Rapid Thermal Runaway Detection of Lithium-Ion Battery via Swelling-Based State-of-Charge Monitoring Using Piezoresistive Sponge Sensor
eTransportation,
Journal Year:
2025,
Volume and Issue:
unknown, P. 100404 - 100404
Published: Feb. 1, 2025
Language: Английский
Multidentate ether-induced reconfiguration of solvation structure in non-flammable phosphate electrolytes for wide-temperature application in lithium-ion batteries
Jia Xie,
No information about this author
Xiankun Yang,
No information about this author
Ziqi Zeng
No information about this author
et al.
Research Square (Research Square),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 13, 2025
Abstract
Conventional
carbonate
electrolytes
fail
to
meet
the
requirements
for
lithium-ion
batteries
(LIBs)
with
wide
temperature
range
and
high
safety.
Diethyl
ethylphosphonate
(DEEP)
has
excellent
flame
retardancy
a
(-83
198°C),
which
holds
promise
developing
non-flammable
electrolyte
wide-temperature
application
in
LIBs.
However,
its
limited
compatibility
graphite
electrodes
slow
ionic
transport
capability
must
be
addressed
effective
application.
Herein,
we
introduce
diethylene
glycol
dimethyl
ether
(DEGDME)
reconfigure
solvation
structure
of
DEEP-based
further
enhance
ion
capacity.
The
film-forming
additives
enable
preserve
98%
capacity
retention
after
150
cycles
Li||Graphite
cells
modified
DEGDME
improved
low-temperature
performance
achieving
71%
50th-cycle
Graphite||LiFePO
4
at
-20°C.
This
work
introduces
new
strategy
designing
phosphate
electrolytes,
enabling
reliable
safe
LIBs
across
range.
Language: Английский
Insights into the doping rules of heteroatom on Ni-rich ternary cathode stability by integrating high throughput calculation and machine learning
Journal of Energy Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 1, 2025
Language: Английский
Thermoresponsive Mono‐Solvent Electrolyte Inhibiting Parasitic Reactions for Safe Lithium Metal Batteries
Advanced Energy Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 10, 2025
Abstract
Solvents
in
liquid
and
gel
polymer
electrolytes
are
recognized
for
contributing
to
high
ionic
conductivity
high‐energy‐density
lithium
metal
batteries.
However,
parasitic
reactions
involving
solvents
induce
safety
risks
under
thermal
abuse
conditions
poor
lifespan
during
room‐temperature
cycles,
which
rarely
investigated.
This
study
introduces
a
thermoresponsive
mono‐solvent
electrolyte
as
built‐in
switch.
The
polymerizes
at
elevated
temperatures,
creating
passivate
network
without
residue
solvents.
exhibits
stability
with
91%
mass
retention
200
°C
significantly
suppresses
side
between
the
electrolyte,
reducing
runaway
risks.
Ah‐level
Li||LiNi
0.8
Co
0.1
Mn
O
2
pouch
batteries
employing
this
can
efficiently
improve
critical
temperature
of
by
75
compared
electrolyte.
At
ambient
promotes
formation
stable
solid
interphase
(SEI)
rich
LiF
Li
O,
effectively
dendrite
growth
on
anode.
Consequently,
0.5
0.2
0.3
cells
retain
capacity
after
152
even
high‐loading
cathodes
(19.7
mg
cm
−2
,
3
mAh
).
research
offers
valuable
insights
into
inhibiting
electrochemical
cycle
runaway,
enhancing
Language: Английский
Consolidating Surface Lattice via Facile Self‐Anchored Oxygen Layer Reconstruction Toward Superior Performance and High Safety Nickel‐Rich Oxide Cathodes
Haoyu Wang,
No information about this author
Qi Shi,
No information about this author
Jinyang Dong
No information about this author
et al.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 10, 2025
Abstract
Nickel‐rich
oxide
materials
have
been
recognized
as
promising
cathodes
for
state‐of‐art
high
energy
lithium‐ion
batteries;
however,
challenges
remain
in
their
commercialization
due
to
chemical
and
structural
degradation,
poor
thermal
stability
related
oxygen
lattice
destabilization.
Herein,
this
work
reports
a
straightforward
approach
stabilizing
the
surface
framework
by
inducing
reconstruction
via
swift
proton
exchange
heat
treatment
argon
atmosphere.
The
robust
structure
with
localized
disordered
phase
domains
effectively
suppresses
interfacial
parasitic
reactions
highly
delithiated
reduces
detrimental
degradation.
Enabled
strongly
anchored
framework,
consolidated
also
reinforces
cathode
featured
higher
decomposition
temperature
reduced
release
under
stress.
In
comparison
unmodified
counterpart,
reconstructed
nickel‐rich
demonstrates
improved
cycling
rate
capability.
