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<p>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 (&lt;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.</p>

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A molecular velcro self-healing cement

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2026年8月1日

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  • Chao Zeng,
  • Zihao Li,
  • Trent R. Graham,
  • Manh Thuong Nguyen,
  • Robert G. Felsted,
  • Xiaoxu Li,
  • William B. Chrisler,
  • Tamas Varga,
  • Lan Li,
  • Quin R. S. Miller,
  • Carlos A. Fernandez

摘要

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.