Issue 3, 2024

Enantiomorphic kagome bands in a two-dimensional covalent organic framework with non-trivial magnetic and topological properties

Abstract

The kagome lattice is one of the most intriguing topics to study. It has a frustrated flat band touching a set of Dirac bands and can possess various promising properties, such as ferromagnetism, superconductivity, and a non-trivial topology. Covalent organic frameworks (COFs) are a rare type of inorganic material, however, they can provide a platform for generating certain required lattices. Based on first-principles density functional theory calculations, we show that a newly synthesized two-dimensional COF named COF-SH has novel enantiomorphic kagome bands, which include two sets of flat bands touching the Dirac bands around the Fermi level. The Bloch wave of the flat-valence band at the K-point shows the kagome nature of the phase interference. Under charge doping, the COF-SH exhibits a ferromagnetic ground state. Moreover, when COF-SH is doped with iodine atoms, a sizable gap in the system is opened between the flat bands and the Dirac bands due to the spin–orbit coupling (SOC) effect. Meanwhile, the spin degeneracy is lifted since the organic layer loses electrons due to the oxidizing property of iodine. In addition, our tight-binding analysis with the SOC effect shows that the flat valence band separates from the Dirac bands and holds a nonzero Chern number. Consequently, this I-doped COF can give rise to a quantum anomalous Hall effect.

Graphical abstract: Enantiomorphic kagome bands in a two-dimensional covalent organic framework with non-trivial magnetic and topological properties

Supplementary files

Article information

Article type
Paper
Submitted
27 Sep 2023
Accepted
15 Nov 2023
First published
21 Nov 2023

Phys. Chem. Chem. Phys., 2024,26, 2066-2072

Enantiomorphic kagome bands in a two-dimensional covalent organic framework with non-trivial magnetic and topological properties

Q. Gao, X. Sun, X. Xu, X. Jiang, Z. Wang, L. Yang, D. Li, B. Cui and D. Liu, Phys. Chem. Chem. Phys., 2024, 26, 2066 DOI: 10.1039/D3CP04688E

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