Small,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 14, 2025
Abstract
Developing
S‐scheme
systems
with
high
photocatalytic
performance
is
crucial
for
long‐term
solar‐to‐hydrogen
conversion.
In
this
study,
hollow
cobalt
tetrasulfide
(Co
3
S
4
)
nanoboxes
(NBs),
synthesized
via
sulfurization
using
zeolitic
imidazolate
framework
(ZIF‐67)
as
a
template,
are
combined
cadmium
sulfide
(CdS)
nanoparticles
(NPs)
to
construct
heterojunction
photocatalysts
under
mild
conditions.
The
optimized
CdS/Co
double‐shelled
(DSNBs)
achieved
superior
hydrogen
production
rate
of
23.45
mmol
h
−1
g
visible
light,
approximately
24
times
greater
than
that
pure
CdS
NPs.
apparent
quantum
efficiency
(AQE)
DSNBs
18.5
%.
distinctive
structure
enhances
visible‐light‐harvesting
by
exposing
active
sites,
enabling
multiple
light
reflections,
and
allowing
the
thin
shells
shorten
transport
distance
charge
carriers,
effectively
minimizing
recombination.
improved
photoactivity
results
from
synergistic
effects
aligned
bandgap
structures,
strong
visible‐light
absorption,
interfacial
interactions
driven
inherent
electric
field
(IEF).
findings
offer
insights
into
designing
efficient
catalysts
sustainable
evolution
through
water
splitting.
ACS Catalysis,
Journal Year:
2025,
Volume and Issue:
unknown, P. 1018 - 1026
Published: Jan. 2, 2025
Polymeric
carbon
nitrides
(PCNs),
usually
the
melon
phase,
have
been
extensively
applied
as
photocatalysts
for
CO2
reduction;
however,
their
performance
is
still
unsatisfactory.
The
condensed
allotrope,
namely,
poly(triazine
imide)
(PTI)
with
extended
conjugation
and
a
crystallized
structure,
indeed
holds
more
favorable
compositional
structural
advantages
photocatalytic
reduction
but
remains
to
be
fully
exploited.
Herein,
hexagonal
prism-shaped
PTI
crystals
were
synthesized
developed
high-performance
photocatalyst
reduction.
With
Co(bpy)32+
cocatalyst,
exhibit
CO
evolution
rate
of
44
μmol
h–1
(i.e.,
1467
g–1
h–1)
93%
selectivity,
markedly
superior
that
counterpart.
Moreover,
manifest
an
apparent
quantum
efficiency
12.9%
at
365
nm,
representing
state-of-the-art
value
by
PCN
CO2-to-CO
without
using
noble
metals.
surface
pyridine
N
species
are
exposed
active
sites
dominate
activation
conversion,
which,
together
high
crystallinity
facilitate
charge
separation
transport,
endows
efficiency.
In
situ
diffuse
reflectance
infrared
Fourier
transform
spectroscopy
determines
key
intermediates
during
reaction
and,
consequently,
constructs
possible
mechanism.
Chemical Reviews,
Journal Year:
2024,
Volume and Issue:
124(21), P. 12006 - 12085
Published: Oct. 31, 2024
Catalytic
COx
(CO
and
CO2)
hydrogenation
to
valued
chemicals
is
one
of
the
promising
approaches
address
challenges
in
energy,
environment,
climate
change.
H2O
an
inevitable
side
product
these
reactions,
where
its
existence
effect
are
often
ignored.
In
fact,
significantly
influences
catalytic
active
centers,
reaction
mechanism,
performance,
preventing
us
from
a
definitive
deep
understanding
on
structure-performance
relationship
authentic
catalysts.
It
necessary,
although
challenging,
clarify
provide
practical
strategies
tune
concentration
distribution
optimize
influence.
this
review,
we
focus
how
induces
structural
evolution
catalysts
assists
processes,
as
well
efforts
understand
underlying
mechanism.
We
summarize
discuss
some
representative
tuning
for
realizing
rapid
removal
or
local
enrichment
around
catalysts,
along
with
brief
techno-economic
analysis
life
cycle
assessment.
