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We analyze a class of bound defect states in the continuum electronic spectrum of bilayer materials, which emerge independent of symmetry protection or additional degrees of freedom. Taking graphene as a prototypical example, our comparative analysis of $AA$- and $AB$-stacked bilayer graphene demonstrates that these states originate from the intrinsic algebraic structure of the tight-binding Hamiltonian when trigonal warping is neglected rather than any underlying symmetry. The inclusion of trigonal warping and higher-order hoppings broadens the bound states into long-lived resonances. This discovery provides a distinct pathway to defect and band-structure engineering. We conclude with a proposed protocol for observing these states in scanning tunneling microscopy experiments.
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Massatt et al. (2025) studied this question.
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