Abstract
The catalytic conversion of methane under mild conditions is an appealing approach to selectively produce value-added products from natural gas. Catalysts which can chemisorb methane can potentially overcome challenges associated with its high stability and achieve facile activation. Although transition metals can activate C-H bonds, chemisorption and lowerature conversion remain elusive on these surfaces. The broad electronic bands of metals can only weakly interact with the methane orbitals, in contrast to specific transition metal oxide and supported metal cluster surfaces which are now recognized to form methane σ-complexes. Here, we report methane chemisorption can, remarkably, occur on metal surfaces via electronic band contraction and localization from metal alloying. From a broad screening including single atom and intermetallic alloys in various substrates, we find early transition metals as promising metal solutes for methane chemisorption and lowerature activation. These findings demonstrate a combinatorial diversity of possible candidates in earth abundant metal alloys with this attractive catalytic behavior.
Original language | English |
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Pages (from-to) | 6057-6066 |
Number of pages | 10 |
Journal | Journal of Materials Chemistry A |
Volume | 8 |
Issue number | 12 |
DOIs | |
State | Published - Mar 28 2020 |
Funding
This work was supported by the Center for Understanding and Control of Acid Gas-Induced Evolution of Materials for Energy (UNCAGE-ME), an Energy Frontier Research Center funded by U.S. Department of Energy (US DoE), Office of Science, Basic Energy Sciences (BES), under Award DE-SC0012577. This work was performed at the Center for Nanophase Materials Sciences, a US Department of Energy Office of Science User Facility. VF was also supported by a Eugene P. Wigner Fellowship at Oak Ridge National Laboratory. This research used resources of the National Energy Research Scientic Computing Center, supported by the Office of Science of the U.S. Department of Energy under Contract No. DE-AC02-05CH11231.