Abstract
Benefiting
from
the
optimal
interaction
strength
between
Cu
and
reactants,
Cu‐based
catalysts
exhibit
a
unique
capability
of
facilitating
formation
various
multi‐carbon
products
in
electricity‐driven
CO
2
reduction
reactions
(CO
ERR).
Nonetheless,
ERR
process
on
these
is
characterized
by
intricate
polyproton‐electron
transfer
mechanisms
that
are
frequently
hindered
high
energy
barriers,
sluggish
reaction
kinetics,
low
C─C
coupling
efficiency.
This
review
employs
advanced
characterization
techniques,
such
as
sum
frequency
generation
technology,
to
provide
comprehensive
analysis
mechanism
surface,
examining
it
both
spatial
temporal
dimensions
proposing
spatial‐temporal
mechanism.
To
improve
efficiency,
series
regulatory
strategies
focused
surface
microenvironment,
catalyst
structure,
internal
electronic
thereby
offering
novel
insights
for
upcoming
design
enhancement
electrocatalysts.
Chemical Reviews,
Год журнала:
2024,
Номер
124(21), С. 12006 - 12085
Опубликована: Окт. 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.
ACS Applied Materials & Interfaces,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 20, 2025
Copper-based
catalysts
demonstrate
distinctive
multicarbon
product
activity
in
the
CO2
electroreduction
reaction
(CO2RR);
however,
their
low
selectivity
presents
significant
challenges
for
practical
applications.
Herein,
we
have
developed
a
multilevel
porous
spherical
Cu2O
structure,
wherein
mesopores
are
enriched
with
catalytic
active
sites
and
effectively
stabilize
Cu+,
while
macropores
facilitate
formation
of
"gas–liquid–solid"
three-phase
interface,
thereby
creating
microenvironment
an
increasing
water
concentration
gradient
from
interior
to
exterior.
Potential-driven
phase
engineering
protonation
synergistically
optimize
pathway,
facilitating
switch
between
CO
C2H4.
At
current
density
100
mA
cm–2,
faradaic
efficiency
(FE)
reaches
impressive
96.97%.
When
increases
1000
FEC2H4
attains
53.05%.
Experiments
theoretical
calculations
indicate
that
at
lower
potentials,
pure
diminishes
adsorption
*CO
intermediates,
weak
inhibits
hydrogen
evolution
reactions,
promoting
production.
Conversely,
more
negative
Cu0/Cu+
interface
strong
generate
locally
elevated
concentrations
*COOH
which
enhance
C–C
coupling
deep
hydrogenation,
ultimately
improving
toward
C2+
products.
This
study
provides
novel
insights
into
rational
design
copper-based
customizable
Journal of the American Chemical Society,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 4, 2025
The
electrochemical
CO2
reduction
reaction
(eCO2RR)
is
a
promising
approach
for
converting
to
useful
chemicals
and,
hence,
achieving
carbon
neutrality.
Though
high
selectivity
and
activity
of
products
have
been
achieved
recently,
all
are
reported
in
neutral
or
alkaline
electrolytes.
Although
these
electrolyte
media
give
activity,
they
face
the
major
challenge
low
utilization
because
carbonate
formation,
which
lowers
overall
efficiency
process.
Conducting
eCO2RR
acidic
can
help
overcome
issue
formation
hence
increase
efficiency.
However,
there
many
challenges
associated
with
eCO2RR.
Two
concerns
highly
competitive
hydrogen
evolution
salt
precipitation
issues.
This
Perspective
focuses
on
fundamentals
eCO2RR,
recent
catalyst
development
strategies,
relevant
problems
that
need
be
addressed
future.
In
end,
we
provide
future
outlook
will
an
idea
about
focus
field
Nano Letters,
Год журнала:
2024,
Номер
24(30), С. 9345 - 9352
Опубликована: Июль 16, 2024
The
electrochemical
CO2
reduction
reaction
(eCO2RR)
to
multicarbon
chemicals
provides
a
promising
avenue
for
storing
renewable
energy.
Herein,
we
synthesized
small
Cu
nanoparticles
featuring
enriched
tiny
grain
boundaries
(RGBs-Cu)
through
spatial
confinement
and
in
situ
electroreduction.
In-situ
spectroscopy
theoretical
calculations
demonstrate
that
small-sized
significantly
enhance
the
adsorption
of
*CO
intermediate,
owing
presence
abundant
low-coordinated
disordered
atoms.
Furthermore,
these
boundaries,
generated
under
high
current
conditions,
exhibit
excellent
stability
during
eCO2RR
process,
thereby
creating
stable
*CO-rich
microenvironment.
