ACS Nano,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 21, 2025
Hydrogen
evolution
reaction
and
Zn
dendrite
growth,
originating
from
high
water
activity
the
adverse
competition
between
electrochemical
kinetics
mass
transfer,
are
main
constraints
for
commercial
applications
of
aqueous
zinc-based
batteries.
Herein,
a
weak
H-bond
interface
with
suspension
electrolyte
is
developed
by
adding
TiO2
nanoparticles
into
electrolytes.
Owing
to
strong
polarity
Ti-O
bonds
in
TiO2,
abundant
hydroxyl
functional
groups
formed
TiO2[110]
active
surface
environment,
which
can
produce
disrupting
initial
networks
molecules,
thereby
accelerating
transfer
Zn2+
reducing
activity.
In
consequence,
Zn||Zn
symmetrical
cells
display
reversible
plating/stripping
behaviors
Coulombic
efficiency
99.7%
over
700
cycles.
Moreover,
TiO2-based
strategy
also
applicable
other
zinc
salt
systems
exhibits
fast
behaviors.
The
enables
long-term
full
cells,
including
Zn||PANI
hybrid
capacitors
Zn||ZnVO
Energy & Environmental Science,
Journal Year:
2024,
Volume and Issue:
17(10), P. 3443 - 3453
Published: Jan. 1, 2024
3-(Hydroxy(phenyl)phosphoryl)propanoic
acid
(HPA)
has
a
strong
coordination
ability
for
Zn
2+
/metal
anodes
which
not
only
form
sphere
micelles
that
promote
the
uniform
transmission
of
but
also
enhance
preferential
adsorption
on
anodes.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
63(18)
Published: March 12, 2024
Abstract
Metallic
zinc
is
a
promising
anode
material
for
rechargeable
aqueous
multivalent
metal‐ion
batteries
due
to
its
high
capacity
and
low
cost.
However,
the
practical
use
always
beset
by
severe
dendrite
growth
parasitic
side
reactions
occurring
at
anode/electrolyte
interface.
Here
we
demonstrate
dynamic
molecular
interphases
caused
trace
dual
electrolyte
additives
of
D‐mannose
sodium
lignosulfonate
ultralong‐lifespan
dendrite‐free
anode.
Triggered
plating
stripping
electric
fields,
species
are
alternately
reversibly
(de‐)adsorbed
on
Zn
metal,
respectively,
accelerate
2+
transportation
uniform
nucleation
deposition
inhibit
Coulombic
efficiency.
As
result,
in
such
dual‐additive
exhibits
highly
reversible
stripping/plating
behaviors
>6400
hours
1
mA
cm
−2
,
which
enables
long‐term
cycling
stability
Zn||Zn
x
MnO
2
full
cell
more
than
2000
cycles.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: July 5, 2024
Abstract
Aqueous
zinc‐ion
batteries
(ZIBs)
have
generated
extensive
research
attention
for
stationary
energy
storage,
due
to
their
advantaged
superiority
in
terms
of
inherent
safety,
low
cost,
and
eco‐friendliness.
However,
uncontrollable
dendrite
growth
side
reactions
the
Zn
anode
affect
cycle
life
ZIBs.
Conventional
separators
are
almost
ineffective
inhibiting
these
issues.
Herein,
a
chitin
nanofiber
membrane
separator
is
developed
tackle
issues
via
simple,
low‐cost,
scalable
strategy.
The
obtained
exhibits
abundant
zincophilic
functional
groups,
homogeneous
nanopores,
excellent
mechanical
properties,
which
facilitate
desolvation
hydrated
2+
ions,
improve
transference
number,
homogenize
ion
flux,
simultaneously.
Moreover,
can
also
reduce
deposition
barrier,
accelerate
kinetics.
Therefore,
dendrites
harmful
effectively
synchronously
suppressed,
enabling
assembled
ZIBs
with
an
ultralong
good
rate
capability.
Impressively,
Zn‐MnO
2
pouch
cell
stability
safety
under
various
external
damages.
above
highlights
mark
significant
step
toward
practical
application
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
36(33)
Published: June 20, 2024
Developing
hydrophobic
interface
has
proven
effective
in
addressing
dendrite
growth
and
side
reactions
during
zinc
(Zn)
plating
aqueous
Zn
batteries.
However,
this
solution
inadvertently
impedes
the
solvation
of
Aqueous
zinc-ion
batteries
(AZIBs)
have
gained
increasing
attention
for
grid
energy
storage
systems.
