Ag/Zn-Ta2C MXene composite as an efficient electrocatalyst for aqueous and non-aqueous CO2 reduction reactions

7Citations
Citations of this article
15Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

This study reports the preparation of an Ag and Zn-based Ta2CTx MXene composite and its electrocatalytic application towards the electrochemical CO2RR in aqueous and non-aqueous (organic) solvents. In aqueous 0.1 M KHCO3, Ag and Zn-based Ta2CTx MXene cathode enables efficient conversion of CO2 to valuable products such as syngas (CO:H2) and formic acid. Ag/Ta2CTx MXene-modified electrode, exhibiting the best CO and H2 (1:1) selectivity at an applied potential of − 0.65 V vs. RHE syngas, was collectively found to be ~ 80%, whereas at the same potential, some formate (20%) was formed. Similar to Zn/Ta2CTx, MXene showed the highest selectivity for CO of 83%. By employing a divided cell setup, CO2RR occurs at lower reduction potentials, enhancing the feasibility of the process. In non-aqueous media, styrene was electrocarboxylated to phenylsuccinic acid (PSA) and phenylpropanoic acid (PPA) using the same cathode, and the selectivity varies Ag/Ta2CTx MXene (45% of PSA) and Zn/Ta2CTx (41% of PPA) with respect to the metal ion present in the composite. Mono- and di-carboxylic acids were produced in quantifiable amounts using the MXene-modified electrodes as the cathode and sacrificial aluminum as the anode. This work highlights the potential of MXene-based electrocatalysts for aqueous CO2RR and selective electrocarboxylation, offering promising pathways for sustainable fuel production and chemical synthesis.

Cite

CITATION STYLE

APA

Vijayaprabhakaran, A., & Kathiresan, M. (2025). Ag/Zn-Ta2C MXene composite as an efficient electrocatalyst for aqueous and non-aqueous CO2 reduction reactions. Advanced Composites and Hybrid Materials, 8(3). https://doi.org/10.1007/s42114-025-01266-5

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