材料科学
纤维素
纳米纤维
生物塑料
韧性
纳米技术
基质(水族馆)
极限抗拉强度
增韧
复合材料
细菌纤维素
聚合物
无定形固体
动力学
纤维
断裂韧性
木质素
超分子化学
高分子科学
纳米纤维素
制作
调制(音乐)
作者
Shi‐Peng Chen,Jing Wang,Dan‐Yang Zhao,Jin‐Long Zhu,Jia‐Cheng Lv,Gan‐Ji Zhong,Hua‐Dong Huang,Zhong‐Ming Li
标识
DOI:10.1002/adfm.202520770
摘要
Abstract Cellulose‐based bioplastic films have long been considered a promising alternative to unrecyclable plastics. However, the failure to harness their full potential of hydroxyl‐rich nature causes weakness and brittleness, restricting their successful applications. Inspired by natural bamboo, a supramolecular engineering strategy is proposed to modulate the self‐assembly kinetics of cellulose chains for simultaneously reinforcing and toughening cellulose films. A loosely‐structured amorphous molecular network is first constructed to enable dynamic rearrangement, and then the stretching field induce the formation of highly‐aligned nanofibers, resembling a natural snap‐fit self‐locking system. As a result, the highly‐aligned and tightly‐stacked nanofiber imparts transparent cellulose films with an increase of exceeding 300% in fracture toughness to 6.82 MJ·m −3 and an impressive tensile strength of 176 MPa, surpassing the most previously reported fully regenerated cellulose films. This pioneering approach of kinetic molecular modulation opens up a new perspective for high‐performance, transparent, and truly sustainable bioplastic films and beyond.
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