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Interpenetrating polymer network (IPN) hydrogels were developed by engineering ionic bridges between carboxylated cellulose nanofibrils (CNFs) and amine-terminated poly(ethylene glycol) (PEG) into a covalent poly(acrylamide) architecture network, and the role of precoordinated CNF-PEG dynamic complexes in the IPN hydrogels viscoelastic dynamics was explored. The results shown that the ionic complexes significantly improved the IPN hydrogels energy dissipation and elastic recovery properties, leading to strain-rate dependent mechanics and notable enhancement in tensile toughness. The uniaxial deformation over a range of strain rates demonstrated that fracture energy peaked at 0.05 s-1 before decreased with further increasing strain rate, consistent with the crack propagation rate result. This straightforward sacrificial bonding strategy validates the hypothesis that elastomers with high toughness and excellent recovery can be achieved by incorporating precoordinated supramolecular associating motifs, which confers control over mechanical properties in a reversible, dynamic, and modular fashion. [ABSTRACT FROM AUTHOR]