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MACROMOLECULAR MATERIALS AND ENGINEERING · 2017 ·Vol. 302 ·期 9 ·1700059 · IF 2.863

Self-Healing Epoxy Coatings via Focused Sunlight Based on Photothermal Effect

Liang Fang,Jiamei Chen,Yuting Zou,Shunping Chen,Tianyu Fang,Chunhua Lu,Zhongzi Xu

Epoxy coatings which can be healed via photothermal effect from focused sunlight are reported. The diamine of m -xylylenediamine (MXDA) and monoamine of 4-(heptadecafluorooctyl)aniline (HFOA) are reacted into the diglycidylether of bisphenol A (DGEBA) network. Via gradual replacement of MXDA with HFOA, the glass transition temperature and crosslinking density of the epoxy network are tuned to achieve the thermally induced healing based on chain diffusion and reentanglement. Aniline black (AB) with well absorptivity for sunlight is used subsequently as the organic photothermal compound, transferring the thermally induced healing into a sunlight responsive one. A common handheld magnifier, which can focus natural sunlight to the required power density (0.6–0.9 W cm −1 ), is used to successfully heal one cracked coating in outdoor circumstance. This study provides a potential approach to achieve the convenient, precise, and timely healing for outdoor epoxy coatings.

CAS / MDL: 68-12-2
研究领域: 材料科学 · 化学工程
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ADVANCED FUNCTIONAL MATERIALS · 2025 · IF 19

Dynamic Na+ Bridges: A 3D Printing Strategy for Hydrogels With High Strength, Low Hysteresis, Strong Adhesion, and Self-Healing

Mengyao Chen,Wenjing Qin,Yanli Wang,Hanlin Zhai,Changshun Gu,Xiangchuan Zhao,Ying Bi,Yixin Xu,Zeyu Ming,Shengrong Li,Shu Hu,Xingyue Zhang,Xiaoye Ma,Shougen Yin

The synergistic optimization of high strength, strong adhesion, high conductivity, and rapid self-healing in hydrogels faces fundamental challenges arising from conflicting mechanisms. Herein, a 3D-printed, ionically conductive interpenetrating double-network hydrogel based on poly (acrylic acid) (PAAc) is developed via the innovative introduction of dynamic Na⁺ bridges. This molecular design enables a unique dual mechanism: the Na⁺ ions not only form reversible ionic bonds that accelerate chain diffusion through bond rupture-recombination but also create an electrostatic shielding effect in the covalent network, which promotes chain extension to improve mechanical strength without sacrificing dynamic properties. Furthermore, Na⁺ ions regulate bound/free water states and reduces energy dissipation during topological rearrangement. These synergistic mechanisms collectively enable the hydrogel to overcome conventional performance trade-offs. The resulting material concurrently enhances mechanical properties (300 kPa tensile, 1.2 MPa compressive strength), adhesion (160 kPa), and self-healing (>90% recovery in 1 h). Biomimetic devices such as an underwater octopus-tentacle gripper, biomimetic crawling suckers, and pressure sensors are fabricated. By integrating hydrogels with 1D convolutional neural network algorithms, a real-time motion behavior recognition system is further developed. The multi-property cooperative design strategy offers a new pathway for the application of intelligent hydrogel materials in soft robotics and flexible electronics.

CAS / MDL: 84434-11-7 79-10-7
研究领域: 材料科学 · 软体机器人 · 柔性电子学 · 水凝胶工程 · 离子导体 · 生物医学器件
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