Journal of Materials Chemistry C,
Journal Year:
2024,
Volume and Issue:
13(5), P. 2388 - 2398
Published: Dec. 9, 2024
A
robust
and
efficient
ion
transport
PTFE-based
separator
with
superior
stability
was
fabricated
for
zinc
hybrid
supercapacitors,
demonstrating
excellent
electrochemical
performance.
Advanced Energy Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 6, 2024
Abstract
The
high
activity
of
water
in
aqueous
electrolyte
causes
drastic
side
reactions
on
the
Zn
anodes,
severely
limiting
electrochemical
performance
zinc
metal
batteries
(AZMBs)
under
extreme
conditions.
Herein,
levulinic
acid
is
developed
as
hydrated
deep
eutectic
solvent
(DES),
to
build
a
novel
non‐flammable
and
cost‐effective
ZnSO
4
‐based
with
triple
regulation
molecules
behavior,
enabling
highly
stable
AZMBs
over
wide
temperature.
In
situ
experiments,
molecular
dynamics
simulations,
spectroscopy
analysis
jointly
reveal
that
DES
capable
comprehensively
lowering
by
simultaneously
controlling
behavior
free,
solvated,
interfacial
within
system.
Consequently,
anodes
exhibit
ultralong
cycling
stability
(4500
h
at
1
mA
cm
−2
/1
),
decent
Coulombic
efficiency
99.39%,
excellent
temperature
tolerance
(−20–50
°C).
Notably,
designed
2.0
Ah
Zn//VOX
pouch
cell
exhibits
recorded
actual
energy
density
37.46
Wh
Kg
−1
95.38
L
whole
level,
remarkable
capacity
retention
81.01%
after
150
cycles,
demonstrating
potential
for
scale‐up
into
real
AZMBs.
This
work
provides
an
in‐depth
understanding
correlation
between
molecule
properties
Small,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 28, 2025
Aqueous
rechargeable
zinc
batteries,
despite
advantages
like
safety
and
performance,
struggle
with
water-based
side
reactions
such
as
hydrogen
evolution
corrosion.
Regulating
the
solvation
structure
of
Zn2+
is
essential
for
stability.
Introducing
n-hexane,
a
nonpolar
alkane,
modifies
coordination
stabilizes
Zn
anode-electrolyte
interface.
The
miscibility
n-hexane
improved
through
formation
an
oil-in-water
macroemulsion
amphiphilic
Zn(OTf)2
β-cyclodextrin.
Macroemulsion
stability
highly
sensitive
to
component
concentrations,
requiring
precise
balance
ensure
proper
electrolyte
function.
However,
designing
multi-component
electrolytes
remains
empirical.
To
address
this,
Bayesian
optimization
framework
presented,
incorporating
physical
relationships
into
machine
learning
efficiently
explore
design
space.
This
approach
rapidly
identifies
critical
concentration
stability,
which
key
maintaining
phase
in
electrolyte.
optimized
maintains
low
overpotential
(30
mV)
over
1300
h
Zn||Zn
symmetric
cell,
current
density
1
mA
cm-2.
Rampant
dendrite
growth
and
severe
parasitic
reactions
at
the
electrode/electrolyte
interface
significantly
limit
cycle
life
of
aqueous
zinc
ion
hybrid
supercapacitors
(ZHSCs).
In
this
study,
sodium
lignosulfonate
(SLS)
as
one
green
polymer
was
introduced
into
ZnSO4
electrolyte
to
construct
a
multifunctional
layer
on
surface
Zn
plates.
Experimental
analyses
theoretical
calculations
show
that
presence
SLS
layer,
rich
in
oxygen-containing
functional
groups
(-SO3-),
can
not
only
modulate
structure
electric
double
(EDL)
suppress
interfacial
side
caused
by
free
H2O
SO42-,
but
also
promote
(101)-oriented
deposition
selectively
controlling
behavior
Zn2+
through
specific
adsorption
different
crystalline
surfaces.
