Lithium-metal
batteries
(LMBs)
have
garnered
widespread
attention
due
to
their
high
energy
density.
Alloy
anodes
are
particularly
notable
for
exceptional
specific
capacity
used
in
LMBs.
However,
alloy
encounter
significant
challenges
interfacial
issues,
which
include
sluggish
reaction
kinetics
and
mechanical
failures
induced
by
force-electric
coupling
at
the
interface.
In
situ
characterization
of
interface
evolution
is
crucial
gain
a
deeper
understanding
fundamental
origins
these
issues.
This
review
systematically
examines
associated
with
highlights
role
techniques
elucidating
kinetics,
mechanisms,
dendrite
formation
anode-electrolyte
The
future
development
this
field
proposed
outlook.
Batteries,
Год журнала:
2024,
Номер
10(1), С. 29 - 29
Опубликована: Янв. 17, 2024
The
primary
goal
of
this
review
is
to
provide
a
comprehensive
overview
the
state-of-the-art
in
solid-state
batteries
(SSBs),
with
focus
on
recent
advancements
solid
electrolytes
and
anodes.
paper
begins
background
evolution
from
liquid
electrolyte
lithium-ion
advanced
SSBs,
highlighting
their
enhanced
safety
energy
density.
It
addresses
increasing
demand
for
efficient,
safe
storage
applications
like
electric
vehicles
portable
electronics.
A
major
part
analyzes
electrolytes,
key
SSB
technology.
classifies
as
polymer-based,
oxide-based,
sulfide-based,
discussing
distinct
properties
application
suitability.
also
covers
anode
materials
exploring
lithium
metal,
silicon,
intermetallic
compounds,
focusing
capacity,
durability,
compatibility
electrolytes.
challenges
integrating
these
materials,
interface
stability
dendrite
growth.
This
includes
discussion
latest
analytical
techniques,
experimental
studies,
computational
models
understand
improve
anode–solid
interface.
These
are
crucial
tackling
interfacial
resistance
ensuring
SSBs’
long-term
efficiency.
Concluding,
suggests
future
research
development
directions,
potential
revolutionizing
technologies.
serves
vital
resource
academics,
researchers,
industry
professionals
battery
technology
development.
offers
detailed
technologies
shaping
future,
providing
insights
into
current
solutions
rapidly
evolving
field.
ACS Energy Letters,
Год журнала:
2025,
Номер
unknown, С. 579 - 587
Опубликована: Янв. 2, 2025
Li-metal-based
batteries
are
considered
as
the
next
alternative
to
Li-ion
owing
their
high
specific
capacity
and
energy
density.
Alleviating
use
of
liquid
electrolytes,
solid-state
using
polymer
electrolytes
have
gained
vast
attention.
However,
Li-metal
major
concerns
regarding
non-total
suppression
dendrites
reactivity
Li
metal
with
certain
polymers
like
polycaprolactones
polycarbonates,
having
main
chain
ester
groups
which
alternatives
PEO-based
matrices.
Herein
we
designed
a
robust
matrix,
namely,
poly(vinyl
butyrate)
starting
from
biodegradable
that
is
highly
stable
metal,
appreciable
ionic
conductivity
single-ion
conducting
properties.
A
first
approach
has
been
made
on
these
types
matrices
not
only
introduces
modified
architecture
for
dry
ester-based
but
also
shows
unprecedented
improvement
in
electrolyte
performance
batteries.
Advanced Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 31, 2025
Solid-state
lithium
(Li)
metal
batteries
(SSLMBs)
have
garnered
considerable
attention
due
to
their
potential
for
high
energy
density
and
intrinsic
safety.
However,
widespread
development
has
been
hindered
by
the
low
ionic
conductivity
of
solid-state
electrolytes.
In
this
contribution,
a
novel
Li-rich
transport
mechanism
is
proposed
achieve
ultrafast
Li-ion
conduction
in
composite
By
incorporating
cation-deficient
dielectric
nanofillers
into
polymer
matrices,
it
found
that
negatively
charged
cation
defects
effectively
intensify
adsorption
Li
ions,
resulting
concentration
enrichment
on
surface
fillers.
More
importantly,
these
formed
layers
are
interconnected
establish
continuous
networks.
The
electrolyte
exhibited
remarkably
ion
activation
(0.17
eV)
achieved
an
unprecedented
approaching
1
×
10⁻3
S
cm⁻1
at
room
temperature.
Li||LiNi0.8Co0.1Mo0.1O2
full
cells
demonstrated
extended
cycling
life
over
200
cycles
with
capacity
retention
70.7%.
This
work
provides
fresh
insight
improving
constructing
networks,
paving
way
high-performance
SSLMBs.
