In the present paper, nanocrystalline samples of NiCrFeO4 were synthesized by the combustion method using different
fuels
such as glycine, urea, and poly(vinyl alcohol) and subjected to heat
treatment at different temperatures of 600, 700, 800, and 1000 °C
for 6 h. The formation of phases with highly crystalline structures
was confirmed by XRD and Rietveld refinement analysis. The optical
band gap of NiCrFeO4 ferrites lies in the visible range,
making them suitable photocatalysts. BET analysis reveals that the
surface area of the phase synthesized using PVA is much higher than
that synthesized using other fuels at each sintering temperature.
In addition, there is a significant decrease in the surface area with
sintering temperature for the catalysts prepared using the fuels PVA
and urea, while it almost remains constant in the case of glycine.
Magnetic studies demonstrate the dependence of saturation magnetization
on the nature of the fuel and on the sintering temperature; moreover,
the coercivity and squareness ratio confirm the single domain nature
of all the synthesized phases. We have also performed photocatalytic
degradation of the highly toxic Rhodamine B (RhB) dye by employing
all the prepared phases as photocatalysts using the mild oxidant H2O2. It is observed that the photocatalyst prepared
using PVA as the fuel exhibited the best photocatalytic activity at
all sintering temperatures. All the three photocatalysts prepared
using different fuels showed a decrease in the photocatalytic activity
with increasing sintering temperature. From the chemical kinetic point
of view, the degradation of RhB by all the photocatalysts was found
to follow pseudo-first-order kinetics.