Advanced Energy Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 30, 2025
Abstract
The
attainment
of
lithium‐ion
batteries
(LIBs)
featuring
high
energy
density
necessitates
the
anode
to
exhibit
substantial
mass
loading
and
thickness.
However,
this
presents
a
formidable
challenge
for
fast
charging
due
inferior
Li‐ion
transport
capability
throughout
electrode
depth,
resulting
in
diminished
capacity,
reduced
lifespan,
potential
safety
hazards.
Here,
an
alternative
strategy
is
put
forth
that
utilizes
electronic/ionic
hybrid
conductive
additive
as
substitution
conventional
reagent.
This
particular
showcases
carbon
black
(CB)
particles
adorned
with
ultrathin
red
phosphorus
nanolayer
(≈2
nm)
(CB‐P),
which
undergo
situ
transformation
into
stable
lithium
phosphide
(Li
3
P)
nanolayer‐coated
CB
during
operation
battery.
Benefiting
from
significant
contribution
Li
+
enhancement,
introduction
P
enables
significantly
increased
apparent
transference
number
similar
ionic
conductivity
compared
(0.67
vs
0.42,
5.2
4.1
mS
cm
−1
).
Notably,
pouch
cell
graphite
CB‐P
demonstrates
capacity
filling
ratio
83.5%
within
15
min
(4C,
relative
at
0.5C)
under
14.4
mg
−2
(4.4
mAh
0.5C).
full
SiO
x
exhibits
82.1%
refilling
4C
rate
(15
min,
0.2C).
In
consideration
superior
compatibility
current
processing,
can
serve
direct
replacement
traditional
additives
existing
boost
implementation
fast‐charging
LIBs
density.
Advanced Materials,
Год журнала:
2024,
Номер
36(35)
Опубликована: Июнь 26, 2024
Sodium-ion
batteries
(SIBs)
have
undergone
rapid
development
as
a
complementary
technology
to
lithium-ion
due
abundant
sodium
resources.
However,
the
extended
charging
time
and
low
energy
density
pose
significant
challenge
widespread
use
of
SIBs
in
electric
vehicles.
To
overcome
this
hurdle,
there
is
considerable
focus
on
developing
fast-charging
anode
materials
with
Na⁺
diffusion
superior
reaction
kinetics.
Here,
key
factors
that
limit
fast
are
examined,
which
provides
comprehensive
overview
major
advances
characteristics
across
various
materials.
Specifically,
it
systematically
dissects
considerations
enhance
rate
performance
materials,
encompassing
aspects
such
porous
engineering,
electrolyte
desolvation
strategies,
electrode/electrolyte
interphase,
electronic
conductivity/ion
diffusivity,
pseudocapacitive
ion
storage.
Finally,
direction
prospects
for
also
proposed,
aiming
provide
valuable
reference
further
advancement
high-power
SIBs.
ACS Nano,
Год журнала:
2024,
Номер
18(21), С. 13662 - 13674
Опубликована: Май 16, 2024
Porous
copper
(Cu)
current
collectors
show
promise
in
stabilizing
Li
metal
anodes
(LMAs).
However,
insufficient
lithiophilicity
of
pure
Cu
and
limited
porosity
three-dimensional
(3D)
porous
structures
led
to
an
inefficient
Li–Cu
composite
preparation
poor
electrochemical
performance
anodes.
Herein,
we
propose
a
Cu-CuZn
(DG-CCZ)
host
for
tackle
these
issues.
This
architecture
features
pore
size
distribution
lithiophilic-lithiophobic
characteristics
designed
gradient
from
the
inside
outside
anode
structure.
dual-gradient
exhibits
exceptional
capillary
wettability
molten
provides
high
up
66.05%.
design
promotes
preferential
deposition
interior
structure
during
battery
operation,
effectively
inhibiting
dendrite
formation.
Consequently,
all
cell
systems
achieve
significantly
improved
cycling
stability,
including
half-cells,
Li–Li
symmetric
cells,
Li-LFP
full
cells.
When
paired
synergistically
with
double-coated
LiFePO4
cathode,
pouch
configured
multiple
electrodes
demonstrates
impressive
discharge
capacity
159.3
mAh
g–1
at
1C.
We
believe
this
study
can
inspire
future
3D
enhanced
utilization
efficiency
facilitate
development
high-energy
batteries.
Chemistry of Materials,
Год журнала:
2024,
Номер
36(19), С. 9299 - 9319
Опубликована: Сен. 18, 2024
With
the
promotion
of
portable
energy
storage
devices
and
popularization
electric
vehicles,
lithium-ion
battery
(LiB)
technology
plays
a
crucial
role
in
modern
systems.
Over
past
decade,
demands
for
LiBs
have
centered
around
high
density
long
cycle
life.
These
parameters
are
often
determined
by
characteristics
active
materials
electrodes.
Given
its
abundance,
environmental
friendliness,
low
cost
capacity,
magnetite
(Fe
Nature Communications,
Год журнала:
2024,
Номер
15(1)
Опубликована: Ноя. 20, 2024
The
numerous
grainboundaries
solid
electrolyte
interface,
whether
naturally
occurring
or
artificially
designed,
leads
to
non-uniform
Li
metal
deposition
and
consequently
results
in
poor
full-battery
performance.
