Integrated Capture and Electrocatalytic Conversion of CO2: A Molecular Electrocatalysts Perspective

1Citations
Citations of this article
10Readers
Mendeley users who have this article in their library.

Abstract

The ever-increasing concentration of atmospheric CO2, primarily driven by anthropogenic activities, has raised urgent environmental concerns, spurring the development of carbon capture and utilization (CCU) technologies. This review focuses on the integrated capture and electrochemical conversion of CO2 (ICECC), a promising approach that combines carbon capture with its direct electroreduction into value-added products. By eliminating energy-intensive steps such as CO2 release, compression, and transportation, ICECC offers a more energy-efficient and cost-effective alternative to conventional CCU methods. In this review, particular attention is given to molecular electrocatalysts, which offer high tunability and selectivity in electrochemical CO2 reduction reaction (eCO2RR). The role of capturing agents, including both external and dual-functional molecular systems, is critically examined to understand their influence on CO2 binding and catalytic efficiency. Whereas ICECC has significant potential, research in this area remains underexplored compared to conventional CO2 reduction methods. The review discusses the mechanistic insights into ICECC processes, highlighting key challenges and potential future research directions for improving catalyst design, enhancing capture efficiency, and scaling up ICECC technologies. These developments can make ICECC a critical component in achieving carbon neutrality and addressing climate change.

Cite

CITATION STYLE

APA

Gupta, N., & Chatterjee, S. (2025, June 2). Integrated Capture and Electrocatalytic Conversion of CO2: A Molecular Electrocatalysts Perspective. Chemistry - An Asian Journal. John Wiley and Sons Ltd. https://doi.org/10.1002/asia.202401611

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free