Deleted Journal,
Год журнала:
2024,
Номер
3(3), С. e9120112 - e9120112
Опубликована: Янв. 18, 2024
Electrocatalytic
carbon
dioxide
reduction
reaction
(CO2RR)
holds
the
promise
of
both
overcoming
greenhouse
effect
and
synthesizing
a
wealth
chemicals.
CO2
toward
carbon-containing
products,
including
C1
products
(carbon
monoxide,
formic
acid,
etc),
C2
(ethylene,
ethanol,
etc.)
multi-carbon
(e.g.,
npropanol),
provides
beneficial
fuel
chemicals
for
industrial
production.
The
complexity
multi-proton
transfer
processes
difficulties
C-C
coupling
in
electrochemical
multi-carbon(C2+)
have
attracted
increasing
concerns
on
design
catalysts
comparison
with
those
products.
In
this
paper,
we
review
main
advances
syntheses
through
electrocatalytic
recent
years,
introduce
basic
principles
CO2RR,
detailly
elucidate
two
widely
accepted
mechanisms
reactions.
Among
abundant
nanomaterials,
copper-based
are
outstanding
preparation
CO2RR
attributing
to
effective
Regarding
different
selectivity
but
extensively
applied
catalysts,
classify
summarize
various
Cu-based
separating
diverse
where
modification
spatial
electronic
structures
is
increase
coverage
CO
or
lower
activation
energy
barrier
forming
CC
bond
form
key
intermediates
production
Challenges
prospects
involving
fundamental
development
also
proposed.
Advanced Materials,
Год журнала:
2023,
Номер
36(5)
Опубликована: Авг. 31, 2023
Abstract
Electrocatalytic
CO
2
reduction
into
value‐added
fuels
and
chemicals
by
renewable
electric
energy
is
one
of
the
important
strategies
to
address
global
shortage
carbon
emission.
Though
classical
H‐type
electrolytic
cell
can
quickly
screen
high‐efficiency
catalysts,
low
current
density
limited
mass
transfer
process
essentially
impede
its
industrial
applications.
The
cells
based
on
electrolyte
flow
system
(flow
cells)
have
shown
great
potential
for
devices,
due
higher
density,
improved
local
concentration,
better
efficiency.
design
optimization
are
significance
further
accelerate
industrialization
electrocatalytic
reaction
(CO
RR).
In
this
review,
progress
RR
C
2+
products
concerned.
Firstly,
main
events
in
development
outlined.
Second,
principles
products,
architectures,
types
summarized.
Third,
optimizing
generate
reviewed
detail,
including
cathode,
anode,
ion
exchange
membrane,
electrolyte.
Finally,
preliminary
attempts,
challenges,
research
prospects
toward
discussed.
Angewandte Chemie International Edition,
Год журнала:
2022,
Номер
62(10)
Опубликована: Дек. 12, 2022
Unrestrained
anthropogenic
activities
have
severely
disrupted
the
global
natural
nitrogen
cycle,
causing
numerous
energy
and
environmental
issues.
Electrocatalytic
transformation
is
a
feasible
promising
strategy
for
achieving
sustainable
economy.
Synergistically
combining
multiple
reactions
can
realize
efficient
renewable
storage
conversion,
restore
balance,
remediate
crises.
Here,
we
provide
unique
aspect
to
discuss
intriguing
electrochemistry
by
linking
three
essential
nitrogen-containing
compounds
(i.e.,
N2
,
NH3
NO3-
)
integrating
four
electrochemical
reactions,
i.e.,
reduction
reaction
(N2
RR),
oxidation
OR),
nitrate
(NO3
ammonia
(NH3
OR).
This
minireview
also
summarizes
acquired
knowledge
of
rational
catalyst
design
underlying
mechanisms
these
interlinked
reactions.
We
further
underscore
associated
clean
technologies
nitrogen-based
ACS Catalysis,
Год журнала:
2023,
Номер
13(7), С. 4221 - 4230
Опубликована: Март 13, 2023
The
atomically
dispersed
iron
site
and
nitrogen
co-doped
carbon
catalysts
(Fe–N–C)
have
demonstrated
promising
performance
in
replacing
Pt
toward
the
oxygen
reduction
reaction
(ORR)
acids
for
proton
exchange
membrane
fuel
cells.
However,
insufficient
durability
of
Fe–N–C
prohibitively
hinders
their
practical
applications.
Herein,
we
report
that
co-doping
Zr
Fe
dual
metal
sites
into
a
ZIF-8-derived
mesoporous
exhibited
significantly
improved
ORR.
Especially,
electrode
assembly
from
ORR
cathode
catalyst
only
lost
25%
voltage
after
20
h
continuous
operation
at
constant
current
density.
After
an
extended
test
up
to
100
h,
Zr-doped
retained
40%
its
initial
performance,
superior
without
doping
with
more
than
70%
activity
loss
h.
also
showed
activity,
achieving
maximum
power
density
0.72
W
cm–2
under
H2/air
conditions.
Extensive
experimental
characterization
functional
theory
calculations
suggested
promoted
catalytic
stability
are
due
formation
Zr-based
active
enhanced
acidic
tolerance
individual
sites.
