Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 30, 2024
Abstract
Aqueous
Zn
ion
batteries
(AZIBs)
have
attracted
considerable
research
interest
because
they
offer
potential
solutions
for
battery
safety
concerns,
enable
long‐duration
energy
storage,
maintain
cost‐effectiveness,
and
support
diverse
application
scenarios.
However,
the
electrochemical
performance
of
AZIBs
is
hampered
by
inherent
issues
arising
from
water
molecules
present
in
water‐based
electrolytes.
Water
are
a
double‐edged
sword
AZIBs,
which
could
serve
not
only
as
rapid
transporter
2+
ions
but
also
instigator
anode
corrosion,
passivation,
hydrogen
precipitation,
narrow
window,
cathode
dissolution,
exacerbation
zinc
dendrite
growth
aqueous
environments.
In
light
these
challenges,
this
review
analyzes
fundamental
principles
underlying
molecules’
role
triggering
water‐related
problems.
It
then
innovatively
summarizes
methods
to
mitigate
activity
alleviate
interface
perspective
“water
repulsing”
trapping”
including
approaches
such
protection,
electrolyte
engineering,
separator
modification,
so
on,
hoping
stimulate
imagination
researchers
playing
with
molecules.
should
be
clarified
that
modification
strategies
do
exist
independently,
complementary
intersections.
Finally,
optimization
mitigating
water‐induced
realize
high‐efficiency
commercially
viable
proposed,
aiming
fresh
perspectives
insights
advance
AZIB
technology.
Journal of the American Chemical Society,
Journal Year:
2024,
Volume and Issue:
146(45), P. 30998 - 31011
Published: Nov. 4, 2024
The
primary
cause
of
the
accelerated
battery
failure
in
aqueous
zinc-ion
batteries
(AZIBs)
is
uncontrollable
evolution
zinc
metal-electrolyte
interface.
In
present
research
on
development
multiadditives
to
ameliorate
interfaces,
it
challenging
elucidate
mechanisms
various
components.
Additionally,
synergy
among
additive
molecules
frequently
disregarded,
resulting
combined
efficacy
that
unlikely
surpass
sum
each
component.
this
study,
"molecular
synergistic
effect"
employed,
which
generated
by
two
nonhomologous
acid
ester
(NAE)
additives
double
electrical
layer
microspace.
Specifically,
ethyl
methyl
carbonate
(EMC)
more
inclined
induce
oriented
deposition
metal
means
targeted
adsorption
with
(002)
crystal
plane.
Methyl
acetate
(MA)
likely
enter
solvated
shell
Zn
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
36(41)
Published: Aug. 13, 2024
Abstract
Dendrite
growth
and
corrosion
issues
have
significantly
hindered
the
usability
of
Zn
anodes,
which
further
restricts
development
aqueous
zinc‐ion
batteries
(AZIBs).
In
this
study,
a
zinc‐philic
hydrophobic
(100)
crystal
plane
end‐capping
reagent
(ECR)
is
introduced
into
electrolyte
to
address
these
challenges
in
AZIBs.
Specifically,
under
mediation
100‐ECR,
electroplated
configures
oriented
dense
deposition
texture,
slows
down
formation
dendrites.
Furthermore,
owing
high
resistance
protective
interface
formed
by
adsorbed
ECR
on
electrode
surface,
anode
demonstrates
enhanced
reversibility
higher
Coulombic
efficiency
modified
electrolyte.
Consequently,
superior
electrochemical
performance
achieved
through
novel
control
strategy
protection
technology.
The
Zn//VO
2
cells
based
maintained
high‐capacity
retention
≈80.6%
after
1350
cycles,
corresponding
low‐capacity
loss
rate
only
0.014%
per
cycle.
This
study
underscores
importance
uniformity
planes
over
their
type.
And
engineering,
high‐quality
constructed,
thereby
expanding
range
options
for
viable
anodes.
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 22, 2024
Abstract
Electrolyte
additives
are
investigated
to
resolve
dendrite
growth,
hydrogen
evolution
reaction,
and
corrosion
of
Zn
metal.
In
particular,
the
electrostatic
shielding
cationic
strategy
is
considered
an
effective
method
regulate
deposition
morphology.
However,
it
very
difficult
for
such
a
simple
modification
avoid
competitive
reactions,
corrosion,
interfacial
pH
fluctuations.
Herein,
multifunctional
potassium
phthalate
(KHP)
based
on
synergistic
design
anionic
chemistry
ultrastable
Zn||I
2
full
batteries
demonstrated.
K
cations,
acting
as
constructed
smooth
HP
anions
can
enter
first
solvation
shell
2+
reduced
activities
H
O,
while
they
remain
in
primary
finally
involved
formation
SEI,
thus
accelerating
charge
transfer
kinetics.
Furthermore,
by
situ
monitoring
near‐surface
electrode,
KHP
effectively
inhibit
accumulation
OH
−
by‐products.
Consequently,
symmetric
cells
achieve
high
stripping–plating
reversibility
over
4500
2600
h
at
1.0
5
mA
cm
−2
,
respectively.
