Crinum asiaticum-assisted green synthesis of TiO2 integrated Ti3C2-MXene@Ag composite electrodes for high-performance supercapacitors

0Citations
Citations of this article
2Readers
Mendeley users who have this article in their library.
Get full text

Abstract

The present study reports fabrication and electrochemical investigations on a partly bio-derived ternary electrode, Ti3C2@Ag/TiO2 (MAT-3), in which TiO2 nanoparticles were green-synthesized from Crinum asiaticum leaf extract and are integrated with Ag-decorated Ti3C2-MXene. The Ag nanoparticles serve as conductive spacers that suppress restacking of Ti3C2-MXene sheets, while the green TiO2 contributes to redox-active sites and further inhibits restacking, raising the BET surface area more than six-fold over pristine Ti3C2-MXene. In 1 M H2SO4, the MAT-3 electrode delivers a specific capacitance of 255.87 F/g at 1 A/g, with lower charge-transfer resistance than its binary and pristine counterparts. Impedance analysis shows that this synergy translates into markedly faster charge-transfer kinetics: relative to pristine Ti3C2-MXene, the ternary electrode exhibits lower solution and a shorter relaxation time (0.318 s to 0.024 s), and a higher ion-diffusion coefficient, indicating efficient interfacial electron transport and rapid ionic access. A symmetric CR2032 cell retains 89.28% of its capacitance after 15,000 cycles at 98.49% coulombic efficiency, and three cells in series power a red LED for ∼8 min. The study underscores the potential of Ti3C2@Ag/TiO2 composite as a promising electrode material for supercapacitors.

Cite

CITATION STYLE

APA

Vidhi, Masih, A., Sadiq, M., Singh, A. K., & Thakur, O. P. (2026). Crinum asiaticum-assisted green synthesis of TiO2 integrated Ti3C2-MXene@Ag composite electrodes for high-performance supercapacitors. Journal of Power Sources, 690. https://doi.org/10.1016/j.jpowsour.2026.240878

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