The kagomé metals RbTi3Bi5 and CsTi3Bi5

Author:

Werhahn Dominik1,Ortiz Brenden R.2,Hay Aurland K.2,Wilson Stephen D.2,Seshadri Ram2,Johrendt Dirk1

Affiliation:

1. Department Chemie , Ludwig-Maximilians-Universität München , Butenandtstraße 5–13 , 81377 München , Germany

2. Materials Department, Materials Research Laboratory and California Nanosystems Institute , University of California Santa Barbara , Santa Barbara , CA 93106 , USA

Abstract

Abstract The kagomé metals RbTi3Bi5 and CsTi3Bi5 were synthesized both as polycrystalline powders by heating the elements in an argon atmosphere and as single crystals grown using a self-flux method. The compounds crystallize in the hexagonal crystal system isotypically to KV3Sb5 (P6/mmm, Z = 1, CsTi3Bi5: a = 5.7873(1), c = 9.2062(1) Å; RbTi3Bi5: a = 5.773(1), c = 9.065(1) Å). The titanium atoms form a kagomé net with bismuth atoms in the hexagons as well as above and below the triangles. The alkali metal atoms are coordinated by 12 bismuth atoms and form AlB2-like slabs between the kagomé layers. Magnetic susceptibility measurements with CsTi3Bi5 and RbTi3Bi5 single crystals reveal Pauli-paramagnetism and traces of superconductivity caused by CsBi2/RbBi2 impurities. Magnetotransport measurements reveal conventional Fermi liquid behavior and quantum oscillations indicative of a single dominant orbit at low temperature. DFT calculations show the characteristic metallic kagomé band structure similar to that of CsV3Sb5 with reduced band filling. A symmetry analysis of the band structure does not reveal an obvious and unique signature of a nontrivial topology.

Funder

German Research Foundation

Bavaria California Technology Center

Publisher

Walter de Gruyter GmbH

Subject

General Chemistry

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