Advanced Functional Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 12, 2025
Abstract
Zn‐ion
batteries
hold
significant
promise
for
large‐scale
energy
storage
systems
owing
to
their
intrinsic
safety
and
cost‐effectiveness.
However,
practical
deployment
is
hindered
by
uncontrolled
dendrite
growth
sluggish
electrode
reaction
kinetics
at
metallic
Zn
anodes.
To
overcome
these
limitations,
a
quasi‐solid
electrolyte
(M@Z)
based
on
MOF@ZnIn
2
S
4
composite
presented.
This
innovative
exhibits
high
room‐temperature
conductivity
(0.99
mS
cm
−1
)
an
improved
2+
transference
number
(0.54).
The
microporous
MOF
component
ensures
uniform
deposition
effectively
suppresses
formation.
Meanwhile,
the
ZnIn
nanosheets
wrapped
around
particles
promote
formation
of
beneficial
In/ZnS‐contained
interphase
anodes
during
cycling,
which
mitigates
side
reactions
accelerates
anode
kinetics.
By
virtue
above
merits,
symmetric
cells
achieve
stabilized
plating/stripping
over
3130
h
with
low
overpotential
tolerate
critical
current
density
10
mA
−2
.
Furthermore,
vanadium‐based
full
assembled
M@Z
deliver
exceptional
cycling
stability,
almost
no
capacity
decay
after
1000
cycles
1.0
A
g
Research Square (Research Square),
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 26, 2025
Abstract
Aqueous
zinc
ion
batteries
(ZIBs)
attract
increasing
attention
as
alternative
energy
storage
technologies
due
to
their
merits
of
safety
and
low
cost.
However,
the
continuous
dissolution
active
materials
in
vanadium
oxide-based
ZIBs
has
posed
an
unavoidable
challenge.
Here,
we
systematically
analyzed
mechanism
using
both
ex-situ
in-situ
methods.
Experimental
theoretical
analyses
revealed
excessive
reduction
valence
following
H+
insertion
at
potentials
above
1.0
V
(vs.
Zn2+/Zn),
primarily
contributing
rather
than
Zn2+
insertion.
Protons
preferentially
form
monodentate
coordination
with
oxygen,
local
electron
density
around
atoms
facilitating
more
transitions
from
1s
higher-energy
3d
states.
This
leads
a
pronounced
V-valence
V-O
bond
breakage.
Specifically,
interlayer-inserted
exhibits
highest
its
significant
binding
compared
surface-inserted
H+.
As
proof
concept,
without
additives
or
cathode
modifications,
electrochemical
improvements
Zn/NH4V4O10
Zn/V2O5
were
achieved
by
reducing
cut-off
voltage
current
high
directly
inhibit
promote
favorable
surface-dominant
We
contend
that
understanding
chemistry
electrochemistry-related
failure
mechanisms
are
crucial
for
designing
Adv.
Mater.
applications.
Chemical Science,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 1, 2025
Aqueous
zinc-ion
batteries
(ZIBs)
are
emerging
as
promising
next-generation
energy
storage
systems
due
to
their
inherent
safety,
environmental
sustainability,
and
cost-effectiveness.
However,
widespread
application
is
hindered
by
challenges
such
dendritic
Zn
growth,
hydrogen
evolution,
corrosion-induced
passivation,
which
compromise
performance
scalability.
To
overcome
these
obstacles,
we
developed
a
novel
dual-interface
modified
zinc
anode
integrating
fluoride
(ZnF2)-silicon
(Si)
interface
using
fluorine-doped
silicon
nanoparticles
encapsulated
within
hollow
mesoporous
carbon
nanospheres
(F-Si@HMCS).
The
in
situ
formation
of
ZnF2
layer
provides
high
electrochemical
stability,
effectively
suppressing
dendrite
formation,
mitigating
corrosion,
reducing
side
reactions
with
the
electrolyte.
silica
further
facilitates
uniform
electrodeposition
forming
Si-O-Zn
bonds,
regulate
electric
field
distribution
lower
nucleation
barriers.
Additionally,
structure
efficient
ion
transport
acts
buffer
against
volume
changes
during
cycling.
Consequently,
F-Si@HMCS@Zn
electrode
exhibits
long
lifespan
over
2500
h
at
5
mA
cm-2
capacity
0.5
symmetrical
cell
test.
When
coupled
α-MnO2
cathodes,
resulting
ZIBs
exhibit
outstanding
stable
cycle
life
2000
cycles
2
A
g-1.
Advanced Functional Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 5, 2025
Abstract
In
past
few
decades,
the
rapid
advancement
of
lithium
battery
technology
has
revolutionized
our
lives
by
powering
portable
electronic
devices
and
vehicles.
However,
increasing
risk
thermal
runaway
(TR)
poses
significant
challenges
to
their
wider
application,
particularly
regarding
detrimental
effects
on
electric
vehicles
large‐scale
energy
storage.
The
separator,
serving
as
a
barrier
between
cathode
anode,
is
critical
in
preventing
active
materials
generate
Joule
heat,
thereby
playing
vital
role
ensuring
safety.
As
understanding
TR
mechanism
deepens,
it
evident
that
numerous
exothermic
reactions
substances
are
closely
linked
separator.
Consequently,
functional
design
development
runaway‐blocking
separators
(TR‐blocking
separators)
regarded
key
strategies
for
mitigating
TR.
intricate
relationships
these
remain
poorly
understood,
making
challenging
gain
progress
targeted
separators.
This
review
presents
an
in‐depth
analysis
regulating
internal
side
batteries
minimize
heat
release
during
TR,
summarize
advancements
TR‐blocking
enhancing
safety
at
different
stages.
Furthermore,
insights
into
presented
based
previous
studies
various
unfavorable
reactions.
Additionally,
future
directions
suggested
Advanced Functional Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 12, 2025
Abstract
Zn‐ion
batteries
hold
significant
promise
for
large‐scale
energy
storage
systems
owing
to
their
intrinsic
safety
and
cost‐effectiveness.
However,
practical
deployment
is
hindered
by
uncontrolled
dendrite
growth
sluggish
electrode
reaction
kinetics
at
metallic
Zn
anodes.
To
overcome
these
limitations,
a
quasi‐solid
electrolyte
(M@Z)
based
on
MOF@ZnIn
2
S
4
composite
presented.
This
innovative
exhibits
high
room‐temperature
conductivity
(0.99
mS
cm
−1
)
an
improved
2+
transference
number
(0.54).
The
microporous
MOF
component
ensures
uniform
deposition
effectively
suppresses
formation.
Meanwhile,
the
ZnIn
nanosheets
wrapped
around
particles
promote
formation
of
beneficial
In/ZnS‐contained
interphase
anodes
during
cycling,
which
mitigates
side
reactions
accelerates
anode
kinetics.
By
virtue
above
merits,
symmetric
cells
achieve
stabilized
plating/stripping
over
3130
h
with
low
overpotential
tolerate
critical
current
density
10
mA
−2
.
Furthermore,
vanadium‐based
full
assembled
M@Z
deliver
exceptional
cycling
stability,
almost
no
capacity
decay
after
1000
cycles
1.0
A
g