Test environment running 7.6.6

Cultural advice

The Australian National University acknowledges, celebrates and pays our respects to the Ngunnawal and Ngambri people of the Canberra region and to all First Nations Australians on whose traditional lands we meet and work, and whose cultures are among the oldest continuing cultures in human history.

Aboriginal and Torres Strait Islander peoples are advised that ANU Library collections may include images, names, voices, and other representations of deceased persons.

Material in the collection may contain terms, language or views that reflect the period in which the item was created and may be considered inappropriate today.

Nitrogen cold plasma treatment stabilizes Cu0/Cu+ electrocatalysts to enhance CO2 to C2 conversion

Abstract

Cu-based materials are ideal catalysts for CO2 electrocatalytic reduction reaction (CO2RR) into multi-carbon products. However, such reactions require stringent conditions on local environments of catalyst surfaces, which currently are the global pressing challenges. Here, a stabilized activation of Cu0/Cu+-on-Ag interface by N2 cold plasma treatment was developed for improving Faradaic efficiency (FE) of CO2RR into C2 products. The resultant Ag@Cu-CuNx exhibits a C2 FE of 72% with a partial current density of −14.9 mA cm−2 at −1.0 V vs. RHE (reversible hydrogen electrode). Combining density functional theory (DFT) and experimental investigations, we unveiled that Cu0/Cu+ species can be controllably tuned by the incorporation of nitrogen to form CuNx on Ag surface, i.e., Ag@Cu-CuNx. This strategy enhances *CO intermediates generation and accelerates C–C coupling both thermodynamically and kinetically. The intermediates O*C*CO, *COOH, and *CO were detected by in-situ attenuated total internal reflection surface enhanced infrared absorption spectroscopy (ATR-SEIRAS). The uncovered CO2RR-into-C2 products were carried out along CO2→ *COOH → *CO → O*C*CO → *C2H3O → *C2H4O → C2H5OH (or *C2H3O → *O + C2H4) paths over Ag@Cu-CuNx electrocatalyst. This work provides a new approach to design Cu-based electrocatalysts with high-efficiency, mild condition, and stable CO2RR to C2 products.

Description

Citation

Source

Journal of Energy Chemistry

Book Title

Entity type

Access Statement

License Rights

Restricted until