However,
ensuring
the
long-term
reversible
operation
of
zinc
anode
remains
a
challenge
due
to
dendrite
growth
and
adverse
side
reactions
during
charge
discharge
cycles.
This
study
investigates
use
d-pantothenic
acid
(D-PA)
as
an
additive
in
2
M
ZnSO4
aqueous
electrolyte
enhance
cycling
stability
AZIBs.
Experimental
results
theoretical
calculations
demonstrate
that
D-PA
reshapes
solvation
structure
Zn2+
by
partially
replacing
coordinated
water
molecules,
transport.
Furthermore,
adsorbs
on
active
sites
anode,
surface
overpotential
(|ηs|),
reducing
nucleation
barrier,
decreasing
critical
nucleus
size
(rcrit),
thus
uniform
deposition.
dual
role
modifying
shell
regulating
effectively
mitigates
suppresses
reactions,
resulting
excellent
anode.
Consequently,
Zn||Zn
symmetrical
cells
with
maintain
stable
over
2000
h
at
1.0
mA
cm–2
cm–2,
nearly
4000
4.0
cm–2.
Additionally,
Zn||Cu
asymmetric
exhibit
300
cycles
0.5
average
Coulombic
efficiency
99.29%.
Moreover,
Zn||V2O5
full
containing
performance
1000
current
density
1
A
g–1,
maintaining
high
capacity
retention.
Specifically,
initial
cell
is
around
161.17
approximately
62.7%
retention
after
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
36(32)
Published: June 12, 2024
Abstract
Aqueous
Zn‐ion
batteries
featuring
with
intrinsic
safety
and
low
cost
are
highly
desirable
for
large‐scale
energy
storage,
but
the
unstable
Zn‐metal
anode
resulting
from
uncontrollable
dendrite
growth
grievous
hydrogen
evolution
reaction
(HER)
shortens
their
cycle
life.
Herein,
a
feasible
in
situ
self‐reconfiguration
strategy
is
developed
to
generate
triple‐gradient
poly(diallyldimethylammonium)
bis(trifluoromethanesulfonyl)imide
(PDDA‐TFSI)‐Zn
5
(OH)
8
Cl
2
·H
O‐Sn
(PT‐ZHC‐Sn)
artificial
layer.
The
interface
consists
of
spherical
top
layer
PT
cation
confinement
H
O
inhibition,
dense
intermediate
ZHC
nanosheet
Zn
2+
conduction
electron
shielding,
bottom
Znophilic
Sn
metal.
well‐designed
interfacial
synergistically
facilitates
rapid
diffusion
regulate
uniform
deposition
accelerates
desolvation
process
while
suppressing
HER.
Consequently,
PT‐ZHC‐Sn@Zn
symmetric
cell
achieves
an
ultralong
lifespan
over
6500
h
at
0.5
mA
cm
−2
mAh
.
Furthermore,
full
battery
coupling
MnO
cathode
exhibits
17.2%
increase
capacity
retention
compared
bare
after
1000
cycles.
also
applied
prepare
PT‐ZHC‐In,
assembled
Zn//Cu
operates
steadily
8400
maintaining
Coulombic
efficiency
99.6%.
This
work
paves
way
designing
multicomponent
gradient
stable
anodes.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
63(41)
Published: July 22, 2024
Abstract
The
practical
application
of
aqueous
zinc‐ion
batteries
(ZIBs)
indeed
faces
challenges
primarily
attributed
to
the
inherent
side
reactions
and
dendrite
growth
associated
with
Zn
anode.
In
present
work,
N‐Methylmethanesulfonamide
(NMS)
is
introduced
optimize
transfer,
desolvation,
reduction
2+
,
achieving
highly
stable
reversible
plating/stripping.
NMS
molecule
can
substitute
one
H
2
O
in
solvation
structure
hydrated
be
preferentially
chemisorbed
on
surface
protect
anode
against
corrosion
hydrogen
evolution
reaction
(HER),
thereby
suppressing
byproducts
formation.
Additionally,
a
robust
N‐rich
organic
inorganic
(ZnS
ZnCO
3
)
hybrid
solid
electrolyte
interphase
situ
generated
due
decomposition
NMS,
resulting
enhanced
transport
kinetics
uniform
deposition.
Consequently,
cells
achieve
long
lifespan
2300
h
at
1
mA
cm
−2
mAh
high
cumulative
plated
capacity
3.25
Ah
excellent
reversibility
an
average
coulombic
efficiency
(CE)
99.7
%
over
800
cycles.