Energy & Environmental Science,
Journal Year:
2021,
Volume and Issue:
14(5), P. 2809 - 2858
Published: Jan. 1, 2021
Non-carbon
supported
SACs
were
classified
into
eight
categories
based
on
the
nature
of
their
substrates
for
first
time,
and
corresponding
anchoring
stabilization
mechanisms
have
been
systematically
summarized
discussed.
Small,
Journal Year:
2021,
Volume and Issue:
17(37)
Published: June 10, 2021
Abstract
Oxygen
evolution
reaction
(OER)
is
an
important
half‐reaction
involved
in
many
electrochemical
applications,
such
as
water
splitting
and
rechargeable
metal–air
batteries.
However,
the
sluggish
kinetics
of
its
four‐electron
transfer
process
becomes
a
bottleneck
to
performance
enhancement.
Thus,
rational
design
electrocatalysts
for
OER
based
on
thorough
understanding
mechanisms
structure‐activity
relationship
vital
significance.
This
review
begins
with
introduction
which
include
conventional
adsorbate
mechanism
lattice‐oxygen‐mediated
mechanism.
The
pathways
related
intermediates
are
discussed
detail,
several
descriptors
greatly
assist
catalyst
screen
optimization
summarized.
Some
parameters
suggested
measurement
criteria
also
mentioned
discussed.
Then,
recent
developments
breakthroughs
experimental
achievements
transition
metal‐based
reviewed
reveal
novel
principles.
Finally,
some
perspectives
future
directions
proposed
further
catalytic
enhancement
deeper
design.
It
believed
that
iterative
improvements
fundamental
principles
essential
realize
applications
efficient
energy
storage
conversion
technologies.
Advanced Energy Materials,
Journal Year:
2019,
Volume and Issue:
9(17)
Published: March 3, 2019
Abstract
The
oxygen
evolution
reaction
(OER)
has
aroused
extensive
interest
from
materials
scientists
in
the
past
decade
by
virtue
of
its
great
significance
energy
storage/conversion
systems
such
as
water
splitting,
rechargeable
metal–air
batteries,
carbon
dioxide
(CO
2
)
reduction,
and
fuel
cells.
Among
all
capable
catalyzing
OER,
layered
double
hydroxides
(LDHs)
stand
out
one
most
effective
electrocatalysts
owing
to
their
compositional
structural
flexibility
well
tenability
simplicity
preparation
process.
For
this
reason,
numerous
efforts
have
been
dedicated
adjusting
structure,
forming
well‐defined
morphology,
developing
methods
LDHs
promote
electrocatalytic
performance.
In
article,
recent
advances
rational
design
LDH‐based
toward
OER
are
summarized.
Specifically,
various
tactics
for
synthetic
methods,
composition
regulations
LDHs,
further
highlighted,
followed
a
discussion
on
influential
factors
Finally,
remaining
challenges
investigate
improve
ability
LDH
stated
indicate
possible
future
development
LDHs.
Advanced Science,
Journal Year:
2018,
Volume and Issue:
5(8)
Published: May 23, 2018
Abstract
Layered
double
hydroxide
(LDH)‐based
materials
have
attracted
widespread
attention
in
various
applications
due
to
their
unique
layered
structure
with
high
specific
surface
area
and
electron
distribution,
resulting
a
good
electrocatalytic
performance.
Moreover,
the
existence
of
multiple
metal
cations
invests
flexible
tunability
host
layers;
intercalation
characteristics
lead
ion
exchange
exfoliation.
Thus,
performance
can
be
tuned
by
regulating
morphology,
composition,
ion,
However,
poor
conductivity
limits
performance,
which
therefore
has
motivated
researchers
combine
them
conductive
improve
Another
factor
hampering
activity
is
large
lateral
size
bulk
thickness
LDHs.
Introducing
defects
tuning
electronic
LDH‐based
are
considered
effective
strategies
increase
number
active
sites
enhance
intrinsic
activity.
Given
advantages
materials,
derivatives
been
also
used
as
advanced
electrocatalysts
for
water
splitting.
Here,
recent
progress
on
LDHs
splitting
summarized,
current
designing
proposed,
significant
challenges
perspectives
discussed.
