ACS Applied Materials & Interfaces,
Journal Year:
2024,
Volume and Issue:
16(3), P. 3368 - 3387
Published: Jan. 12, 2024
The
electrochemical
synthesis
of
syngas
(CO
and
H2)
has
garnered
considerable
attention
in
the
context
Fischer–Tropsch
(FT)
employing
thermal
catalysts.
Nonetheless,
need
for
a
novel,
cost-effective
technique
persists.
In
this
investigation,
we
introduce
direct
(dEC)
approach
FT
that
functions
under
ambient
conditions
by
utilizing
p-block
element
(Sn
In)
overlaid
Cu
electrode.
Surface
*CO
H*
species
were
obtained
an
electrolytic
medium
through
CO2
+
H+
e–
→
HOOCad
(or
CO
adsorption)
reactions,
respectively.
We
have
observed
C2–7
long-chain
hydrocarbons
with
CnH2n+2/CnH2n
ratio
1–3,
observation
can
be
explained
process
C–C
coupling
chain
growth
conventional
synthesis,
based
on
linearity
Anderson-Schulz–Flory
equation
plots.
Thick
Sn
overlayers
resulted
dominant
production
formate,
while
C2H4
found
to
proportional
inversely
correlated
H2,
C2H6,
C3–7
hydrocarbon
production.
EC
CO2/CO
reduction
used
dEC
offers
valuable
insights
into
mechanism
C2+
holds
promise
as
eco-friendly
producing
energy
environmental
purposes.
Chemical Reviews,
Journal Year:
2019,
Volume and Issue:
119(12), P. 7610 - 7672
Published: May 22, 2019
To
date,
copper
is
the
only
heterogeneous
catalyst
that
has
shown
a
propensity
to
produce
valuable
hydrocarbons
and
alcohols,
such
as
ethylene
ethanol,
from
electrochemical
CO2
reduction
(CO2R).
There
are
variety
of
factors
impact
CO2R
activity
selectivity,
including
surface
structure,
morphology,
composition,
choice
electrolyte
ions
pH,
cell
design.
Many
these
often
intertwined,
which
can
complicate
discovery
design
efforts.
Here
we
take
broad
historical
view
different
aspects
their
complex
interplay
in
catalysis
on
Cu,
with
purpose
providing
new
insights,
critical
evaluations,
guidance
field
regard
research
directions
best
practices.
First,
describe
various
experimental
probes
complementary
theoretical
methods
have
been
used
discern
mechanisms
by
products
formed,
next
present
our
current
understanding
reaction
networks
for
Cu.
We
then
analyze
two
key
attempts
alter
selectivity
Cu:
nanostructuring
formation
bimetallic
electrodes.
Finally,
offer
some
perspectives
future
outlook
CO2R.
ACS Energy Letters,
Journal Year:
2020,
Volume and Issue:
5(4), P. 1044 - 1053
Published: Feb. 6, 2020
We
report
single-atom
Cu
catalysts
dispersed
on
nitrogen-doped
carbon
by
a
nitrogen-coordination
strategy.
The
presence
of
nitrogen
enabled
good
dispersion
and
attachment
atomic
species
the
frameworks
with
Cu–Nx
configurations.
doping
concentrations
configurations
were
well-tuned
pyrolysis
temperature.
At
high
concentration
4.9%mol,
distance
between
neighboring
was
close
enough
to
enable
C–C
coupling
produce
C2H4.
In
contrast,
at
lower
than
2.4%mol,
large
so
that
electrocatalyst
favored
formation
CH4
as
C1
products.
Density
functional
theory
calculations
further
confirmed
capability
producing
C2H4
two
CO
intermediates
binding
adjacent
Cu–N2
sites,
while
isolated
Cu–N4,
sites
led
CH4.
Our
work
demonstrates
facile
approach
tuning
active
for
CO2
electroreduction
different
hydrocarbons.
ACS Catalysis,
Journal Year:
2019,
Volume and Issue:
9(3), P. 2018 - 2062
Published: Jan. 15, 2019
Structurally
ordered
intermetallic
compounds
possess
unique
chemical
and
physical
properties,
making
them
an
interesting
class
of
materials
for
application
in
electrocatalytic
reactions.
This
Review
comprises
the
work
on
used
energy
relevant
electrocatalysis
is
structured
by
reactions
scope,
which
are
hydrogen
evolution
reaction
(HER),
electrochemical
carbondioxide
reduction
(eCO2RR),
oxygen
(ORR),
oxidation
(HOR)
as
well
formic
acid
(FAOR),
methanol
(MOR),
ethanol
(EtOR).
Optimization
pathways
electrocatalysts,
based
adjustability
materials,
highlighted,
experimental
data
provided
a
comparative
manner,
to
provide
overview,
foundation,
reference
further
development.
