Abstract

Self-healing functional polymer surfaces, designed with an intrinsic and spontaneous mechanism which replenishes the damaged surfaces with the original chemical functionalities, are of great interest to maintain a high performance of the functionality and extend the life-time of materials. We report self-replenishing UV-cured hydrophobic polymer films prepared through the incorporation of methacrylate-terminated perfluorinated-dangling chains into poly(ethylene glycol diacrylate) (PEGDA)-based networks. The films are able to spontaneously and fully self-replenish the surface hydrophobicity, multiple times, upon consecutive intentional damages. The rate of recovery was found to be dependent on the glass transition temperature (Tg) of the networks, which directly correlates to the PEG block length in the PEGDA oligomer used. This study demonstrates that an intrinsic self-replenishing mechanism can be implemented in new network architectures, created rapidly and efficiently by free radical UV-polymerization, which allows preparing self-healing functional polymer films in a faster and eco-friendlier way.

Keywords:
Polymer Materials science Ethylene glycol Polymerization Oligomer Methacrylate Self-healing Polymer chemistry Chemical engineering Photopolymer Glass transition Radical polymerization Polymer science Composite material

Metrics

22
Cited By
2.82
FWCI (Field Weighted Citation Impact)
56
Refs
0.90
Citation Normalized Percentile
Is in top 1%
Is in top 10%

Citation History

Topics

Polymer composites and self-healing
Physical Sciences →  Materials Science →  Polymers and Plastics
Surface Modification and Superhydrophobicity
Physical Sciences →  Materials Science →  Surfaces, Coatings and Films
Advanced Sensor and Energy Harvesting Materials
Physical Sciences →  Engineering →  Biomedical Engineering
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