The present work explores the electrochemical
energy storage performance
of Ti3C2T
x
(MXene)
and 1T-VS2 nanosheet hybrids synthesized by a simple in
situ hydrothermal method. Different analytical methods such as X-ray
diffraction, field emission scanning electron microscopy, Fourier
transform infrared, Raman spectroscopy, and Brunauer–Emmett–Teller
were employed to explore the structural and morphological properties
and composition of electrode materials. Furthermore, the electrochemical
characterization of 1T-VS2/MXene hybrid electrode materials
with different concentrations of MXene was investigated systematically.
The all pseudocapacitive asymmetric supercapacitor cell was fabricated
by combining the best performing 1T-VS2/MXene and MXene,
which displayed the highest specific capacitance of 115.7 F/g at a
current density of 0.8 A/g in an expanded potential range of 1.6 V.
Additionally, the highest energy density achieved was 41.13 W h kg–1 at a maximum power density of 793.50 W kg–1. The asymmetric supercapacitor was able to achieve a high capacitance
retention of 85% and a coulombic efficiency of 100% after 5000 galvanostatic
charge–discharge cycles. Moreover, the synergistic effect and
charge storage kinetics of the 1T-VS2/MXene hybrid pseudocapacitive
electrode material were investigated in detail using experimental
and density functional theory calculations. Based on the results,
we have further demonstrated the usage of 1T-VS2/MXene
and MXene as a high-performance energy storage material for supercapacitor
application with the dominating intercalation mechanism. The lower
diffusion energy barrier for electrolytic ions in the case of hybrid
1T-VS2/MXene supports the higher charge storage. The enhanced
density of states and lower diffusion barrier justify the superior
charge storage performance for hybrid 1T-VS2/MXene.