Proceedings of the National Academy of Sciences,
Год журнала:
2024,
Номер
121(42)
Опубликована: Окт. 10, 2024
Catalytic
oxidation
through
the
transfer
of
lattice
oxygen
from
metal
oxides
to
reactants,
namely
Mars-van
Krevelen
mechanism,
has
been
widely
reported.
In
this
study,
we
evidence
overlooked
route
that
features
in
situ
formation
surface
OH
species
on
Cu
catalysts
and
its
selective
addition
reactant
carbonyl
group.
We
observed
glucose
gluconic
acid
air
(21%
O
Advanced Energy Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Июнь 27, 2024
Abstract
Artificial
photosynthesis
emerges
as
a
strategic
pathway
to
produce
hydrogen
peroxide
(H
2
O
),
an
environmentally
benign
oxidant
and
clean
energy
carrier.
Nonetheless,
in
many
heterojunction‐based
artificial
photosynthetic
systems,
the
H
productivity
is
significantly
hindered
by
poor
carrier
transport,
narrow
spectral
light
absorption,
lack
of
adequate
active
sites
for
two‐electron
oxygen
reduction
reaction.
Herein,
catalyst
architecture
with
iso‐elemental
heterojunction
formed
interfacing
Zn
3
In
S
6
nano‐flowers
ZnIn
4
nanosheets
proposed.
This
exhibits
production
rate
high
23.47
µmol
g
−1
min
under
UV–vis
irradiation,
which
attributed
minimized
contact
barrier
enhanced
lattice
match
at
/Zn
interface
thanks
aids
efficient
separation
transfer
photogenerated
carriers.
Theoretical
simulations
alongside
comprehensive
in‐situ
ex‐situ
characterizations
confirm
photo‐redox
generation
effective
dynamics
across
surface.
Moreover,
substituting
one
reduction‐type
other
non‐iso‐elemental
catalysts
like
CdIn
,
TiO
CdS
further
confirms
feasibility
superiority
proposed
configuration.
work
offers
new
perspective
on
designing
.
ACS Applied Nano Materials,
Год журнала:
2024,
Номер
7(8), С. 8716 - 8729
Опубликована: Апрель 12, 2024
Synergetic
photocatalytic
H2
production
by
organic
dye
photodegradation
is
always
a
goal.
However,
the
related
research
has
been
hindered
due
to
uncontrollability
of
this
process.
This
study
prepares
ZnO/Bi-QDs/BiOBr
photocatalyst,
and
hole
(h+)
aggregation
phase
(ZnO)
constructed
into
lamellar
porous
structure
improve
its
adsorption
capacity
for
dyes
based
on
energy
level
composite.
By
method,
reactive
groups
used
are
controlled
h+
•OH,
e–
production,
synergistic
effect
realized.
Under
action
photocatalyst
visible
light,
rhodamine
B
(RhB)
completely
degraded
in
8
min,
time
can
be
reduced
2
min
when
pH
5,
it
realize
complete
degradation
RhB
120
under
natural
sunlight.
The
rate
reaches
1678
μmol·g–1·h–1
(h+
scavenger)
aqueous
solution
light.
provides
an
effective
method
design
idea
photocatalysts
with
during
dyes.
Advanced Functional Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Окт. 14, 2024
Abstract
The
photocatalytic
oxygen
reduction
reaction
(ORR)
is
a
key
pathway
for
producing
hydrogen
peroxide
(H
2
O
).
While
most
previous
studies
have
focused
on
the
two‐step
2e
−
ORR
process,
one‐step
two‐electron
route
offers
thermodynamic
and
kinetic
advantages
that
can
significantly
enhance
activity
selectivity.
In
this
study,
photocatalyst
design
reported
by
incorporating
cadmium
into
vacancy‐rich
Zn
3
S
6
(Cd‐S
V
/ZIS).
This
catalyst
enables
H
production
via
process
without
use
of
sacrificial
agents,
achieving
high
yield
39.42
µmol
g
−1
min
under
UV–vis
light
irradiation,
outperforming
ZIS‐based
photocatalysts.
Theoretical
simulations
experimental
results
demonstrate
Cd
doping
improves
carrier
kinetics
catalyst,
broadens
its
absorption
range,
promotes
Yeager
adsorption
configuration
,
leading
to
highly
active
selective
generation.
study
provides
insights
efficient
photocatalysts
production.
The
metal
indium
sulfides
have
attracted
extensive
research
interest
in
photocatalysis
due
to
regulable
atomic
configuration
and
excellent
optoelectronic
properties.
However,
the
synthesis
of
sulfide
layers
is
still
challenging
since
intrinsic
non-van-der-Waals
layered
structures
some
components.
Here,
a
surfactant
self-assembly
growth
mechanism
proposed
controllably
synthesize
layers.
Eleven
types
with
tunable
compositions,
thickness,
defect
concentrations
are
successfully
achieved
namely
In
ACS Nano,
Год журнала:
2024,
Номер
18(32), С. 21585 - 21592
Опубликована: Авг. 5, 2024
Building
a
polarization
center
is
an
effective
avenue
to
boost
charge
separation
and
molecular
activation
in
photocatalysis.
However,
limited
number
of
centers
are
usually
created.
Here,
plane
based
on
two-dimensional
(2D)
atomic
layers
designed
maximize
the
surface
centers.
The
Mn
2D
crystal
lattice
etched
from
MnIn2S4
build
consecutive
symmetry-breaking
structure
isolated
InO1S5
sites.
More
charges
aggregate
around
O,
making
sites
highly
polarized.
Due
formation
plane,
enormous
polarized
electric
field
formed
perpendicular
carrier
lifetime
can
be
prolonged
93.2
ps
1130
amorphous
MnxIn2Sy.
Meantime,
large
density
gradient
favors
coupling
small
molecules.
Benefiting
these
features,
good
NH3
photosynthesis
performance
(515.8
μmol
g–1
h–1)
realized
over
MnxIn2Sy,
roughly
2.5
48.9
times
higher
than
those
bulk
MnIn2S4,
respectively.
apparent
quantum
yields
reach
5.4
3.3%
at
380
400
nm,
Meanwhile,
greatly
improved
CO2
reduction
activity
also
achieved
This
strategy
provides
accessible
pathway
for
designing
asymmetrical
motivate
photocatalysis
optimization.
ACS Nano,
Год журнала:
2024,
Номер
18(52), С. 35749 - 35757
Опубликована: Дек. 18, 2024
We
present
an
effective
strategy
for
developing
the
dispersing
strong-binding
metal
In
on
surface
of
weak-binding
Zn,
which
modulates
binding
energy
reaction
intermediates
and
further
facilitates
efficient
conversion
CO2
to
formate.
The
In-Zn
interface
(In-Zn2)
benefits
from
formation
active
sites
through
favorable
orbital
interactions,
leading
a
Faradaic
efficiency
82.7%
formate
partial
current
density
12.39
mA
cm-2,
along
with
stable
performance
over
15
h
at
-1.0
V
versus
reversible
hydrogen
electrode.
Both
in
situ
Fourier
transform
infrared
spectroscopy
functional
theory
calculations
show
that
bimetallic
catalyst
can
deliver
superior
*OCHO
intermediate,
thereby
fundamentally
accelerating
addition,
exposed
promotes
capture
activation
molecules
dynamics
within
significantly
reduce
barrier
associated
generation
HCOO-,
thus
augmenting
selectivity
catalytic
activity
generation.