Chemical Society Reviews,
Journal Year:
2020,
Volume and Issue:
49(10), P. 2937 - 3004
Published: Jan. 1, 2020
Catalytic
conversion
of
CO2
to
produce
fuels
and
chemicals
is
attractive
in
prospect
because
it
provides
an
alternative
fossil
feedstocks
the
benefit
converting
cycling
greenhouse
gas
on
a
large
scale.
In
today's
technology,
converted
into
hydrocarbon
Fischer-Tropsch
synthesis
via
water
shift
reaction,
but
processes
for
direct
such
as
methane,
methanol,
C2+
hydrocarbons
or
syngas
are
still
far
from
large-scale
applications
processing
challenges
that
may
be
best
addressed
by
discovery
improved
catalysts-those
with
enhanced
activity,
selectivity,
stability.
Core-shell
structured
catalysts
relatively
new
class
nanomaterials
allow
controlled
integration
functions
complementary
materials
optimised
compositions
morphologies.
For
conversion,
core-shell
can
provide
distinctive
advantages
addressing
catalyst
sintering
activity
loss
reforming
processes,
insufficient
product
selectivity
thermocatalytic
hydrogenation,
low
efficiency
photocatalytic
electrocatalytic
hydrogenation.
preceding
decade,
substantial
progress
has
been
made
synthesis,
characterization,
evaluation
potential
applications.
Nonetheless,
remain
inexpensive,
robust,
regenerable
this
class.
This
review
in-depth
assessment
these
thermocatalytic,
photocatalytic,
valuable
hydrocarbons.
Advanced Functional Materials,
Journal Year:
2020,
Volume and Issue:
30(31)
Published: June 9, 2020
Abstract
The
recent
advances
in
electrocatalysis
for
oxygen
reduction
reaction
(ORR),
evolution
(OER),
hydrogen
(HER),
oxidation
(HOR),
carbon
dioxide
(CO
2
RR),
and
nitrogen
(NRR)
are
thoroughly
reviewed.
This
comprehensive
review
focuses
on
the
single‐atom
catalysts
(SACs)
including
Sc,
Cr,
Mn,
Fe,
Co,
Ni,
Cu,
Zn,
Mo,
Sn,
W,
Bi,
Ru,
Rh,
Pd,
Ag,
Ir,
Pt,
Au
with
single‐metal
sites
or
dual‐metal
sites.
development
of
electrocatalysts
novel
configurations
compositions
is
documented.
understanding
process–structure–property
relationships
highlighted.
For
SACs,
their
electrocatalytic
performance
stability
fuel
cells,
zinc–air
batteries,
electrolyzers,
CO
RR,
NRR
summarized.
challenges
perspectives
emerging
field
discussed.
Accounts of Chemical Research,
Journal Year:
2020,
Volume and Issue:
53(1), P. 255 - 264
Published: Jan. 8, 2020
Due
to
increasing
worldwide
fossil
fuel
consumption,
carbon
dioxide
levels
have
increased
in
the
atmosphere
with
increasingly
important
impacts
on
environment.
Renewable
and
clean
sources
of
energy
been
proposed,
including
wind
solar,
but
they
are
intermittent
require
efficient
scalable
storage
technologies.
Electrochemical
CO2
reduction
reaction
(CO2RR)
provides
a
valuable
approach
this
area.
It
combines
solar-
or
wind-generated
electrical
production
chemical
bonds
carbon-based
fuels.
can
provide
ways
integrate
capture,
utilization,
cycles
while
maintaining
controlled
atmospheric
CO2.
Electrochemistry
allows
for
utilization
an
input
drive
reactions.
Because
is
kinetically
inert,
highly
active
catalysts
required
decrease
barriers
sufficiently
so
that
rates
be
achieved
sufficient
electrochemical
reduction.
Given
associated
multiple
electron-proton
CO,
formaldehyde
(HC(O)H),
formic
acid,
formate
(HC(O)OH,
HC(O)O-),
more
reduced
forms
carbon,
there
also
demand
high
selectivity
catalysis.
