Nano-Micro Letters,
Journal Year:
2025,
Volume and Issue:
17(1)
Published: March 26, 2025
Silicon
stands
as
a
key
anode
material
in
lithium-ion
battery
ascribing
to
its
high
energy
density.
Nevertheless,
the
poor
rate
performance
and
limited
cycling
life
remain
unresolved
through
conventional
approaches
that
involve
carbon
composites
or
nanostructures,
primarily
due
un-controllable
effects
arising
from
substantial
formation
of
solid
electrolyte
interphase
(SEI)
during
cycling.
Here,
an
ultra-thin
homogeneous
Ti
doping
alumina
oxide
catalytic
interface
is
meticulously
applied
on
porous
Si
synergistic
etching
hydrolysis
process.
This
defect-rich
promotes
selective
adsorption
fluoroethylene
carbonate,
leading
reaction
can
be
aptly
described
"molecular
concentration-in
situ
conversion".
The
resultant
inorganic-rich
SEI
layer
electrochemical
stable
favors
ion-transport,
particularly
at
high-rate
temperature.
robustly
shielded
Si,
with
large
surface
area,
achieves
initial
Coulombic
efficiency
84.7%
delivers
exceptional
25
A
g-1
(692
mAh
g-1)
99.7%
over
1000
cycles.
robust
constructed
precious
promises
significant
advantages
for
fast
development
silicon-based
fast-charging
batteries.
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
36(21)
Published: Feb. 13, 2024
Abstract
With
the
continuously
growing
demand
for
wide‐range
applications,
lithium‐ion
batteries
(LIBs)
are
increasingly
required
to
work
under
conditions
that
deviate
from
room
temperature
(RT).
However,
commercial
electrolytes
exhibit
low
thermal
stability
at
high
temperatures
(HT)
and
poor
dynamic
properties
(LT),
hindering
operation
of
LIBs
extreme
conditions.
The
bottleneck
restricting
practical
applications
has
promoted
researchers
pay
more
attention
developing
a
series
innovative
electrolytes.
This
review
primarily
covers
design
adaptability
perspective.
First,
fundamentals
concerning
temperature,
including
donor
number
(DN),
dielectric
constant,
viscosity,
conductivity,
ionic
transport,
theoretical
calculations
elaborated.
Second,
prototypical
examples,
such
as
lithium
salts,
solvent
structures,
additives,
interfacial
layers
in
both
liquid
solid
electrolytes,
presented
explain
how
these
factors
can
affect
electrochemical
behavior
or
temperatures.
Meanwhile,
principles
limitations
electrolyte
discussed
corresponding
Finally,
summary
outlook
regarding
extend
proposed.
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
36(35)
Published: June 28, 2024
In
situ
polymerized
solid-state
electrolytes
have
attracted
much
attention
due
to
high
Li-ion
conductivity,
conformal
interface
contact,
and
low
resistance,
but
are
plagued
by
lithium
dendrite,
degradation,
inferior
thermal
stability,
which
thereby
leads
limited
lifespan
severe
safety
hazards
for
high-energy
metal
batteries
(LMBs).
Herein,
an
in
electrolyte
is
proposed
copolymerization
of
1,3-dioxolane
with
1,3,5-tri
glycidyl
isocyanurate
(TGIC)
as
a
cross-linking
agent,
realizes
synergy
battery
compatibility
Li
anode.
Functional
TGIC
enhances
the
polymeric
level.
The
unique
carbon-formation
mechanism
facilitates
flame
retardancy
eliminates
fire
risk.
meantime,
TGIC-derived
inorganic-rich
interphase
inhibits
side
reactions
promotes
uniform
plating.
Intrinsically
safe
LMBs
nonflammability
outstanding
electrochemical
performances
under
extreme
temperatures
(130
°C)
achieved.
This
functional
polymer
design
shows
promising
prospect
development
LMBs.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: July 24, 2024
Abstract
Lithium
(Li)
metal
is
considered
as
a
promising
anode
material
for
high‐energy
batteries;
yet,
its
practical
application
hindered
by
uncontrolled
Li
dendrite
growth,
especially
at
high
rate.
Herein,
dual
conductive
gradient
V
2
CT
x
/MoO
3
(DG‐V
)
host
that
integrates
electronic/ionic
gradients
and
lithiophilicity
prepared
layer‐by‐layer
assembly
dendrite‐free
anodes.
Gradient
LiF
deriving
from
different
amount
of
endows
good
ionic
gradient;
while,
MoO
regarded
spacer
to
avoid
the
restacking
,
increasing
space
deposition.
The
effectively
optimize
current
density
+
flux
distribution
bottom,
achieving
fast
reduction
“bottom–up”
deposition
mode.
Meanwhile,
lithiophilic
guide
homogeneous
growth.
As
result,
symmetrical
half‐cells
based
on
DG‐V
@Li
anodes
conduct
700
h
5
mAh
cm
−2
20
mA
.
@Li||LiFePO
4
full‐cells
maintain
capacity
retention
85.4%
after
1350
cycles
C.
Remarkably,
@Li||LiNi
0.6
Co
0.2
Mn
O
can
run
150
with
80.6%
even
harsh
conditions.
well‐adjusted
materials
structures
both
properties
will
bring
inspiration
novel
design
other
batteries.
ACS Nano,
Journal Year:
2024,
Volume and Issue:
18(28), P. 18622 - 18634
Published: July 1, 2024
Advancing
the
high-voltage
stability
of
O3-type
layered
cathodes
for
sodium-ion
batteries
is
critical
to
boost
their
progress
in
energy
storage
applications.