These
fundamental
understandings
further
extended
reactions
CO
CO2
reduction
under
external
field
(light,
electricity,
plasma).
also
present
suggestions
prospects
deciphering
controlling
applications.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 15, 2024
The
regulation
of
peroxymonosulfate
(PMS)
activation
by
photo-assisted
heterogeneous
catalysis
is
under
in-depth
investigation
with
potential
as
a
replaceable
advanced
oxidation
process
in
water
purification,
yet
it
remains
significant
challenge.
Herein,
we
demonstrate
strategy
to
construct
polyethylene
glycol
(PEG)
well-coupled
dual-defect
V
Journal of Materials Chemistry A,
Journal Year:
2024,
Volume and Issue:
12(24), P. 14646 - 14658
Published: Jan. 1, 2024
Multichannel-optimized
MoS
2
/Sv-ZnIn
S
4
/Cu(OH)
composites,
integrating
sulfur
vacancy,
Ohmic
junction
and
Schottky
junction,
were
synthesized
by
an
in
situ
technique.
Benefiting
from
the
synergistic
effect,
staggered
composites
exhibited
enhanced
photocatalytic
hydrogen
production
activity.
Chemistry of Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 4, 2024
The
interface
electronic
structure
of
heterogeneous
catalysts
can
be
modulated
by
changing
the
surface
coordination
configuration,
which
is
crucial
to
their
catalytic
activity.
Herein,
a
phosphorus-grafted
Ti3C2Tx
MXene
platform
anchored
with
an
MoS2
nanoflake
heterojunction
electrocatalyst
was
assembled
through
simple
phosphorus-hydrothermal
method.
An
charge
"bridge"
has
been
created
grafting
uniform
P
atoms
coordinated
O
(P-Ti3C2Tx),
resulting
in
charge-transfer
channel
between
P-Ti3C2Tx
and
MoS2.
Based
on
ultrafast
transient
absorption
spectroscopy,
fastest
electron-transfer
kinetics
from
(1.7
ps)
slowest
electron–hole
recombination
speed
(28
were
obtained
over
MoS2@P-Ti3C2Tx
than
those
MoS2@O-Ti3C2Tx
MoS2@OP-Ti3C2Tx.
Benefiting
lower
carrier
transport
activation
energy,
exhibited
stirring
electrocatalytic
activity
toward
hydrogen
evolution
all-pH
media,
delivered
three
low
overpotentials
48.6,
63.2,
70.5
mV
at
10
mA
cm–2
alkaline,
acid,
neutral
respectively.
Grafting
atomic
scale
create
proposes
new
strategy
design
efficient
pH-universal
electrocatalyst.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 27, 2024
Abstract
Photocatalytic
CO
2
reduction
serves
as
an
important
technology
for
value‐added
solar
fuel
production,
however,
it
is
generally
limited
by
interfacial
charge
transport.
To
address
this
limitation,
a
two‐dimensional/two‐dimensional
(2D/2D)
p‐n
heterojunction
CuS‐Bi
WO
6
(CS‐BWO)
with
highly
connected
and
matched
lattices
was
designed
in
work
via
two‐step
hydrothermal
tandem
synthesis
strategy.
The
integration
of
CuS
BWO
created
robust
interface
electric
field
provided
fast
transfer
channels
due
to
the
function
difference,
well
lattices.
combination
promoted
electron
from
Cu
Bi
sites,
leading
coordination
sites
high
electronic
density
low
oxidation
state.
nanosheets
facilitated
adsorption
activation
,
generation
high‐coverage
key
intermediate
b‐CO
3
2−
while
(CS)
acted
broad
light‐harvesting
material
provide
abundant
photoinduced
electrons
that
were
injected
into
conduction
band
photoreduction
reaction.
Remarkably,
CS‐BWO
exhibited
average
CH
4
yields
33.9
16.4
μmol
g
−1
h
respectively,
which
significantly
higher
than
those
CS,
BWO,
physical
mixture
samples.
This
innovative
design
strategy
developing
high‐activity
photocatalyst
converting
fuels.