Journal of Materials Chemistry A,
Год журнала:
2023,
Номер
11(6), С. 2780 - 2792
Опубликована: Янв. 1, 2023
This
work
provides
a
composite
solid
electrolyte
combining
dendritic
SPES
nanofibers
and
LaCoO
3
nanowires
for
ASSLIBs.
Benefitting
from
the
promotion
of
electrolytes
on
rapid
ion
deposition,
pouch
cell
possesses
excellent
cycle
performance.
Advanced Materials,
Год журнала:
2023,
Номер
35(38)
Опубликована: Июнь 2, 2023
Solid-state
batteries
can
ensure
high
energy
density
and
safety
in
lithium
metal
batteries,
while
polymer
electrolytes
are
plagued
by
slow
ion
kinetics
low
selective
transport
of
Li+
.
Metal-organic
frameworks
(MOFs)
proposed
as
emerging
fillers
for
solid-state
poly(ethylene
oxide)(PEO)
electrolytes,
however,
developing
functionalized
MOFs
understanding
their
roles
on
transfer
has
proven
challenging.
Herein,
combining
computational
experimental
results,
the
functional
group
regulation
effectively
change
surficial
charge
distribution
limit
anion
movement
is
revealed,
providing
a
potential
solution
to
these
issues.
Specifically,
2D
MOF
sheets
designed
through
molecular
engineering
construct
high-performance
composite
where
electron-donating
effect
substituents
2D-MOFs
limits
ClO4-
promotes
mechanical
properties
migration
numbers
(0.36
up
0.64)
PEO.
As
result,
Li/Li
cells
with
electrolyte
exhibit
superior
cyclability
1000
h
at
current
0.2
mA
cm-2
Meanwhile,
solid
LiFePO4
/Li
battery
delivers
highly
reversible
capacities
148.8
mAh
g-1
after
200
cycles.
These
findings
highlight
new
approach
confinement
use
electronic
effects,
leading
enhanced
ionic
conductivity,
feasible
direction
batteries.
Energy & Environmental Science,
Год журнала:
2024,
Номер
17(13), С. 4426 - 4460
Опубликована: Янв. 1, 2024
The
practical
application
of
commercialized
lithium-ion
batteries
(LIBs)
currently
faces
challenges
due
to
using
liquid
electrolytes
(LEs),
including
limited
energy
density
and
insufficient
safety
performance.
Advanced Energy Materials,
Год журнала:
2023,
Номер
13(13)
Опубликована: Фев. 24, 2023
Abstract
Nanocomposite
solid
polymer
electrolytes
are
considered
as
a
promising
strategy
for
solid‐state
lithium
metal
batteries
(SSLMBs).
However,
the
randomly
dispersed
fillers
in
matrix
with
limited
Li
+
transference
number
and
insufficient
ionic
conductivity
severely
sacrifice
ion
transport
capacity,
thus
restricting
their
practical
application.
To
tackle
these
issues,
magnetic
field‐assisted
alignment
is
proposed
to
disperse
vertically
aligned
akaganéite
nanotube
an
inorganic‐polymer
nanocomposite
electrolyte
ultra‐stable
SSLMBs.
The
cations
Lewis
acid
sites
can
grab
anions
promote
dissociation
of
salts
while
sufficient
oxygen
hydroxyl
functional
group
offer
abundant
Li‐ion
migration
favored
transportation.
At
same
time,
akaganéite/polymer
interface
combined
above
synergistic
effects
establish
oriented
channels
inside
electrolyte,
which
significantly
elevates
its
conductivity.
Specially,
organic‐inorganic
dual‐layer
solid‐electrolyte
formed
uniform
deposition
suppress
dendrite
growth.
beneficial
effect
network
also
demonstrated
full
cell
pouch
where
remarkable
2000
cycles
capacity
decay
0.012%
per
cycle
be
achieved.
Advanced Energy Materials,
Год журнала:
2024,
Номер
14(11)
Опубликована: Янв. 8, 2024
Abstract
All‐solid‐state
lithium
metal
batteries
(ASSLMBs)
hold
great
promise
for
the
development
of
next‐generation
high‐safety,
high‐energy‐density
batteries,
but
still
face
challenges
dendrite
growth
and
thickness.
Herein,
ultrathin
PEO‐based
composite
solid
polymer
electrolyte
(denoted
as
PAL)
supported
by
a
low‐density
self‐supporting
aramid
nanofiber
(ANF)
aerogel
framework
is
developed.
The
ANF
obtained
novel
CO
2
‐assisted
induced
self‐assembly
method
has
well‐designed
bilayer
structure
with
double
cross‐linking
degree.
Benefiting
from
intermolecular
interaction
between
ANFs
PEO,
PAL
achieves
an
thickness
(20
µm)
excellent
thermal
stability
mechanical
strength.
Meanwhile,
due
to
modulation
ionic
pathways
functionalized
ANF,
uniform
deposition
without
dendrites,
resulting
in
stable
long
cycling
(1400
h)
symmetric
cells.
Consequently,
Li|PAL|LiFePO
4
(LFP)
cell
long‐term
(1
C,
>700
cycles,
Coulombic
efficiency
>
99.8%)
fast
charge/discharge
performance
(rate,
10
C).
More
practically,
Li|PAL|LFP
energy
density
180
Wh
kg
−1
ability
match
high‐loading
(8
mg
cm
−2
)
cathode.
Furthermore,
double‐layer
pouch
demonstrates
flexibility
safety
abuse
tests.
Angewandte Chemie International Edition,
Год журнала:
2024,
Номер
63(18)
Опубликована: Фев. 20, 2024
Abstract
Poly(ethylene
oxide)
(PEO)‐based
electrolytes
are
often
used
for
Li
+
conduction
as
they
can
dissociate
the
salts
efficiently.
However,
high
entanglement
of
chains
and
lack
pathways
rapid
ion
diffusion
limit
their
applications
in
advanced
batteries.
Recent
developments
ionic
covalent
organic
frameworks
(iCOFs)
showed
that
highly
ordered
structures
provide
efficient
transport,
solving
limitations
traditional
PEO‐based
electrolytes.
Here,
we
present
imidazolate
COFs,
PI‐TMEFB‐COFs,
having
methoxyethoxy
chains,
synthesized
by
Debus–Radziszewski
multicomponent
reactions
ionized
form,
@PI‐TMEFB‐COFs,
showing
a
conductivity
8.81
mS
cm
−1
transference
number
0.974.
The
mechanism
such
excellent
electrochemical
properties
is
LiClO
4
,
making
free
then
those
transported
through
COFs’
pores.
@PI‐TMEFB‐COFs
formed
stable
interface
with
metal.
Thus,
employing
solid
electrolyte
to
assemble
LiFePO
batteries
an
initial
discharge
capacity
119.2
mAh
g
at
0.5
C,
82.0
%
99.9
Coulombic
efficiency
were
maintained
after
400
cycles.
These
results
show
iCOFs
ether
via
create
new
chapter
rechargeable
Solid-state
batteries
(SSBs)
are
under
development
as
high-priority
technologies
for
safe
and
energy-dense
next-generation
electrochemical
energy
storage
systems
operating
over
a
wide
temperature
range.
electrolytes
(SSEs)
exhibit
high
thermal
stability
and,
in
some
cases,
the
ability
to
prevent
dendrite
growth
through
physical
barrier,
compatibility
with
"holy
grail"
metallic
lithium.
These
unique
advantages
of
SSEs
have
spurred
significant
research
interests
during
last
decade.
Garnet-type
SSEs,
that
is,
Li