| Issue |
MATEC Web Conf.
Volume 420, 2026
International Conference on Material Physics, Chemistry and New Energy (MPCNE 2026)
|
|
|---|---|---|
| Article Number | 02005 | |
| Number of page(s) | 8 | |
| Section | Hydrogen Energy, Fuel Cells, and Catalysis | |
| DOI | https://doi.org/10.1051/matecconf/202642002005 | |
| Published online | 08 May 2026 | |
Progress in Electrochemical CO2 Reduction Reaction (Eco2RR) for Multi-Carbon Product Synthesis
School of Chemical Engineering and Technology, Tianjin University, Tianjin, 300354, China
* Corresponding author: This email address is being protected from spambots. You need JavaScript enabled to view it.
Abstract
Motivated by the worldwide goal of carbon neutrality, electrochemical CO2 reduction reaction (eCO2RR) is an environmentally friendly technology that converts CO2 to useful chemical products using renewalelectricity, is of significant interest both in academia and industry. Multi-carbon products (C2+) are expected to have clearer resource-based benefits compared with traditional CCS due to the higher energy content and value. This review outlines the recent advances of eCO2 RR towards C2 + products. The basic reaction mechanism is introduced first in this article, and then describes catalyst research in terms of categories (including a discussion on the dominance of copperbased catalysts), the promise of complementarity with non-copper options, and the design of tandem approaches. Besides the energy conversion efficiency, current problems of this area concerning selectivity and stability are also discussed. In the end, perspectives about industrialization pathways and future research trends are given. These developments improved greatly the performance for C2 + products as well as the applicability of eCO2RR systems, laying groundwork for use of dilute CO2. The purpose of this work is to support the shift towards sustainable energy as well as contributing toward achieving global net-zero emissions, developing the green chemical industry.
© The Authors, published by EDP Sciences, 2026
This is an Open Access article distributed under the terms of the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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