Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
34(46)
Published: July 17, 2024
Abstract
VO
2
is
considered
as
one
of
the
most
likely
cathode
materials
to
be
commercialized
for
large‐scale
application
in
AZIBs
and
at
forefront
aqueous
batteries,
but
its
lower
electrical
conductivity,
slower
Zn
2+
mobility,
well
voltage
degradation
structural
collapse
due
vanadium
solubilization
have
limited
further
development.
Herein,
a
Co‐substitution
engineering
strategy
proposed,
which
introducing
heteroatom
Co
doping
substitution
oxygen
vacancy
stabilize
structure
promote
ionic/electronic
leading
an
enhanced
ion
storage
behavior.
The
Co‐substituted
(Co
0.03
V
0.97
O
2‐x
,
denote
v
‐CoVO)
reported
this
paper,
inhibits
dissolution
AZIBs,
even
acetionitrile
system.
DFT
calculations
show
that
‐CoVO
has
more
stable
faster
electronic/ionic
conductivity.
Consequently,
‐CoVO||ZnOTF||Zn
battery
(aqueous)
can
deliver
remarkable
capacity
475
mAh
g
−1
0.2
A
with
99.1%
retention
after
200
cycles,
still
maintains
excellent
cycling
stability
‐CoVO||ZnTFSI||Zn
(acetionitrile
electrolyte)
0.1
.
In
addition,
compared
charge
transfer
resistance
iffusion
coefficient
are
significantly
enhanced.
This
work
broadens
scope
research
high
performance
ZIBs.
Advanced Functional Materials,
Journal Year:
2023,
Volume and Issue:
34(8)
Published: Nov. 12, 2023
Abstract
The
electrochemical
performance
of
aqueous
zinc
metal
batteries
(AZMBs)
is
highly
dependent
on
the
electric
double
layer
(EDL)
properties
at
Zn
electrode/electrolyte
interface.
Herein,
a
novel
reconfigured
EDL
constructed
via
double‐charged
theanine
(TN)
additive
for
super‐stable
and
deep‐rechargeable
AZMBs.
Experiments
theoretical
computations
unravel
that
positively
charged
TN
not
only
serves
as
preferential
anchor
to
form
water‐poor
Helmholtz
plane
onto
anode,
but
also
its
anionic
end
could
coordinate
with
2+
tailor
solvation
structure
in
diffusion
further
reconstruct
inner
H‐bonds
networks,
thus
effectively
guiding
uniform
deposition
suppressing
water‐induced
side
reactions.
Consequently,
Zn//Zn
cells
acquire
outstanding
cycling
stabilities
nearly
800
h
high
depth
discharge
80%.
Moreover,
Zn//VOX
full
deliver
substantial
capacity
retention
(94.12%
after
1400
cycles
2
A
g
−1
)
under
practical
conditions.
Importantly,
designed
2.7
Ah
pouch
cell
harvests
recorded
energy
density
42.3
Wh
Kg
79.5
L
–1
,
remarkable
85.93%
220
50
mA
.
This
innovative
design
concept
reshape
chemistry
would
inject
fresh
vitality
into
developing
advanced
AZMBs
beyond.
Advanced Materials,
Journal Year:
2023,
Volume and Issue:
36(11)
Published: Dec. 13, 2023
Abstract
The
practical
implementation
of
aqueous
zinc‐ion
batteries
(AZIBs)
encounters
challenges
such
as
dendrite
growth,
parasitic
reactions,
and
severe
decay
in
battery
performance
under
harsh
environments.
Here,
a
novel
hydrated
eutectic
electrolyte
(HEE)
composed
Zn(ClO
4
)
2
·6H
O,
ethylene
glycol
(EG),
InCl
3
solution
is
introduced
to
effectively
extend
the
lifespan
AZIBs
over
wide
temperature
range
from
−50
50
°C.
Molecular
dynamics
simulations
spectroscopy
analysis
demonstrate
that
H
O
molecules
are
confined
within
liquid
network
through
dual‐interaction,
involving
coordination
with
Zn
2+
hydrogen
bonding
EG,
thus
weakening
activity
free
water
extending
electrochemical
window.
Importantly,
cryo‐transmission
electron
microscopy
techniques
reveal
HEE
situ
forms
zincophobic/zincophilic
bilayer
interphase
by
dissociation‐reduction
molecules.
