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Gyromorphs: A New Class of Functional Disordered Materials

Mathias Casiulis1,2,*, Aaron Shih3,1,*, and Stefano Martiniani3,1,2,4,†

  • 1Center for Soft Matter Research, Department of Physics, New York University, New York, New York 10003, USA
  • 2Simons Center for Computational Physical Chemistry, Department of Chemistry, New York University, New York, New York 10003, USA
  • 3Courant Institute of Mathematical Sciences, New York University, New York, New York 10003, USA
  • 4Center for Neural Science, New York University, New York, New York 10003, USA

  • *These authors contributed equally to this work.
  • †Contact author: sm7683@nyu.edu

Phys. Rev. Lett. 135, 196101 – Published 6 November, 2025

DOI: https://doi.org/10.1103/gqrx-7mn2

Abstract

We introduce a new class of functional correlated disordered materials, termed gyromorphs, which uniquely combine liquidlike translational disorder with quasi-long-range rotational order, induced by a ring of G delta peaks in their structure factor. We generate gyromorphs in 2D and 3D by spectral optimization methods, verifying that they display strong discrete rotational order but no long-range translational order, while maintaining rotational isotropy at short range for sufficiently large G. Using a coupled dipoles approximation, we numerically show that these structures outperform quasicrystals, stealthy hyperuniformity, and Vogel spirals in the formation of low-index-contrast isotropic band gaps in 2D, for both scalar and vector waves, and open complete isotropic band gaps in 3D. This claim is further supported by analytical effective-medium theory and by numerical estimates of scattering mean-free paths. Finally, we introduce “polygyromorphs” with several rotational symmetries at different length scales (i.e., multiple rings of delta peaks), enabling the formation of multiple band gaps in a single structure, thereby paving the way for fine control over optical properties.

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