Enhanced titanium carbide MXene structure with CuO quantum dots as an electrode for advanced supercapacitor applications

Abstract

Ti3C2 : CuO quantum dot composites with different mass ratios (1 : 0.5, 1 : 1 and 1 : 2) were successfully synthesized through hydrofluoric acid etching of Ti3AlC2 (MAX phase) to obtain Ti3C2 MXene, followed by sonication-assisted intercalation of quantum dots. The incorporation of CuO quantum dots was found to effectively prevent MXene restacking, enhance ion accessibility, and introduce additional redox-active sites, thereby improving the electrochemical properties of the electrode material. Among the tested composites, the Ti3C2 : CuO QDs (1 : 1) composite delivered the highest specific capacitance of 108.1 F g−1 in a three-electrode configuration, significantly outperforming pristine Ti3C2 (74.2 F g−1) in 1 M H2SO4. An asymmetric supercapacitor (SC) device was further fabricated using Ti3C2 : CuO QDs (1 : 1) as the negative electrode and human hair-derived activated carbon as the positive electrode. The device exhibited a high coulombic efficiency of 94.8%, excellent cycling stability with 82.6% capacitance retention after 10 000 cycles, a specific energy of 5.4 W h kg−1, and a power density of 410 W kg−1 at 1 A g−1. These findings highlight the synergistic benefits of CuO quantum dot intercalation and confirm the promise of Ti3C2 : CuO QDs composites as advanced electrode materials for high-performance supercapacitors.

Graphical abstract: Enhanced titanium carbide MXene structure with CuO quantum dots as an electrode for advanced supercapacitor applications

Supplementary files

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Article information

Article type
Paper
Submitted
21 Jan 2026
Accepted
31 Mar 2026
First published
22 Apr 2026
This article is Open Access
Creative Commons BY-NC license

New J. Chem., 2026, Advance Article

Enhanced titanium carbide MXene structure with CuO quantum dots as an electrode for advanced supercapacitor applications

M. Rantsotlhe, K. Otun, R. A. M. Adam, G. Rutavi, S. Chigome and N. Manyala, New J. Chem., 2026, Advance Article , DOI: 10.1039/D6NJ00232C

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