Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 5, 2024
Abstract
Aqueous
zinc‐ion
batteries
are
widely
recognized
as
promising
alternatives
to
lithium
due
their
excellent
safety,
environmental
compatibility,
and
cost‐effectiveness.
Nonetheless,
the
formation
of
dendrites,
corrosion,
undesirable
side
reactions
on
zinc
surface
pose
significant
challenges
cycling
stability
batteries.
In
this
study,
polar
propylene
carbonate
(PC)
is
paired
with
tetrafluoroborate
anions
establish
a
strong
ion‐dipole
interaction.
Strong
interaction
can
not
only
alter
solvation
structure
ions
but
also
facilitate
dynamic
double
electric
layer
electrode,
suppressing
ZnF
2
interface
carbonate,
thereby
facilitating
uniform
ion
deposition,
consequently
improving
battery
over
broad
temperature
range.
Concretely,
formulated
electrolyte
enhances
wide
range
−30
40
°C,
accompanied
by
capacity
retention
≈100%
even
after
10
000
cycles
at
°C.
The
symmetrical
utilizing
exhibits
stable
performance
for
1200
h
25
°C
1900
respectively.
findings
provide
direction
development
long‐cycle
capable
operating
Advanced Energy Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 9, 2025
Abstract
Aqueous
zinc‐ion
batteries
have
garnered
significant
attention
due
to
their
abundant
materials,
low
production
costs,
and
safety.
However,
these
suffer
from
severe
side
reactions,
which
are
closely
associated
with
the
presence
of
a
substantial
amount
solvent
at
electrode
surfaces.
Herein,
1,4,7,10,13,16‐hexaoxacyclooctadecane
(18‐crown‐6)
is
added
electrolyte
illustrate
both
theoretically
experimentally
its
contribution
rapid
desolvation
aspect.
It
shown
that
addition
18‐crown‐6
greatly
facilitates
solvated
structure
prevents
collection
molecules
on
surface
zinc
anode,
thus
inhibiting
hydrogen
precipitation
reaction.
also
enhances
transference
number
ions,
makes
interfacial
electric
field
anode
stable
promotes
orderly
diffusion
uniform
nucleation
Zn
2+
,
inhibits
growth
dendrites.
As
result,
containing
as
additives
shows
cycle
life,
Zn||Zn
symmetric
cell
cycled
for
nearly
1700
h
1
mA
cm
−2
showing
improvement
in
Coulombic
efficiency.
The
assembled
Zn||NH
4
V
O
10
exhibits
excellent
electrochemical
performance,
reaching
capacity
100.9
mAh
g
−1
even
after
4000
cycles
10.0
A
.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 6, 2024
Abstract
Due
to
their
cost‐effectiveness,
high
safety,
and
environmental
friendliness,
aqueous
zinc‐ion
batteries
(AZIBs)
are
among
the
most
promising
technologies
for
next‐generation
energy
storage
systems.
Nonetheless,
dendrite
growth,
hydrogen
evolution,
corrosion
at
zinc
(Zn)
anode
severely
hinder
practical
application.
In
this
study,
a
combination
of
molecular
self‐assembly
engineering,
squeegee
coating,
air
spraying
process
is
employed
create
superhydrophobic
highly
flexible
artificial
solid‐electrolyte‐interface
layer
on
Zn
(denoted
as
SFM/Zn).
Self‐assembled
monolayer
triethoxy‐3‐aminopropylsilane
optimizes
2+
migration
kinetics.
The
interface,
formed
by
polydimethylsiloxane
(PDMS)
trimethoxy(octadecyl)silane
(OTS)‐modified
nanosilicon
dioxide
particles,
inhibits
water‐related
side
reactions.
Furthermore,
PDMS
serves
dynamic
adaptive
interface
anode,
effectively
alleviating
“tip
effect”.
Consequently,
SFM/Zn||SFM/Zn
symmetrical
cells
enable
reversible
stable
plating/stripping
both
ultralow
current
density
(0.2
mA
cm
−2
)
ultrahigh
(45
).
assembled
Zn‐vanadium
(SFM/Zn||NH
4
V
O
10
cell
deliver
average
Coulombic
efficiency
(nearly
100%)
ultralong
cycling
stability
(135.5
mAh
g
−1
after
500
cycles
5
A
173.2
1000
2
This
innovative
three‐layered
strategy
sheds
new
light
designing
durable
high‐performance
AZIBs.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 3, 2024
Abstract
Uncontrolled
dendrite
growth
and
electrolyte‐induced
intricate
parasitic
reactions
are
two
great
challenges
that
hinder
the
commercial
applications
of
aqueous
zinc‐ion
batteries.
Herein,
a
synchronous
modulation
strategy
for
Zn
2+
interfacial
migration
behavior
electrolyte
microenvironment
is
proposed
by
constructing
functional
lanthanum
hydroxide
aerogel
(LAG)
interface
layer
on
anode
surface.