Carbon Neutralization,
Год журнала:
2024,
Номер
3(3), С. 386 - 395
Опубликована: Апрель 22, 2024
Abstract
Due
to
its
high
energy
density
and
low
interface
impedance,
in
situ
polymerized
gel
electrolytes
were
considered
as
a
promising
electrolyte
candidate
for
lithium
metal
batteries
(LMBs).
In
this
work,
new
flame‐retardant
was
prepared
via
ring‐opening
polymerization
of
DOL
TEP.
The
PDOL–TEP
exhibits
excellent
room
temperature
ionic
conductivity
(0.38
mS
cm
−1
),
wide
electrochemical
window
(4.4
V),
Li
+
transference
number
(0.57),
enhanced
safety.
Thus,
the
NCM811||Li
cells
with
exhibit
cycle
stability
(82.7%
capacity
retention
rate
after
300
cycles
at
0.5
C)
performance
(156
119
mAh
g
1
C).
Furthermore,
phosphorus
radicals
decomposed
from
TEP
can
combine
hydrogen
block
combustion
reaction.
This
work
provides
an
effective
method
preparation
solid‐state
LMBs
voltage,
density,
Advanced Functional Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Май 6, 2024
Abstract
High‐performance
optoelectronic
bifunctional
cathode
materials
may
simultaneously
seize
and
store
solar
energy
in
lithium‐ion
batteries
to
boost
their
storage
capacity.
However,
such
photoactive
cathodes
with
typical
intrinsic
features
are
generally
limited
for
UV
light
applications
offer
poor
sunlight
harvesting
which
results
lower
density.
Here,
the
assembly
of
two
oligomers,
poly(vat
blue
6)
(PVB6)
6
sulfide)
(PVB6S)
is
reported,
through
polymerization
extend
conjugated
structure
organic
small
molecules.
These
oligomers
effectively
employed
as
photo‐assisted
batteries.
The
extended
narrows
gap,
promoting
exciton
dissociation
expanding
absorption
region.
PVB6S
possesses
a
narrow
gap
1.565
eV,
discharge‐specific
capacity
battery
enhanced
from
203
411
mAh
g
−1
under
illumination,
approximately
twice
original
This
demonstrates
charge
separation
cell,
synergistically
contributes
rational
design
complementary
enhances
performance
Nano-Micro Letters,
Год журнала:
2025,
Номер
17(1)
Опубликована: Янв. 28, 2025
Abstract
All-solid-state
batteries
(ASSBs)
are
pursued
due
to
their
potential
for
better
safety
and
high
energy
density.
However,
the
density
of
cathode
ASSBs
does
not
seem
be
satisfactory
low
utilization
active
materials
(AMs)
at
loading.
With
small
amount
solid
electrolyte
(SE)
powder
in
cathode,
poor
electrochemical
performance
is
often
observed
contact
loss
non-homogeneous
distribution
AMs
SEs,
leading
tortuosity
limitation
lithium
electron
transport
pathways.
Here,
we
propose
a
novel
design
that
can
achieve
volumetric
1258
Wh
L
−1
AM
content
85
wt%
by
synergizing
merits
AM@SE
core–shell
composite
particles
with
conformally
coated
thin
SE
shell
prepared
from
mechanofusion
process
particles.
The
structure
an
intimate
guarantees
ionic
conduction
pathway
while
unharming
electronic
conduction.
In
addition,
play
role
filler
reduces
packing
porosity
electrode
as
well
between
separator
layer.
systematic
demonstration
optimization
may
provide
understanding
guidance
on
electrodes
density,
capacity,
ultimately
ACS Applied Materials & Interfaces,
Год журнала:
2024,
Номер
16(24), С. 31191 - 31200
Опубликована: Июнь 6, 2024
Garnet-based
electrolytes
with
high
ionic
conductivity
and
excellent
stability
against
lithium
metal
anodes
are
promising
for
commercial
applications
in
solid-state
batteries
(SSLBs).
However,
the
further
development
of
SSLBs
is
inhibited
by
issues
such
as
low
uncontrolled
dendrite
growth.
Herein,
we
report
synthesis
fluorine-doped
Li7La3Zr2O12
(LLZO-F0.2)
fibers
electrospinning
subsequent
calcination
at
temperatures.
The
solid
composite
electrolyte
LLZO-F0.2
exhibits
an
5.37
×
10–4
S
cm–1
a
lithium-ion
transference
number
0.61
room
temperature.
Meanwhile,
it
lower
resistance
more
uniform
stripping
deposition
symmetric
cells.
full
cell
LiFePO4
cathode
rate
capability
cycling
800
cycles
0.5
C
discharge
specific
capacity
retention
97.7%.
This
fibrous
garnet-type
provides
viable
option
preparing
high-performance
SSLBs.