单层
双层
材料科学
聚合物
模数
分子
共价键
弹性模量
纳米技术
结晶学
联锁
自组装
复合材料
脂质双层力学
两亲性
表面力仪
脂质双层
嵌入
作者
Ye Yang,André Knapp,David Bodesheim,Alexander Croy,Mike Hambsch,Ilka Hermes,Chandrasekhar Naisa,Darius Pohl,Bernd Rellinghaus,Changsheng Zhao,Stefan C. B. Mannsfeld,Gianaurelio Cuniberti,Zhiyong Wang,Renhao Dong,Andreas Fery,Xinliang Feng
标识
DOI:10.1038/s44160-025-00930-4
摘要
Abstract Two-dimensional polymers (2DPs), comprising mono- or multilayer covalent polymeric networks with long-range order in two orthogonal directions, are of considerable interest due to their unique physicochemical properties. However, achieving precise thickness control from monolayer to bilayer, crucial for exploring proximity effect-driven phenomena beyond the monolayer limit, remains synthetically challenging. Here we report the on-water surface synthesis of crystalline mechanically interlocked monolayer and bilayer 2DP (MI-M2DP and MI-B2DP) films by embedding macrocyclic molecules with one and two cavities into 2DP backbones. The incorporation of bulky macrocyclic molecules introduces periodic mechanical bonds that precisely control interlayer interlocking, enabling selective monolayer or bilayer 2DP formation. Both MI-M2DP and MI-B2DP exhibit homogeneous, large-area films with ordered hexagonal pores and high modulus. MI-B2DP demonstrates an exceptionally high effective Young’s modulus of 151 ± 16 GPa (indentation method), surpassing MI-M2DP (90 ± 14 GPa), van der Waals-stacked MI-M2DPs (46 ± 11 GPa) and other reported multilayer 2DPs (<50 GPa). Modelling confirms that the mechanical interlocking minimizes interlayer sliding and reinforces the structure.
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