材料科学
自愈水凝胶
可重构性
解耦(概率)
超分子化学
稳健性(进化)
结合属性
消散
纳米技术
生物系统
化学物理
流变学
应力松弛
热稳定性
联想代换
离解(化学)
分子动力学
软机器人
软物质
放松(心理学)
热的
计算机科学
催化作用
平版印刷术
拓扑(电路)
智能材料
化学工程
复杂系统
材料设计
作者
Pierre Le Bourdonnec,Charafeddine Ferkous,Léo Comunale,Luca Cipelletti,Rémi Merindol
标识
DOI:10.1002/adma.202516741
摘要
The design of hydrogels that combine mechanical robustness with dynamic reconfigurability remains a fundamental challenge, as increasing crosslink dissociation rates compromise network integrity. This limitation is addressed through the incorporation of an associative crosslink exchange into DNA-based supramolecular hydrogels, enabling the decoupling of network relaxation behavior from crosslink stability. The hydrogels are constructed from enzyme-synthesized single-stranded DNA that self-assembles via hybridization between complementary domains. These crosslinks can reorganize through dissociative melting or associative strand displacement reaction, yielding networks with tunable relaxation timescales spanning over three orders of magnitude. Rheological measurements and thermodynamic modeling confirm that associative exchange facilitates efficient stress dissipation without diminishing rupture strength or thermal stability. In contrast, dissociative systems inherently trade increased dynamics with mechanical weakening. This decoupling is achieved through the implementation of a catalytic reorganization pathway governed by the composition of the sample, independently of the crosslink strength. These findings establish the mechanism of reorganization as a key design parameter for engineering adaptive soft materials that combine resilience and responsiveness.
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