Band Structure Engineering of Coupled-Resonator Phononic Polyacetylene and Polyaminoborane
B. Manjarrez-Monta\~nez, R. A. M\'endez-S\'anchez, Y. Betancur-Ocampo, A. Mart\'inez-Arg\"uello

TL;DR
This paper introduces a method to engineer band structures in coupled-resonator phononic metamaterials by designing artificial analogs of molecular structures, revealing topologically protected states in the process.
Contribution
It presents a novel approach to construct and analyze phononic metamaterials based on molecular analogs using tight-binding models and topological concepts.
Findings
Successful design of phononic analogs of trans-polyacetylene and trans-polyaminoborane.
Identification of topologically protected states in the artificial trans-polyacetylene.
Application of SSH model and $$-deformed Dirac equation to analyze band structures.
Abstract
A methodology for constructing a quasi-one-dimensional coupled-resonator phononic metamaterial is presented. This is achieved through the design of artificial phononic analogs of two molecular structures: trans-polyacetylene and trans-polyaminoborane. The band structure of trans-polyacetylene is analyzed in relation to the Su-Schrieffer-Heeger (SSH) model, while that of trans-polyaminoborane is examined using the -deformed Dirac equation, both within a tight-binding framework. Additionally, the obtained finite realization of the artificial trans-polyacetylene exhibits topologically protected states.
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