Herein,
a
lithium-ion
selective
transport
layer
is
reported
achieve
highly
efficient
dendrite-free
lithium
anode.
layer-by-layer
assembled
protonated
carbon
nitride
nanosheets
present
uniform
macroscopical
structure
without
grainboundaries.
with
ordered
pores
basal
plane
provides
high-speed
channels
low
tortuosity.
Consequently,
the
324
Wh
kg−1
pouch
cell
exhibits
300
stable
cycles
capacity
retention
of
90.0%
an
average
Coulombic
efficiency
up
99.7%.
ultra-dense
anode
makes
current
collector-free
possible,
achieving
high
energy
density
long
cycle
life
7
Ah
(506
kg−1,
160
cycles).
Thus,
it
proved
that
macroscopically
interface
conductive
could
battery
promising
application
potential.
Here,
authors
report
grain
boundary-free
microscopic
+
-selective
enables
deposition,
resulting
kg−1)
(160
cycles)
Advanced Energy Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 21, 2025
Abstract
Layered
transition
metal
dichalcogenides
(LTMDs),
such
as
MoS
2
,
are
promising
anode
materials
for
high‐energy‐density
lithium‐ion
batteries
(LIBs)
due
to
their
high
specific
capacities.
However,
practical
applications
hindered
by
poor
cycling
stability
resulting
from
the
instable
structure
during
charge/discharge
and
inherently
low
electronic
conductivity.
To
tackle
these
issues,
herein,
this
study
presents
design
synthesis
of
spongy
silicon‐doped
induced
long‐chain
molecules
in
mesopores.
The
material
consists
few‐layered
nanofragments
with
porosity,
abundant
edge
sites
sulfur
vacancies.
These
structural
features
can
promote
Li
+
transport
accommodate
electrode
volume
changes
charge/discharge.
Electrochemical
theoretical
analyses
reveal
that
silicon
doping
enhances
conductivity
while
nanostructure
enables
reversible
Li⁺
diffusion
along
edges,
distinct
storage
interlayers
conventional
anodes.
Notably,
delivers
a
capacity
767.9
mAh
g
−1
at
0.1
A
exhibits
remarkable
rate
capability.
Moreover,
it
demonstrates
superior
over
83%
retention
even
after
1000
cycles
1.0
outperforming
most
existing
‐based
materials.
This
work
paves
new
way
designing
high‐performance
LTMD‐based
anodes
LIBs
beyond.
The
SiOx
anode
exhibits
a
high
specific
capacity
and
commendable
durability
for
lithium-ion
batteries
(LIBs).
However,
its
practical
application
is
hindered
by
significant
volumetric
fluctuations
during
lithiation/delithiation,
alongside
metastable
nature,
which
induces
mechanical
instability
irreversible
lithium
consumption,
ultimately
impairing
long-term
retention
in
full-battery
cell
configurations.
In
this
study,
we
present
phase-engineering
approach
designed
to
improve
the
structural
stability
of
anodes
LIB
applications.
By
incorporating
fluoride,
amorphous
undergoes
partial
transformation
into
quartz-like
phase,
enhances
integrity
mitigates
loss.
This
modified
demonstrates
significantly
improved
prolonged
cycle
lifespan.
Through
combination
multiscale
simulations
situ
characterizations,
elucidate
stabilization
mechanisms
conferred
quartz
providing
critical
insights
role
SiOx's
crystal
structure
influencing
degradation
pathways.
work
introduces
an
accessible
efficient
method
controlling
crystallinity
SiOx,
offering
solution
enhance
high-energy-density
LIBs.
ACS Applied Materials & Interfaces,
Год журнала:
2024,
Номер
16(5), С. 5915 - 5925
Опубликована: Янв. 26, 2024
The
development
of
a
high-rate
SiO
lithium-ion
battery
anode
is
seriously
limited
by
its
low
intrinsic
conductivity,
sluggish
interfacial
charge
transfer
(ICT),
and
unstable
dynamic
interface.
To
tackle
the
above
issues,
encapsulation
engineering
for
effectively
regulating
reaction
thus
realizing
stable
solid
electrolyte
interphase
significantly
important.
Hybrid
coating,
which
aims
to
enhance
coupled
e-/Li+
transport
via
employment
dual
layers,
has
emerged
as
promising
strategy.
Herein,
we
construct
hybrid
MXene-graphene
oxide
(GO)
coating
layer
on
microparticles.
In
design,
Ti3C2Tx
MXene
acts
"bridge",
forms
close
covalent
connection
with
GO
through
Ti-O-Si
Ti-O-C
bonds,
respectively,
greatly
reducing
ICT
resistance.
Moreover,
rich
surface
groups
(e.g.,
-OH,
-F)
outer
layers
an
intertwined
porous
framework
synergistically
enable
pseudocapacitance
dominated
behavior,
beneficial
fast
storage.
Accordingly,
as-made
Si@MXene@GO
exhibits
considerably
reinforced
storage
performance
in
terms
superior
rate
(1175.9
mA
h
g-1
at
5
A
g-1)
long
cycling
stability
(1087.6
capacity
retained
after
1000
cycles
2.0
g-1).
In-depth
chemical
composition
analysis
further
reveals
that
inorganically
gradient
distribution
LiF
Li2O
formed
electrolyte/anode
interface
ensures
mechanical
during
repeated
cycles.
This
work
paves
feasible
way
maximizing
potential
anodes
toward
fast-charging
batteries.