Journal of Materials Chemistry A,
Год журнала:
2024,
Номер
unknown
Опубликована: Дек. 17, 2024
The
multifarious
aromatic
sulfone-decorated
conjugated
polymers
(CPs)
have
recently
been
developed
to
enable
them
be
employed
in
artificial
photocatalysis
with
encouraging
achievements.
Abstract
The
exploration
of
photocatalytic
materials
with
efficient
charge
separation
has
always
been
a
prominent
area
research
in
photocatalysis.
In
the
preceding
years,
strategy
constructing
donor–acceptor
(D–A)
structured
gradually
developed
systems,
becoming
new
crossroads
and
attracting
extensive
interdisciplinary
focus.
Polymeric
carbon
nitride
(PCN)
recognized
as
primary
material
for
D–A
structures
due
to
its
attractive
exceptional
physicochemical
stability,
electronic
band
structure,
cost‐effectiveness.
However,
few
reports
have
summarized
on
type
PCN
at
molecular
level.
This
review
focuses
level
design
strategies
performance
enhancement
mechanisms
are
emphasized
from
two
main
aspects:
intramolecular
intermolecular
D–A.
addition,
concept
dual
is
introduced,
proposing
direction
advancing
efficacy
photocatalysts.
Subsequently,
this
summarizes
application
scenarios
energy
transformation
environmental
amelioration.
Finally,
by
elaborating
difficulties
opportunities
hot
field,
can
provide
inspiration
innovative
developing
resolving
issues.
Although
the
design
of
photocatalysts
incorporating
donor-acceptor
units
has
garnered
significant
attention
for
its
potential
to
enhance
efficiency
photocatalysis
process,
primary
bottleneck
lies
in
challenge
generating
long-lived
charge
separation
states
during
exciton
separation.
Therefore,
a
novel
Janus-nanomicelles
photocatalyst
is
developed
using
carbazole
(Cz)
as
donor
unit,
perylene-3,4,9,10-tetracarboxydiimide
(PDI)
with
long-excited
state
acceptor
unit
and
polyethylene
glycol
(PEG)
hydrophilic
segment
through
ROMP
polymerization.
After
optimizing
ratio,
Cz19-PDI18-PEG10
rapidly
adsorbs
bisphenol
A
(BPA)
within
10
s
π-π
interaction,
hydrogen-bonding
hydrophobic
interaction
between
BPA
blocks
when
exposed
aqueous
humor
efficiently
photodegrades
(50
ppm)
120
min
water
purification
purposes
due
achieving
highest
reported
so
far.
Mechanistic
studies
have
shown
that
this
excellent
performance
can
be
attributed
synergistic
interactions
highly
efficient
adsorption
capacity
photocatalysis.
This
strategy
holds
promise
an
effective
candidate
purification.
ACS Applied Nano Materials,
Год журнала:
2025,
Номер
8(4), С. 1882 - 1892
Опубликована: Янв. 21, 2025
Given
its
multifaceted
important
roles
such
as
aqueous
oxidant,
chemical
platform
for
environmental
remediation,
possible
liquid
fuel,
and
so
on,
environmentally
friendly
approaches
to
produce
hydrogen
peroxide
(H2O2)
are
highly
desirable.
In
this
context,
the
photocatalytic
generation
of
from
water
oxidation
has
emerged
a
promising
method,
phenol–formaldehyde-based
functional
resins
have
been
established
an
excellent
developing
photocatalysts
oxidation.
The
present
work
reports
development
resorcinol–formaldehyde
(RF)
TiO2
(RF/TiO2)
composites
efficient
heterogeneous
production
H2O2
through
synthesis
RF/TiO2
was
accomplished
following
simple
high-temperature
hydrothermal
it
characterized
study
microstructures
optical
properties.
role
optimum
amount
in
improving
activity
resin
by
with
varied
amounts
TiO2.
As
experimentally
established,
prepared
1.1–1.6%
(w/w)
feed
respect
resorcinol
at
temperature
200
°C
under
conditions
were
found
be
most
ones
study.
Out
these
composites,
RF/TiO2-1.2%
RF/TiO2-1.3%
resulted
∼500
∼530
μmol
per
gram
catalyst,
respectively,
upon
5
h
continuous
photoirradiation
experimental
reaction
∼30–35
°C.
It
observed
that
rate
can
enhanced
increasing
temperature.
Advanced Functional Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 24, 2025
Abstract
The
sluggish
interfacial
charge
transfer
and
constrained
intrinsic
catalytic
activity
in
photocatalytic
systems
are
major
obstacles
to
the
efficiency
selectivity
of
CO
2
photoreduction
(CO
PR).
Herein,
a
novel
organic–inorganic
supramolecular
assembly
heterojunction
(NiAl‐ZnTCPP)
comprising
single
molecules
2D
matrix
is
presented,
featuring
high‐quality
contact
achieved
through
electrostatic
interactions
hydrogen
bonding.
This
comprehensive
investigations
unveil
formation
an
effective
built‐in
electric
field
(BEF)
directed
from
NiAl‐LDH
toward
ZnTCPP,
which
significantly
boosts
PR.
NiAl‐ZnTCPP
achieves
impressive
yield
1568.6
µmol
g
−1
h
,
exceeding
yields
ZnTCPP
by
25
5.6
times,
respectively,
while
maintaining
remarkable
98%
extremely
low
selectivity.
Utilizing
advanced
experimental
technologies,
including
diverse
operando
characterizations
theoretical
simulations,
bifunctionality
BEF
elucidated,
not
only
accelerates
photogenerated
carriers
photosensitizer
NiAl‐ZnTCPP,
but
also
enhances
modulating
electronic
structure
nickel
active
sites
(specifically
lowering
energy
barrier
for
*
COOH
conversion
improving
transport
capability).
work
provides
new
insights
into
application
molecule/2D
junctions
generate
fields
that
enhance
performance.