence spinel family as an under-explored platform for discovering unconventional, correlated ground states.
Unconventional polaronic ground state in superconducting LiTi2O4 / Hasan, Z., Pan, G.A., Labollita, H., Kaczmarek, A., Sung, S.H., Sharma, S., Balakrishnan, P.P., Mercer, E., Bhartiya, V., N'Diaye, A.T., Salman, Z., Prokscha, T., Suter, A., Grutter, A.J., Garcia-Fernandez, M., Zhou, K., Pelliciari, J., Bisogni, V., El Baggari, I., Schlom, D.G., et al.. - In: NATURE COMMUNICATIONS. - ISSN 2041-1723. - 17:1(2026), pp. 1-9. [10.1038/s41467-025-68068-7]
Unconventional polaronic ground state in superconducting LiTi2O4
Pelliciari, Jonathan;
2026
Abstract
Geometrically frustrated lattices can display a range of correlated phenomena, ranging from spin frustration and charge order to dispersionless flat bands due to quantum interference. One particularly compelling family of such materials is the half-valence spinel LiB2O4 materials. On the B-site frustrated pyrochlore sublattice, the interplay of correlated metallic behavior and charge frustration leads to a superconducting state in LiTi2O4 and heavy fermion behavior in LiV2O4. To date, however, LiTi2O4 has primarily been understood as a conventional BCS superconductor despite a lattice structure that could host more exotic ground states. Here, we present a multimodal investigation of LiTi2O4, combining ARPES, RIXS, proximate magnetic probes, and ab-initio many-body theoretical calculations. Our data reveals a novel mobile polaronic ground state with spectroscopic signatures that underlie co-dominant electron-phonon coupling and electron-electron correlations also found in the lightly doped cuprates. The cooperation between the two interaction scales distinguishes LiTi2O4 from other superconducting titanates, suggesting an unconventional origin to superconductivity in LiTi2O4. Our work deepens our understanding of the rare interplay of electron-electron correlations and electron-phonon coupling in unconventional superconducting systems. In particular, our work identifies the geometrically frustrated, mixed-valence spinel family as an under-explored platform for discovering unconventional, correlated ground states.| File | Dimensione | Formato | |
|---|---|---|---|
|
s41467-025-68068-7.pdf
Open access
Tipologia:
VOR - Versione pubblicata dall'editore
Dimensione
2.31 MB
Formato
Adobe PDF
|
2.31 MB | Adobe PDF | Visualizza/Apri |
Pubblicazioni consigliate

I metadati presenti in IRIS UNIMORE sono rilasciati con licenza Creative Commons CC0 1.0 Universal, mentre i file delle pubblicazioni sono rilasciati con licenza Attribuzione 4.0 Internazionale (CC BY 4.0), salvo diversa indicazione.
In caso di violazione di copyright, contattare Supporto Iris