However,
this
type
cathode
often
suffers
from
intricate
phase
transition
and
structural
degradation
at
high
voltages
(i.e.,
>4.0
V
vs
Na+/Na),
resulting
rapid
capacity
decay.
Here,
we
present
a
Li/Ti
cosubstitution
strategy
modify
electronic
configuration
oxygen
elements
oxide
cathode.
This
deliberate
modulation
simultaneously
mitigates
transitions
counteracts
weakening
shielding
effect
extraction
sodium
ions,
thus
enhancing
electrostatic
bonding
within
TM
layer
inducing
optimizing
O3-OP2
occurring
voltage
range
2.0-4.3
V.
Consequently,
cosubstituted
NaLi1/9Ni1/3Mn4/9Ti1/9O2
exhibits
an
astounding
161.2
mAh
g-1
1C,
stable
cycling
up
100
cycles
has
been
achieved.
work
shows
impact
mechanism
element
substitution
on
interlayer
forces
transitions,
providing
crucial
reference
optimization
materials.
Energy & Environmental Science,
Journal Year:
2024,
Volume and Issue:
17(20), P. 7699 - 7711
Published: Jan. 1, 2024
We
present
a
simple
and
scalable
surface
chemical
approach
of
spraying
dilute
DFFSA
solution
on
the
Li
to
eliminate
native
passivation
layer
form
multi-component
SEI,
enabling
stable
cycling
460
W
h
kg
−1
metal
pouch
cell.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 23, 2025
Abstract
Commercialization
of
lithium–sulfur
(Li–S)
batteries
is
largely
limited
by
polysulfide
shuttling
and
sluggish
kinetics.
Herein,
2D
nanochannel
interlayer
composed
alternatively‐stacked
porous
silica
nanosheets
(PSN)
Ti
3
C
2
T
x
‐MXene
are
developed.
The
nanochannels
with
selective
cation
transport
characteristics
facilitate
lithium
ion
rapid
transport,
while
reject
the
translocation
anions
across
separator.
hydroxylated
MXene
shifts
p
‐band
center
surface
O
on
PSN
closer
to
Fermi
level,
leading
strong
absorptive/catalytic
effect
for
polysulfides
thus
fast
transformation
Together
ion/electron
bi‐conduction
function
PSN/MXene,
Li–S
deliver
high
initial
capacity
1443
mAh
g
−1
at
0.1
C,
low‐capacity
decay
rate
0.049%
per
cycle
over
800
cycles
excellent
capability.
At
a
sulfur
loading
5.2
mg
cm
−2
,
cells
present
higher
areal
specific
than
commercial
batteries.
pouch
lean
electrolyte
(E/S
=
3.9
µL
)
yield
2‐Ah
100
mA,
energy
density
cycling
stability.
This
contribution
opens
up
new
avenues
expanding
application
nanofluidics
in
electrochemical
storage
conversion.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 10, 2025
Abstract
The
artificial
solid
electrolyte
interphase
(SEI)
layer
is
capable
of
protecting
lithium
anodes
and
preventing
side
reactions
with
electrolytes.
development
inorganic/organic
composite
hybrid
SEI
can
be
considered
as
an
efficient
strategy
to
combine
the
merits
high
ion
conductivity,
mechanical
modulus,
flexibility.
However,
it
still
poses
a
great
challenge
solve
agglomeration
problem
in
these
maintain
strong
interaction
between
metal.
Herein,
bilayer
ultra‐thin
(P‐FEM@Li)
derivative
from
reactive
fluorinated
copolymer
(P‐FEM)
prepared
shows
ultra‐large
Young's
modulus
(>
75
GPa).
robust
inorganic
LiF‐rich
provides
superior
ionic
conductivity
large
while
flexible
organic
polymer
regulates
ions
transport
compatibility.
P‐FEM
induced
demonstrate
stable
cycles
for
more
than
4400
h
at
1
mA
cm
−2
average
coulombic
efficiency
(CE)
Li||P‐FEM@Cu
99.78%
after
100
cycles.
Moreover,
P‐FEM@Li||NCM811
punch
cell
428
Wh
kg
−1
exhibits
high‐capacity
retention
73%
175
This
work
new
way
prepare
practical
anodes.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 10, 2025
Abstract
Practical
application
of
Li
metal
anodes
(LMAs)
is
restricted
by
growth
dendrites.
Achieving
uniform
deposition
with
high
practically
available
specific
capacity
vital
to
obtain
advanced
LMAs.
Herein,
an
ultralight
V
2
CT
x
/bacterial
cellulose
(U‐V
/BC)
foam
a
volume
density
0.039
g
cm
−3
guided
tertiary
butanol
avoid
restacking
both
and
BC.
The
lithiophilic
functional
groups
BC
synergistically
induce
the
nucleation.
loose
stacking
structure
U‐V
/BC
provides
3D
ion
channels
for
accelerating
+
diffusion,
homogeneous
flux,
as
well
enough
sites
interspace
deposition.
As
result,
/BC@Li
exhibits
superior
stability
2800
h
at
5
mAh
−2
mA
ultrahigh
2040
−1
.
Furthermore,
full‐cells
paired
LiFePO
4
cathodes
possess
remarkable
retention
80.7%
after
800
cycles
1
C.
Even
harsh
conditions,
/BC@Li||LiFePO
can
also
run
100
0.3
C
84.9%.
This
work
sheds
light
on
surface
engineering
multiscale
architecture
design
LMAs
capacity.