In this article, we have judiciously
interfaced copper oxides with
graphitic carbon nitride (g-C
3
N
4
) from thermal
reaction of melamine and copper sulfate in a one-pot protocol and
manipulated the perforated sheet morphology thereafter. The CCN-
X
(
X
= 30, 40, 50, 60, and 70, depending
on the wt % of CuSO
4
·5H
2
O) nanocomposites
were prepared by homogenously mixing different percentages of CuSO
4
·5H
2
O with melamine from a solid-state thermal
reaction in a furnace in air. Drastic lowering of CuSO
4
decomposition temperature due to Cu(II)–amine complex formation
and subsequent reduction of Cu(II) species by in situ produced ammonia
(NH
3
) resulted in the production of CuO and catalytic amount
of Cu
2
O, homogeneously dispersed within the perforated
g-C
3
N
4
nanosheet. How perforated sheet morphology
evolved by combined effect of NH
3
, released from thermal
condensation of melamine ensuring two-dimensional (2D) growth, and
sulfur trioxide (SO
3
), expelled from CuSO
4
·5H
2
O facilitating the perforation, yielding better catalytic
performance, has been elucidated. Excess NH
3
from added
NH
4
Cl removed perforation and ensued a marked decrease
in efficacy. However, a high proportion of CuSO
4
·5H
2
O ruptured the framework of 2D sheets because of excess SO
3
evolution. Among the different nanocomposites synthesized,
CCN-40 (CuO–Cu
2
O/g-C
3
N
4
) showed
the highest catalytic activity for 4-nitrophenol reduction. Thus,
enhanced efficiency of the copper oxide catalyst by interfacing it
with an otherwise inactive g-C
3
N
4
platform was
achieved.