{"title":"Strong and Ultra-Tough Hydrogel with Hierarchical Cross-Linking Network Architecture Constructed by a Hyperbranched Topological Structure","authors":"Ying Zhu, Hanjing Zhang, Qinwen Tan, Yangfei Wu, Mengting Du, Nikos Hadjichristidis, Yu Jiang, Daohong Zhang","doi":"10.1021/acs.macromol.5c00513","DOIUrl":null,"url":null,"abstract":"Natural biological tissues such as jellyfish integrate hierarchical architectures with multifunctionality (e.g., bioluminescence, mechanical resilience, and responsiveness), yet replicating such synergy in synthetic hydrogels remains a significant challenge. Here, we present a bioinspired hydrogel engineer that employs a hyperbranched macro-cross-linker as a topological regulator to precisely manipulate the hierarchical cross-linking network architecture. Compared to the linear macro-cross-linker, the introduction of a hyperbranched topological structure has endowed the hydrogel with excellent mechanical properties. By systematically tuning branching parameters (DB and <i>S</i><sub>n</sub>), we further achieve simultaneous modulation of both the microphase separation morphology and multistage cross-linking networks. With moderate DB and <i>S</i><sub>n</sub>, the hydrogel exhibits an optimal hierarchical structure and the most uniform microphase separation, achieving the integration of excellent mechanical performance, remarkable unconventional fluorescence emission, and notable conductivity. Furthermore, the hydrogel demonstrates highly sensitive dual optical–electrical responsive behaviors when used as a strain sensor. This strategy provides a universal platform for designing hierarchical hydrogels with programmable functionality, offering promising material for advanced applications in bioelectronics and soft robotics.","PeriodicalId":51,"journal":{"name":"Macromolecules","volume":"45 1","pages":""},"PeriodicalIF":5.1000,"publicationDate":"2025-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Macromolecules","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.macromol.5c00513","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
Natural biological tissues such as jellyfish integrate hierarchical architectures with multifunctionality (e.g., bioluminescence, mechanical resilience, and responsiveness), yet replicating such synergy in synthetic hydrogels remains a significant challenge. Here, we present a bioinspired hydrogel engineer that employs a hyperbranched macro-cross-linker as a topological regulator to precisely manipulate the hierarchical cross-linking network architecture. Compared to the linear macro-cross-linker, the introduction of a hyperbranched topological structure has endowed the hydrogel with excellent mechanical properties. By systematically tuning branching parameters (DB and Sn), we further achieve simultaneous modulation of both the microphase separation morphology and multistage cross-linking networks. With moderate DB and Sn, the hydrogel exhibits an optimal hierarchical structure and the most uniform microphase separation, achieving the integration of excellent mechanical performance, remarkable unconventional fluorescence emission, and notable conductivity. Furthermore, the hydrogel demonstrates highly sensitive dual optical–electrical responsive behaviors when used as a strain sensor. This strategy provides a universal platform for designing hierarchical hydrogels with programmable functionality, offering promising material for advanced applications in bioelectronics and soft robotics.
期刊介绍:
Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.