Advanced Energy Materials,
Год журнала:
2024,
Номер
14(43)
Опубликована: Авг. 22, 2024
Abstract
Exploiting
the
synergy
between
organic
polymer
electrolytes
and
inorganic
via
development
of
composite
can
suggest
solutions
to
current
challenges
next‐generation
solid‐state
lithium‐metal
batteries
(SSLMBs).
Depending
upon
a
mass
fraction
fillers
polymers,
are
broadly
classified
into
“ceramic‐in‐polymer”
(CIP)
“polymer‐in‐ceramic”
(PIC)
categories,
inheriting
distinct
structure
electrochemical
properties.
Since
stability
characteristics
phase
superior
those
for
lithium‐ion
conduction,
applying
lithium‐enrich
active
filler
in
PIC
seems
more
promising.
The
preserves
primary
migratory
channels
electrolyte,
while
viscoelastic
properties
attempt
be
introduced
from
binder
or
host.
present
work
overviews
studies
on
state‐of‐the‐art
electrolytes,
fundamental
mechanism
ionic
preparation
methods,
progress
materials
SSLMBs.
In
addition,
modification
strategies
improving
electrode–electrolyte
interface
also
emphasized.
Moreover,
it
further
prospects
effective
future
PICs‐based
CPEs
accelerate
practical
application
This
review
examines
outlook
PIC‐based
lithium
batteries.
Nano-Micro Letters,
Год журнала:
2023,
Номер
16(1)
Опубликована: Ноя. 20, 2023
The
widespread
adoption
of
lithium-ion
batteries
has
been
driven
by
the
proliferation
portable
electronic
devices
and
electric
vehicles,
which
have
increasingly
stringent
energy
density
requirements.
Lithium
metal
(LMBs),
with
their
ultralow
reduction
potential
high
theoretical
capacity,
are
widely
regarded
as
most
promising
technical
pathway
for
achieving
batteries.
In
this
review,
we
provide
a
comprehensive
overview
fundamental
issues
related
to
reactivity
migrated
interfaces
in
LMBs.
Furthermore,
propose
improved
strategies
involving
interface
engineering,
3D
current
collector
design,
electrolyte
optimization,
separator
modification,
application
alloyed
anodes,
external
field
regulation
address
these
challenges.
utilization
solid-state
electrolytes
can
significantly
enhance
safety
LMBs
represents
only
viable
approach
advancing
them.
This
review
also
encompasses
variation
design
transition
from
liquid
solid
electrolytes.
Particularly
noteworthy
is
that
introduction
SSEs
will
exacerbate
differences
electrochemical
mechanical
properties
at
interface,
leading
increased
inhomogeneity-a
critical
factor
contributing
failure
all-solid-state
lithium
Based
on
recent
research
works,
perspective
highlights
status
developing
high-performance
Gel
polymer
electrolytes
(GPEs)
hold
tremendous
potential
for
advancing
high-energy-density
and
safe
rechargeable
solid-state
batteries,
making
them
a
transformative
technology
electric
vehicles.
GPEs
offer
high
ionic
conductivity
mechanical
stability,
enabling
their
use
in
quasi-solid-state
batteries
that
combine
interfaces
with
liquid-like
behavior.
Various
based
on
different
materials,
including
flame-retardant
GPEs,
dendrite-free
gel
electrolytes,
hybrid
3D
printable
have
been
developed.
Significant
efforts
also
directed
toward
improving
the
interface
between
electrodes.
The
integration
of
gel-based
into
electrochemical
devices
has
to
revolutionize
energy
storage
solutions
by
offering
improved
efficiency
reliability.
These
advancements
find
applications
across
diverse
industries,
particularly
vehicles
renewable
energy.
This
review
comprehensively
discusses
as
battery
systems,
such
lithium-ion
(LiBs),
lithium
metal
(LMBs),
lithium–oxygen
lithium–sulfur
zinc-based
sodium–ion
dual-ion
batteries.
highlights
materials
being
explored
GPE
development,
polymers,
inorganic
compounds,
liquids.
