Simultaneous Stabilization of Copper Species and Regulation of the Cu+/Cu0 Balance on SiO2 for Selective Ethanol Dehydrogenation
Abstract Selective ethanol dehydrogenation is a promising route for acetaldehyde production; however, achieving stable copper catalysts on inert supports with a well-balanced Cu+/Cu0 ratio remains challenging. Herein, we report a urea-assisted strategy to simultaneously stabilize copper species and regulate the Cu+/Cu0 balance on a silica support. The gradual release of ammonia promotes the formation of interfacial Cu–O–Si linkages and basic copper nitrate species, which serve as precursors for Cu+ and Cu0, respectively. The resulting catalyst exhibits highly dispersed copper species with a balanced Cu+/Cu0 distribution, delivering high activity, >95% acetaldehyde selectivity, and stable performance in ethanol dehydrogenation. Mechanistic studies reveal that Cu+ sites facilitate ethanol activation, while Cu0 sites promote C–H bond cleavage. However, excessive Cu+ species lead to the formation of strongly adsorbed enolic intermediates, which trigger C–C coupling and byproduct formation. This work highlights the importance of Cu+/Cu0 synergy and provides a general strategy for designing stable and selective copper-based catalysts on inert supports.
Authors
- Marc Heggen (ORCID: https://orcid.org/0000-0002-2646-0078)
- Feng Wang (ORCID: https://orcid.org/0000-0002-9167-8743)
- Yinpan Zhang
- Rafal E. Dunin–Borkowski (ORCID: https://orcid.org/0000-0001-8082-0647)
- Pengfei Cao (ORCID: https://orcid.org/0000-0002-8360-4541)
- Qiang Guo (ORCID: https://orcid.org/0009-0000-6141-466X)
- Jian Zhang
- Jincong Wang
Institutions
- University of Science and Technology of China (CN)
- Forschungszentrum Jülich (DE)
- Dalian Institute of Chemical Physics (CN)
- Chinese Academy of Sciences (CN)
- Dalian University of Technology (CN)
- University of Chinese Academy of Sciences (CN)
- Southwest Jiaotong University (CN)
Publication Details
- Journal
- ACS Catalysis
- Published
- 2026-10-28
- DOI
- https://doi.org/10.1021/acscatal.6c06988
- Primary Topic
- Catalytic Processes in Materials Science
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China
- National Key Research and Development Program of China