Volume 56, Issue 43 pp. 13406-13410
Communication

Selective C−H Bond Cleavage in Methane by Small Gold Clusters

Dr. Sandra M. Lang

Corresponding Author

Dr. Sandra M. Lang

Institute of Surface Chemistry and Catalysis, University of Ulm, Albert-Einstein-Allee 47, 89069 Ulm, Germany

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Prof. Dr. Thorsten M. Bernhardt

Prof. Dr. Thorsten M. Bernhardt

Institute of Surface Chemistry and Catalysis, University of Ulm, Albert-Einstein-Allee 47, 89069 Ulm, Germany

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Valeriy Chernyy

Valeriy Chernyy

Institute for Molecules and Materials, FELIX Laboratory, Radboud University, 6525 ED, Nijmegen, The Netherlands

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Dr. Joost M. Bakker

Dr. Joost M. Bakker

Institute for Molecules and Materials, FELIX Laboratory, Radboud University, 6525 ED, Nijmegen, The Netherlands

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Dr. Robert N. Barnett

Dr. Robert N. Barnett

School of Physics, Georgia Institute of Technology, Atlanta, GA, 30332-0430 USA

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Prof. Dr. Uzi Landman

Corresponding Author

Prof. Dr. Uzi Landman

School of Physics, Georgia Institute of Technology, Atlanta, GA, 30332-0430 USA

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First published: 04 September 2017
Citations: 82

Graphical Abstract

Selection by gold: Vibrational spectroscopy in conjunction with first-principle calculations demonstrate that small gold clusters can mediate the selective dissociation of one of the four C−H bonds of methane, which thus represents the first step towards its conversion into higher-quality chemicals. The distinct selectivity of these gold clusters originates from their finely balanced electronic structure. Au yellow, C gray, H white.

Abstract

Methane represents the major constituent of natural gas. It is primarily used only as a source of energy by means of combustion, but could also serve as an abundant hydrocarbon feedstock for high quality chemicals. One of the major challenges in catalysis research nowadays is therefore the development of materials that selectively cleave one of the four C−H bonds of methane and thus make it amenable for further chemical conversion into valuable compounds. By employing infrared spectroscopy and first-principles calculations it is uncovered herein that the interaction of methane with small gold cluster cations leads to selective C−H bond dissociation and the formation of hydrido methyl complexes, H-Aux+-CH3. The distinctive selectivity offered by these gold clusters originates from a fine interplay between the closed-shell nature of the d states and relativistic effects in gold. Such fine balance in fundamental interactions could prove to be a tunable feature in the rational design of a catalyst.

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