Also,
could
suppress
H2O2
other
free
radicals,
thus
mitigating
degradation.
possible
Fe/Zr
dual-metal
sites,
i.e.,
N2(N)–Fe–N2–Zr–N2(O2),
likely
intrinsic
relative
conventional
FeNx
Advanced Energy Materials,
Год журнала:
2023,
Номер
13(28)
Опубликована: Июнь 8, 2023
Abstract
Single‐atom
catalysts
(SACs)
have
been
emerging
as
attractive
catalytic
materials
in
electrocatalysis
for
sustainable
energy
storage
and
conversion.
To
realize
the
practical
implementation
of
SACs,
reliable
support
is
highly
imperative
to
stabilize
atomically
dispersed
metals
with
strong
metal–support
interaction,
tunable
local
electronic
environment,
favorable
electron/mass
transport.
Thanks
great
designability
tunability
composition,
structure,
morphology,
porous
organic
polymers
(POPs)
demonstrated
grand
promise
appropriate
platforms
toward
design
SACs
at
molecular
level
fabrication
a
controlled
manner.
Herein,
comprehensive
overview
recent
advances
elucidation
general
principles,
effective
synthesis
approaches,
fundamental
mechanisms
boosting
development
high‐performance
POPs‐based
electrocatalytic
transformations
provided.
The
authors
first
outline
rationales
using
supports
principles
electrocatalysis,
followed
by
discussing
approaches
utilizing
POPs
POPs‐derived
nanocarbons
host
single‐atom
metals.
Then,
state‐of‐the‐art
their
applications
heterogeneous
(ORR,
OER,
HER,
CO
2
RR,
NRR)
are
discussed,
which
focus
on
revealing
structure–performance
correlation
mechanisms.
Finally,
challenges
strategies
associated
rational
suggested.
Advanced Energy Materials,
Год журнала:
2023,
Номер
13(34)
Опубликована: Июль 27, 2023
Abstract
The
efficient
conversion
of
CO
2
to
value‐added
products
represents
one
the
most
attractive
solutions
mitigate
climate
change
and
tackle
associated
environmental
issues.
In
particular,
electrochemical
reduction
fuels
chemicals
has
garnered
tremendous
interest
over
last
decades.
Among
all
from
reduction,
formic
acid
is
considered
economically
vital
products.
P‐block
metals
(especially
Bi,
Sn,
In,
Pb)
have
been
extensively
investigated
recognized
as
catalytic
materials
for
electroreduction
formate.
Despite
remarkable
progress,
future
implementation
this
technology
at
industrial‐scale
hinges
on
ability
solve
remaining
roadblocks.
review,
current
research
status,
challenges,
prospects
p‐block
metal‐based
catalysts
primarily
formate
are
comprehensively
reviewed.
rational
design
nanostructure
engineering
these
metal
optimization
their
performances
discussed
in
detail.
Subsequently,
recent
progress
development
state‐of‐the‐art
operando
characterization
techniques
together
with
advanced
cells
uncover
intrinsic
catalysis
mechanism
discussed.
Lastly,
a
perspective
directions
including
tackling
critical
challenges
realize
its
early
industrial
presented.
Journal of the American Chemical Society,
Год журнала:
2024,
Номер
146(2), С. 1423 - 1434
Опубликована: Янв. 3, 2024
Cu-based
catalysts
hold
promise
for
electrifying
CO2
to
produce
methane,
an
extensively
used
fuel.
However,
the
activity
and
selectivity
remain
insufficient
due
lack
of
catalyst
design
principles
steer
complex
reduction
pathways.
Herein,
we
develop
a
concept
carbon-supported
Cu
by
regulating
active
sites'
atomic-scale
structures
engineering
carbon
support's
mesoscale
architecture.
This
aims
provide
favorable
local
reaction
microenvironment
selective
pathway
methane.
In
situ
X-ray
absorption
Raman
spectroscopy
analyses
reveal
dynamic
reconstruction
nitrogen
hydroxyl-immobilized
Cu3
(N,OH-Cu3)
clusters
derived
from
atomically
dispersed
Cu–N3
sites
under
realistic
conditions.
The
N,OH-Cu3
possess
moderate
*CO
adsorption
affinity
low
barrier
hydrogenation,
enabling
intrinsically
CO2-to-CH4
compared
C–C
coupling
with
high
energy
barrier.
Importantly,
block
copolymer-derived
fiber
support
interconnected
mesopores
is
constructed.
unique
long-range
mesochannels
offer
H2O-deficient
prolong
transport
path
CO
intermediate,
which
could
suppress
hydrogen
evolution
favor
deep
toward
methane
formation.
Thus,
newly
developed
consisting
in
constructed
embedded
into
bicontinuous
achieved
unprecedented
Faradaic
efficiency
74.2%
at
industry-level
current
density
300
mA
cm–2.
work
explores
effective
concepts
steering
desirable
pathways
interfacial
catalytic
systems
via
modulating
site
atomic
level
pore
architectures
supports
on
create
microenvironments.