Issue 6, 2025

Anchoring Co–Fe alloy nano-grains on carbon fibers by an in situ alloying strategy to boost the catalytic performance for rapid oxidative degradation of emerging contaminants

Abstract

Advanced oxidation is regarded as the most promising pathway for the purification of hard-to-degrade contaminants. In this study, novel CoFe alloy-decorated carbon nanofibers (CoFe/CF) were constructed utilizing an alloy engineering strategy, which achieved the complete degradation of tetracycline with the rate constant reaching 97.92 × 10−3 min−1. Integrated experimental analysis and density functional theory (DFT) simulations revealed that the synergistic integration of Fe and Co within the nanoalloy endowed the catalyst with an optimized electronic structure and distinct redox characteristics, markedly improving its capacity for peroxymonosulfate (PMS) activation. The low ecotoxicity and phytotoxicity of the intermediates during TC degradation confirmed the robust capability of CoFe/CF-800/PMS for the mineralization of TC-containing wastewater. Moreover, the pivotal role of CoFe nanoalloys for the generation of oxidative radicals was confirmed through an integrated experimental analysis, and a plausible mechanism for TC degradation was ultimately hypothesized. This work provides a case study about the electronic structure customization of bimetallic catalysts through alloy engineering and expands their applications for the elimination of hard-to-degrade pollutants.

Graphical abstract: Anchoring Co–Fe alloy nano-grains on carbon fibers by an in situ alloying strategy to boost the catalytic performance for rapid oxidative degradation of emerging contaminants

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Article information

Article type
Paper
Submitted
05 Dec 2024
Accepted
20 Dec 2024
First published
23 Dec 2024

J. Mater. Chem. A, 2025,13, 4329-4342

Anchoring Co–Fe alloy nano-grains on carbon fibers by an in situ alloying strategy to boost the catalytic performance for rapid oxidative degradation of emerging contaminants

M. Yang, X. Cheng, F. Geng, W. Han, P. Niu, L. Xie, Z. Li, Y. Zhang, D. Zhang, J. Xu, X. Zhang and L. Geng, J. Mater. Chem. A, 2025, 13, 4329 DOI: 10.1039/D4TA08657K

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