Catalysis Today,
Journal Year:
2024,
Volume and Issue:
434, P. 114674 - 114674
Published: March 27, 2024
The
use
of
graphitic
carbon
nitrides
(g-C3N4)
as
photocatalysts
for
the
reduction
p-nitrobenzoic
acid
(PNBA)
under
simulated
sunlight
has
been
investigated.
were
synthesized
through
thermal
polymerization
melamine
and
urea.
effects
g-C3N4
precursor
employed
in
synthesis,
exfoliation
treatment,
addition
sacrificial
agents,
pH
conditions
evaluated.
It
was
found
that
presence
carboxylic
acids
electron
donors
required
to
attain
photocatalytic
PNBA,
while
amines
or
alcohols
did
not
lead
any
activity
this
purpose.
Furthermore,
it
observed
used
synthesis
nitride
had
a
slight
influence
on
activity,
whereas
treatment
bulk
materials
exhibited
favourable
effect.
best
results
obtained
upon
oxalic
at
=
3
using
exfoliated
materials,
achieving
these
complete
removal
PNBA
after
ca.
60
min
irradiation.
Time
resolved
profiles
p-aminobenzoic
(PABA)
agree
with
an
initial
form
compound,
followed
by
oxidation
PABA
reactive
oxygen
species
formed
reaction
medium.
RSC Advances,
Journal Year:
2024,
Volume and Issue:
14(35), P. 25629 - 25662
Published: Jan. 1, 2024
Graphitic
carbon
nitride
(g-C
3
N
4
)-based
materials
have
emerged
as
promising
photocatalysts
due
to
their
unique
band
structure,
excellent
stability,
and
environmental
friendliness.
Advanced Energy Materials,
Journal Year:
2024,
Volume and Issue:
14(39)
Published: July 22, 2024
Abstract
Graphitic
carbon
nitride
(g‐C
3
N
4
)
assisted
photocatalytic
production
of
hydrogen
peroxide
(H
2
O
has
already
attracted
the
interest
many
researchers
due
to
its
environmental
sustainability.
Nevertheless,
inherent
drawbacks
g‐C
limit
progress.
Metal‐free
modification
strategies,
including
nanostructure
design,
defect
introduction,
doping,
and
heterojunction
construction,
have
been
developed
improve
efficiency
H
production.
Compared
metal
modification,
metal‐free
strategies
avoid
use
precious
metals
leaching
heavy
ions,
which
advantages
good
stability
friendliness.
However,
a
comprehensive
review
from
modified
by
is
still
lacking.
This
first
recaps
mechanism
,
photoexcitation,
carrier
separation
redox
reactions.
Then,
perspective
advances
in
photocatalysts
are
presented,
with
special
focus
on
kernel
connection
between
different
based
pivotal
stages
Subsequently,
recent
applications
‐based
for
situ
generated
mainly
water
purification
organic
synthesis,
briefly
discussed.
Finally,
prospects
envisioned
hope
that
it
will
“something
do”
field
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
34(28)
Published: Feb. 15, 2024
Abstract
Photocatalytic
oxygen
(O
2
)
reduction
to
hydrogen
peroxide
(H
O
is
considered
be
a
promising
method
for
energy
storage.
However,
it
suffers
from
the
rapid
recombination
of
carriers,
limited
solubility
and
slow
diffusion
,
self‐decomposition
H
in
traditional
diphase
systems.
Here,
self‐floating
carbon
dots/conjugated
microporous
polymer
(CDs/CMP)
photocatalytic
system
established
production
organic
synthesis.
Due
D–π–A
structure,
porous
hydrophobicity,
CMP
induced
intramolecular
charge
transfer,
exposed
abundant
reaction
sites,
enhanced
adsorption.
CDs
act
as
“bridges”
electron
transmission
regulate
surface
hydrophobicity
CMP,
further
improving
transfer
optimizing
interface.
CDs/CMP
exhibits
high
8542.6
µmol
g
−1
h
concurrent
furoic
acid
at
2.22
m
.
