聚合物
氢键
材料科学
分子
产量(工程)
化学物理
结晶
之字形的
氢
化学工程
纳米技术
化学
复合材料
有机化学
工程类
数学
几何学
作者
Yu Yanagisawa,Yiling Nan,Kou Okuro,Takuzo Aida
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2017-12-14
卷期号:359 (6371): 72-76
被引量:823
标识
DOI:10.1126/science.aam7588
摘要
A healing squeeze The very long molecules found in synthetic polymers, and their tendency to entangle and partially crystallize, impart many of the polymers' useful properties. However, these same characteristics also mean that chain dynamics are slow, which impedes potential self-healing. Yanagisawa et al. developed a family of ether-thiourea linear polymers that form hydrogen-bonded networks and still manage to stay amorphous. The polymers are stiff, showing the strength of the hydrogen bonding; however, because these bonds can easily reform, the polymer is also able to self-heal when compressed. Science , this issue p. 72
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