Small,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 24, 2025
Abstract
Recently,
the
enzyme‐inspired
nanoconfinement
effect
has
garnered
significant
attention
for
enhancing
efficiency
of
electrocatalysts
and
photocatalysts.
Despite
substantial
progress
in
these
fields,
there
remains
a
notable
absence
comprehensive
insightful
articles
providing
clear
understanding
nanoconfined
catalysts.
This
review
addresses
this
gap
by
delving
into
catalysts
electrocatalytic
photocatalytic
energy
conversion.
Initially,
on
thermodynamics
kinetics
reactions
is
explored.
Subsequently,
primary
secondary
structures
are
categorized,
their
properties
outlined,
typical
methods
construction
summarized.
Furthermore,
an
overview
state‐of‐the‐art
applications
provided,
focusing
hydrogen
oxygen
evolution,
reduction,
carbon
dioxide
peroxide
production,
nitrogen
reduction.
Finally,
current
challenges
future
prospects
discussed.
aims
to
provide
in‐depth
insights
guidelines
advance
development
conversion
technology
Angewandte Chemie International Edition,
Journal Year:
2023,
Volume and Issue:
62(43)
Published: June 20, 2023
Upgrading
CO2
into
multi-carbon
(C2+)
compounds
through
the
reduction
reaction
(CO2
RR)
offers
a
practical
approach
to
mitigate
atmospheric
while
simultaneously
producing
high
value
chemicals.
The
pathways
for
C2+
production
involve
multi-step
proton-coupled
electron
transfer
(PCET)
and
C-C
coupling
processes.
By
increasing
surface
coverage
of
adsorbed
protons
(*Had
)
*CO
intermediates,
kinetics
PCET
can
be
accelerated,
thereby
promoting
production.
However,
*Had
are
competitively
intermediates
on
monocomponent
catalysts,
making
it
difficult
break
linear
scaling
relationship
between
adsorption
energies
/*CO
intermediate.
Recently,
tandem
catalysts
consisting
multicomponents
have
been
developed
improve
or
by
enhancing
water
dissociation
-to-CO
auxiliary
sites.
In
this
context,
we
provide
comprehensive
overview
design
principles
based
products.
Moreover,
development
cascade
RR
catalytic
systems
that
integrate
with
downstream
catalysis
has
expanded
range
potential
upgrading
Therefore,
also
discuss
recent
advancements
in
systems,
highlighting
challenges
perspectives
these
systems.
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 13, 2024
Single-atom
electrocatalysts
(SACs)
are
a
class
of
promising
materials
for
driving
electrochemical
energy
conversion
reactions
due
to
their
intrinsic
advantages,
including
maximum
metal
utilization,
well-defined
active
structures,
and
strong
interface
effects.
However,
SACs
have
not
reached
full
commercialization
broad
industrial
applications.
This
review
summarizes
recent
research
achievements
in
the
design
crucial
electrocatalytic
on
sites,
coordination,
substrates,
as
well
synthesis
methods.
The
key
challenges
facing
activity,
selectivity,
stability,
scalability,
highlighted.
Furthermore,
it
is
pointed
out
new
strategies
address
these
increasing
activity
enhancing
utilization
improving
optimizing
local
environment,
developing
fabrication
techniques,
leveraging
insights
from
theoretical
studies,
expanding
potential
Finally,
views
offered
future
direction
single-atom
electrocatalysis
toward
commercialization.
ACS Applied Materials & Interfaces,
Journal Year:
2024,
Volume and Issue:
16(22), P. 29060 - 29068
Published: May 20, 2024
Highly
efficient
electrochemical
CO2-to-CO
conversion
is
a
promising
approach
for
achieving
carbon
neutrality.
While
nonmetallic
electrocatalysts
have
shown
potential
utilization
in
H-type
cells,
flow
cells
at
an
industrial
scale
remains
challenging.
In
this
study,
we
present
cost-effective
synthesis
strategy
preparing
ultrathin
2D
nanosheet
catalysts
through
simple
amine
functionalization.
The
optimized
catalyst,
NCNs-2.5,
demonstrates
exceptional
CO
selectivity
with
maximum
Faradaic
efficiency
of
98%
and
achieves
high
current
density
55
mA
cm-2
cell.
Furthermore,
the
catalyst
exhibits
excellent
long-term
stability,
operating
continuously
50
h
while
maintaining
above
90%.
superior
catalytic
activity
NCNs-2.5
attributed
to
presence
amine-N
active
sites
within
lattice
structure.
This
work
establishes
foundation
rational
design
as
sustainable
alternatives
metals
energy
systems.
ACS Energy Letters,
Journal Year:
2025,
Volume and Issue:
10(1), P. 620 - 628
Published: Jan. 3, 2025
Polymeric
ionomers
near
the
catalyst
surface
of
CO2
reduction
reaction
(CO2RR)
electrodes
affect
their
efficiency;
however,
multifaceted
properties
complicate
structure–activity
relationship
elucidation.
Here,
we
synthesized
polycarbazole-based
anion-exchange
(QPC)
bearing
varying
functionalized
side
chains
to
explore
this
relationship.
