Operando TEM study of a working copper catalyst during ethylene oxidation

Yu, Wenqian; Yue, Shengnan; Yang, Minghe; Hashimoto, Masahiro; Liu, Panpan; Zhu, Li; Xie, Wangjing; Jones, Travis Elliott Loyd; Willinger, Marc; Huang, Xing

doi:10.1038/s41467-025-57418-0

Title: Operando TEM study of a working copper catalyst during ethylene oxidation

Journal Article · 26 February 2025 · Nature Communications

DOI: https://doi.org/10.1038/s41467-025-57418-0 · OSTI ID:2530358

Yu, Wenqian ^[1];

^[1]; Yang, Minghe ^[1]; Hashimoto, Masahiro ^[2]; Liu, Panpan ^[1]; Zhu, Li ^[1]; Xie, Wangjing ^[1];

^[3];

^[4];

^[5]

Fuzhou Univ. (China); Qingyuan Innovation Laboratory (China)
JEOL (EUROPE) SAS (France)
Los Alamos National Laboratory (LANL), Los Alamos, NM (United States)
Technical Univ. of Munich (Germany); Eidgenoessische Technische Hochschule (ETH), Zurich (Switzerland)
Fuzhou Univ. (China); Qingyuan Innovation Laboratory (China); Eidgenoessische Technische Hochschule (ETH), Zurich (Switzerland)

Active catalysts are typically metastable, and their surface state depends on the gas-phase chemical potential and reaction kinetics. To gain relevant insights into structure-performance relationships, it is essential to investigate catalysts under their operational conditions. Here, we use operando TEM combining real-time observations with online mass spectrometry (MS) to study a Cu catalyst during ethylene oxidation. We identify three distinct regimes characterized by varying structures and states that show different selectivities with temperature, and elucidate the reaction pathways with the aid of theoretical calculations. Our findings reveal that quasi-static Cu₂O at low temperatures is selective towards ethylene oxide (EO) and acetaldehyde (AcH) via an oxometallacycle (OMC) pathway. In the dynamic Cu⁰/Cu₂O oscillation regime at medium temperatures, partially reduced and strained oxides decrease the activation energies associated with partial oxidation. At high temperatures, the catalyst is predominantly Cu⁰, partially covered by a monolayer Cu₂O. While Cu⁰ is extremely efficient in dehydrogenation and eventual combustion, the monolayer oxide favors direct EO formation. These results challenge conclusions drawn from ultra-high vacuum studies that suggested metallic copper would be a selective epoxidation catalyst and highlight the need for operando study under realistic conditions.

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Research Organization:: Los Alamos National Laboratory (LANL), Los Alamos, NM (United States)

Sponsoring Organization:: USDOE

Grant/Contract Number:: 89233218CNA000001

OSTI ID:: 2530358

Report Number(s):: LA-UR--24-32577

Journal Information:: Nature Communications, Journal Name: Nature Communications Journal Issue: 1 Vol. 16; ISSN 2041-1723

Publisher:: Nature Publishing GroupCopyright Statement

Country of Publication:: United States

Language:: English

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37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
catalytic mechanisms
heterogeneous catalysis
transmission electron microscopy

Title: Operando TEM study of a working copper catalyst during ethylene oxidation

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