Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 12, 2024
Abstract
The
application
of
aqueous
zinc‐ion
batteries
in
large‐scale
energy
storage
systems
is
significantly
limited
by
the
hydrogen
evolution
reaction
(HER).
Although
conventional
pH‐adjusting
additives
can
reduce
overpotential
HER,
it
imperative
to
simultaneously
modulate
composition
solid
electrolyte
interphase
(SEI)
and
electrical
double
layer
(EDL)
structure
enhance
utilization
zinc
metal.
This
research
develops
a
multifunctional
pH‐controlling
additive,
bis(2‐hydroxyethyl)amino‐tris(hydroxymethyl)methane
(BT).
First,
addition
BT
increases
pH
5.9,
which
within
its
effective
buffer
zone,
reduces
HER
potential
−1.107
V
versus
Ag/AgCl.
Second,
inhibitory
effect
on
be
further
enhanced
preferential
adsorption
molecules
containing
multiple
hydroxyl
functional
groups
anode,
leading
reduction
number
active
water
EDL.
Third,
participate
solvation
accomplish
reduction,
promotes
uniform
deposition
Zn
2+
ions
forming
nitrogen‐containing
SEI.
Ultimately,
symmetric
battery
accomplishes
2700
stable
cycles
BT‐3
electrolyte.
More
crucially,
corresponding
Zn//MnO
2
full
(1
A
g
−1
)
able
release
specific
capacity
117.2
mA
h
after
600
cycles.
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
36(38)
Published: July 17, 2024
Electrolyte
additives
are
efficient
to
improve
the
performance
of
aqueous
zinc-ion
batteries
(AZIBs),
yet
current
electrolyte
limited
fully
water-soluble
(FWAs)
and
water-insoluble
(WIAs).
Herein,
trace
slightly
(SWAs)
zinc
acetylacetonate
(ZAA)
were
introduced
ZnSO
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:
2025,
Volume and Issue:
unknown
Published: Jan. 21, 2025
Abstract
Anode‐free
sodium
batteries
(AFSBs)
hold
great
promise
for
high‐density
energy
storage.
However,
high‐voltage
AFSBs,
especially
those
can
stably
cycle
at
a
wide
temperature
range
are
challenging
due
to
the
poor
electrolyte
compatibility
toward
both
cathode
and
anode.
Herein,
AFSBs
with
cycling
ability
in
(−20–60
°C)
realized
first
time
via
sole‐solvent
high‐entropy
based
on
diethylene
glycol
dibutyl
ether
solvent
(D2)
NaPF
6
salt.
The
unique
solvent‐ions
effect
of
strong
anion
interaction
weak
cation
solvation
enables
entropy‐driven
salt
disassociation
high‐concentration
contact
ion
pairs,
thus
simultaneously
forming
stable
anion‐derived
electrode–electrolyte
interphases
Moreover,
liquid
D2
further
extends
extremes
battery.
Consequently,
ampere‐hour
(Ah)‐level
anode‐free
pouch
cells
cyclability
−20–60
°C
realized.
Impressively,
cell
achieves
leadingly
high
cell‐level
density
209
Wh
kg
−1
capacity
retention
83.1%
after
100
cycles
25
°C.
This
work
provides
inspirations
designing
advanced
electrolytes
practical
AFSBs.
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 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
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 2, 2025
Abstract
Interface
issues
such
as
parasitic
reactions
and
dendrite
growth
have
long
been
major
obstacles
hindering
the
longevity
of
aqueous
zinc‐ion
batteries
(AZIBs).
The
quest
for
more
effective
strategies
to
regulate
highly
active
interface
remains
a
focal
point
in
AZIBs.
Herein,
novel
interface‐targeted
additive
N‐Acetoacetylmorpholine
(NHM)
is
introduced,
by
lowering
interfacial
tension
modifying
electrical
double
layer,
improve
performance
This
reconfiguration
results
H
2
O‐poor
inner
Helmholtz
plane,
which
suppresses
reactions,
accelerates
kinetics,
fosters
uniform
zinc
deposition.
Consequently,
anode
demonstrates
impressive
cycling
durability,
exceeding
3800
h
plating/stripping
process
400
steady
cycle
at
high
depth
discharge
(DOD)
60%.
Zn/NH
4
V
O
10
full
cell
superior
performance,
achieving
80%
capacity
retention
after
1500
cycles.
Moreover,
pouch
cells
with
highloading
cathodes
(13.5
mg
cm
−2
)
can
maintain
70%
300
cycles
0.5
A
g
−1
.
controlled
N/P
ratio
(2.63:1)
shows
excellent
stability
130
These
findings
provide
valuable
insights
into
design
offer
promising
enhancing
practicality
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 20, 2025
Aqueous
zinc
ion
batteries
(AZIBs)
face
challenges
due
to
the
limited
interface
stability
of
Zn
anode,
which
includes
uncontrolled
hydrogen
evolution
reaction
(HER)
and
excessive
dendrite
growth.
In
this
study,
a
natural
binary
additive
composed
saponin
anisaldehyde
is
introduced
create
stable
interfacial
adsorption
layer
for
protection
via
reshaping
electric
double
(EDL)
structure.
Saponin
with
rich
hydroxyl
carboxyl
groups
serves
as
"anchor
points",
promoting
through
intermolecular
bonding.
Meanwhile,
anisaldehyde,
unique
aldehyde
group,
enhances
HER
suppression
by
preferentially
facilitating
electrocatalytic
coupling
H*
in
EDL,
leading
formation
robust
inorganic
solid
electrolyte
interphase
that
prevents
formation,
structural
during
deposition
process
verified.
As
result,
Zn||Zn
symmetric
cells
present
an
ultra-long
cycling
lifespan
3
400
h
at
1
mA
cm-2
700
10
cm-2.
Even
current
density
20
cm-2,
demonstrate
reversible
operations
450
h.
Furthermore,
Zn-ion
hybrid
capacitors
exhibit
remarkable
100
000
cycles.
This
work
presents
simple
synergetic
strategy
enhance
anode/electrolyte
stability,
highlighting
its
potential
anode
high-performance
AZIBs.