Specifically,
zincophilic
reduces
energy
barrier
for
nucleation,
promoting
uniform
deposition,
while
zincophobic
prevents
active
contacting
surface,
inhibiting
side
reactions.
Furthermore,
relationships
between
structural
evolution
interfacial
chemistry
at
electrode/electrolyte
further
discussed
this
work.
scalability
design
strategy
can
bring
benefits
operating
range.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
34(18)
Published: Jan. 25, 2024
Abstract
Rechargeable
aqueous
zinc
(Zn)
batteries
are
a
promising
candidate
for
large‐scale
energy
storage,
but
the
noncompact
and
dendritic
Zn
deposition,
water‐induced
parasitic
reaction,
narrow
operating
temperature
range
severely
hinder
their
practical
application.
Here,
it
is
demonstrated
that
these
challenges
can
be
conquered
by
introducing
low‐cost
acetamide
(Ace)
into
electrolytes.
The
non‐sacrificial
Ace
molecules
with
both
donor
acceptor
groups
disrupt
original
H‐bonded
network
of
water,
replace
solvating‐H
2
O
in
2+
‐solvation
sheath,
form
dynamic
adsorption
on
Zn,
create
an
H
O‐poor
electrical
double‐layer.
Consequently,
presence
suppresses
water
erosion
homogenizes
nucleation/growth,
reduces
reactivity,
depresses
freezing
point
electrolyte.
formulated
Ace‐containing
electrolyte
features
wide
from
−20
to
60
°C
enables
highly
compact
dendrite‐free
electrodeposition
even
at
25
mAh
cm
−2
using
non‐pressure
electrolytic
cell.
Moreover,
allows
electrodes
achieve
long‐term
lifespan
across
−20–60
excellent
deep
cycling
stability
under
85.3%
depth‐of‐discharge
(25
)
over
400
h,
supports
stable
operation
Zn–Iodine
full
harsh
conditions.
Chemical Society Reviews,
Journal Year:
2024,
Volume and Issue:
53(10), P. 5291 - 5337
Published: Jan. 1, 2024
Design
principles,
engineering
strategies,
challenges,
and
opportunities
of
gel
polymer
electrolytes
for
rechargeable
batteries
toward
wide-temperature
applications
are
thoroughly
reviewed.
Advanced Energy Materials,
Journal Year:
2023,
Volume and Issue:
14(8)
Published: Dec. 28, 2023
Abstract
Low‐temperature
vanadium‐based
zinc
ion
batteries
(LT‐VZIBs)
have
attracted
much
attention
in
recent
years
due
to
their
excellent
theoretical
specific
capacities,
low
cost,
and
electrochemical
structural
stability.
However,
working
temperature
surrounding
often
results
retarded
transport
not
only
the
frozen
aqueous
electrolyte,
but
also
at/across
cathode/electrolyte
interface
inside
cathode
interior,
significantly
limiting
performance
of
LT‐VZIBs
for
practical
applications.
In
this
review,
a
variety
strategies
solve
these
issues,
mainly
including
interface/bulk
structure
engineering
electrolyte
optimizations,
are
categorially
discussed
systematically
summarized
from
design
principles
in‐depth
characterizations
mechanisms.
end,
several
issues
about
future
research
directions
advancements
characterization
tools
prospected,
aiming
facilitate
scientific
commercial
development
LT‐VZIBs.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
34(30)
Published: March 25, 2024
Abstract
Aqueous
zinc
ion
batteries
hold
promise
as
alternative
systems
to
lithium‐based
batteries.
However,
practical
development
faces
critical
challenges
due
parasitic
side
reactions
and
dendrite
growth
in
anodes.
While
introducing
electrolyte
additives
is
promising,
monofunctional
offer
limited
protection
the
anode
from
a
single
aspect.
Herein,
disodium
succinate
additive
presented
establish
hydrophobic
zincophilic
dual
electric
layer
structure
on
Zn
surface,
regulate
solvation
of
2+
,
act
pH
buffer
during
cycling.
As
result,
symmetrical
cell
with
an
containing
0.2
m
SADS
shows
durable
life
over
2200
h,
Zn||MnO
2
full
still
maintains
80%
capacity
retention
after
1000
cycles.
