On-surface synthesis of covalent coordination polymers on micrometer scale

被引:21
|
作者
Koudia, Mathieu [1 ]
Nardi, Elena [1 ]
Siri, Olivier [2 ]
Abel, Mathieu [1 ]
机构
[1] Aix Marseille Univ, CNRS, UMR 7334, IM2NP, F-13397 Marseille, France
[2] Aix Marseille Univ, CNRS, UMR 7325, CINaM, F-13288 Marseille, France
关键词
on-surface synthesis; scanning tunneling microscopy (STM); two-dimensional polymer; covalent organic frameworks; META-QUINONOID MOLECULES; ELECTRONIC-STRUCTURE; BOND FORMATION; ZWITTERION; CHEMISTRY; NETWORKS; REACTIVITY; PHTHALOCYANINE; COMPLEXES; DIPOLE;
D O I
10.1007/s12274-016-1352-y
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
On-surface synthesis under ultrahigh vacuum provides a promising strategy to control matter at the atomic level, with important implications for the design of new two-dimensional materials having remarkable electronic, magnetic, or catalytic properties. This strategy must address the problem of limited extension of the domains due to the irreversible nature of covalent bonds, which prevents the ripening of defects. We show here that extended materials can be produced by a controlled co-deposition process. In particular, co-deposition of quinoid zwitterion molecules with iron atoms on a Ag(111) surface held at 570 K allows the formation of micrometer-sized domains based on covalent coordination bonds. This work opens up the construction of micrometer-scale single-layer covalent coordination materials under vacuum conditions.
引用
收藏
页码:933 / 940
页数:8
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