ACS Catalysis,
Journal Year:
2019,
Volume and Issue:
9(5), P. 3783 - 3791
Published: March 18, 2019
Earth-abundant
electrocatalysts
are
desirable
for
the
efficient
and
selective
reduction
of
CO2
to
value-added
chemicals.
Here,
a
low-cost
porous
Zn
electrocatalyst
is
synthesized
using
facile
electrodeposition
method
boost
performance
electrocatalytic
reaction
(CO2RR).
In
an
H-cell
reactor,
catalyst
can
convert
CO
at
remarkably
high
faradaic
efficiency
(FE,
∼95%)
current
density
(27
mA
cm–2)
−0.95
V
versus
reversible
hydrogen
electrode.
Detailed
electrokinetic
studies
demonstrate
that
instead
enhanced
intrinsic
activity,
dramatically
increased
active
sites
play
decisive
role
in
improving
catalytic
activity.
addition,
local
pH
induced
by
highly
structure
results
selectivity
because
suppressed
H2
evolution.
Furthermore,
we
present
straightforward
strategy
transform
electrode
into
gas
diffusion
This
way,
CO2RR
be
boosted
200
cm–2
with
∼84%
FE
−0.64
flow-cell
which
is,
date,
best
observed
over
non-noble
catalysts.
Advanced Materials,
Journal Year:
2020,
Volume and Issue:
32(17)
Published: March 5, 2020
Abstract
Electrochemical
reduction
of
carbon
dioxide
(CO
2
RR)
product
distribution
has
been
identified
to
be
dependent
on
various
surface
factors,
including
the
Cu
facet,
morphology,
chemical
states,
doping,
etc.,
which
can
alter
binding
strength
key
intermediates
such
as
*CO
and
*OCCO
during
reduction.
Therefore,
in‐depth
knowledge
catalyst
identification
active
species
under
reaction
conditions
aid
in
designing
efficient
Cu‐based
electrocatalysts.
This
progress
report
categorizes
electrocatalysts
into
four
main
groups,
namely
metallic
Cu,
alloys,
compounds
(Cu
+
non‐metal),
supported
catalysts
by
carbon,
metal
oxides,
or
polymers).
The
detailed
mechanisms
for
selective
CO
RR
are
presented,
followed
recent
relevant
developments
synthetic
procedures
preparing
nanoparticles.
Herein,
potential
link
between
performance
is
highlighted,
especially
terms
but
other
significant
factors
defective
sites
roughened
morphology
equally
considered
discussion
current
studies
with
fully
understand
origin
enhancement
toward
C
formation.
concludes
providing
suggestions
future
designs
highly
stable
RR.
Advanced Materials,
Journal Year:
2021,
Volume and Issue:
33(32)
Published: May 29, 2021
With
the
capability
of
inducing
intense
electromagnetic
field,
energetic
charge
carriers,
and
photothermal
effect,
plasmonic
metals
provide
a
unique
opportunity
for
efficient
light
utilization
chemical
transformation.
Earth-abundant
low-cost
Cu
possesses
tunable
localized
surface
plasmon
resonance
from
ultraviolet-visible
to
near
infrared
region.
Moreover,
essentially
exhibits
remarkable
catalytic
performance
toward
various
reactions
owing
its
intriguing
physical
properties.
Coupling
with
light-harvesting
ability
function,
serves
as
promising
platform
light-driven
reaction.
Herein,
recent
advancements
Cu-based
photocatalysis
are
systematically
summarized,
including
designing
synthetic
strategies
catalysts,
performance,
mechanistic
understanding
over
catalysts.
What's
more,
approaches
enhancement
efficiency
construction
active
centers
on
catalysts
highlighted
discussed
in
detail,
such
morphology
size
control,
regulation
electronic
structure,
defect
strain
engineering,
etc.
Remaining
challenges
future
perspectives
further
development
catalysis
also
proposed.
Small Methods,
Journal Year:
2018,
Volume and Issue:
3(3)
Published: Dec. 12, 2018
Abstract
Electrochemical
reduction
of
CO
2
into
value‐added
chemicals
or
fuels,
driven
by
renewable
energy,
presents
a
promising
solution
to
depletion
fossil
fuels
and
greenhouse
effects
caused
excessive
carbon
emissions.
In
the
past
few
years,
great
efforts
have
been
dedicated
promote
research
in
this
field.
Herein,
review
focuses
on
recent
advances
underlying
mechanistic
studies
novel
heterogeneous
catalyst
constructions
for
electrochemical
aqueous
media,
targeting
at
presenting
full
landscape
current
stage.
The
outlook
future
development
is
also
included
end
review.