Chao Zeng, Zihao Li, Trent R. Graham, Manh‐Thuong Nguyen, Robert G. Felsted, Xiaoxu Li, William Chrisler, Tamás Varga, Lan Li, Quin R. S. Miller, Carlos A. Fernandez
Cracking fundamentally limits the durability of cementitious materials, while most self-healing strategies rely on encapsulated agents or high additive loadings that restrict repeatability, scalability, or mechanical performance. Here we report a cement composite incorporating an ultra-low polymer concentration (<0.15 wt%) that enables autonomous, multi-cycle crack healing without capsules or vascular networks and with minimal impact on hydration, setting, or workability. The system forms an in-situ poly(acrylic acid)/poly(ethylene oxide)/branched poly(ethylene imine) complex that establishes reversible electrostatic and hydrogen-bonding interactions with both itself and cement hydration products, creating a molecular-scale “Velcro” network. High-resolution X-ray computed tomography and optical microscopy reveal rapid polymer redistribution and crack sealing, including closure through a ~ 2 mm-deep fracture within ~4 h, corresponding to healing rates of ~10 mm·day⁻¹. Time-resolved confocal Raman spectroscopy identifies bi-exponential kinetics with characteristic times of ~10 min and ~9 h, consistent with multi-stage polymer transport and interfacial reorganization, and corroborated by identical-location SEM–EDS observations. Mechanical testing under a severe post-peak loading protocol (20% strength loss beyond the maximum) shows strength recovery of up to 62% in compression and 59% in direct tension, with sustained recovery across multiple damage–healing cycles. These results demonstrate that reversible polymer–cement interactions coupled with efficient pore-scale transport enable rapid, repeatable self-healing at exceptionally low additive concentrations, providing a scalable pathway toward longer-lived and more sustainable concrete infrastructure. A “molecular Velcro” cement with trace amounts of polymer rapidly heals cracks through reversible molecular interactions and pore-scale transport, restoring strength across damage cycles and offering a scalable path to longer-lasting concrete.