This
local
concentration
around
catalyst
surface
can
reduce
energy
barrier
C–C
coupling
increase
Faradaic
efficiency
(FE)
products
across
both
neutral
alkaline
electrolytes.
Specifically,
developed
RGBs-Cu
electrocatalyst
achieved
peak
FE
77.3%
maintained
more
than
134
h
at
constant
density
−500
mA
cm–2.
Abstract
The
electrochemical
activation
of
inert
CO
2
molecules
through
C─C
coupling
reactions
under
ambient
conditions
remains
a
significant
challenge
but
holds
great
promise
for
sustainable
development
and
the
reduction
emission.
Lewis
pairs
can
capture
react
with
,
offering
novel
strategy
electrosynthesis
high‐value‐added
C2
products.
Herein,
an
electron‐beam
irradiation
is
presented
rapidly
synthesizing
metal–organic
framework
(MOF)
well‐defined
(i.e.,
Cu‐
N
pyridinic
).
synthesized
MOFs
exhibit
total
product
faradic
efficiency
70.0%
at
−0.88
V
versus
RHE.
In
situ
attenuated
reflection
Fourier
transform
infrared
Raman
spectra
reveal
that
electron‐deficient
acidic
Cu
sites
electron‐rich
basic
in
ligand
facilitate
targeted
chemisorption,
activation,
conversion
molecules.
DFT
calculations
further
elucidate
electronic
interactions
key
intermediates
reaction.
work
not
only
advances
pair‐site
as
new
platform
conversion,
also
provides
pioneering
insights
into
underlying
mechanisms
irradiated
synthesis
advanced
nanomaterials.
Carbon
dioxide
reduction
reaction
(CO2RR)
is
an
efficacious
method
to
mitigate
carbon
emissions
and
simultaneously
convert
CO2
into
high-value
products.
The
efficiency
of
CO2RR
depends
on
the
development
highly
active
selective
catalysts.
Copper
(Cu)-based
catalysts
can
effectively
reduce
hydrocarbons
oxygen-containing
compounds
because
their
unique
geometric
electronic
structures.
Most
importantly,
Cu
multiple
products
(C2+).
Therefore,
this
review
aims
outline
recent
research
progress
in
Cu-based
for
CO2RR.
After
introducing
mechanism
electroreduction
reaction,
we
summarize
influence
size,
morphology,
coordination
environment
single
component
performance,
especially
performance
control
that
contain
nano
or
single-atom
sites.
Then,
synergistic
regulation
strategies
doping
other
metals
are
summarized.
Finally,
supports
used
reviewed.
prospects
challenges
discussed.
Heterogeneous
catalysis
is
a
surface
phenomenon
where
the
adsorption,
desorption,
and
transfer
of
reactants
products
are
critical
for
catalytic
performance.
Recent
results
show
that
catalyst
wettability
strongly
related
to
products.
In
this
review,
we
briefly
summarize
strategies
regulating
enrich
reactants,
accelerate
desorption
products,
promote
mass
in
heterogeneous
catalysis.
addition,
explore
insights
into
enhancement
Finally,
concerns
challenges
subject
outlined,
practical
proposed
regulation
wettability.
We
hope
review
will
be
helpful
designing
highly
efficient
catalysts
future.
The
interaction
between
liquids
and
surfaces
is
a
common
phenomenon
in
nature
has
attracted
extensive
scientific
attention.
Among
these
interactions,
the
dynamic
behavior
of
on
superspreading
exhibits
significant
diversity,
which
can
be
categorized
into
four
processes:
impact,
spreading,
film
formation,
phase
transition.
Traditional
characterization
using
equilibrium
contact
angle
(CA)
proves
insufficient
for
describing
liquid
behaviors.
Recent
studies
introduce
time
(ST)
curve
radius
versus
spreading
(SRST),
providing
comprehensive
understanding
processes.
This
review
systematically
analyzes
behaviors
surfaces,
including
their
underlying
mechanisms
associated
influencing
factors.
Furthermore,
we
discuss
applications
by
categorizing
them
unsteady-state
films
steady-state
films.
leverage
processes,
such
as
transition,
to
enhance
thermal
management
efficiency,
bubble
detachment,
photothermal
conversion,
convective
heat
transfer.
In
contrast,
focus
stable
thin
formation
use
areas
antifouling
coatings,
drag
reduction,
biomaterial
enhancement,
uniform
fabrication.
Finally,
highlight
existing
challenges
liquid-solid
fundamental
research
industrial
applications.
provides
insights
both
practical
arousing
attention
field
strengthen
mechanism
promote