Crystal water-driven ion pathways in layered vanadium oxide for improved supercapacitor performance
摘要
Designing a stable and efficient charge storage system presents a persistent bottleneck due to limitations in structural integrity and ion transport over prolonged cycles. Modifying the interlayer region within layered host materials has offered a promising avenue, although the underlying structure–function correlation is largely unexplored. In this study, we demonstrate hydrothermally synthesized V6O13.nH2O with an intercalated water network as a promising electrode material for supercapacitor applications. Structural and surface analyses using X-ray diffraction. X-ray photoelectron spectroscopy, scanning electron microscopy and transmission electron microscopy validate the mixed-valence nature and layered framework of the hydrated vanadium oxide. The phase composition and effects of water intercalation were studied using FTIR spectroscopy, Raman spectroscopy and thermogravimetry. The extended hydrogen-bonded network formed by the interlayer water increases the interlayer spacing, allowing efficient proton transport and enhanced pseudo-capacitance behaviour, while the water pillars enhance crystal structural stability. Electrochemical investigations of the electrode exhibited a significant specific capacitance of ~ 232 F g−1, power density of ~ 0.9 kW kg−1 and energy density of ~ 29 Wh kg−1 at 0.5 A g−1. The electrode showcased good rate capability and cycling performance, retaining ~ 87% of its capacitance over 2000 cycles.
Graphical abstract