纤维素
胶粘剂
微纤维
图层(电子)
化学
粘附
化学工程
多糖
粘接
材料科学
表面改性
纳米纤维素
原子力显微镜
工程木材
高分子化学
按需
组分(热力学)
能源需求
机制(生物学)
粘结强度
分子
作者
Yuan Sun,Liu Y,Long Bai,Shouxin Liu,Zhangmin Wan,Zhaolin Yang,Liwen Yu,Siqi Huan,Chengyu Wang,Zhiguo Li,Yi Lu,Orlando J Rojas
标识
DOI:10.1038/s41467-026-72609-z
摘要
Wood panels are extensively applied in furniture, construction fields, where their versatility and cost-effectiveness make them indispensable, but their assembly relies on adhesives that emit toxic formaldehyde, demand energy-intensive curing, and form weak interfacial bonds. Inspired by wood's self-repair via cellulose microfibril reorganization, we develop a cellulose-based homologous active adhesive (HAA) derived from wood components. HAA cures under ambient hydration, eliminating toxic emissions and reducing energy consumption by >80%. Its mechanism activates wood surface hydroxyl groups and regenerates cellulose to create a seamless transition layer that enhances load transfer and resistance. This architecture enables specific bonding strength up to 100× greater than conventional adhesives, despite ultra-low solid content (<5%). Using molecular dynamics simulations, AFM nanomechanics, spectroscopy, and life-cycle assessment, we reveal that HAA outperforms commercial resins, offering pot life >30 days, full biodegradability, and >70% lower environmental impacts. HAA establishes a biomimetic, circular pathway for sustainable, high-strength wood bonding.
科研通智能强力驱动
Strongly Powered by AbleSci AI