Journal of the American Chemical Society,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 28, 2025
The
broad
temperature
adaptability
associated
with
the
desolvation
process
remains
a
formidable
challenge
for
organic
electrolytes
in
rechargeable
metal
batteries,
especially
under
low-temperature
(LT)
conditions.
Although
traditional
approach
involves
utilizing
high
degree
of
anion
participation
solvation
structure,
known
as
weakly
(WSEs),
structure
these
is
highly
susceptible
to
fluctuations,
potentially
undermining
their
LT
performance.
To
address
this
limitation,
we
have
devised
an
innovative
electrolyte
that
harnesses
interplay
between
solvent
molecules,
effectively
blending
strong
and
weak
solvents
while
incorporating
mostly
unchanged
by
variations.
Remarkably,
competitive
coordination
two
molecules
introduces
local
disorder,
which
not
only
boosts
ionic
conductivity
but
also
prevents
salt
precipitation
solidification.
Therefore,
has
3.12
mS
cm-1
at
-40
°C.
Na3V2(PO4)3||Na
cells
demonstrated
reversible
capacity
95.9
mAh
g-1
°C,
87.6%
room
temperature,
well
stable
cycling
3400
cycles
retention
98.2%
-20
°C
5
C
600
96.1%
1
C.
This
study
provides
new
perspective
on
designing
regulating
temperature-robust
structures.
Advanced Materials,
Год журнала:
2024,
Номер
36(41)
Опубликована: Авг. 13, 2024
Abstract
Developing
rechargeable
batteries
with
high
power
delivery
at
low
temperatures
(LT)
below
0
°C
is
significant
for
cold‐climate
applications.
Initial
anode‐free
sodium
metal
(AFSMBs)
promise
LT
performances
because
of
the
de‐solvation
energy
and
smaller
Stokes
radius
Na
+
,
nondiffusion‐limited
plating/stripping
electrochemistry,
maximized
density.
However,
severe
reduction
in
electrolyte
ionic
conductivity
formation
unstable
solid
interphase
(SEI)
hinder
their
practical
applications
LT.
In
this
study,
a
2‐methyltetrahydrofuran‐based
dilute
designed
to
concurrently
achieve
an
anion‐coordinated
solvation
structure
impressive
3.58
mS
cm
−1
−40
°C.
The
dominant
aggregate
solvates
enable
highly
efficient
LT‐resistant
hopping
channels
electrolyte.
Moreover,
methyl‐regulated
electronic
2‐methyltetrahydrofuran
induces
gradient
decomposition
toward
inorganic‐organic
bilayer
SEI
mobility,
composition
homogeneity,
mechanical
robustness.
As
such,
record‐high
Coulombic
efficiency
beyond
99.9%
achieved
even
as‐constructed
AFSMBs
sustain
300
cycles
80%
capacity
maintained,
0.5‐Ah
level
pouch
cell
delivers
85%
over
180
−25
This
study
affords
new
insights
into
formulation
fast
conduction
superior
reversibility
ultralow
temperatures.
Angewandte Chemie International Edition,
Год журнала:
2024,
Номер
63(12)
Опубликована: Янв. 29, 2024
Room-temperature
sodium-sulfur
(RT
Na-S)
batteries
are
promising
for
low-cost
and
large-scale
energy
storage
applications.
However,
these
plagued
by
safety
concerns
due
to
the
highly
flammable
nature
of
conventional
electrolytes.
Although
non-flammable
electrolytes
eliminate
risk
fire,
they
often
result
in
compromised
battery
performance
poor
compatibility
with
sodium
metal
anode
sulfur
cathode.
Herein,
we
develop
an
additive
tin
trifluoromethanesulfonate
(Sn(OTf)
Advanced Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 26, 2025
Abstract
Sodium‐based
rechargeable
batteries
are
some
of
the
most
promising
candidates
for
electric
energy
storage
with
abundant
sodium
reserves,
particularly,
sodium‐based
dual‐ion
(SDIBs)
perform
advantages
in
high
work
voltage
(≈5.0
V),
high‐power
density,
and
potentially
low
cost.
However,
irreversible
electrolyte
decomposition
co‐intercalation
solvent
molecules
at
electrode
interface
under
a
charge
state
blocking
their
development.
Herein,
high‐salt
concentration
microenvironment
is
created
proposed
by
tailoring
solvation
structures
carriers
including
both
cations
anions,
which
maintains
highly
oxidation‐resistant
contact
ion
pairs
aggregates
provides
conductivity.
The
tailored
structure
makes
great
contribution
to
protecting
graphite
cathode
from
oxidation,
co‐intercalation,
structural
degradation
constructing
robust
cathode‐electrolyte
interphase
standout
electrochemical
stability.
Based
on
this,
SDIBs
achieved
an
excellent
high‐voltage
cycling
stability
81%
capacity
retention
after
10
000
cycles
battery
showed
improved
rate
performance
97.4
mAh
g
−1
maintained
100
C.
It
identified
that
regulating
anion
responsible
stable
chemistry
enhanced
reaction
kinetics,
deep
insight
into
compatibility
design
between
specialized
electrodes.
The
interfacial
wettability
between
electrodes
and
electrolytes
could
ensure
sufficient
physical
contact
fast
mass
transfer
at
the
gas-solid-liquid,
solid-liquid,
solid-solid
interfaces,
which
improve
reaction
kinetics
cycle
stability
of
rechargeable
metal-based
batteries
(RMBs).
Herein,
engineering
multiphase
interfaces
is
summarized
from
electrolyte
electrode
aspects
to
promote
interface
rate
durability
RMBs,
illustrates
revolution
that
taking
place
in
this
field
thus
provides
inspiration
for
future
developments
RMBs.
Specifically,
review
presents
principle
macro-
microscale
summarizes
emerging
applications
concerning
effect
on
Moreover,
deep
insight
into
development
provided
outlook.
Therefore,
not
only
insights
but
also
offers
strategic
guidance
modification
optimization
toward
stable
electrode-electrolyte
Journal of the American Chemical Society,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 28, 2025
The
broad
temperature
adaptability
associated
with
the
desolvation
process
remains
a
formidable
challenge
for
organic
electrolytes
in
rechargeable
metal
batteries,
especially
under
low-temperature
(LT)
conditions.
Although
traditional
approach
involves
utilizing
high
degree
of
anion
participation
solvation
structure,
known
as
weakly
(WSEs),
structure
these
is
highly
susceptible
to
fluctuations,
potentially
undermining
their
LT
performance.
To
address
this
limitation,
we
have
devised
an
innovative
electrolyte
that
harnesses
interplay
between
solvent
molecules,
effectively
blending
strong
and
weak
solvents
while
incorporating
mostly
unchanged
by
variations.
Remarkably,
competitive
coordination
two
molecules
introduces
local
disorder,
which
not
only
boosts
ionic
conductivity
but
also
prevents
salt
precipitation
solidification.
Therefore,
has
3.12
mS
cm-1
at
-40
°C.
Na3V2(PO4)3||Na
cells
demonstrated
reversible
capacity
95.9
mAh
g-1
°C,
87.6%
room
temperature,
well
stable
cycling
3400
cycles
retention
98.2%
-20
°C
5
C
600
96.1%
1
C.
This
study
provides
new
perspective
on
designing
regulating
temperature-robust
structures.