RESUMO
Electrochemical reduction of carbon dioxide into ethylene, as opposed to traditional industrial methods, represents a more environmentally friendly and promising technical approach. However, achieving high activity of ethylene remains a huge challenge due to the numerous possible reaction pathways. Here, we construct a hierarchical nanoelectrode composed of CuO treated with dodecanethiol to achieve elevated ethylene activity with a Faradaic efficiency reaching 79.5%. Through on in situ investigations, it is observed that dodecanethiol modification not only facilitates CO2 transfer and enhances *CO coverage on the catalyst surfaces, but also stabilizes Cu(100) facet. Density functional theory calculations of activation energy barriers of the asymmetrical C-C coupling between *CO and *CHO further support that the greatly increased selectivity of ethylene is attributed to the thiol-stabilized Cu(100). Our findings not only provide an effective strategy to design and construct Cu-based catalysts for highly selective CO2 to ethylene, but also offer deep insights into the mechanism of CO2 to ethylene.
RESUMO
The homogeneous distribution of carbon nanotubes (CNTs) in the Cu matrix and good interfacial bonding are the key factors to obtain excellent properties of carbon nanotube-reinforced Cu-based composites (CNT/Cu). In this work, silver-modified carbon nanotubes (Ag-CNTs) were prepared by a simple, efficient and reducer-free method (ultrasonic chemical synthesis), and Ag-CNTs-reinforced copper matrix composites (Ag-CNTs/Cu) were fabricated by powder metallurgy. The dispersion and interfacial bonding of CNTs were effectively improved by Ag modification. Compared to CNTs/Cu counterparts, the properties of Ag-CNTs/Cu samples were significantly improved, with the electrical conductivity of 94.9% IACS (International Annealed Copper Standard), thermal conductivity of 416 W/m·k and tensile strength (315 MPa). The strengthening mechanisms are also discussed.