The
in
situ
derivation
ion‐conducting
zinc
sulfate
(ZHS)
from
LAG
results
spontaneous
generation
hierarchic
during
plating
process,
where
high
selectivity
upper
dense
ZHS
can
limit
SO
4
2−
allow
fast
kinetics,
while
with
well‐defined
nanochannels
near
side
homogenize
distribution,
thus
leading
to
effective
suppression
both
dendrites
reactions.
Additionally,
pH
acidic
be
synchronously
regulated
slightly
soluble
La(OH)
3
aerogel,
further
inhibiting
corrosion
HER.
Consequently,
modified
delivers
highly
reversible
plating/stripping
low‐voltage
hysteresis,
areal‐capacity
Zn||MnO
2
full
cells
demonstrate
considerable
electrochemical
performances
under
utilization
conditions.
This
aerogel‐driven
provides
new
insight
stabilizing
metal
anodes.
Small,
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 14, 2024
Abstract
Aqueous
Zn
metal
batteries
are
attracting
tremendous
interest
as
promising
energy
storage
systems
due
to
their
intrinsic
safety
and
cost‐effectiveness.
Nevertheless,
the
reversibility
of
anodes
(ZMAs)
is
hindered
by
water‐induced
parasitic
reactions
dendrite
growth.
Herein,
a
novel
hydrated
eutectic
electrolyte
(HEE)
consisting
Zn(BF
4
)
2
·xH
O
sulfolane
(SL)
developed
prevent
side
achieve
outstanding
cyclability
ZMAs.
The
strong
coordination
between
2+
SL
triggers
feature,
enabling
low‐temperature
availability
HEEs.
restriction
BF
−
hydrolysis
in
system
can
realize
favorable
compatibility
‐based
Besides,
newly‐established
solvation
structure
with
participation
SL,
H
O,
,
induce
situ
formation
desirable
SEI
gradient
B,O‐rich
species,
ZnS,
ZnF
offer
satisfactory
protection
toward
Consequently,
HEE
allows
Zn||Zn
symmetric
cell
cycle
over
1650
h
at
mA
cm
−2
1
.
Moreover,
Zn||NH
V
10
full
deliver
prolonged
lifespan
for
1000
cycles
high
capacity
retention
83.4%.
This
work
represents
feasible
approach
elaborate
design
advanced
next‐generation
batteries.
Energy & Environmental Science,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
This
work
proposes
a
novel
electrolyte
additive,
sulfobutylether-β-cyclodextrin,
which
remarkably
improves
the
cycling
stability
of
AZIBs
with
synergistic
effect
its
zincophilic
functional
groups
and
unique
adsorption
configuration.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 7, 2025
Abstract
Long‐standing
challenges
including
notorious
side
reactions
at
the
Zn
anode,
low
anode
utilization,
and
rapid
cathode
degradation
current
densities
hinder
advancement
of
aqueous
zinc‐ion
batteries
(AZIBs).
Inspired
by
critical
role
capping
agents
in
nanomaterials
synthesis
bulk
crystal
growth,
a
series
are
employed
to
demonstrate
their
applicability
AZIBs.
Here,
it
is
shown
that
preferential
adsorption
on
different
planes,
coordination
between
2+
ions,
interactions
with
metal
oxide
cathodes
enable
preferred
(002)
deposition,
water‐deficient
ion
solvation
structure,
dynamic
cathode‐electrolyte
interface.
Benefiting
from
multi‐functional
agents,
dendrite‐free
plating
stripping
an
improved
Coulombic
efficiency
99.2%
enhanced
long‐term
cycling
stability
realized.
Remarkable
capacity
retention
91%
achieved
for
after
more
than
500
cycles
under
density
200
mA
g
−1
,
marking
one
best
stabilities
date.
This
work
provides
proof‐of‐concept
manipulating
electrochemical
behaviors,
which
should
inspire
pave
new
avenue
research
address
practical
energy
storage
beyond
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 9, 2025
Abstract
Achieving
highly
ordered
and
compact
assembly
of
zinc
(Zn)
deposits,
side‐reaction‐free,
no
by‐product
deposition
manner
Zn
anodes
is
crucial
to
avoid
the
premature
failure
for
Zn‐ion
batteries,
which
jointly
determined
by
state
polycrystalline
substrates,
interfacial
microenvironment,
epitaxial
growth,
crystal
orientation,
their
interaction.
Herein,
progressive
electrochemical
behavior
anodes,
regulated
converted
species
l
‐theanine
(THE)
molecules
from
hydrogel
matrix,
uncovered.
THE
are
capable
accommodating
electrolyte
environment
provide
a
weakly
acidic
condition
at
infancy
stage
electrodeposition,
induces
an
in
situ
acid
etching
process
releasing
residual
stress
substrates.
This
achieves
lattice
match
between
substrate
overgrowth
crystals,
renders
crystals
seamlessly
amalgamate
with
form
oriented
densely
packed
deposit
via
homoepitaxial
growth
combined
+
cations.
Concomitantly,
adsorbed
cations
facilitate
formation
inorganic–organic
hybrid
solid
interphase
layer.
Consequently,
Zn||Zn
cell
THE‐filled
significantly
long
cycling
stability
2000
cycles,
ultrahigh
average
Coulombic
efficiency
99.0%
over
1000
cycles.