Advanced Functional Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Сен. 2, 2024
Abstract
The
application
of
alloying‐typed
red
phosphorus
(red
P)
anode
in
potassium‐ion
batteries
(KIBs)
with
ultra‐high
theoretical
capacity
is
hindered
by
the
limited
and
fast
decay
due
to
poor
electronic
conductivity
huge
volume
change.
Herein,
a
facile
efficient
strategy
fluorine
(F)
doping
innovatively
developed
modulate
pore
structure
carbon
matrix
(F‐CNS)
encapsulate
P
enhanced
potassium
storage
capability.
Theoretical
calculations
reveal
that
F
induces
additional
defects
within
layer,
which
facilitates
4
molecules
embedding
into
F‐doping‐induced
micropores,
enhances
adsorption
ability
toward
K
atoms
molecules,
improves
electrochemical
kinetics
assisted
more
charge
transfer
obtained
from
electron
density
difference,
thus
enabling
robust
capability
for
such
unique
Red
P@F‐CNS
anode.
Accordingly,
demonstrates
outstanding
cycling
stability
(90%
retention
after
800
cycles
at
2A
g
−1
),
full
cell
(Red
P@F‐CNS//KFeHCF)
exhibits
exceptional
long‐term
performance
(129
mAh
2500
5
A
only
0.014%
per
cycle).
In
situ
characterizations
confirm
superior
structural
integrity
carbon‐based
matrix.
This
study
offers
rational
design
principle
engineering
high‐performance
carbon‐supported
anodes
KIBs.
Chemical Society Reviews,
Год журнала:
2024,
Номер
53(13), С. 7202 - 7298
Опубликована: Янв. 1, 2024
The
growing
global
energy
demand
necessitates
the
development
of
renewable
solutions
to
mitigate
greenhouse
gas
emissions
and
air
pollution.
To
efficiently
utilize
yet
intermittent
sources
such
as
solar
wind
power,
there
is
a
critical
need
for
large-scale
storage
systems
(EES)
with
high
electrochemical
performance.
While
lithium-ion
batteries
(LIBs)
have
been
successfully
used
EES,
surging
price,
coupled
limited
supply
crucial
metals
like
lithium
cobalt,
raised
concerns
about
future
sustainability.
In
this
context,
potassium-ion
(PIBs)
emerged
promising
alternatives
commercial
LIBs.
Leveraging
low
cost
potassium
resources,
abundant
natural
reserves,
similar
chemical
properties
potassium,
PIBs
exhibit
excellent
ion
transport
kinetics
in
electrolytes.
This
review
starts
from
fundamental
principles
structural
regulation
PIBs,
offering
comprehensive
overview
their
current
research
status.
It
covers
cathode
materials,
anode
electrolytes,
binders,
separators,
combining
insights
full
battery
performance,
degradation
mechanisms,
Interdisciplinary materials,
Год журнала:
2023,
Номер
2(4), С. 635 - 663
Опубликована: Июль 1, 2023
Abstract
Silicon
(Si)‐based
solid‐state
batteries
(Si‐SSBs)
are
attracting
tremendous
attention
because
of
their
high
energy
density
and
unprecedented
safety,
making
them
become
promising
candidates
for
next‐generation
storage
systems.
Nevertheless,
the
commercialization
Si‐SSBs
is
significantly
impeded
by
enormous
challenges
including
large
volume
variation,
severe
interfacial
problems,
elusive
fundamental
mechanisms,
unsatisfied
electrochemical
performance.
Besides,
some
unknown
processes
in
Si‐based
anode,
electrolytes
(SSEs),
anode/SSE
interfaces
still
needed
to
be
explored,
while
an
in‐depth
understanding
solid–solid
chemistry
insufficient
Si‐SSBs.
This
review
aims
summarize
current
scientific
technological
advances
insights
into
tackling
promote
deployment
First,
differences
between
various
conventional
liquid
electrolyte‐dominated
lithium‐ion
(LIBs)
with
discussed.
Subsequently,
mechanical
contact
model,
chemical
reaction
properties,
charge
transfer
kinetics
(mechanical–chemical
kinetics)
anode
three
different
SSEs
(inorganic
(oxides)
SSEs,
organic–inorganic
composite
inorganic
(sulfides)
SSEs)
systemically
reviewed,
respectively.
