Volume 1, 2023

Ultra-high-rate CO2 reduction reactions to multicarbon products with a current density of 1.7 A cm−2 in neutral electrolytes

Abstract

CO2 electrolysis to value-added products is a promising technology to close the carbon cycle and sequester anthropogenic CO2 into chemical feedstocks; an increase of the current density for multicarbon products is one of the requirements for practical implementation. We have successfully increased the partial current density for gaseous CO2 reduction reactions to multicarbon products (C2+) over Cu nanoparticles on gas diffusion electrodes in neutral electrolytes to a record value of 1.7 A cm−2. The faradaic efficiency for multicarbon products increased with the current density below total current density of 2000 mA cm−2 and reached 76% at a total current density of 1600 mA cm−2. The turnover frequency for the production of C2+ per Cu atoms exceeded 1.1 s−1. Optimizing the standard components and their assembly as the cathode elicits the high-turnover frequency of oxide-derived Cu catalysts, resulting in the record partial current density for C2+. Especially, we demonstrated that the thickness of catalyst layers was one highly sensitive factor in determining the maximum current density for C2+.

Graphical abstract: Ultra-high-rate CO2 reduction reactions to multicarbon products with a current density of 1.7 A cm−2 in neutral electrolytes

Supplementary files

Article information

Article type
Communication
Submitted
01 Sep. 2022
Accepted
01 Nov. 2022
First published
03 Nov. 2022
This article is Open Access
Creative Commons BY-NC license

EES. Catal., 2023,1, 9-16

Ultra-high-rate CO2 reduction reactions to multicarbon products with a current density of 1.7 A cm−2 in neutral electrolytes

A. Inoue, T. Harada, S. Nakanishi and K. Kamiya, EES. Catal., 2023, 1, 9 DOI: 10.1039/D2EY00035K

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements