| Literature DB >> 28092430 |
Guoxi Xu1, Zihan Huang1, Pengyu Chen1, Tianqi Cui1, Xinghua Zhang2, Bing Miao3, Li-Tang Yan1.
Abstract
Structurally dynamic polymers are recognized as a key potential to revolutionize technologies ranging from design of self-healing materials to numerous biomedical applications. Despite intense research in this area, optimizing reactivity and thereby improving self-healing ability at the most fundamental level pose urgent issue for wider applications of such emerging materials. Here, the authors report the first mechanistic investigation of the fundamental principle for the dependence of reactivity and self-healing capabilities on the properties inherent to dynamic polymers by combining large-scale computer simulation, theoretical analysis, and experimental discussion. The results allow to reveal how chain stiffness and spatial organization regulate reactivity of dynamic polymers grafted on Janus nanoparticles and mechanically mediated reaction in their reverse chemistry, and, particularly, identify that semiflexible dynamic polymers possess the optimal reactivity and self-healing ability. The authors also develop an analytical model of blob theory of polymer chains to complement the simulation results and reveal essential scaling laws for optimal reactivity. The findings offer new insights into the physical mechanism in various systems involving reverse/dynamic chemistry. These studies highlight molecular engineering of polymer architecture and intrinsic property as a versatile strategy in control over the structural responses and functionalities of emerging materials with optimized self-healing capabilities.Entities:
Keywords: dynamic bond; self-healing ability; structurally dynamic polymers; supracolloidal reaction; theory and simulation
Year: 2017 PMID: 28092430 DOI: 10.1002/smll.201603155
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281