Hybrid Supercapacitor Performance Through Electrode Composites: Ti 3 C 2 T x Anode and Fe 3 O 4 @Activated Carbon Cathode Integration

View at publisher
Authors: Prashant M. Kakade, Avinash R. Kachere, Sukhada S. Pandey, Rahul Aher, Shrikrishna Dattatraya Sartale, Sandesh R. Jadkar, Priyanka Ruz, V. Sudharshan, Rajendrakumar Sharma, Hansol Kim, Nandkumar T. Mandlik, Ravindra N. Bulakhe
+1 more JI Man Kim
Cited by: 1
References: 89

Abstract

Here, we report the performance of an asymmetric supercapacitor (ASC) fabricated using a chemically synthesized Ti 3 C 2 T x MXene as an anode, a ferric oxide (Fe 3 O 4 ) (magnetite), and biomass‐derived activated carbon (AC) composite (MAC composite) as a cathode, 2 M potassium hydroxide (KOH) as an electrolyte. Ti 3 C 2 T x MXene synthesis was carried out using chemical etching processes using synthesized Ti 3 AlC 2 MAX phase. AC was synthesized using biomass (coconut shell) by carbonization and activation processes. Whereas MAC composite was prepared using the solvothermal method. Physiochemical characteristics of all samples were analyzed using X‐ray diffraction, Raman spectroscopy, field emission scanning microscopy, and HR‐TEM techniques. Specific surface areas of Ti 3 C 2 T x MXene and MAC‐7.5 was found to be 85.37 and 434.35 m 2 g −1 , respectively. The attained specific capacitance values for bare Ti 3 C 2 T x MXene and MAC‐7.5 composite are 173 F g −1 at 1 A g −1 and 1722 A g −1 at 2 A g −1 current density, respectively. Electrochemical performance of the developed ASC device displayed a 133.47 F g −1 specific capacitance at a current density of 1 A g −1 with the maximum energy and a power density of 41.71 and 512 W kg −1 , respectively. Stability performance of the ASC showed the highest retention rate of 94% after 5000 cycles.

Fields of Study & Subjects

MXene and MAX Phase Materials Supercapacitor Materials and Fabrication Advancements in Battery Materials

Publication details

Journal / source
Energy Technology
Publisher
Wiley
Volume
14
Issue
1
Publication date
1 January 2026
Language
EN