Hydrogen
peroxide
(H2O2)
production
via
oxygen
(O2)
reduction
reaction
(ORR)
in
pure
water
(H2O)
through
graphitic
carbon
nitrides
(g-C3N4)-based
piezo-photocatalysts
is
an
exciting
approach
many
current
studies.
However,
the
low
Lewis-acid
properties
of
g-C3N4
limited
catalytic
performance
because
O2
adsorption
efficacy.
To
overcome
this
challenge,
we
utilized
interaction
precursors
with
various
solvents
to
synthesize
g-C3N4,
possessing
multiple
nitrogen-vacant
species
thermal
shocking
polymerization.
Our
results
suggest
that
lack
nitrogen
and
incident
introduction
oxygen-functional
groups
enhance
Lewis
acid-base
interactions
polarize
lattices,
leading
enormous
enhancement,
roughly
7
times
from
optimal
samples
compared
pristine
piezo-photocatalysis.
Meanwhile,
also
observed
correlation
between
charge
separation
kinetic
crystalline
degree
synthesized
materials,
which
can
elucidate
how
defects
impacted
outcomes.
Furthermore,
mechanisms
were
thoroughly
studied,
formation
H2O2
proceeding
radical
oxidation
pathways,
roles
light
ultrasound
carefully
investigated.
Thus,
our
findings
not
only
reinforce
potential
view
metal-free
photocatalysts,
accelerating
understanding
working
principles
generate
based
on
reactions,
but
propose
a
facile
one-step
way
for
fabricating
highly
efficient
scalable
photocatalysts
produce
without
using
sacrificial
agents,
pushing
practical
application
in-situ
solar
toward
real-world
scenarios.
Small Methods,
Journal Year:
2024,
Volume and Issue:
unknown
Published: July 31, 2024
Abstract
Hydrogen
peroxide
(H
2
O
)
production
via
oxygen
(O
reduction
reaction
(ORR)
in
pure
water
O)
through
graphitic
carbon
nitrides
(g‐C
3
N
4
)‐based
piezo‐photocatalysts
is
an
exciting
approach
many
current
studies.
However,
the
low
Lewis‐acid
properties
of
g‐C
limited
catalytic
performance
because
adsorption
efficacy.
To
overcome
this
challenge,
interaction
precursors
with
various
solvents
are
utilized
to
synthesize
,
possessing
multiple
nitrogen‐vacant
species
thermal
shocking
polymerization.
These
results
suggest
that
lack
nitrogen
and
incident
introduction
oxygen‐functional
groups
enhance
Lewis
acid‐base
interactions
polarize
lattices,
leading
enormous
enhancement.
Furthermore,
mechanisms
thoroughly
studied,
formation
H
proceeding
radical
oxidation
pathways,
which
roles
light
ultrasound
carefully
investigated.
Thus,
these
findings
not
only
reinforce
potential
view
metal‐free
photocatalysts,
accelerating
understanding
working
principles
generate
based
on
reactions,
but
also
propose
a
facile
one‐step
way
for
fabricating
highly
efficient
scalable
photocatalysts
produce
without
using
sacrificial
agents,
pushing
practical
application
situ
solar
toward
real‐world
scenarios.