Small,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 10, 2024
Aqueous
Zinc-iodine
batteries
(ZIBs)
are
widely
viewed
as
promising
energy
storage
devices
due
to
their
high
density
and
intrinsic
safety.
However,
they
encounter
great
challenges
such
grievous
polyiodides
shuttle
sluggish
iodine
(I
ACS Nano,
Journal Year:
2024,
Volume and Issue:
18(42), P. 28557 - 28574
Published: Oct. 9, 2024
Aqueous
zinc–iodine
batteries
(ZIBs)
based
on
the
reversible
conversion
between
various
iodine
species
have
garnered
global
attention
due
to
their
advantages
of
fast
redox
kinetics,
good
reversibility,
and
multielectron
feasibility.
Although
significant
progress
has
been
achieved
in
ZIBs
with
two-electron
I–/I2
pathway
(2eZIBs),
relatively
low
energy
density
hindered
practical
application.
Recently,
four-electron
I–/I2/I+
electrochemistry
(4eZIBs)
shown
a
improvement
density.
Nonetheless,
use
4eZIBs
is
challenged
by
poor
reversibility
polyiodide
shuttling
during
I+
hydrolysis
I2/I+
conversion.
In
this
Review,
we
thoroughly
summarize
fundamental
understanding
two
ZIBs,
including
reaction
mechanisms,
limitations,
strategies.
Importantly,
provide
an
intuitive
evaluation
assess
potential
highlight
critical
impacts
Zn
utilization
rate.
Finally,
emphasize
cost
issues
associated
electrodes
propose
closed-loop
recycling
routes
for
sustainable
storage
ZIBs.
These
findings
aim
motivate
application
advanced
promote
storage.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 31, 2025
Aqueous
zinc
iodine
(Zn-I2)
batteries
have
attracted
attention
due
to
their
low
cost,
environmental
compatibility,
and
high
specific
capacity.
However,
development
is
hindered
by
the
severe
shuttle
effect
of
polyiodides
slow
redox
conversion
kinetics
(I2)
cathode.
Herein,
a
long-life
Zn-I2
battery
developed
anchoring
within
an
edible
fungus
slag-derived
carbon
matrix
encapsulated
with
Zn
single-atom
catalysts
(SAZn@CFS).
The
N
content
microporous
structure
SAZn@CFS
provide
strong
confinement,
while
Zn-N4-C
sites
chemical
interact
effectively
mitigating
dissolution
polyiodide
effect.
Additionally,
uniformly
distributed
SAZn
significantly
enhance
efficiency
I-/I3
-/I5
-/I2,
leading
improved
At
current
density
10
A
g-1,
designed
delivers
excellent
capacity
147.2
mAh
g-1
long
lifespan
over
80
000
cycles
93.6%
retention.
Furthermore,
exhibits
stable
operation
for
3500
times
even
at
50
°C,
demonstrating
significant
advances
in
reversible
storage.
This
synergistic
strategy
optimizes
composite
structure,
offering
practical
approach
meet
requirements
high-performance
batteries.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 4, 2025
Abstract
Zinc–iodine
batteries
(ZIBs)
are
promising
energy
storage
devices
due
to
their
nonflammable
aqueous
electrolyte
and
intrinsically
safe
zinc
(Zn)
anode
but
encounters
thorny
challenges,
including
soluble
polyiodides
shuttling
sluggish
iodine
redox
kinetics.
Here,
an
ionic
porous
organic
polymers
(iPOPs)
with
Lewis
acid–base
pairs
(e.g.,
pyridine
cation
free
Br
−
)
Zn
single‐atom
sites
(iPOP‐TPyPZn)
is
developed
as
advanced
I
2
host
notably
enhance
the
performance
of
ZIBs.
The
iPOP‐TPyPZn
can
not
only
significantly
prevent
via
synergy
also
expedite
kinetics
species
through
combined
action
acid
catalytic
sites.
Benefiting
from
double
synergistic
mechanism,
assembled
ZIBs
loaded
cathode
exhibit
outstanding
electrochemical
ultra‐high
cycling
stability
over
40
000
cycles
at
8
A
g
−1
.
Combined
in/ex
situ
spectral
characterizations
theoretical
calculations
clearly
reveal
reversible
reaction
mechanism
vital
role
in
enhancing
performance.
This
work
provides
a
path
for
precise
preparation
hosts
offers
new
insights
into
toward
metal–I
batteries.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 13, 2025
Abstract
The
energy
efficiency
of
aqueous
Zn‐I
2
batteries
(AZIBs)
is
traditionally
enhanced
by
cathode
host
catalysts
with
high
electron
affinity,
based
on
the
consensus
that
stronger
affinity
improves
electron‐rich
polyiodides
adsorption
and
prevents
shuttle
effects,
thus
promoting
I
/I⁻
conversion
reaction.
Herein,
carbon‐coated
Mo
C
nanocrystals
supported
carbon
spheres
(CS/Mo
C@C)
as
an
iodine
catalyst
developed.
Interestingly,
a
deviation
from
expectation
observed:
moderate
CS/Mo
C@C,
rather
than
higher
C,
actually
leads
to
faster
reaction
kinetics,
while
maintaining
stable
species.
This
phenomenon
can
be
attributed
optimal
electron‐donating
properties
charge
transfer
dynamics
associated
lower
affinity.
