| Literature DB >> 33837619 |
Hefei Li1,2, Tianfu Liu1, Pengfei Wei1,2, Long Lin1,2, Dunfeng Gao1, Guoxiong Wang1, Xinhe Bao1.
Abstract
Electrochemical CO2 reduction reaction (CO2 RR) to multicarbon hydrocarbon and oxygenate (C2+ ) products with high energy density and wide availability is of great importance, as it provides a promising way to achieve the renewable energy storage and close the carbon cycle. Herein we design a Cu-CuI composite catalyst with abundant Cu0 /Cu+ interfaces by physically mixing Cu nanoparticles and CuI powders. The composite catalyst achieves a remarkable C2+ partial current density of 591 mA cm-2 at -1.0 V vs. reversible hydrogen electrode in a flow cell, substantially higher than Cu (329 mA cm-2 ) and CuI (96 mA cm-2 ) counterparts. Induced by alkaline electrolyte and applied potential, the Cu-CuI composite catalyst undergoes significant reconstruction under CO2 RR conditions. The high-rate C2+ production over Cu-CuI is ascribed to the presence of residual Cu+ and adsorbed iodine species which improve CO adsorption and facilitate C-C coupling.Entities:
Keywords: CO2 electroreduction; Cu-CuI composite catalysts; adsorbed iodine; multicarbon products
Year: 2021 PMID: 33837619 DOI: 10.1002/anie.202102657
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336