Nature Communications,
Год журнала:
2025,
Номер
16(1)
Опубликована: Май 25, 2025
Ideal
silicon
negative
electrodes
for
high-energy
lithium-ion
batteries
are
expected
to
feature
high
capacity,
minimal
expansion,
long
lifespan,
and
fast
charging.
Yet,
engineered
materials
face
a
fundamental
paradox
associated
with
particle
deformation
charge
transfer,
which
hinders
the
industrial
use
of
advanced
electrode
materials.
Here
we
show
sieving-pore
design
carbon
supports
that
overcomes
these
mechano-kinetic
limitations
enable
stable,
(de)alloying
chemistries
electrodes.
Such
structure
features
an
inner
nanopore
body
reserved
voids
accommodate
high-mass-content
outer
sub-nanopore
entrance
induce
both
pre-desolvation
intrapore
transport
ions
during
cycling.
Importantly,
sieving
effect
yields
inorganic-rich
solid
electrolyte
interphases
mechanically
confine
in-pore
silicon,
producing
stress-voltage
coupling
mitigates
formation
detrimental
crystalline
Li15Si4.
As
result,
this
enables
low
expansion
(58%
at
specific
capacity
1773
mAh
g-1
areal
4
cm-2),
initial/cyclic
Coulombic
efficiency
(93.6%/99.9%),
decay
(0.015%
per
cycle).
A
practical
pouch
cell
such
delivers
80%
retention
over
1700
cycles
2
as
well
10-min
charging
capability.
Advanced Energy Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 17, 2025
Abstract
Silicon
(Si)
holds
immense
promise
as
viable
anode
for
next‐generation
high‐energy‐density
Li‐ion
batteries
(LIBs).
However,
its
poor
ionic/electronic
conductivity
and
significant
volumetric
changes
during
cycling
lead
to
rapidly
deteriorated
LIB
performance.
Here,
a
novel
multifunctional
coating
featuring
ultrafine
SiO
2
nanoparticles
(<7
nm)
embedded
carbon
on
Si
(termed
Si@uSiO
‐C)
resolve
these
challenges
is
proposed.
This
unique
uSiO
‐C
provides
high‐efficient
electron
ion
transport
pathways,
while
also
improves
interfacial
stability
mitigates
volume
cycling,
thereby
enhancing
the
structural
integrity
of
‐C,
corroborated
by
extensive
experimental
computational
studies.
In
addition,
abundant
interfaces
in
facilitate
Li
+
evenly
distributed
impart
high
electrochemical
reactivity
mechanical
robustness.
Consequently,
achieves
reversible
capacity
2093
mAh
g
−1
at
0.2
A
,
with
initial
Coulombic
efficiency
88.3%,
superior
rate
capability
durability
(1000
cycles,
928
1.0
75%
retention).
Full
cells
paired
commercial
LiFePO
4
cathodes
demonstrate
cyclability,
maintaining
80%
retention
over
500
cycles
C.
work
highlights
vital
role
promoting
performance
Si‐based
anodes
high‐performance
LIBs.
Advanced Materials,
Год журнала:
2024,
Номер
36(35)
Опубликована: Июнь 25, 2024
Polyoxometalates
(POMs)
have
been
considered
one
of
the
most
promising
anode
candidates
for
lithium-ion
batteries
(LIBs)
in
virtue
their
high
theoretical
capacity
and
reversible
multielectron
redox
properties.
However,
poor
intrinsic
electronic
conductivity,
low
specific
surface
area,
solubility
organic
electrolytes
hinder
widespread
applications
LIBs.
Herein,
a
novel
hybrid
nanomaterial
is
synthesized
by
co-assembling
POMs
porphyrins
(PMo
Chemical Science,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 1, 2025
Silicon
(Si)
is
considered
a
promising
anode
material
for
next-generation
lithium-ion
batteries
due
to
its
high
theoretical
specific
capacity
and
earth-abundancy.
However,
challenges
such
as
significant
volume
expansion,
unstable
solid
electrolyte
interphase
(SEI)
formation
in
incompatible
electrolytes,
slow
transport
lead
poor
cycling
rate
performance.
In
this
work,
it
demonstrated
that
superior
cyclability
capability
of
Si
anodes
can
be
achieved
using
ethyl
fluoroacetate
(EFA)
fluoroethylene
carbonate
(FEC)
solvents
with
low
binding
energy
Li+
but
sufficiently
relative
dielectric
constants.
By
weakening
the
interaction
between
solvent,
barrier
desolvation
process
lowered,
while
ensuring
conductivity
diffusion
Li+.
As
result,
silicon-carbon
optimized
exhibits
excellent
performance,
work
reversibly
1709.1
mAh
g-1
proceeds
over
250
cycles
retains
85.2%
at
0.2C.
Furthermore,
Si/C‖LiFePO4
(LFP)
full
cell
shows
an
extended
service
life
more
than
500
cycles.
This
offers
valuable
insights
into
design
weakly
solvating
electrolytes
high-performance
Si-based
batteries.
