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Quantum Matter Seminar

Monday, June 30, 2025
4:00pm to 5:00pm
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East Bridge 114
From Massless to Super Heavy Electrons in Kagome Metals
Haim Beidenkopf, Professor, Condensed Matter Physics, Weizmann Institute of Science,

The kagome lattice structure of corner-sharing triangles hosts a variety of electronic motifs that challenge Fermi liquid theory and give rise to exotic responses. On the heavy side, the kagome band structure hosts a pair of saddle points that correspond to van Hove singularities with a diverging density of states. Destructive interference further yields a flat band of localized moments. On the light side, it hosts a symmetry-protected Dirac band of massless electrons that, under certain layer stacking schemes, gives rise to three-dimensional massless Weyl electrons. We studied the three motifs on the atomic scale using scanning tunneling spectroscopy. We visualized Weyl electrons on the surface of the kagome-stacked ferromagnet Co3Sn2S2. On its kagome Co3Sn termination, we identified a new mechanism under which a breathing distortion turns the kagome van Hove singularity into a higher-order one at the Fermi energy. The strong interactions result in a spontaneous formation of a nematic state under a Pomeranchuk instability. In the kagome metal Ni3In, the kagome flat band is tuned to the Fermi energy, resulting in the breakdown of Fermi liquid theory signified by a strange metal non-linear temperature dependence of resistivity. We identify spectroscopically the localized degrees of freedom and their strong interactions with Dirac light bands pertaining to heavy-Fermion systems. Our studies thus reveal the exciting opportunities put forward by kagome metals for the investigation of exotic electronic states ranging from massless Dirac-particles, through moderately heavy states exhibiting spontaneous symmetry breaking, to super-heavy ones at which the interaction energy surpasses the bandwidth extending the universality of the heavy Fermion paradigm to kagome flat bands.

For more information, please contact Annika Keating by email at [email protected].