The
deliver
ultralong
term
stability
1400
cycles
with
high‐capacity
retention
78.5%.
ACS Nano,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 24, 2024
Zn
metal
anodes
experience
dendritic
growth
and
hydrogen
evolution
reactions
(HER)
in
aqueous
batteries.
Herein,
we
propose
an
interface
regulation
strategy
with
a
trace
(1.4
×
10
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 10, 2024
Aqueous
zinc
batteries
(AZBs)
hold
great
potential
for
green
grid-scale
energy
storage
due
to
their
affordability,
resource
abundance,
safety,
and
environmental
friendliness.
However,
practical
deployment
is
hindered
by
challenges
related
the
electrode,
electrolyte,
interface.
Functional
hydrogels
offer
a
promising
solution
address
such
owing
broad
electrochemical
window,
tunable
structures,
pressure-responsive
mechanical
properties.
In
this
review,
key
properties
that
functional
must
possess
advancing
AZBs,
including
strength,
ionic
conductivity,
swelling
behavior,
degradability,
from
perspective
of
full
life
cycle
in
AZBs
are
summarized.
Current
modification
strategies
aimed
at
enhancing
these
improving
AZB
performance
also
explored.
The
design
considerations
integrating
with
electrodes
interface
discussed.
end,
limitations
future
directions
bridge
gap
between
academia
industries
successful
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 19, 2025
Abstract
The
sustained
hydrogen
evolution
and
zinc
(Zn)
dendrite
growth
greatly
impede
the
practical
application
of
low‐cost
aqueous
Zn
metal
batteries
(ZMBs).
Herein,
for
first
time,
a
microphase
separation
strategy
is
proposed
to
construct
″water‐in‐oil
(W/O)
electrolyte
endow
durable
ZMBs.
As
validated
by
theoretical
modeling
experimental
characterizations,
unique
reverse
micelle
structure
within
not
only
disrupts
water
bonding
efficiently
inhibits
consumption
at
anode,
but
also
undergoes
directed
movement
reversible
demulsification
under
electric
field,
thus
enhancing
anode
desolvation
kinetics
inhibiting
interfacial
side
reactions.
Owing
simultaneous
regulation
molecules
in
both
bulk
interface,
this
W/O
achieves
high
plating/stripping
Coulombic
efficiency
99.76%
over
6000
cycles,
maintains
an
extend
lifespan
Zn||V
10
O
24
·12H
2
(VOH)
cells
with
negligible
formation.
These
key
findings
are
expected
promote
engineering
toward
ACS Nano,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 26, 2025
The
interfacial
wettability
between
electrodes
and
electrolytes
could
ensure
sufficient
physical
contact
fast
mass
transfer
at
the
gas-solid-liquid,
solid-liquid,
solid-solid
interfaces,
which
improve
reaction
kinetics
cycle
stability
of
rechargeable
metal-based
batteries
(RMBs).
Herein,
engineering
multiphase
interfaces
is
summarized
from
electrolyte
electrode
aspects
to
promote
interface
rate
durability
RMBs,
illustrates
revolution
that
taking
place
in
this
field
thus
provides
inspiration
for
future
developments
RMBs.
Specifically,
review
presents
principle
macro-
microscale
summarizes
emerging
applications
concerning
effect
on
Moreover,
deep
insight
into
development
provided
outlook.
Therefore,
not
only
insights
but
also
offers
strategic
guidance
modification
optimization
toward
stable
electrode-electrolyte
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 28, 2025
Abstract
Zincophilic
additives
have
been
widely
applied
to
stabilize
Zn
metal
anodes
owing
their
efficacy
in
regulating
2+
diffusion.
However,
high
zincophilicity
causes
elevated
desolvation
barriers,
contributing
increased
polarization
and
reduced
stability,
particularly
under
high‐current
conditions.
Herein,
a
novel
molecular
engineering
approach
is
proposed
that
integrates
steric
hindrance
H‐bond
interactions
promote
the
of
zincophilic
additives,
thereby
achieving
high‐rate
with
minimized
polarization.
As
proof‐of‐concept,
N,N‐di‐(2‐picolyl)ethylenediamine
(NDPA),
additive
comprising
potent
chelating
sites
polar
amino
tail
group
designed.
NDPA
boasts
four
solvation
sites,
which
not
only
contribute
exceptional
zincophilicity,
effectively
diffusion
but
also
exhibit
significant
hindrance,
reducing
number
H₂O
molecules,
lowering
dehydration
energy.
Additionally,
NDPA's
free
groups
form
H‐bonds
facilitating
dissociation
coordinated
additives.
Consequently,
at
current
density
20
mA
cm
−2
,
addition
Zn||Zn
symmetric
cell
improves
lifespan
from
37
h
over
2000
reduces
voltage
137
82
mV.
This
work
presents
strategy
overcome
zincophilicity‐desolvation
dilemma
electrolyte
for
developing
durable
zinc
anodes.