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Structural criterion for the onset of rigidity in a colloidal gel

C. S. Dias1,2,*, J. C. Neves1,2,†, M. M. Telo da Gama1,2,‡, E. Del Gado3,§, and N. A. M. Araújo1,2,∥

  • 1Centro de Física Teórica e Computacional, Faculdade de Ciências, Universidade de Lisboa, 1749-016 Lisboa, Portugal
  • 2Departamento de Física, Faculdade de Ciências, Universidade de Lisboa, 1749-016 Lisboa, Portugal
  • 3Department of Physics, Institute for Soft Matter Synthesis and Metrology, Georgetown University, Washington, DC 20057, USA

  • *Contact author: csdias@fc.ul.pt
  • †Contact author: fc51402@alunos.fc.ul.pt
  • ‡Contact author: mmgama@fc.ul.pt
  • §Contact author: emanuela.del.gado@georgetown.edu
  • ∥Contact author: nmaraujo@fc.ul.pt

Phys. Rev. E 112, L033401 – Published 5 September, 2025

DOI: https://doi.org/10.1103/gw42-dks6

Abstract

Identifying the conditions for rigidity onset in gels is challenging. We propose a model that distinguishes attractive bonds from repulsive steric constraints, allowing the systematic variation of the number of bonded and nonbonded neighbors. Using simulations, rheology, and percolation analysis, we find that rigidity coincides with the percolation of particles with three or more bonds, occurring after connectivity percolation. This interplay of bonding and steric interactions, which is not a local but a large-scale effect, provides the mechanism for the rigidity of low-valence colloidal gels.

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See Also

Rigid m-percolation in limited-valence gels

J. C. Neves, J. M. Tavares, N. A. M. Araújo, and C. S. Dias
Phys. Rev. E 112, 035406 (2025)

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