The Journal of Physical Chemistry C,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 19, 2024
The
contact
loss
and
interface
impedance
of
all-solid-state
lithium-ion
batteries
(ASSLBs)
have
greatly
restricted
their
commercial
applications.
This
study
simulates
the
ASSLB
composed
a
LiNi0.8Co0.1Mn0.1O2
(NMC811)
cathode,
silicon–carbon
composite
(SiC)
anode,
Li10GeP2S12
(LGPS)
solid
electrolyte
analyzes
interfacial
electrochemical
mechanical
behavior.
electrical
resistance
stress
are
obtained
by
fractal
network
model
mechanics
theory.
According
to
reaction
kinetics
Nernst–Planck–Poisson
equations,
analytical
electric
field
space
charge
layer
(SCL)
in
case
symmetric
carrier
movement
is
acquired.
In
addition,
optimization
effect
coating
porous
poly(ethylene
oxide)
(PEO)
on
studied
theoretically.
Based
equivalent
circuit
(ECM),
spectra
(EIS)
whole
cell
simulated
Comsol
Multiphysics.
To
investigate
evolution
SCL
capacitance,
resistance,
impedance,
relevant
physical
parameters
reasonably
regulated.
results
show
that
when
buffer
higher
initial
porosity
taken
with
thickness
1.5–2.5
×
10–7m,
can
be
relieved
actual
improved.
What's
more,
relative
permittivity
electrolytes
range
10–50
reduce
as
well.
Carbon Neutralization,
Journal Year:
2025,
Volume and Issue:
4(1)
Published: Jan. 1, 2025
ABSTRACT
Solid‐state
lithium
batteries
have
attracted
increasing
attention
due
to
their
high
ionic
conductivity,
potential
safety
performance,
and
energy
density.
However,
practical
application
is
limited
by
a
series
of
interface
issues.
In
recent
years,
many
efforts
been
dedicated
solving
these
problems
via
engineering
providing
feasible
strategies
for
the
optimization
lithiumion
solid‐state
battery
interfaces.
This
paper
reviews
developments
in
addressing
interfacial
The
existing
are
first
systematically
summarized,
including
poor
contact,
electrochemical
instability,
dendrites,
space‐charge
layers,
element
diffusion.
Then,
corresponding
characteristics
thoroughly
analyzed
from
perspective
cathode/electrolyte
interface,
anode/electrolyte
structure
design.
Finally,
future
research
directions
modification
discussed.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 29, 2024
Abstract
Designing
solid
polymer
electrolytes
(SPEs)
with
high
ionic
conductivity
for
room‐temperature
operation
is
essential
advancing
flexible
all‐solid‐state
energy
storage
devices.
Innovative
strategies
are
urgently
required
to
develop
SPEs
that
safe,
stable,
and
high‐performing.
In
this
work,
we
introduce
photoexcitation‐modulated
heterojunctions
as
catalytically
active
fillers
within
SPEs,
guided
by
photocatalytic
design
principles,
meanwhile
employ
natural
bacterial
cellulose
improve
the
compatibility
poly(ethylene
oxide),
coordination
environment
of
lithium
salts,
optimize
both
ion
transport
mechanical
properties.
situ
photothermal
experiments
theoretical
calculations
reveal
strong
photogenerated
electric
field
produced
trace
oxide)
under
photoexcitation
significantly
enhances
salt
dissociation,
increasing
concentration
mobile
Li
+
.
This
results
in
a
substantial
increase
conductivity,
reaching
0.135
mS
cm
−1
at
25
°C,
transference
number
0.46.
The
lithium‐metal
pouch
cells
exhibit
an
impressive
discharge
capacity
178.8
mAh
g
even
after
repeated
bending
folding,
demonstrate
exceptional
long‐term
cycling
stability,
retaining
86.7
%
their
initial
250
cycles
1
C
(25
°C).
research
offers
novel
approach
developing
high‐performance
batteries.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
63(44)
Published: Aug. 2, 2024
Abstract
Polyethylene
oxide
(PEO)‐based
all‐solid‐state
lithium
metal
batteries
(ASSLMBs)
are
strongly
hindered
by
the
fast
dendrite
growth
at
Li
metal/electrolyte
interface,
especially
under
large
rates.
The
above
issue
stems
from
suboptimal
interfacial
chemistry
and
poor
+
transport
kinetics
during
cycling.
