Issue 37, 2022

In situ regeneration of copper catalysts for long-term electrochemical CO2 reduction to multiple carbon products

Abstract

The valorization of carbon dioxide (CO2) via electrochemical CO2 reduction (ECR) has attracted great interest as a pragmatic approach to tackle greenhouse gas emissions. Multiple carbon (C2+) products, such as ethylene (C2H4), ethanol (C2H5OH), and propanol (C3H7OH), are highly valuable chemicals and of great demand. Copper (Cu)-based catalysts are so far the only electrocatalytic materials that allow CO2 reduction to C2+ products at industrially relevant current densities (≥100 mA cm−2). However, most Cu-based catalysts are unstable in long-term reactions (>100 hours), with the main reasons being the potential-induced surface reconstruction, deposition of impurities, and catalyst aggregation and leaching, among others. Herein, we report an in situ catalyst regeneration strategy that can extend the operation time of Cu-based catalysts. By periodically adding segments of anodic currents to electrolysis, a Cu catalyst is partially oxidized to CuOx in each cycle, as confirmed by in situ Raman studies, leading to the restoration of the catalytically active sites for C2+ products. We found that the oxidation current density and time significantly affect the selectivity and stability of Cu catalysts. Applying this strategy to a Cu catalyst – which is stable for ∼5 h towards C2+ products during a continuous electroreduction under neutral-pH conditions, we were able to extend the operating time to ∼120 h in a flow cell system. The catalyst maintained a high faradaic efficiency (FE) for C2H4 of ≥50% at a fixed cathodic current density of 150 mA cm−2 for over 60 h and continued to operate with a C2H4 FE ≥ 40% for the entire length of the reaction time. This work opens up an avenue to enhance the stability of Cu electrocatalysts, via controlling the operating procedure during electrolysis.

Graphical abstract: In situ regeneration of copper catalysts for long-term electrochemical CO2 reduction to multiple carbon products

Supplementary files

Article information

Article type
Paper
Submitted
04 apr. 2022
Accepted
19 júl. 2022
First published
19 júl. 2022

J. Mater. Chem. A, 2022,10, 20059-20070

In situ regeneration of copper catalysts for long-term electrochemical CO2 reduction to multiple carbon products

C. A. Obasanjo, A. S. Zeraati, H. S. Shiran, T. N. Nguyen, S. Md. Sadaf, M. G. Kibria and C. Dinh, J. Mater. Chem. A, 2022, 10, 20059 DOI: 10.1039/D2TA02709G

To request permission to reproduce material from this article, 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 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