Engineered nanomaterials are emerging
in the field of environmental
chemistry. This study involves the analysis of the structural, electronic,
crystallinity, and morphological changes in graphitic carbon nitride
(g-C
3
N
4
), an engineered nanomaterial, under
rapid cooling conditions. X-ray diffraction, scanning electron microscopy,
high-resolution transmission electron microscopy, Brunauer–Emmett–Teller,
Fourier transform infrared, Raman, band gap, and Mott–Schottky
analyses strongly proved that the liquid N
2
-quenched sample
of g-C
3
N
4
has structural distortion. The photocatalytic
efficiency of engineered g-C
3
N
4
nanostructures
was analyzed through the degradation of reactive red 120 (RR120),
methylene blue (MB), rhodamine B, and bromophenol as a representative
dye. The photocatalytic dye degradation efficiency was analyzed by
UV–vis spectroscopy and total organic carbon (TOC) analysis.
The photocatalytic efficiency of g-C
3
N
4
under
different quenching conditions included quenching at room temperature
in ice and liquid N
2
. The degradation efficiencies are
found to be 4.2, 14.7, and 82.33% for room-temperature, ice, and liquid
N
2
conditions, respectively. The pseudo-first-order reaction
rate of N
2
-quenched g-C
3
N
4
is 9 times
greater than the ice-quenched g-C
3
N
4
. Further,
the TOC analysis showed that 55% (MB) and 59% (RR120) of photocatalytic
mineralization were achieved within a time duration of 120 min by
the liquid N
2
-quenched g-C
3
N
4
nanostructure.
In addition, the quenched g-C
3
N
4
electrocatalytic
behavior was examined via the hydrogen (H
2
) evolution reaction
in acidic medium. The liquid N
2
-quenched g-C
3
N
4
catalyst showed a lower overpotential with high H
2
evolution when compared with the other two g-C
3
N
4
-quenched samples. The results obtained provide an insight
and extend the scope for the application of engineered g-C
3
N
4
nanostructures in the degradation of organic pollutants
as well as for H
2
evolution.