The
optimized
allows
stable
Zn//Zn
symmetric
cells
achieve
cumulative
plating
capacity
exceeding
4
Ah
cm-2
high
areal
5
mAh
cm-2,
cycling
for
more
than
1000
cycles
with
an
excellent
average
Coulombic
efficiency
99.34%
Zn//Cu
asymmetric
cells.
Zn//AC
ZHSC
exhibits
ultralong
stability
over
40,000
electrolyte,
decay
rate
low
0.000285%
per
cycle.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 17, 2025
Abstract
Aqueous
zinc‐ion
batteries
(AZIBs),
candidates
for
large‐scale
energy
storage,
face
limitations
due
to
the
poor
reversibility
of
zinc
anodes.
It
reports
on
pyridine
derivatives
with
high
donor
characteristics,
including
2‐chloro‐1‐methylpyridinium
iodide
(CMPI)
and
pyridine‐2‐acetaldoxime
methyl
(PAMI),
as
effective
additives.
At
lower
concentrations,
these
additives
markedly
curtail
dendrites
formation
evolution
hydrogen
anode,
thereby
prolonging
AZIBs
life.
Through
a
combination
theory
experiments,
impact
side‐chain
groups
kinetic
process
depositioni
is
elucidated.
In
contrast
PAM
+
,
CMPI
demonstrates
enhanced
adsorption
self‐assembles
at
anode‐electrolyte
interface,
forming
barrier
free
water
protective
ZnI
layer
via
I
−
ion
integration.
This
dual‐layer
strategy
boosts
plating/stripping
by
100‐fold
achieves
coulombic
efficiency
99.7%
in
zinc–copper
half‐
batteries.
The
findings
advance
understanding
electrolyte
additive
structures
deposition,
providing
molecular
framework
screening
aqueous
metal‐ion
Small,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 3, 2025
Abstract
Electrolyte
additives
are
commonly
employed
in
aqueous
zinc‐ion
batteries
(ZIBs)
to
suppress
dendrite
growth,
corrosion,
and
hydrogen
evolution.
However,
rational
design
principles
systematic
mechanistic
studies
for
selecting
suitable
regulate
reversible
Zn
plating/stripping
chemistry
worth
in‐depth
study.
Using
L‐ascorbic
acid
sodium
(LAAS)
as
the
representative,
theoretical
calculations
combined
with
situ
experimental
analyses
manifest
that
polyhydroxy‐sodium‐salts
preferentially
chemisorbed
on
surface
construct
H
2
O‐poor
interfacial
microenvironment,
suppressing
undesirable
water‐related
side
reactions.
Concurrently,
ions
provide
an
armor
shielding
layer
electric
field
guide
(002)
deposition
texture.
Specifically,
sodium‐salts
replace
O
molecules
coordinated
shell
of
hydrated
2+
ions,
improving
electrochemical
stability
window
(ESW)
extend
working
voltage
ZIBs.
Therefore,
Zn||Zn
symmetric
cell
additive
exhibits
impressive
cumulative
capacity
7875
mAh
cm
−2
at
high
current
density
30
mA
.
Even
when
discharge
expands
1.8
V,
Zn||V
5
full
realizes
a
retention
98.26%
over
500
cycles.
This
work
quickens
advanced
ZIBs
by
green
cheap
electrolyte
additive,
which
is
expected
herald
innovative
phase
research
high‐stability
batteries.
Advanced Energy Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 3, 2025
Abstract
An
all‐aqueous
membrane‐free
Zn–Mn
redox
flow
battery
utilizing
deposition
chemistry
can
be
an
excellent
alternative
to
conventional
aqueous
batteries
for
reducing
costs
and
improving
stability.
In
the
neutral/mildly
acidic
electrolyte
environment
of
batteries,
anode
still
suffers
from
issues
such
as
zinc
dendrite
growth
corrosion,
while
cathode
struggles
with
poor
reversibility.
