Abstract
Tandem carbon dioxide reduction reaction (CO 2 RR) to multicarbon products (CO 2 -CO-C 2+ ) such as ethylene represents a pivotal strategy for carbon valorization. However, conventional alkaline or neutral tandem systems limit the carbon dioxide utilization and stability due to severe (bi)carbonate formation. Here, we design a durable acidic-alkaline tandem system to efficiently synthesize C 2+ products, especially ethylene. In the acidic CO 2 RR step, a catalyst with precisely controlled metal site distance was used to regulate *COOH adsorption. Typically, a 99.7 ± 0.4% carbon monoxide Faradaic efficiency (FE) at 1.4 amperes per square centimeter can be achieved using a catalyst with 0.5-nanometer nickel sites, surpassing the previously reported metal catalysts. When this catalyst was integrated into the acidic-alkaline tandem system and coupled with the alkaline carbon monoxide electroreduction, the ethylene and C 2+ FE reached 75.3 ± 1.2 and 92.5 ± 1.3% at 10 amperes, respectively, and remained stable for 400 hours. Our work provides solutions for the durable conversion of carbon dioxide to C 2+ products from catalyst and electrolyzer design.
Funding Information
  • National Natural Science Foundation of China (224B2510)
  • National Natural Science Foundation of China (22422506; 22201271; 22221003; 22425302)
  • Natural Science Foundation of Anhui Province (2208085UD04)
  • China Ministry of Science and Technology (2021YFA1500404)
  • Major Frontier Research Project of the University of Science and Technology of China (LS2060000002)
  • Major Frontier Research Project of the University of Science and Technology of China (LS2060000002)
  • National Natural Science Foundation of China (U23A2081)
  • Anhui Provincial Key Research and Development Project (2023z04020010)
  • Natural Science Foundation of Anhui Province (2108085UD06)
  • China Ministry of Science and Technology (2021YFA1501003)
  • USTC Research Funds of the Double First-Class Initiative (YD2060006005)

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