This
rate
≈90%
higher
than
that
system,
exceeding
all
previously
reported
photocatalysts
triphase
Notably,
achieves
relative
separation
suppressing
generated
self‐decomposition.
Theoretical
calculations
situ
characterizations
reveal
mechanism
evolution.
provides
insights
into
exploring
application
metal‐free
heterogeneous
reactions.
Carbon Energy,
Journal Year:
2024,
Volume and Issue:
6(11)
Published: July 9, 2024
Abstract
Hydrogen
peroxide
(H
2
O
)
is
one
of
the
100
most
important
chemicals
in
world
with
high
energy
density
and
environmental
friendliness.
Compared
anthraquinone
oxidation,
direct
synthesis
H
hydrogen
oxygen
(O
),
electrochemical
methods,
photocatalysis
has
characteristics
low
consumption,
easy
operation
less
pollution,
broad
application
prospects
generation.
Various
photocatalysts,
such
as
titanium
dioxide
(TiO
graphitic
carbon
nitride
(g‐C
3
N
4
metal‐organic
materials,
nonmetallic
have
been
studied
for
production.
Among
them,
g‐C
which
are
simple
to
synthesize
functionalize,
attracted
wide
attention.
The
electronic
band
structure
shows
a
bandgap
2.77
eV,
valence
maximum
1.44
V,
conduction
minimum
−1.33
theoretically
meets
requirements
In
comparison
semiconductor
materials
like
TiO
(3.2
eV),
this
material
smaller
bandgap,
results
more
efficient
response
visible
light.
However,
photocatalytic
activity
yield
were
severely
inhibited
by
electron‐hole
pair
recombination
rate,
utilization
rate
light,
poor
selectivity
products.
Although
previous
reviews
also
presented
various
strategies
improve
production,
they
did
not
systematically
elaborate
inherent
relationship
between
control
their
structure.
From
point
view,
article
focuses
on
engineering
latest
research
progress
On
basis,
strategy
production
proposed
through
morphology
control,
crystallinity
defect,
doping,
combined
other
strategies.
Finally,
challenges
industrialization
discussed
envisioned.
Inorganic Chemistry Frontiers,
Journal Year:
2024,
Volume and Issue:
11(16), P. 4914 - 4973
Published: Jan. 1, 2024
This
review
summarizes
advancements
in
g-C
3
N
4
-based
direct
Z
and
S-scheme
heterostructures
for
solar
H
2
O
synthesis,
exploring
advanced
characterization
methods
to
verify
the
charge
transfer
mechanism.
ACS Sustainable Chemistry & Engineering,
Journal Year:
2024,
Volume and Issue:
12(30), P. 11409 - 11418
Published: July 16, 2024
The
production
of
hydrogen
peroxide
(H2O2)
by
combining
photocatalytic
oxygen
(O2)
reduction
with
water
(H2O)
oxidation
is
a
satisfactory
substitute
for
the
industrial
anthraquinone
process.
But
efficiency
H2O2
generation
still
low,
especially
in
heterogeneous
reactions,
owing
to
poor
mass
transfer
and
weak
H2O
oxidation.
Hereby,
porous
organic
framework
(BPYTEA-POF)
hexagonal
hollow
nanotube
structure
was
synthesized
through
5,5′-dibromo-2,2′-bipyridine
(BPY)
reacting
tris(4-ethynylphenyl)amine
(TEA)
Sonogashira
coupling
reaction
without
template,
which
contains
2,2′-bipyridine
active
site.
BPYTEA-POF
morphology
hierarchical
wall
beneficial
and/or
diffusion
substrate
via
siphonic
effect;
meanwhile,
it
benefits
exposure
catalytic
site,
boosts
contact
O2
site
rapidly
dissociates
generated
H2O2,
thus
improving
efficiency.
At
same
time,
moiety
capable
effectually
weakening
O–H
bonds
promoting
produce
proton
(H+);
then,
produced
H+
were
used
efficient
under
additive-free
condition.
definite
specific
sites
enhance
initial
rate
up
3446
μmol
gcat–1
h–1,
condition
visible-light
irradiation
(λ
≥
400
nm)
any
additional
additive.