摘要
The on-surface self-assembly of inorganic atomic clusters and organic molecules offers significant opportunities to design novel hybrid materials with tailored functionalities.By adopting the advantages from both inorganic and organic components,the hybrid self-assembly molecules have shown great potential in future optoelectrical devices.Herein,we report the co-deposition of 4,8-diethynylbenzo[1,2-d-4,5-d0]bisoxazole(DEBBA)and Se atoms to produce a motif-adjustable organic–inorganic hybrid self-assembly system via the non-covalent interactions.By controlling the coverage of Se atoms,various chiral molecular networks containing Se,Se_(6),Se_(8),and terminal alkynes evolved on the Ag(111)surface.In particular,with the highest coverage of Se atoms,phase segregation into alternating one-dimensional chains of non-covalently bonded Se_(8) clusters and organic ligands has been noticed.The atom-coverage dependent evolution of self-assembly structures reflects the remarkable structural adaptability of Se clusters as building blocks based on the spontaneous resize to reach the maximum non-covalent interactions.This work has significantly extended the possibilities of flexible control in self-assembly nanostructures to enable more potential functions for broad applications.
基金
the Guangdong Basic and Applied Basic Research Foundation(Nos.2019A1515110819 and 2020A1515010767)
NRF-CRP grant“Two Dimensional Covalent Organic Framework:Synthesis and Applications”(No.NRF-CRP16-2015-02,funded by National Research Foundation,Prime Minister’s Office,Singapore)
the Shenzhen Peacock Plan(No.KQTD2016053112042971)
the National Natural Science Foundation of China(Nos.21802067 and 21771156).
