This
paper details an approach for the synthesis of stable electroactive
Au–V2O5–MnO2 nanoflower
composites using a simple redox-mediated methodology under modified
hydrothermal (MHT) conditions. The nanocomposite was characterized
by various techniques like X-ray diffraction, scanning electron microscopy,
high-resolution transmisson electron microscopy, and X-ray photoelectron
spectroscopy. MnO2 and Au formed a profitable hierarchical
network morphology in the interstitial sites of V2O5, and this kind of synergetic architecture exhibits an elevated
specific capacitance (388 F g–1 at 1 A g–1) compared to commercial V2O5 (85 F g–1 at 1 A g–1) in a neutral electrolyte. The as-synthesized
nanocomposite contributed more to energy storage with superior energy
density (49 Wh kg–1 at 1 A g–1 current density) and power density (4 kW kg–1 at
10 A g–1 current density) and demonstrated improved
stability compared to commercial V2O5 of up
to 2000 continuous charge/discharge cycles in a two-electrode system.
Temperature- and field-dependent [both direct-current (dc) and alternating-current
(ac)] studies exhibited enhanced conductance due to the incorporation
of Au and MnO2 and non-Ohmic electrical conduction, characterized
by the onset voltage V
0 (dc) and onset
frequency f
0 (ac). These two onset parameters
followed power-law behavior with Ohmic conductance with two onset
exponents (x
V and x
f). Such electrical transport properties were explained using
intrachain hopping conduction of charge carriers within the layers
of pristine V2O5 and hopping of charge carriers
between the layers of V2O5 in the Au–V2O5–MnO2 nanocomposite and supported
the interstitial incorporation of the compounds.