Furthermore,
it
underscores
impact
role
enhancing
performance
safety
devices.
Angewandte Chemie International Edition,
Год журнала:
2024,
Номер
63(18)
Опубликована: Март 2, 2024
Abstract
The
solid‐state
electrolyte
interface
(SEI)
between
the
polymer
and
lithium
metal
anode
dramatically
affects
overall
battery
performance.
Increasing
content
of
fluoride
(LiF)
in
SEI
can
help
uniform
deposition
inhibit
growth
dendrites,
thus
improving
cycle
stability
performance
batteries.
Currently,
most
methods
constructing
LiF
involve
decomposing
salt
by
polar
groups
filler.
However,
there
is
a
lack
research
reports
on
how
to
affect
layer
Li‐ion
batteries
increasing
charge
transfer
number.
In
this
study,
porous
organic
with
“charge
storage”
properties
was
prepared
doped
into
composite
solid
study
effect
sufficient
decomposition
salts.
results
show
contrast
porphyrins,
unique
structure
POF
allows
for
each
individual
porphyrin.
Therefore,
during
TFSI
−
formation
LiF,
obtain
charge,
thereby
promoting
break
C−F
forming
LiF‐rich
SEI.
Compared
single
porphyrin
(0.423
e
),
provides
2.7
times
more
LiTFSI
(1.147
).
experimental
that
Li//Li
symmetric
equipped
PEO‐POF
be
operated
stably
than
2700
h
at
60
°C.
Even
(45
μm)
cells
are
stable
1100
0.1
mA
cm
−1
.
addition,
LiFePO
4
//PEO‐POF//Li
have
excellent
cycling
2
C
(80
%
capacity
retention
after
750
cycles).
1
(96
300
when
PEO‐base
replaced
PEG‐base
PVDF‐base,
cell
still
significantly
improved.
we
believe
concept
offers
novel
perspective
preparation
high‐performance
assemblies.
Nano-Micro Letters,
Год журнала:
2024,
Номер
16(1)
Опубликована: Янв. 12, 2024
Composite
solid
electrolytes
(CSEs)
have
emerged
as
promising
candidates
for
safe
and
high-energy-density
solid-state
lithium
metal
batteries
(SSLMBs).
However,
concurrently
achieving
exceptional
ionic
conductivity
interface
compatibility
between
the
electrolyte
electrode
presents
a
significant
challenge
in
development
of
high-performance
CSEs
SSLMBs.
To
overcome
these
challenges,
we
present
method
involving
in-situ
polymerization
monomer
within
self-supported
porous
Li
Advanced Functional Materials,
Год журнала:
2024,
Номер
34(24)
Опубликована: Фев. 16, 2024
Abstract
Polyethylene
oxide
(PEO)
solid
electrolytes
are
regarded
as
a
promising
candidate
for
all‐solid‐state
lithium
batteries
owing
to
their
high
safety
and
interfacial
compatibility.
However,
PEO
electrolyte
is
plagued
by
relatively
weak
structural
strength
unsatisfactory
Li
+
conductivity.
Herein,
mechanically
strong
conductively
favorable
cellulosic
scaffold
of
fabricated
through
amino
(‐NH
2
)
modification
g‐C
3
N
4
(CN)
incorporation
bacterial
cellulose
(BC)
under
microbial
circumstance.
The
biologically
‐NH
modified
BC
(B‐NBC)
entangled
with
CN
nanosheets
(CN@B‐NBC)
an
in
situ
secretion
nanocellulose
followed
hydrogen
bond‐induced
self‐assembly.
groups
from
B‐NBC
weaken
the
complexation
its
counterpart,
thus
facilitating
release
more
free
.
C‐N
covalence
extra
lone
electrons
further
strengthens
skeleton
meanwhile
offers
sufficient
anchors
migration.