Catalysts
explored
include
homogeneous
solution,
immobilized
surfaces,
heterogeneous
catalysts.
In
catalysis,
occurs
following
diffusion
catalyst
electrode
where
proton
coupled
electron
transfer
occurs.
Useful
area
typically
transition-metal
complexes
organic
ligands
properties
utilize
combinations
metal
ligand
redox
levels.
As
way
limit
amount
catalyst,
device-like
configurations,
added
surfaces
conductive
substrates
by
surface
binding,
polymeric
films,
molecular
structures
electronic
configurations
related
solution.
Immobilized,
suffer
from
performance
losses
even
decomposition
during
long-term
cycles,
amenable
detailed
mechanistic
investigations.
parallel
efforts,
nanocatalysts
detail
development
facile
synthetic
procedures
offer
catalytic
areas.
Their
activity
stability
attracted
significant
level
investigation,
possible
exploitation
large-scale
applications.
However,
translation
reactivity
creates
new
environment
complicates
elucidation
details
identification
site
exploring
pathways.
Here,
results
previous
studies
based
complex
electroreduction
summarized.
Early
showed
Ru,
Ir,
Rh,
Os,
well-defined
structures,
all
capable
catalyzing
CO
formate.
Derivatives
were
attached
conducting
electrodes
bonding,
noncovalent
polymerization.
The
concept
binding
has
extended
preparation
chemically
deposition
nanostructured
such
as
nano
tin,
copper,
which
shown
selectivities
activities
toward
our
presentation,
we
end
Account
recent
advances
perspective
about
application
electrocatalysis
Angewandte Chemie International Edition,
Journal Year:
2021,
Volume and Issue:
60(36), P. 19572 - 19590
Published: Feb. 19, 2021
Abstract
Compared
to
modern
fossil‐fuel‐based
refineries,
the
emerging
electrocatalytic
refinery
(e‐refinery)
is
a
more
sustainable
and
environmentally
benign
strategy
convert
renewable
feedstocks
energy
sources
into
transportable
fuels
value‐added
chemicals.
A
crucial
step
in
conducting
e‐refinery
processes
development
of
appropriate
reactions
optimal
electrocatalysts
for
efficient
cleavage
formation
chemical
bonds.
However,
compared
well‐studied
primary
(e.g.,
O
2
reduction,
water
splitting),
mechanistic
aspects
materials
design
complex
are
yet
be
settled.
To
address
this
challenge,
herein,
we
first
present
fundamentals
heterogeneous
electrocatalysis
some
reactions,
then
implement
these
establish
framework
by
coupling
situ
generated
intermediates
(integrated
reactions)
or
products
(tandem
reactions).
We
also
set
principles
strategies
efficiently
manipulate
reaction
pathways.
Nature Communications,
Journal Year:
2019,
Volume and Issue:
10(1)
Published: Aug. 9, 2019
Abstract
Molecular
catalysts
that
combine
high
product
selectivity
and
current
density
for
CO
2
electrochemical
reduction
to
or
other
chemical
feedstocks
are
urgently
needed.
While
earth-abundant
metal-based
molecular
electrocatalysts
with
conversion
known,
they
characterized
by
densities
significantly
lower
than
those
obtained
solid-state
metal
materials.
Here,
we
report
a
cobalt
phthalocyanine
bearing
trimethyl
ammonium
group
appended
the
macrocycle
is
capable
of
reducing
in
water
activity
over
broad
pH
range
from
4
14.
In
flow
cell
configuration
operating
basic
conditions,
production
occurs
excellent
(ca.
95%),
good
stability
maximum
partial
165
mA
cm
−2
(at
−0.92
V
vs.
RHE),
matching
most
active
noble
nanocatalysts.
These
results
represent
state-of-the-art
performance
electrolytic
carbon
dioxide
catalyst.