The demand for high-performance energy storage systems has increased, highlighting the need to improve the pore structure and specific surface area of electrode materials for both supercapacitors and lithium-ion batteries. Supercapacitors offer high p...
The demand for high-performance energy storage systems has increased, highlighting the need to improve the pore structure and specific surface area of electrode materials for both supercapacitors and lithium-ion batteries. Supercapacitors offer high power density, but their energy density must be improved by enlarging the active surface area and optimizing ion transport pathways. Lithium-ion batteries provide high energy density however, their rate capability and cycling stability depend on reducing diffusion resistance and increasing the number of electrochemically active sites. Therefore, controlling porosity and surface area is a key strategy for enhancing the performance of both devices. In this study, we fabricated electrode materials based on the carbide derived two dimensional material Ti3C2Tx MXene. The Al layer of Ti3AlC2 MAX phase was etched using a LiF/HCl solution instead of conventional HF. The LiF/HCl method offers milder and more uniform etching, improving safety and providing higher reaction controllability. As a result, single-layer Ti3C2Tx MXene sheets with a thickness of about 1.6 nm were successfully obtained. To further improve the electrochemical performance, MXene was combined with zinc oxide (ZnO), which has a wurtzite structure and preferential c-axis growth, allowing ZnO nanostructures to grow uniformly on the MXene surface. The MXene@ZnO composite was synthesized using a precipitation process, which requires no additional equipment and allows easy control of particle size and growth time. Structural characterization using SEM and XRD confirmed that the layered MXene structure was preserved and that ZnO nanoparticles were uniformly formed on the MXene sheets. BET analysis showed that the composite synthesized for 2 hours exhibited the largest specific surface area of 43.639 cm3 g-1, indicating the most effective pore structure formation. In supercapacitor measurements, the 2 hour composite exhibited the highest performance, with a specific capacitance of 139.0 F g-1 and the longest discharge time of 172.6 s. These results are attributed to the expanded pore structure and the increased active surface area. For lithium-ion battery anode performance, the 3 hour composite showed a high initial capacity but poor rate capability, with a capacity retention below 70% at high scan rates. In contrast, the 2 hour composite showed better stability, achieving 38% rate retention and 52% charge–discharge capacity retention. Overall, the LiF/HCl-etched Ti3C2Tx MXene combined with ZnO effectively enhanced structural stability, ion transport pathways, and electrochemically active surface area. This study confirms that the Ti3C2Tx MXene@ZnO composite is a promising electrode material for high power and high stability energy storage applications.