Ionomers modulate the microenvironment in electrocatalytic CO2 reduction

Abstract

The global shift toward a low-carbon society has accelerated the development of electrocatalytic CO2 reduction reaction (CO2RR) technology, which shows great potential in simultaneously addressing environmental pollution and energy crises. In the CO2RR system, microenvironment modulation can effectively enhance catalytic activity, product selectivity, operational stability, and energy efficiency. The introduction of ionomers into catalyst layers enables precise control of the microenvironment at the catalyst surface through their unique structural properties, significantly improving CO2RR performance. In this review, we first provide a concise overview of the key components and main influencing factors of the reaction microenvironment and the structures together with the functional mechanisms of commonly used ionomers. We then systematically discuss how various ionomers modulate the microenvironment, including their effects on CO2 mass transport, stabilization and diffusion of intermediates, ion species and concentrations at the surface (affecting the pH, K+ distribution and interfacial electric field), surface morphology and hydrophobicity of catalysts, and structures of interfacial water. Finally, we present a comprehensive summary that identifies current practical challenges of ionomer applications from multiple perspectives while proposing feasible solutions and outlining future research directions for this field.

Graphical abstract: Ionomers modulate the microenvironment in electrocatalytic CO2 reduction

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Article information

Article type
Review Article
Submitted
27 Sep 2025
Accepted
20 Nov 2025
First published
22 Nov 2025
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2025, Advance Article

Ionomers modulate the microenvironment in electrocatalytic CO2 reduction

S. Ruan, G. Tang, Z. Zhang, Q. Zhang, Y. Wang and S. Xie, Chem. Sci., 2025, Advance Article , DOI: 10.1039/D5SC07515G

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