High-Rate CO2 Electroreduction to C2+ Products over a Copper-Copper Iodide Catalyst.
Hefei LiTianfu LiuPengfei WeiLong LinDunfeng GaoGuoxiong WangXinhe BaoPublished in: Angewandte Chemie (International ed. in English) (2021)
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.
Keyphrases
- metal organic framework
- aqueous solution
- ionic liquid
- room temperature
- reduced graphene oxide
- stem cells
- carbon dioxide
- magnetic resonance imaging
- visible light
- cell therapy
- computed tomography
- single cell
- bone marrow
- high resolution
- mesenchymal stem cells
- oxide nanoparticles
- genetic diversity
- tandem mass spectrometry