Moreover,
progress
SSE‐based
on
aspects
electrode
constitution,
three‐dimensional
structured
electrodes,
external
stack
pressure
highlighted,
Finally,
future
research
directions
prospects
development
proposed.
Journal of the American Chemical Society,
Год журнала:
2024,
Номер
146(10), С. 6753 - 6762
Опубликована: Фев. 27, 2024
High-temperature
rechargeable
batteries
are
essential
for
energy
storage
in
elevated-temperature
situations.
Due
to
the
resource
abundance
of
potassium,
high-temperature
K-ion
drawing
increasing
research
interest.
However,
raising
working
temperature
would
aggravate
chemical
and
mechanical
instability
KIB
anode,
resulting
very
fast
capacity
fading,
especially
when
high
is
pursued.
Here,
we
demonstrated
that
a
porous
conductive
metal–organic
framework
(MOF),
which
constructed
by
N-rich
aromatic
molecules
CuO4
units
via
π–d
conjugation,
could
provide
multiple
accessible
redox-active
sites
promised
robust
structure
stability
efficient
potassium
at
temperatures.
Even
60
°C,
this
MOF
anode
deliver
initial
(455
mAh
g–1),
impressive
rate,
extraordinary
cyclability
(96.7%
retention
1600
cycles),
much
better
than
those
reported
anodes.
The
mechanistic
study
revealed
C═N
groups
contributed
abundant
sites;
synergistic
effect
conjugated
character
reticular
architecture
facilitated
K+/e–
transport
ensured
an
insoluble
electrode
with
small
volume
deformation,
thus
achieving
stable
high-capacity
storage.
Abstract
The
development
of
highly
efficient
sodium‐ion
batteries
depends
critically
on
the
successful
exploitation
advanced
anode
hosts
that
is
capable
overcoming
sluggish
reaction
kinetics
while
also
withstanding
severe
structural
deformation
triggered
by
large
radius
Na
+
‐insertion.
Herein,
a
hierarchically
hybrid
material
with
hetero‐Co
3
S
4
/NiS
hollow
nanosphere
packaged
into
densified
N‐doped
carbon
matrix
(Co
/NiS@N‐C)
was
designed
and
fabricated
utilizing
CoNi‐glycerate
as
self‐sacrifice
template,
making
utmost
synergistic
effect
strong
electric
field
rich
active‐sites
together
outer‐carbon
scaffolds
remarkable
electronic
conductivity
robust
mechanical
toughness.
As
anticipated,
as‐fabricated
Co
/NiS@N‐C
affords
specific
capacity,
prolonged
cycle
lifespan
up
to
2
400
cycles
an
only
0.05%
fading
each
at
20.0
A
g
−1
,
excellent
rate
feature
(354.9
mAh
30.0
),
one
best
performances
for
most
existing
/NiS‐based
anodes.
Ex
situ
characterizations
in
tandem
theoretical
analysis
demonstrate
reversible
insertion‐conversion
mechanism
initially
proceeding
de‐/intercalation
superior
heterogeneous
interfacial
behavior
‐adsorption
ability.
Further,
full
cell
capacitor
based
exhibit
impressive
electrochemical
characteristics
cycling
performance
capability,
showcasing
its
outstanding
feasibility
toward
practical
use.
Journal of the American Chemical Society,
Год журнала:
2024,
Номер
146(7), С. 4752 - 4761
Опубликована: Фев. 9, 2024
Alloy
anode
materials
have
garnered
unprecedented
attention
for
potassium
storage
due
to
their
high
theoretical
capacity.
However,
the
substantial
structural
strain
associated
with
deep
potassiation
results
in
serious
electrode
fragmentation
and
inadequate
K-alloying
reactions.
Effectively
reconciling
trade-off
between
low-strain
deep-potassiation
alloy
anodes
poses
a
considerable
challenge
larger
size
of
K-ions
compared
Li/Na-ions.
In
this
study,
we
propose
chemical
bonding
modulation
strategy
through
single-atom
modification
address
volume
expansion
during
potassiation.
Using
black
phosphorus
(BP)
as
representative
generalizing
other
anodes,
established
robust
P–S
covalent
network
via
sulfur
doping.
