超分子化学
结晶度
单层
分子间力
共价键
剥脱关节
材料科学
结晶学
离子键合
纳米技术
化学
分子
化学物理
晶体结构
石墨烯
有机化学
离子
作者
Jinqiao Dong,Lingmei Liu,Chunxia Tan,Qisong Xu,Jiachen Zhang,Zhiwei Qiao,Dandan Chu,Yan Liu,Qun Zhang,Jianwen Jiang,Yu Han,Anthony P. Davis,Yong Cui
出处
期刊:Nature
[Springer Nature]
日期:2022-02-23
卷期号:602 (7898): 606-611
被引量:87
标识
DOI:10.1038/s41586-022-04407-8
摘要
Two-dimensional materials with monolayer thickness and extreme aspect ratios are sought for their high surface areas and unusual physicochemical properties1. Liquid exfoliation is a straightforward and scalable means of accessing such materials2, but has been restricted to sheets maintained by strong covalent, coordination or ionic interactions3-10. The exfoliation of molecular crystals, in which repeat units are held together by weak non-covalent bonding, could generate a greatly expanded range of two-dimensional crystalline materials with diverse surfaces and structural features. However, at first sight, these weak forces would seem incapable of supporting such intrinsically fragile morphologies. Against this expectation, we show here that crystals composed of discrete supramolecular coordination complexes can be exfoliated by sonication to give free-standing monolayers approximately 2.3 nanometres thick with aspect ratios up to approximately 2,500:1, sustained purely by apolar intermolecular interactions. These nanosheets are characterized by atomic force microscopy and high-resolution transmission electron microscopy, confirming their crystallinity. The monolayers possess complex chiral surfaces derived partly from individual supramolecular coordination complex components but also from interactions with neighbours. In this respect, they represent a distinct type of material in which molecular components are all equally exposed to their environment, as if in solution, yet with properties arising from cooperation between molecules, because of crystallinity. This unusual nature is reflected in the molecular recognition properties of the materials, which bind carbohydrates with strongly enhanced enantiodiscrimination relative to individual molecules or bulk three-dimensional crystals.
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