Nature Communications,
Journal Year:
2019,
Volume and Issue:
10(1)
Published: Dec. 6, 2019
Abstract
Efficient
generation
of
hydrogen
from
water-splitting
is
an
underpinning
chemistry
to
realize
the
economy.
Low
cost,
transition
metals
such
as
nickel
and
iron-based
oxides/hydroxides
have
been
regarded
promising
catalysts
for
oxygen
evolution
reaction
in
alkaline
media
with
overpotentials
low
~200
mV
achieve
10
mA
cm
−2
,
however,
they
are
generally
unsuitable
reaction.
Herein,
we
show
a
Janus
nanoparticle
catalyst
nickel–iron
oxide
interface
multi-site
functionality
highly
efficient
comparable
performance
benchmark
platinum
on
carbon
catalyst.
Density
functional
theory
calculations
reveal
that
catalytic
activity
induced
by
strong
electronic
coupling
effect
between
iron
at
interface.
Remarkably,
also
exhibits
extraordinary
activity,
enabling
active
stable
bi-functional
whole
cell
with,
best
our
knowledge,
highest
energy
efficiency
(83.7%)
reported
date.
Advanced Functional Materials,
Journal Year:
2020,
Volume and Issue:
30(34)
Published: June 29, 2020
Abstract
Reducing
green
hydrogen
production
costs
is
essential
for
developing
a
economy.
Developing
cost‐effective
electrocatalysts
water
electrolysis
thus
of
great
research
interest.
Among
various
material
candidates,
transition
metal
phosphides
(TMP)
have
emerged
as
robust
bifunctional
both
the
evolution
reaction
(HER)
and
oxygen
(OER)
due
to
their
phases
tunable
electronic
structure.
Recently,
heterostructured
catalysts
exhibited
significantly
enhanced
activities
toward
HER/OER.
The
enhancement
can
be
attributed
increased
amount
accessible
active
sites,
accelerated
mass/charge
transfer,
optimized
adsorption
intermediates,
which
arise
from
synergistic
effects
heterostructure.
Herein,
comprehensive
overview
recent
progress
TMP‐based
heterostructure
introduced
provide
an
insight
into
preparation
corresponding
mechanisms.
It
starts
with
summarizing
general
fundamental
aspects
HER/OER
effect
heterostructures
catalytic
activity.
Next,
innovational
strategies
design
construct
overall
splitting
activity,
well
related
mechanisms,
are
discussed
in
detail.
Finally,
summary
perspective
further
opportunities
challenges
highlighted
development
points
practical
application
mechanistic
studies.
Advanced Functional Materials,
Journal Year:
2020,
Volume and Issue:
31(1)
Published: Sept. 28, 2020
Abstract
Developing
high‐performance
and
cost‐effective
bifunctional
electrocatalysts
for
large‐scale
water
electrolysis
is
desirable
but
remains
a
significant
challenge.
Most
existing
nano‐
micro‐structured
require
complex
synthetic
procedures,
making
scale‐up
highly
challenging.
Here,
heterogeneous
Ni
2
P‐Fe
P
microsheet
synthesized
by
directly
soaking
foam
in
hydrochloric
acid
an
iron
nitrate
solution,
followed
phosphidation.
Benefiting
from
high
intrinsic
activity,
abundant
active
sites,
superior
transfer
coefficient,
this
self‐supported
electrocatalyst
shows
superb
catalytic
activity
toward
overall
splitting,
requiring
low
voltages
of
1.682
1.865
V
to
attain
current
densities
100
500
mA
cm
−2
1
m
KOH,
respectively.
Such
performance
the
benchmark
IrO
||
Pt/C
pair
also
places
among
best
catalysts
reported
thus
far.
Furthermore,
its
enhanced
corrosion
resistance
hydrophilic
surface
make
it
suitable
seawater
splitting.
It
able
achieve
KOH
at
1.811
2.004
V,
respectively,
which,
together
with
robust
durability,
demonstrates
great
potential
realistic
electrolysis.
This
work
presents
general
economic
approach
fabrication
metallic
phosphide
water/seawater
electrocatalysis.