Bottom-Up Synthesis of Metalated Carbyne

被引:109
|
作者
Sun, Qiang [1 ]
Cai, Liangliang [1 ]
Wang, Shiyong [2 ]
Widmer, Roland [2 ]
Ju, Huanxin [3 ]
Zhu, Junfa [3 ]
Li, Lei [4 ]
He, Yunbin [4 ]
Ruffieux, Pascal [2 ]
Fasel, Roman [2 ,5 ]
Xu, Wei [1 ]
机构
[1] Tongji Univ, Coll Mat Sci & Engn, Tongji Aarhus Joint Res Ctr Nanostruct & Funct Na, Caoan Rd 4800, Shanghai 201804, Peoples R China
[2] Empa Swiss Fed Labs Mat Sci & Technol, CH-8600 Dubendorf, Switzerland
[3] Univ Sci & Technol China, Natl Synchrotron Radiat Lab, Hefei 230029, Peoples R China
[4] Hubei Univ, Fac Mat Sci & Engn, Key Lab Green Preparat & Applicat Funct Mat, Minist Educ, Wuhan 430062, Peoples R China
[5] Univ Bern, Dept Chem & Biochem, CH-3012 Bern, Switzerland
基金
瑞士国家科学基金会; 中国国家自然科学基金;
关键词
ORGANOMETALLIC INTERMEDIATE; TERMINAL ALKYNES; GRAPHENE FILMS; SURFACE; COVALENT; CYCLODEHYDROGENATION; SUPERCONDUCTIVITY; POLYYNES; CU(110); MODEL;
D O I
10.1021/jacs.5b10725
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Because of stability issues, carbyne, a one-dimensional chain of carbon atoms, has been much less investigated than other recent carbon allotropes such as graphene. Beyond that, metalation of such a linear carbon nanostructure with regularly distributed metal atoms is even more challenging. Here we report a successful on surface synthesis of metalated carbyne chains by dehydrogenative coupling of ethyne molecules and copper atoms on a Cu(110) surface under ultrahigh-vacuum conditions. The length of the fabricated metalated carbyne chains was found to extend to the submicron scale (with the longest ones up to similar to 120 nm). We expect that the herein-developed on-surface synthesis strategy for the efficient synthesis of organometallic carbon-based nano structures will inspire more extensive experimental investigations of their physicochemical properties and explorations of their potential with respect to technological applications.
引用
收藏
页码:1106 / 1109
页数:4
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