Strain Engineering of Cu<sub>2</sub>O@C<sub>2</sub>N for Enhanced Methane-to-Methanol Conversion
Inspired by the active site of methane monooxygenase, we designed a Cu<sub>2</sub>O cluster anchored in the six-membered nitrogen cavity of a C<sub>2</sub>N monolayer (Cu<sub>2</sub>O@C<sub>2</sub>N) as a stable and efficient enzyme-like catalyst. Dens...
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| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2025-07-01
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| Series: | Molecules |
| Subjects: | |
| Online Access: | https://www.mdpi.com/1420-3049/30/15/3073 |
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| Summary: | Inspired by the active site of methane monooxygenase, we designed a Cu<sub>2</sub>O cluster anchored in the six-membered nitrogen cavity of a C<sub>2</sub>N monolayer (Cu<sub>2</sub>O@C<sub>2</sub>N) as a stable and efficient enzyme-like catalyst. Density functional theory (DFT) calculations reveal that the bridged Cu-O-Cu structure within C<sub>2</sub>N exhibits strong electronic coupling, which is favorable for methanol formation. Two competing mechanisms—the concerted and radical-rebound pathways—were systematically investigated, with the former being energetically preferred due to lower energy barriers and more stable intermediate states. Furthermore, strain engineering was employed to tune the geometric and electronic structure of the Cu-O-Cu site. Biaxial strain modulates the Cu-O-Cu bond angle, adsorption properties, and d-band center alignment, thereby selectively enhancing the concerted pathway. A volcano-like trend was observed between the applied strain and the methanol formation barrier, with 1% tensile strain yielding the overall energy barrier to methanol formation (ΔG<sub>overall</sub>) as low as 1.31 eV. N<sub>2</sub>O effectively regenerated the active site and demonstrated strain-responsive kinetics. The electronic descriptor Δε (ε<sub>d</sub> − ε<sub>p</sub>) captured the structure–activity relationship, confirming the role of strain in regulating catalytic performance. This work highlights the synergy between geometric confinement and mechanical modulation, offering a rational design strategy for advanced C1 activation catalysts. |
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| ISSN: | 1420-3049 |