Through
systematic
electrochemical
spectroscopic
analysis,
it
uncovered
conformal
layer
covering
key
adjusting
capability,
enhancing
transfer,
improving
interfacial
kinetics
C@C
catalyst.
Consequently,
assembled
AZIBs
employing
C@C/I
demonstrate
smaller
overpotential
gap
(0.06
V)
superior
cyclic
stability
(89.6%
capacity
retention
after
25
000
cycles
at
5
A
g⁻
1
)
compared
C/I
(0.09
V/40.6%
5000
cycles).
study
highlights
significance
modulating
surface
in
design
for
high‐efficiency
AZIBs.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 25, 2025
Abstract
The
industrial
development
of
Zn‐ion
batteries
requires
high
performance
even
with
lean‐electrolyte.
Nevertheless,
lean‐electrolyte
can
exacerbate
concentration
polarization
at
the
interface
electrode/electrolyte,
leading
to
significant
Zn
corrosion
and
battery
failure.
Here,
a
stable
ion‐rich
protective
layer
(TMAO‐Zn)
is
constructed
by
unique
zwitterion
structure
trimethylamine
N‐oxide
(TMAO).
TMAO
characterized
direct
connection
between
positive
negative
charges
(N
+
‐O
−
)
minimal
dipole
moment,
which
renders
weak
interactions
form
TMAO‐Zn
2+
,
thereby
reducing
promoting
rapid
uniform
deposition
.
Furthermore,
O
exhibits
higher
electrophilic
index,
indicating
stronger
propensity
for
hydrogen
bond
active
free
water
in
inner
Helmholtz
(IHL),
mitigating
under
extreme
conditions
low
electrolyte‐to‐capacity
ratio
(E/C
ratio).
Consequently,
symmetrical
enables
cycling
over
250
h
15
µL
mA
−1
Additionally,
Zn/I₂
pouch
E/C
21.2
provides
ultra‐high
specific
capacity
96
cycles
(capacity
retention
rate
98.3%).
This
study
offers
new
concept
propel
practical
application
Journal of the American Chemical Society,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 5, 2025
Aqueous
zinc-iodine
(Zn-I2)
batteries
with
four-electron
(4e)
I-/I0/I+
conversion
(4eZIBs)
offer
high
energy
density
but
face
significant
challenges
for
application,
including
the
polyiodide
shuttle
effect
and
I+
hydrolysis
I2
cathodes
poor
reversibility
Zn
anodes.
Here,
we
report
a
coordination
chemistry
strategy
to
address
these
issues
simultaneously
by
introducing
hexamethylenetetramine
(HMTA)
as
an
electrolyte
additive.
In
aqueous
electrolytes,
HMTA
undergoes
protonation
form
positively
charged
nitrogen
moieties
that
effectively
precipitate
polyiodides
species
(ICl2-)
mitigate
hydrolysis.
This
enables
4eZIBs
achieve
near-theoretical
specific
capacity
of
425
mA
h
g-1
(based
on
mass
iodine)
Coulombic
efficiency
(CE)
exceeding
99%.
On
anode,
preferentially
adsorbs
onto
its
surface,
inhibiting
competitive
water
adsorption
suppress
both
dendrite
formation
hydrogen
evolution.
As
result,
first
time,
durable
4eZIB
performance
in
pouch-cell
configurations
limited
supply.
A
0.5
pouch
cell
15%
utilization
exhibits
113.0
W
kg-1
anodes)
excellent
cycling
stability
over
1400
cycles,
highlighting
potential
next-generation
storage
systems.
Journal of Materials Chemistry A,
Journal Year:
2024,
Volume and Issue:
12(37), P. 24746 - 24760
Published: Jan. 1, 2024
Aqueous
zinc–halogen
batteries
(AZHBs)
are
promising
energy-storage
systems
but
suffer
from
shuttle
effect
and
poor
redox
kinetics.
This
review
summarizes
the
mechanism
research
status
of
AZHBs
provides
solutions
to
overcome
challenges.
Advanced Energy Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 16, 2024
Abstract
Achieving
both
high
iodine
loading
cathode
and
Zn
anode
depth
of
discharge
(DOD)
is
pivotal
to
unlocking
the
full
potential
energy‐dense
Zn‐I
2
batteries.
However,
this
combination
exacerbates
detrimental
shuttle
effect
polyiodide
intermediates,
significantly
impairing
battery's
reversibility
stability.
Herein,
study
reports
an
advanced
high‐loading
(denoted
as
MX‐AB@I)
enabled
by
a
multifunctional
Ti
3
C
T
x
MXene
modulator,
which
presents
stability
energy
density
in
Through
comprehensive
experimental
theoretical
analyses,
intrinsic
regulating
mechanisms
are
elucidated
modulator
effectively
suppresses
shuttling,
enhances
conversion
kinetics,
dramatically
improves
reversibility.
With
aid
MX‐AB@I
composite
achieves
mass
23
mg
cm
−2
realizes
practically
areal
capacity
4.0
mAh
.
When
paired
with
thin
(10
µm),
configuration
DOD
78.7%
171.3
Wh
kg
−1
,
surpassing
majority
battery
systems
reported
literature.
This
effective
approach
designing
cathodes
for
batteries
leveraging
modulators
regulate
critical
electrochemical
reaction
processes.