Abstract
Unstable
solid‐electrolyte
interphase
(SEI)
film
resulting
from
chemically
active
surface
state
and
huge
volume
fluctuation
limits
the
development
of
Si‐based
anode
materials
in
lithium‐ion
batteries.
Herein,
a
photo‐initiated
polypyrrole
(PPy)
coating
is
manufactured
on
Si
nanoparticles
to
guide
situ
generation
PPy‐integrated
hybrid
SEI
(hSEI).
The
hSEI
shows
excellent
structure
stability
optimized
component
composition
for
lithium
storage.
More
promisingly,
precursor
with
more
uniform
thickness,
stronger
interaction
inner
particles,
higher
mechanical
strength
further
enables
structural
integrity
film.
highly
ordered
interchain
can
maintain
effective
Li
+
transport
during
electrochemical
cycling.
Consequently,
SiNPs@hSEI‐L
maintains
reversible
capacity
1044.7
mAh
g
−1
after
500
cycles
at
2
A
,
manifesting
superior
This
work
proposes
novel
polymer‐integrated
formation
provides
an
reference
optimization
semiconductor
materials.
Advanced Functional Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 21, 2025
Abstract
The
electrochemical
performance
of
Si
anodes
for
lithium‐ion
batteries
(LIBs)
is
primarily
influenced
by
the
stress–strain
and
transport
dynamics.
However,
traditional
Si/carbon
composites
often
fail
to
well
balance
these
two
factors.
Herein,
a
hierarchically
porous
silicon/carbon
composite
(denoted
as
pSi@void@NMC)
with
high
lithium
storage
capacity
developed
under
guidance
finite
element
analysis,
where
(pSi)
nitrogen‐doped
mesoporous
carbon
(NMC)
used
yolk
shell,
respectively.
internal
external
cultivation
design
endows
pSi@void@NMC
fast
transfer
kinetics,
effective
stress‐buffering,
low
volume
expansion,
superior
mechanical
stability.
Compared
core–shell
pSi@NMC
bare
pSi
electrodes,
resulting
anode
demonstrates
reversible
1769.8
mAh
g
−1
after
300
cycles
at
0.2
A
exceptional
cycling
stability
only
0.016%
decay
rate
per
cycle.
In
situ
ex
characterization
results
further
confirm
its
reversibility
Li
+
insertion/extraction
during
reactions
benefiting
from
formation
inorganic
LiF‐rich
SEI
film.
Moreover,
also
shows
good
potential
full‐cell
applications.
These
findings
provide
facile
concept
research
strategy
addressing
stress
fractures
inadequate
kinetics
Si‐based
materials
high‐performance
LIBs.
Advanced Energy Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Ноя. 19, 2024
Abstract
The
unstable
interface
between
reactive
anodes
and
electrolytes
in
batteries
has
been
identified
as
a
critical
factor
limiting
the
long‐cycle
stability
of
batteries.
An
effective
solution
is
to
build
solid
electrolyte
interphase
(SEI)
that
acts
passivation
layer
mitigate
side
reactions
electrolytes.
mechanical
SEI
important
because
with
poor
cannot
survive
volume
topography
fluctuation
anode
upon
cycling.
stress
built‐up
would
cause
failure
SEI,
resulting
exposure
fresh
surface
electrolyte,
consuming
limited
active
materials
electrolytes,
inducing
rapid
battery
decay.
Therefore,
understanding
regulating
imperative
for
improving
cycle
life.
In
this
review,
properties
are
discussed.
Then,
advanced
characterization
tools
measure
introduced.
Additionally,
recent
progress
on
presented
terms
situ
ex
modifications
SEI.
Finally,
an
insightful
outlook
provided
further
understand
regulate
performance.
Advanced Energy Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Дек. 20, 2024
Abstract
Balancing
interfacial
interactions
is
critical
to
the
reversibility
and
cycle
stability
of
Zn
ion
batteries,
as
severe
chemical
corrosion
undesirable
hydrogen
evolution
reaction
(HER)
are
inevitable
for
anode
in
aqueous
electrolytes
during
charge/discharge
process.
Herein,
a
multi‐functional
copolymeric
solid/electrolyte
interface
(SEI)
layer,
self‐assembling
on
based
click
between
epoxy
silane
thioalcohol,
employed
eliminate
these
side
reactions.
The
dense
robust
SEI
layer
can
not
only
physically
repel
water
from
surface
effectively
inhibit
HER
but
also
facilitate
desolvation
2+
accelerate
kinetic
Additionally,
it
regulate
flux
induce
preferred
plating
with
(002)
crystallographic
orientation,
enabling
dendrite‐free
deposition.
As
result,
stable
long
life
≈200
h
at
depth
discharge
(DoD)
60%
achieved.
Zn||V
2
O
5
full
cell
delivers
high
specific
capacity
165.2
mAh
g
−1
after
600
cycles
an
ultralow
N/P
ratio
(the
negative
electrode
positive
electrode)
2.5.
construction
this
provides
new
pathway
development
practical
batteries.