Comprehensive
analysis
in
physicochemical
properties,
electrochemical
activity,
and
operando
ATR-SEIRAS
revealed
that
functional
group
modification
significantly
influenced
intrinsic
ionomer
thereby
affecting
Ag
microenvironments
interfacial
water
structures,
kinetics
protonation
step
for
CO2RR
hydrogen
evolution
(HER).
Notably,
QPC-trimethyl
phosphonium
(TMP)
induced
favorable
having
a
high
proportion
strong
H-bonded
with
low
Stark
tuning
slopes,
which
inhibit
HER
promote
CO2RR.
A
CO
Faradaic
efficiency
(>90%)
was
maintained
using
QPC-TMP
membrane
electrode
assembly,
even
under
concentrations
(100–15%)
elevated
temperatures
(28–72
°C).
These
findings
suggest
catalytic
environment
can
be
optimized
by
fine-tuning
structure,
contributing
advancement
high-performance
ionomers.
Advanced Functional Materials,
Journal Year:
2023,
Volume and Issue:
33(25)
Published: March 10, 2023
Abstract
It
is
highly
desired
yet
challenging
to
strategically
steer
carbon
dioxide
(CO
2
)
electroreduction
reaction
ER)
toward
ethanol
(EtOH)
with
high
activity,
which
provides
a
promising
way
for
intermittent
renewable
energy
reservation.
Controlling
spatial
distance
between
the
adjoining
active
centers
and
promoting
CC
coupling
progress
are
crucial
realize
this
purpose.
Herein,
ultrathin
2D
Cu
2‐x
Se
prepared
abundant
vacancies,
where
CuCu
around
vacancies
effectively
shortened
because
of
lattice
stress.
Besides,
moderate
induced
by
can
significantly
decrease
Gibbs
free
asymmetric
*CO*CHO
progress,
change
local
charge
distribution,
valence
state
atoms
increase
electron‐donating
capacity
dual
sites.
Combining
experimental
observations
density
functional
theory
simulations,
sites
2.51
Å
in
V
‐Cu
sample
catalyze
CO
ER
EtOH
selectivity
potential
range
from
−0.4
−1.6
V,
reach
highest
faradaic
efficiency
68.1%
at
−0.8
V.
This
work
reveals
influence
spacing
effect
on
selectivity,
new
idea
future
design
catalysts
chain
elongation
reaction,
bring
extensive
attention.
Advanced Functional Materials,
Journal Year:
2023,
Volume and Issue:
33(32)
Published: April 25, 2023
Abstract
Electrochemical
carbon
dioxide
(CO
2
)
conversion
technologies
have
become
new
favorites
for
addressing
environmental
and
energy
issues,
especially
with
direct
electrocatalytic
reduction
of
CO
(ECO
RR)
alkali
metal‐CO
(M–CO
batteries
as
representatives.
They
are
poised
to
create
economic
drivers
while
also
paving
the
way
a
cleaner
more
sustainable
future
humanity.
Although
still
far
from
practical
application,
ECO
RR
has
been
intensively
investigated
over
last
few
years,
some
achievements.
In
stark
contrast,
M–CO
batteries,
aqueous
hybrid
offer
potential
combine
storage
into
an
integrated
system,
but
their
research
is
in
early
stages.
This
article
gives
insightful
review,
comparison,
analysis
recent
advances
illustrating
similarities
differences,
aiming
advance
development
innovation.
Considering
crucial
role
well‐designed
functional
materials
facilitating
special
attention
paid
rational
design
strategies
components,
such
electrodes/catalysts,
electrolytes,
membranes/separators,
at
industrial
level
impact
on
conversion.
Moreover,
perspectives
suggestions
presented
facilitate
applications.
ACS Sustainable Chemistry & Engineering,
Journal Year:
2023,
Volume and Issue:
11(24), P. 9057 - 9064
Published: June 6, 2023
As
a
nitrogen-containing
source,
nitrate
is
regarded
as
promising
precursor
for
generating
ammonia
(NH3)
through
electrochemical
processes
that
can
potentially
mitigate
the
problem
of
groundwater
contamination
and
hydrogen-carrier
energy
crisis.
Herein,
we
report
cobalt
zeolitic
imidazolate
framework
(ZIF-67)-derived
catalyst
CoNi
alloys
incorporated
in
N-doped
carbon
frameworks
electroreduction.
Computational
results
obtained
using
density
functional
theory
give
deep
insight
structure
embedded
skeleton
inhibit
production
hydrogen
facilitate
hydrogenation
*NO
intermediates.
The
enriched
active
sites
from
ZIF-67-derived
introduction
Ni
afford
desirable
electrocatalytic
performance.
Finally,
optimized
CoNi@NC
hybrid
achieve
an
168
mmol
gcat–1
h–1
Faradaic
efficiency
∼93%
at
potential
low
−0.1
V
vs
reversible
electrode
(RHE).
highest
yield
rate
1254
be
detected
−0.6
RHE.
This
study
inspire
further
development
non-noble
metal-based
electrocatalysts
reduction
also
anticipation
into
sustainable
synthesis
carbon-related
fuels
CO2
reduction.