Herein,
a
SnF
2
‐catalyzed
lithiophilic‐lithiophobic
gradient
solid
electrolyte
interphase
(SCG‐SEI)
of
x
Sn
y
/LiF‐Li
O
is
in
situ
formed.
superior
ionic
LiF‐Li
rich
upper
layer
(17.1
nm)
possesses
high
energy
diffusion
channels,
wherein
lithiophilic
alloy
(8.4
could
highly
reduce
nucleation
overpotential
with
lower
barrier
promote
rapid
electron
transportation
for
reversible
plating/stripping.
Simultaneously,
insoluble
‐coordinated
PEO
promotes
ion
bulk
phase.
As
result,
an
over
46.7
3.5
times
improvements
lifespan
critical
current
density
symmetrical
cells
achieved,
respectively.
Furthermore,
LiFePO
4
‐based
ASSLMBs
deliver
recorded
cycling
performance
5
C
(over
1000
cycles
capacity
retention
80.0
%).
More
importantly,
impressive
electrochemical
performances
safety
tests
LiNi
0.8
Mn
0.1
Co
pouch
cell
,
even
extreme
conditions
(i.e.,
100
°C),
also
demonstrated,
reconfirmed
importance
design
high‐rate
applications.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
unknown
Published: July 26, 2024
Deep
eutectic
electrolytes
(DEEs)
are
regarded
as
one
of
the
next-generation
to
promote
development
lithium
metal
batteries
(LMBs)
due
their
unparalleled
advantages
compared
both
liquid
and
solid
electrolytes.
However,
its
application
in
LMBs
is
limited
by
electrode
interface
compatibility.
Here,
we
introduce
a
novel
dimethylmalononitrile
(DMMN)-based
DEE
induced
N
coordination
dissociate
LiTFSI.
We
confirmed
that
DMMN
molecule
can
dissociation
LiTFSI
interaction
between
atom
Li
InfoMat,
Journal Year:
2024,
Volume and Issue:
unknown
Published: July 30, 2024
Abstract
Solid‐state
Li
metal
battery
has
attracted
increasing
interests
for
its
potentially
high
energy
density
and
excellent
safety
assurance,
which
is
a
promising
candidate
next
generation
system.
However,
the
low
ionic
conductivity
+
transport
number
of
solid‐state
polymer
electrolytes
limit
their
practical
application.
Herein,
composite
electrolyte
with
self‐inserted
structure
proposed
using
layered
double
hydroxides
(LDHs)
as
dopant
to
achieve
fast
channel
in
poly(vinylidene‐co‐trifluoroethylene)
[P(VDF‐TrFE)]
based
electrolyte.
In
such
electrolyte,
P(VDF‐TrFE)
an
all‐trans
conformation,
all
fluorine
atoms
locate
on
one
side
chain,
providing
highways.
Meanwhile,
LDH
can
immobilize
anions
salts
electrostatic
interactions,
promoting
dissociation
salts,
thereby
enhancing
(6.4
×
10
−4
S
cm
−1
)
transference
(0.76).
The
anion
immobilization
effect
realize
uniform
electric
field
distribution
at
anode
surface
suppress
dendritic
growth.
Moreover,
hydrogen
bonding
interaction
between
chains
also
endows
strong
mechanical
properties.
Thus,
room
temperature,
||
symmetric
cells
be
stably
cycled
over
1000
h
current
0.2
mA
−2
,
full
LiFePO
4
cathode
deliver
capacity
retention
(>95%)
after
200
cycles.
This
work
offers
route
construct
transport.
image
Journal of the American Chemical Society,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 3, 2025
Engineering
aqueous
electrolytes
with
an
ionic
liquid
(IL)
for
the
zinc
(Zn)
metal
anode
has
been
reported
to
enhance
electrochemical
performances
of
Zn
batteries
(ZMBs).
Despite
these
advancements,
effects
IL
and
mechanisms
involving
their
anions
cations
have
scarcely
investigated.
Here,
we
introduce
a
novel
electrolyte
design
strategy
that
synergizes
anion-cation
chemistry
using
halogen-based
elucidates
underlying
mechanism.
The
strongly
preferentially
adsorbed
halogen
guide
formation
water-poor
electrical
double
layer
(EDL)
by
imidazole-based
cations,
resulting
in
halide-rich
inorganic
interphase.
This
synergistic
interaction
significantly
mitigates
corrosion
at
anode-electrolyte
interface,
while
interphase
promotes
dense
deposition.
Consequently,
battery
exhibits
superior
performance,
including
high
reversibility
(99.74%)
ultralong
cycle
life
(20,000
cycles).
combines
traditional
single
solid
classic
EDL
mechanism,
substantially
enhancing
performance
ZMBs.