Insights into an autonomously formed oxygen-evacuated Cu2O electrode for the selective production of C2H4 from CO2. Issue 2 (9th October 2014)

• Record Type: Journal Article
• Authors: Kim, Dahee; Lee, Seunghwa; Ocon, Joey D.; Jeong, Beomgyun; Lee, Jae Kwang; Lee, Jaeyoung
• Is Part Of: Physical chemistry chemical physics. Volume 17:Issue 2(2015)
• Page Start: 824
• Page End: 830
• Publication Date: 2014-10-09
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c4cp03172e
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : In situ transformation of bulk Cu2 O to a Cu2 O-derived bulk structure with oxygen-vacant sites, with the oxide layer still on the surface, resulted in highly active, stable, and selective production of ethylene from carbon dioxide. Abstract : Electrochemical conversion of carbon dioxide (CO2 ) to small organic fuels ( e.g. formate, methanol, ethylene, ethanol) is touted as one of the most promising approaches for solving the problems of climate change and energy security. In this study, we report the highly efficient electrochemical reduction of CO2 using cuprous oxide (Cu2 O) electrodes to produce ethylene (C2 H4 ) primarily. During CO2 electrolysis using electrodeposited Cu2 O on a carbon electrode, we observe the transformation of a compact metal oxide layer to a metal oxide structure with oxygen vacant sites at the bulk region. In contrast to previous studies, our results clearly indicate that Cu2 O remains at the surface of the catalyst and it efficiently catalyzes the conversion process of CO2 at low overpotential, exhibiting a high selective faradaic efficiency of over 20% towards C2 H4 formation even in long-term electrolysis.