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In relation to this article, we declare that there is no conflict of interest.
Publication history
Received December 16, 2025
Revised January 5, 2026
Accepted January 7, 2026
Available online April 25, 2026
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Urea-Assisted Carbonyl Functionalization of Carbon Nanotubes for Enhanced Vanadium Redox Reaction Kinetics

epartment of IT⋅Energy Convergence , Korea National University of Transportation 1Department of Chemical and Biological Engineering , Korea National University of Transportation
ychung@ut.ac.kr
Korean Journal of Chemical Engineering, April 2026, 43(5), 1425-1436(12)
https://doi.org/10.1007/s11814-026-00649-8

Abstract

Carbon nanotubes (CNTs) are promising electrocatalysts for vanadium redox fl ow batteries (VRFBs); however, their 

inherent hydrophobicity poses challenges for practical application. In this study, we introduce a straightforward and industrially

feasible urea-assisted treatment that facilitates carbonyl-rich oxygen functionalization on CNT surfaces through 

mild oxidation, while maintaining the integrity of the graphitic framework. X-ray photoelectron spectroscopy confi rms a 

signifi cant enrichment of carbonyl (C = O) species, resulting in a marked enhancement in surface wettability, with only 

a moderate reduction in electrical conductivity. Electrochemical analyses demonstrate a substantial increase in catalytic 

activity towards both VO 2+ /VO 2+ and V 2+ /V 3+ redox couples, with anodic peak current densities approximately 2.32 times 

greater than those of pristine CNTs and a decreased charge-transfer resistance (66.1% post-treatment). When applied to 

graphite felt electrodes, CNT/urea exhibits improved single-cell VRFB performance, achieving an energy effi ciency of 

approximately 64.5% and a discharge capacity of 25.77 Ah L⁻¹ at 400 mA cm⁻², along with stable operation over 1,000 

cycles. This research highlights urea-assisted carbonyl functionalization as a cost-eff ective and scalable approach for 

developing hydrophilic, catalytically active CNT electrodes for practical VRFB applications. 

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