Suppr超能文献

基于可控自聚集的支化低聚物基可逆粘合剂

Branched Oligomer-Based Reversible Adhesives Enabled by Controllable Self-Aggregation.

作者信息

Qin Chenxi, Yang Hao, Li Bin, Xing Zhencai, Yu Bo, Cai Meirong, Pei Xiaowei, Ma Yanfei, Zhou Feng, Liu Weimin

机构信息

State Key Laboratory of Solid Lubrication, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou, 730000, China.

Center of Materials Science and Optoelectronics Engineering, University of Chinese Academy of Sciences, Beijing, 100049, China.

出版信息

Adv Mater. 2024 Sep;36(39):e2408330. doi: 10.1002/adma.202408330. Epub 2024 Aug 3.

Abstract

Supramolecular adhesion material systems based on small molecules have shown great potential to unite the great contradiction between strong adhesion and reversibility. However, these material systems suffer from low adhesion strength/narrow adhesion span, limited designability, and single interaction due to fewer covalent bond content and action sites in small molecules. Herein, an ultrahigh-strength and large-span reversible adhesive enabled by a branched oligomer controllable self-aggregation strategy is developed. The dense covalent bonds present in the branched oligomers greatly enhance adhesion strength without compromising reversibility. The resulting adhesive exhibits a large-span reversible adhesion of ≈140 times, switching between ultra-strong and tough adhesion strength (5.58 MPa and 5093.92 N m) and ultralow adhesion (0.04 MPa and 87.656 N m) with alternating temperature. Moreover, reversible dynamic double cross-linking endows the adhesive with stable reversible adhesion transitions even after 100 cycles. This reversible adhesion property can also be remotely controlled via a voltage of 8 V, with a loading voltage duration of 45 s. This work paves the way for the design of reversible adhesives with long-span outstanding properties using covalent polymers and offers a pathway for the rational design of high-performance adhesives featuring both robust toughness and exceptional reversibility.

摘要

基于小分子的超分子粘附材料体系已显示出巨大潜力,有望化解强粘附性与可逆性之间的巨大矛盾。然而,由于小分子中较少的共价键含量和作用位点,这些材料体系存在粘附强度低/粘附跨度窄、可设计性有限以及相互作用单一的问题。在此,通过支化低聚物可控自聚集策略开发了一种具有超高强度和大跨度可逆性的粘合剂。支化低聚物中存在的密集共价键在不影响可逆性的情况下极大地提高了粘附强度。所得粘合剂表现出约140倍的大跨度可逆粘附性,随着温度交替在超强和坚韧的粘附强度(5.58兆帕和5093.92牛米)与超低粘附性(0.04兆帕和87.656牛米)之间切换。此外,可逆动态双交联赋予粘合剂即使在100次循环后仍具有稳定的可逆粘附转变。这种可逆粘附特性还可以通过8伏电压进行远程控制,加载电压持续时间为45秒。这项工作为使用共价聚合物设计具有大跨度优异性能的可逆粘合剂铺平了道路,并为合理设计兼具强大韧性和卓越可逆性的高性能粘合剂提供了一条途径。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验