4.6 Article

Atomic-thin hexagonal CuCo nanocrystals with d-band tuning for CO2 reduction

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 9, Issue 12, Pages 7496-7502

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0ta12022g

Keywords

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Funding

  1. Fundamental Research Funds for the Central Universities
  2. Natural Science Foundation of China [62005216]
  3. University Science and Technology Association Talent Promotion Program of Shaanxi [20200102]
  4. AcRF Tier 1 grant by Ministry of Education in Singapore [RG105/19]

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The study focuses on using ultrathin CuCo nanocrystals for CO2 reduction to ethylene, achieving a high faradaic efficiency. By tailoring the d-band states and synergistic cooperation between Cu and Co, the activity can be boosted while lowering energy barriers for the reaction.
Regenerative energy replacing CO2-releasing fossil fuels has drawn widespread attention in wind/solar energy storage and conversion. In particular, CO2 reduction to valuable chemicals using renewable energy is attractive and alleviates global warming. Cu is prominent for CO2 reduction to derive multi-carbon products, such as ethylene. However, the productivity, energy efficiency, and cost-effectiveness of Cu-based electrocatalysts remain unsatisfactory in meeting industrial requirements. Hence, ultrathin CuCo nanocrystals are exploited for CO2 reduction to ethylene, delivering a high faradaic efficiency of 81.3% at a potential of -1.5 V vs. reversible hydrogen electrode (RHE). Tailoring the d-band states and synergistic cooperation between Cu and Co are significant to boost activity via controlling the intermediate binding energy and lowering the reaction energy barriers.

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