In
addition,
both
show
wide
applicability
match
NVO
I
cathode.
This
work
provides
low‐cost
multifunctional
additive,
facilitating
high‐performance
aqueous
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
63(14)
Published: Feb. 3, 2024
Abstract
Aqueous
zinc‐ion
batteries
are
regarded
as
promising
and
efficient
energy
storage
systems
owing
to
remarkable
safety
satisfactory
capacity.
Nevertheless,
the
instability
of
zinc
metal
anodes,
characterized
by
issues
such
dendrite
growth
parasitic
side
reactions,
poses
a
significant
barrier
widespread
applications.
Herein,
we
address
this
challenge
designing
localized
conjugated
structure
comprising
cyclic
polyacrylonitrile
polymer
(CPANZ),
induced
Zn
2+
‐based
Lewis
acid
(zinc
trifluoromethylsulfonate)
at
temperature
120
°C.
The
CPANZ
layer
on
anode,
enriched
with
appropriate
pyridine
nitrogen‐rich
groups
(conjugated
−C=N−),
exhibits
notable
affinity
for
ample
deposition
sites.
This
zincophilic
skeleton
not
only
serves
protective
guide
but
also
functions
proton
channel
blocker,
regulating
flux
mitigate
hydrogen
evolution.
Additionally,
strong
adhesion
strength
guarantees
its
sustained
protection
during
long‐term
cycling.
As
result,
modified
electrode
demonstrates
long
cycle
life
high
durability
in
both
half‐cell
pouch
cells.
These
findings
present
feasible
approach
performance
aqueous
anodes
introducing
layer.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
34(29)
Published: March 10, 2024
Abstract
The
practical
applications
of
aqueous
Zn/I
2
batteries
(AZIBs)
operating
within
a
wide
temperature
range
are
severely
hindered
by
the
uncontrolled
shutting
polyiodide
ions
(I
3
−
/
I
5
)
and
rampant
side
reactions.
In
this
study,
tolerant
polyanionic
hydrogel
(borax‐bacteria
cellulose
p
(AMPS‐AM))
with
ion
selective
permeability
is
designed
for
inhibiting
effect
reactions
under
extreme
temperatures
from
−50
to
50
°C.
zincophilic
R−SO
significantly
enhances
transport
Zn
2+
cations
promotes
uniform
growth
metal
along
(002)
plane.
Moreover,
abundant
hydrophilic
groups
in
hydrogels
effectively
suppress
both
hydrogen
evolution
reaction
formation
by‐products
reducing
water
reactivity.
Furthermore,
theoretical
calculations,
visualization
experiment
situ
Raman
spectroscopy
confirm
that
group
hinders
shuttle
process
/I
anions
through
electrostatic
repulsion.
Consequently,
gel
electrolyte
facilitates
ultra‐stable
full
cell
at
low
current
density
C
over
100
A
pouch
negative/positive
capacity
ratio
3.3
exhibits
stable
performance
350
cycles
an
impressive
high‐areal
2.03
mA
h
cm
−2
,
thereby
establishing
solid
foundation
its
applications.
Nano-Micro Letters,
Journal Year:
2024,
Volume and Issue:
16(1)
Published: May 14, 2024
Aqueous
zinc-ion
batteries
(AZIBs)
are
one
of
the
most
compelling
alternatives
lithium-ion
due
to
their
inherent
safety
and
economics
viability.
In
response
growing
demand
for
green
sustainable
energy
storage
solutions,
organic
electrodes
with
scalability
from
inexpensive
starting
materials
potential
biodegradation
after
use
have
become
a
prominent
choice
AZIBs.
Despite
gratifying
progresses
molecules
electrochemical
performance
in
AZIBs,
research
is
still
infancy
hampered
by
certain
issues
underlying
complex
electrochemistry.
Strategies
designing
electrode
AZIBs
high
specific
capacity
long
cycling
life
discussed
detail
this
review.
Specifically,
we
put
emphasis
on
unique
electrochemistry
different
redox-active
structures
provide
in-depth
understanding
working
mechanisms.
addition,
highlight
importance
molecular
size/dimension
regarding
profound
impact
performances.
Finally,
challenges
perspectives
developing
point
view
future
We
hope
valuable
evaluation
our
context
give
inspiration
rational
design
high-performance