The
same
arise
in
that
use
a
combined
electrolyte,
where
both
anolyte
catholyte
are
combined.
Therefore,
it
is
possible
simultaneously
address
by
using
single
additive
electrolyte.
Here,
aspartic
acid
introduced
universal
battery.
bonded
Zn
surface,
2+
ions,
Mn
resolving
almost
all
side
reactions.
Impressively,
demonstrated
remarkable
cycling
stability
300
cycles
at
areal
capacity
10
mAh
cm
−2
.
A
new
efficient
strategy
proposed
controlling
overall
reactions
simple
addition
integrated
this
report.
Advanced Energy Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 10, 2025
Abstract
The
electrode/electrolyte
interfacial
side
reaction
is
a
critical
issue
for
aqueous
zinc
ion
batteries
(ZIBs).
In
this
study,
it
presents
an
innovative
electrolyte
designed
to
utilize
steric
hindrance
effects
modulate
Zn
deposition
behavior
while
mitigating
undesirable
hydrogen
evolution
reactions.
incorporation
of
sugar
alcohols
into
the
facilitates
reconfiguration
bonding
network,
alters
solvation
structure
2
⁺
ions,
and
promotes
rapid
desolvation
process,
resulting
in
enhanced
transport
kinetics.
Additionally,
xylitol
molecules
preferentially
adsorb
onto
(100)
crystalline
surface,
inducing
structural
changes
promote
(101)
growth.
Consequently,
configuration
enables
anode
achieve
impressive
operational
lifespan
2100
h
exceptional
Coulombic
efficiency
99.8%.
Furthermore,
when
paired
with
ZnHCF
as
anode,
full
cell
operates
at
high
voltage
1.75
V,
illustrating
promising
pathway
practical
application
ZIBs.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 30, 2025
Abstract
Vanadium
oxides
hold
great
promise
for
aqueous
zinc‐ion
batteries
(AZIBs)
due
to
their
multiple
oxidation
states,
diverse
crystalline
structures,
and
high
vanadium
abundance.
However,
applications
are
limited
by
narrow
interlayer
spacing,
poor
reversibility,
solubility.
To
address
these
issues,
an
inorganic–organic
co‐intercalated
[Al
0.16
(C
5
H
14
ON)
0.12
]V
2
O
·0.39H
cathode
(IO‐V
)
is
reported
with
enlarged
spacing
(13.7
Å)
enhanced
structure
stability
better
AZIBs.
Serving
as
structural
pillars,
Al
3+
,
betaine
create
a
fast
2D
channel
Zn
2+
transport.
The
positively
charged
quaternary
ammonium
groups
in
strongly
interact
the
lattice
oxygen
of
V
further
stabilizing
layered
structure.
polar
carboxylic
acid
weaken
interaction
between
V─O
bonds
thus
improve
diffusion
kinetics
lowered
energy
barriers.
Consequently,
IO‐V
delivers
specific
capacity
(549.5
mAh
g
−1
at
0.2
A
),
ion
rate
(10
−8
∼10
−7
cm
s
superior
cycle
life
(80.1%
retention
after
20,000
cycles
30
ultrahigh
density
(416.3
Wh
kg
becoming
state‐of‐the‐art
systems
comprehensive
metrics.
This
study
provides
promising
direction
design
vanadium‐based
materials
advanced
Small,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 30, 2024
Aqueous
zinc-ion
batteries
(AZIBs)
stand
out
among
many
energy
storage
systems
due
to
their
merits,
and
it's
expected
become
an
alternative
the
prevailing
alkali
metal
ion
batteries.
Nevertheless,
cumbersome
manufacturing
process
high
cost
of
conventional
separators
make
them
unfavorable
for
large-scale
applications.
Herein,
inspired
by
unique
nature
cellulose
ZrO