Biomimetic growth in polymer gels.

By modeling gels growing in confined environments, we uncover a biomimetic feedback mechanism between the evolving gel and confining walls that enables significant control over the properties of the grown gel. Our new model describes the monomer adsorption, polymerization and cross-linking involved in forming new networks and the resultant morphology and mechanical behavior of the grown gel. Confined between two hard walls, a thin, flat "parent" gel undergoes buckling; removal of the walls returns the gel to the flat structure. Polymerization and cross-linking in the confined parent generates the next stage of growth, forming a random copolymer network (RCN). When the walls are removed, the RCN remains in the buckled state, simultaneously "locking in" these patterns and increasing the Young's modulus by two orders of magnitude. Confinement of thicker gels between harder or softer 3D walls leads to controllable mechanical heterogeneities, where the Young's modulus between specific domains can differ by three orders of magnitude. These systems effectively replicate the feedback between mechanics and morphology in biological growth, where mechanical forces guide the structure formation throughout stages of growth. The findings provide new guidelines for shaping "growing materials" and introducing new approaches to matching form and function in synthetic systems.