期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 138, 期 4, 页码 1106-1109出版社
AMER CHEMICAL SOC
DOI: 10.1021/jacs.5b10725
关键词
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资金
- National Natural Science Foundation of China [21473123, 21473178, 61274010]
- Research Fund for Doctoral Program of Higher Education of China [20120072110045]
- Swiss National Science Foundation (SNSF)
- Office of Naval Research BRC Program
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.
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