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Updated: Aug 31, 2025

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
Published on: February 7, 2017
Unprecedented toughness in transparent, luminescent, self-healing polymers enabled via hierarchical rigid domain
Di Zhao1, Xinzhe Zhou1, Qianrui Li1
1National-Local Joint Engineering Laboratory for Energy Conservation in Chemical Process Integration and Resources Utilization, Tianjin Key Laboratory of Chemical Process Safety, School of Chemical Engineering and Technology, Hebei University of Technology, GuangRong Dao 8, Hongqiao District, Tianjin, 300130, P. R. China. lihuanrong@hebut.edu.cn.
Abstract:
The preparation of luminescent self-healing materials simultaneously featuring superior integrated mechanical properties is still a great challenge because the relationship between self-healing ability and mechanical capacities is conflicted. Here, transparent luminescent materials with balanced self-healing behavior, extreme toughness, and fast elastic recovery are prepared via hierarchical rigid domain design by coordinating lanthanide (Ln3+) to terpyridine (TPy) moieties linked to the polymer chains formed through polymerization of tolylene-2,4-diisocyanate-terminated polypropylene glycol (PPG-NCO) and 1,6-hexanediamine (HDA). The hierarchical rigid domain containing lanthanide-terpyridine (Ln3+-TPy) coordination interactions and H-bonds formed by urea and urethane leads to a tough network that features unprecedented toughness of 133.35 MJ m-3, which reaches 83% of that of typical spider silk (≈ 160 MJ m-3) and is also dynamic for fast self-healing at ambient temperature. Besides, the multi-color emission, ranging from red through orange and yellow to green, can be achieved via adjusting the molar ratio of Eu3+/Tb3+. We believe that the strategy applied in this work provides some insights for the preparation of high mechanical strength luminescence materials with self-healing properties.
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