This
reveals
critical
role
of
regulating
on
electrochemical
performance
behaviors,
explores
potential
feasible
modification
advanced
batteries.
Language: Английский
Fire-Proofing, Mechanic-Reinforcing, Electrostatic-Spinning Strategies Toward Fabricating Porous Separator for Superior and Safer Lithium-Ion Batteries
Junling Wang,
No information about this author
Chuang He,
No information about this author
Yunfeng Jia
No information about this author
et al.
ACS Applied Polymer Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 8, 2025
Language: Английский
Chelating Solvent Mediated Solvation Structure Enables High‐Rate Operation of Ah‐Level Li‐Ion Batteries in Nonflammable Phosphate Electrolyte
Mengchuang Liu,
No information about this author
Wei Liu,
No information about this author
Ziqi Zeng
No information about this author
et al.
Advanced Energy Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 25, 2025
Abstract
Highly
flammable
carbonate
electrolytes
induce
significant
safety
risk
for
lithium‐ion
batteries
(LIBs),
raising
concerns
about
their
suitability
large‐scale
applications.
In
contrast,
non‐flammable
phosphate
offer
a
potential
solution,
yet
the
untamed
strong
interaction
of
Li
+
‐phosphates
and
inefficient
diffusion
result
in
sluggish
reaction
kinetics,
which
restricts
operation
Ah‐level
LIBs
to
rates
below
0.2C.
Herein,
chelating
solvent‐mediated
ion‐solvent
coordinated
structure
is
designed
modulate
interaction.
This
innovative
approach
enables
high‐efficiency
pseduo‐structrural
diffusion,
similar
that
observed
high
concentration
electrolytes,
while
maintaining
standard
1
mol
L
−1
achieving
Li⁺
conductivity.
The
operating
rate
graphite|LiFePO
4
cells
increased
from
0.2C
2C,
with
Ah
25
retaining
73.9%
71.0%
capacity
after
1000
600
cycles,
respectively.
Additionally,
maximum
temperature
during
nail
penetration
significantly
reduced
338.9
200
°C.
strategy
provides
promising
tuition
developing
advanced
electrolytes.
Language: Английский
Temperature‐Inert Interface Enables Safe and Practical Energy‐Dense LiNi0.91Co0.07Mn0.02O2 Pouch Cells
Junxian Hou,
No information about this author
Qinyu Shi,
No information about this author
Xuning Feng
No information about this author
et al.
Advanced Energy Materials,
Journal Year:
2024,
Volume and Issue:
14(40)
Published: July 20, 2024
Abstract
Safety
concerns
significantly
hinder
the
practical
implementation
of
ultrahigh‐nickel
cathodes
in
lithium‐ion
batteries.
The
solid
electrolyte
interphase
(SEI)
derived
from
conventional
ester‐based
is
susceptible
to
thermal
decomposition,
resulting
battery
safety
degradation.
Herein,
a
temperature‐inert
and
inorganic‐rich
SEI
developed
for
LiNi
0.91
Co
0.07
Mn
0.02
O
2
|graphite
(NCM91|Gr)
by
employing
flame‐retardant
diluted
weakly
solvated
electrolyte.
Temperature‐dependent
X‐ray
photoelectron
spectroscopy
reveals
that
SEI's
inorganic
components
LiF,
Li
SO
3
,
4
N
exhibit
exceptional
thermotolerance
under
attack.
Further
evidence
temperature‐dependent
diffraction
indicates
this
thermally
stable
interface
effectively
mitigates
anode
phase
transition
original
LiC
6
12
state,
remarkable
improvement
intrinsic
32%
reduction
gas
emission
battery.
1.2
Ah
NCM91|Gr
pouch
cell
exhibits
failure
onset
temperature
as
high
183.1
°C
maintains
stability
at
180
60
min.
Furthermore,
360
Wh
kg
−1
12.3
0.92
0.06
|graphite@20%
silicon
dioxide
experiences
no
runaway
even
200
°C.
also
delivers
outstanding
capacity
retention
90.5%
after
1200
cycles
with
enhanced
electrochemical
performance.
This
study
provides
promising
approach
developing
safer
energy‐dense
batteries
through
design.
Language: Английский
Cation migration of layered oxide cathodes for sodium-ion batteries: fundamental failure mechanisms and practical modulation strategies
Zhuang‐Chun Jian,
No information about this author
Jun-Xu Guo,
No information about this author
Yi‐Feng Liu
No information about this author
et al.
Chemical Science,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Jan. 1, 2024
We
comprehensively
review
the
research
advances
in
cation
migration
of
sodium
layered
oxides,
systematically
revealing
fundamental
mechanisms
and
practical
modulation
strategies
for
irreversible
leading
to
battery
failure.
Language: Английский