Cascade Dual Sites Modulate Local CO Coverage and Hydrogen-Binding Strength to Boost CO 2 Electroreduction to Ethylene
Tianjin University · Southeast University · +8 more institutions
Abstract
Rationally modulating the binding strength of reaction intermediates on surface sites of copper-based catalysts could facilitate C–C coupling to generate multicarbon products in an electrochemical CO2 reduction reaction. Herein, theoretical calculations reveal that cascade Ag–Cu dual sites could synergistically increase local CO coverage and lower the kinetic barrier for CO protonation, leading to enhanced asymmetric C–C coupling to generate C2H4. As a proof of concept, the Cu3N-Ag nanocubes (NCs) with Ag located in partial Cu sites and a Cu3N unit center are successfully synthesized. The Faraday efficiency and partial current density of C2H4 over Cu3N-Ag NCs are 7.8 and 9.0 times those of Cu3N NCs,…
Citation impact
- FWCI
- 16.41
- Percentile
- 100%
- References
- 42
Authors
16Topics & keywords
- Chemistry
- Catalysis
- Cascade
- Electrochemistry
- Protonation
- Selectivity
- Hydrogen
- Copper
Funding
- NRNational Research Foundation SingaporeAwards: LCERFI01-0017, NRF-NRFF11-2019-0002
- NNNational Natural Science Foundation of ChinaAwards: 22325101, 22375142, 22071172
- TUTianjin UniversityAward: B2-2022-002
- BRBasic Research Program of Jiangsu ProvinceAward: BK20220800
- FRFundamental Research Funds for the Central UniversitiesAward: 3207022307A2