The Origin of Aromaticity: Aromatic Compounds as Intrinsic Topological Superconductors with Majorana Fermion
Kyoung Hwan Choi, Dong Hack Suh

TL;DR
This paper reveals that polyaromatic hydrocarbons are topological superconductors with Majorana states, reinterpreting aromaticity through topological concepts and suggesting new applications in quantum computing.
Contribution
It demonstrates that aromatic compounds like benzene are topological superconductors, linking aromaticity to topological invariants and Majorana fermions, which is a novel perspective.
Findings
Polyaromatic hydrocarbons are topological superconductors.
Aromaticity can be reinterpreted via topological invariants.
Potential application in quantum computing.
Abstract
Topological superconductors have been discovered with recent advances in understanding the topological properties of condensed matters. These states have a full pairing gap in the bulk and gapless counter-propagating Majorana states at the boundary. A pair of Majorana zero modes is associated with each vortex. This understanding had a great influence on the theory of superconductivity and their following experiments, but its relevantce to organic compounds was not closely observed. Here, we analyze the topological states of various polyaromatic hydrocarbons (PAHs), including benzene, and reveal that they are topological superconductors. We have analyzed the momentum vectors of benzene and other PAHs through a semi-classical approach to confirm their non-trivial state. Their unique properties might be originated from the odd number of Kramers doublets in PAHs. The H\"uckel rule…
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Taxonomy
TopicsTopological Materials and Phenomena · Graphene research and applications · Quantum Mechanics and Non-Hermitian Physics