After
infiltrating
LiTFSI/PEO
(LP),
LP/CN@B‐NBC
composite
(CSE)
exhibits
transference
number
ionic
Upon
coupling
LiFePO
cathode,
full
battery
remarkably
specific
capacity,
superior
rate
capability,
decent
cycling
stability.
This
work
pioneers
attempts
chemical
decoration
ingredient
architecture
CSE
aid
bottom‐up
biosynthetic
avenue.
Angewandte Chemie,
Год журнала:
2024,
Номер
136(18)
Опубликована: Март 2, 2024
Abstract
The
solid‐state
electrolyte
interface
(SEI)
between
the
polymer
and
lithium
metal
anode
dramatically
affects
overall
battery
performance.
Increasing
content
of
fluoride
(LiF)
in
SEI
can
help
uniform
deposition
inhibit
growth
dendrites,
thus
improving
cycle
stability
performance
batteries.
Currently,
most
methods
constructing
LiF
involve
decomposing
salt
by
polar
groups
filler.
However,
there
is
a
lack
research
reports
on
how
to
affect
layer
Li‐ion
batteries
increasing
charge
transfer
number.
In
this
study,
porous
organic
with
“charge
storage”
properties
was
prepared
doped
into
composite
solid
study
effect
sufficient
decomposition
salts.
results
show
contrast
porphyrins,
unique
structure
POF
allows
for
each
individual
porphyrin.
Therefore,
during
TFSI
−
formation
LiF,
obtain
charge,
thereby
promoting
break
C−F
forming
LiF‐rich
SEI.
Compared
single
porphyrin
(0.423
e
),
provides
2.7
times
more
LiTFSI
(1.147
).
experimental
that
Li//Li
symmetric
equipped
PEO‐POF
be
operated
stably
than
2700
h
at
60
°C.
Even
(45
μm)
cells
are
stable
1100
0.1
mA
cm
−1
.
addition,
LiFePO
4
//PEO‐POF//Li
have
excellent
cycling
2
C
(80
%
capacity
retention
after
750
cycles).
1
(96
300
when
PEO‐base
replaced
PEG‐base
PVDF‐base,
cell
still
significantly
improved.
we
believe
concept
offers
novel
perspective
preparation
high‐performance
assemblies.
Advanced Functional Materials,
Год журнала:
2023,
Номер
33(50)
Опубликована: Сен. 7, 2023
Abstract
The
practical
application
of
solid‐state
lithium‐metal
batteries
(SSLMBs)
based
on
polymer
solid
electrolytes
has
been
hampered
by
their
low
ion
conductivity
and
lithium‐dendrite‐induced
short
circuits.
This
study
innovatively
introduces
1D
ferroelectric
ceramic‐based
Bi
4
Ti
3
O
12
‐BiOBr
heterojunction
nanofibers
(BIT‐BOB
HNFs)
into
poly(ethylene
oxide)
(PEO)
matrix,
constructing
lithium‐ion
conduction
highways
with
“dissociators”
“accelerating
regions.”
BIT‐BOB
HNFs,
as
ceramic
fillers,
not
only
can
construct
long‐range
organic/inorganic
interfaces
transport
pathways,
but
also
install
regions”
for
these
pathways
through
the
electric
dipole
layer
built‐in
field
promoting
dissociation
lithium
salts
transfer
ions.
working
mechanisms
HNFs
in
matrix
are
verified
experimental
tests
density
functional
theory
calculations.
obtained
composite
exhibit
excellent
migration
number
(6.67
×
10
−4
S
cm
−1
0.54
at
50
°C,
respectively).
assembled
symmetric
battery
achieves
good
cycling
stability
over
4500
h.
LiFePO
||Li
full
delivers
a
high
Coulombic
efficiency
(>99.9%)
discharge
capacity
retention
rate
(>87%)
after
2200
cycles.
In
addition,
prepared
electrolyte
demonstrates
potential
flexible
pouch
batteries.