This
exhibits
sustained
stability
across
discharge–charge
cycles,
elevating
modulus
K–P
compounds
by
74%,
effectively
withstanding
induced
process.
Additionally,
reduces
formation
energies
phosphides,
facilitating
deeper
BP
anode.
As
result,
modified
reversible
capacity
extended
operational
lifespan,
coupled
areal
work
introduces
new
perspective
on
overcoming
development
high-energy
stable
potassium-ion
batteries.
Abstract
The
electrolyte‐wettability
at
electrode
material/electrolyte
interface
is
a
critical
factor
that
governs
the
fundamental
mechanisms
of
electrochemical
reaction
efficiency
and
kinetics
materials
in
practical
energy
storage.
Therefore,
design
construction
material
surfaces
with
improved
has
been
demonstrated
to
be
important
optimize
storage
performance
material.
Here,
we
comprehensively
summarize
advanced
strategies
key
progresses
surface
chemical
modification
for
enhancing
materials,
including
polar
atom
doping
by
post
treatment,
introducing
functional
groups,
grafting
molecular
brushes,
coating
situ
reaction.
Specifically,
basic
principles,
characteristics,
challenges
these
improving
are
discussed
detail.
Finally,
potential
research
directions
regarding
characterization
techniques
future
provided.
This
review
not
only
insights
into
but
also
provides
strategic
guidance
optimization
pursuing
high‐performance
devices.
image
ACS Applied Materials & Interfaces,
Год журнала:
2024,
Номер
16(14), С. 17553 - 17562
Опубликована: Март 27, 2024
The
pore
structure
of
carbon
anodes
plays
a
crucial
role
in
enhancing
the
sodium
storage
capacity.
Designing
more
confined
pores
is
accepted
as
an
effective
strategy.
However,
current
design
strategies
for
fail
to
achieve
both
high
capacity
and
initial
Coulombic
efficiency
(ICE)
simultaneously.
Herein,
we
develop
strategy
utilizing
repeated
impregnation
precarbonization
method
liquid
pitch
regulate
activated
(AC)
material.
Driven
by
capillary
coalescence,
impregnated
into
AC,
which
reduces
specific
surface
area
During
carbonization
process,
numerous
with
diameters
less
than
1
nm
are
formed,
resulting
improved
ICE
anode.
Moreover,
ordered
layers
derived
from
also
enhance
electrical
conductivity,
thereby
improving
rate
capability
as-obtained
anodes.
This
enables
fabricated
material
(XA-4T-1300)
have
91.1%
383.0
mA
h
g–1
at
30
g–1.
retention
95.5%
after
300
cycles
A
study
proposes
practical
approach
adjust
microcrystalline
structures
performance
sodium-ion
materials.
Abstract
The
high
potassization/depotassization
energy
barriers
and
lack
of
efficient
ion
diffusion
pathways
are
two
serious
obstacles
for
carbon‐based
materials
to
achieve
satisfactory
potassium
storage
performance.
Herein,
a
facile
controllable
one‐step
exfoliation‐doping‐etching
strategy
is
proposed
construct
heteroatoms
(N,
O,
S)‐doped
mesoporous
few‐layer
carbon
nanosheets
(NOS‐C).
mixed
molten
salts
KCl/K
2
SO
4
innovatively
used
as
the
exfoliators,
dopants,
etching
agents,
which
enable
NOS‐C
with
expanded
interlayer
spacing
uniformly
distributed
mesopores
adjusted
electronic
structure
surrounding
atoms,
contributing
dual
(vertical
horizontal)
K‐ion
pathways,
low
abundant
active
sites.
Thus,
NOS
anodes
reversible
capacity
516.8
mAh
g
−1
at
0.05
A
,
superior
rate
capability
202.8
5
excellent
long‐term
cyclic
stability,
their
practical
application
potential
demonstrated
by
assembled
potassium‐ion
full
batteries.
Moreover,
surface‐interlayer
synergetic
K
+
mechanism
revealed
combined
theoretical
experimental
approach
including
in
situ
EIS,
Raman,
ex
XPS,
SEM
analysis.
unique
structural
engineering
provide
new
pathway
devices
even
beyond.