位阻效应
自愈水凝胶
量子纠缠
材料科学
化学物理
物理
凝聚态物理
纳米技术
化学
聚合物
光电子学
作者
Zimo Pang,Sijia Li,Muqing Si,Yujie Chen,Ping He,Chuan Wei Zhang,Chengzhen Du,Xiujun Han,Mingzhi Wei,Ximin He,Hezhou Liu
标识
DOI:10.1038/s41467-026-73850-2
摘要
Damping hydrogels play a crucial role in dissipating vibrational and impact energy, thereby ensuring material durability. However, the increasingly diverse and complex application scenarios impose different requirements on damping hydrogels, and it remains a challenge to develop hydrogels that exhibit excellent multidimensional damping performance along with robust mechanical properties. Here, we propose a friction-amplification strategy based on synergistic entanglement domains and steric hindrance, which simultaneously increases the frictional resistance to chain sliding, expands the frictional interfaces, and enhances chains interactions. In this design, the entanglement domains act as amplifiers that significantly elevate the energy barriers for chain sliding imposed by steric hindrance. This approach differs from conventional methods that rely solely on increasing the density of binary entanglement points, which offer limited energy dissipation performance. This strategy achieves an order-of-magnitude enhancement in damping capacity (610-fold increase) of hydrogels while maintaining high damping efficiency (96.3%) and considerable loss factor. We further demonstrate that it substantially improves the mechanical properties of hydrogels, exhibits broad universality, and shows promise for impact protection and vibration suppression. Damping hydrogels have potential in protection from impact and vibration, but combining this performance with desirable mechanical properties is challenging. Here, the authors report the development of hydrogels with entangled domains for resistance to chain sliding, giving favourable performance.
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