Spatial and anchoring effects of zirconia-doped 3D scaffolds for stable zinc anodes
Jinqiu Ye,
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Tiancheng Ge,
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Xin Qu
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et al.
Chemical Engineering Journal,
Journal Year:
2025,
Volume and Issue:
505, P. 159397 - 159397
Published: Jan. 10, 2025
Language: Английский
Unveiling the Origin of Oxygen Framework Stability in Ultra‐High Nickel Layered Oxide Cathodes
Fangyan Liu,
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Shihao Li,
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Chihon Leung
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et al.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 6, 2025
Ultra-high
nickel
layered
oxides
are
recognized
as
promising
cathode
candidates
for
high-energy-density
lithium-ion
batteries
due
to
their
enhanced
overall
capacity
and
elevated
operating
voltage.
However,
the
interlayer
sliding
of
transition
metal-oxygen
octahedra
(TMO6)
instability
lattice
oxygen
at
high
voltages
ultra-high
oxide
cathodes
pose
significant
challenges
development.
Herein,
origin
framework
stability
is
investigated
by
incorporating
high-covalent
element
Mo
in
both
bulk
surface
using
a
one-step
integrated
method
material
LiNi0.92Co0.08O2.
It
revealed
that
apart
from
isolation
protection
effect
Mo-enriched
layer,
suppression
Li/Ni
antisite
defects
Mo6+
with
strong
covalency
plays
critical
role
reducing
configurations
activated
anionic
redox
reaction
stabilizing
structure.
Benefiting
this,
reversibility
significantly
enhanced,
enabling
more
oxidized
exist
form
dimer
ions
O2n-$O_2^{n
-
}$
rather
than
being
lost
gaseous
O2.
Consequently,
modified
demonstrates
improved
diffusion
kinetics
optimized
electrochemical
performance
Language: Английский
Integrated Lithium-Rich yLi2MnO3∙(1-y)LiNi1/3Co1/3Mn1/3O2 Layered Cathode Nanomaterials for Lithium-ion Batteries
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(3), P. 1346 - 1346
Published: Feb. 5, 2025
Integrated
Li-
and
Mn-rich
layered
cathodes
yLi2MnO3∙(1-y)LiMO2
(M
=
Mn,
Co,
Ni)
have
shown
their
ability
to
deliver
specific
capacities
close
300
mAh
g−1,
but
significant
drawbacks
are
capacity
fading
voltage
decay
during
cycling.
In
this
study,
new
stoichiometric
high-voltage
Li-rich
oxides
with
y
0.0,
0.3,
0.5
synthesized
in
identical
conditions
using
a
sol–gel
method.
These
compositions
were
analyzed
determine
optimal
configuration
understand
extraordinary
behavior.
Their
nanostructural
properties
investigated
XRD
Raman
spectroscopy,
while
the
morphology
grain-size
distribution
of
samples
characterized
by
BET,
SEM
HRTEM
analyses.
The
electrochemical
performances
integrated
compounds
evaluated
through
galvanostatic
cycling
impedance
spectroscopy.
best
cathode
material
0.5Li2MnO3∙0.5LiNi1/3Co1/3Mn1/3O2
had
retention
83.6%
after
100
cycles
potential
range
2.0–4.8
V
vs.
Li+/Li.
Language: Английский
Potential-dependent interfacial specific adsorption accelerates charge transfer in sodium-ion batteries
Yao Xiao,
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Shaowen Xu,
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Wei Liu
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et al.
Research Square (Research Square),
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 10, 2025
Abstract
Fast-charging
capabilities
of
sodium-ion
batteries
have
emerged
as
a
pivotal
objective
within
the
energy
storage
fields.
Sodium
layered
P2-type
oxide
cathodes
most
potential
for
fast
charging
due
to
their
inherent
Na
+
mobility.
However,
electrochemical
polarization
and
interfacial
charge
transfer
especially
at
high
state
are
limiting
factors
in
quick
kinetic
response
large
current.
Herein,
we
demonstrate
that
typical
cathode
(Na
0.7Ni
0.27Mn
0.53Cu
0.04Fe
0.08Ti
0.08O
2)
achieves
high-rate
capacities
through
avoiding
octahedral
stacking
faults,
maintaining
lattice
oxygen
activity
controlling
anion-specific
adsorption.
The
intermediate
Z-phase
intergrowth
structure
mitigate
hysteresis
thermodynamic
by
simultaneously
suppressing
detrimental
P2−O2
phase
evolution
irreversible
redox.
potential-dependent
competitive
adsorption
mechanism
between
anions
solvent
molecules
is
revealed
inner
Helmholtz
plane
(IHP),
where
optimized
elevates
difference
IHP,
accelerating
across
electrode/electrolyte
interface.
Furthermore,
F-rich
cathode/electrolyte
interphase
generated
from
IHP
avoids
transition
metal
dissolution
surface
collapse
stable
long-term
cycling.
This
study
highlights
synergistic
coupling
interaction
bulk
stability
environment
optimization
ensuring
Na
+/charge
transport
kinetics
batteries.
Language: Английский
Enhancing Lithium‐Ion Battery Performance With Ultra‐Thin LiF Coating: A Study on Surface Vapor Deposition for LiNi0.9Co0.05Mn0.05O2 Cathode Material Stabilization
Wenna Xie,
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Xiaoqian Ma,
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J. Y. Shi
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et al.
Battery energy,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 7, 2025
ABSTRACT
High‐nickel
ternary
cathode
(HNCM)
materials
are
regarded
as
the
primary
choice
for
lithium‐ion
batteries
(LIBs)
due
to
their
high
energy
density.
However,
development
is
limited
by
lithium–nickel
mixing,
microcrack
generation,
and
surface
side
reactions.
Herein,
a
combined
roll‐to‐roll
vacuum
vapor
deposition
process
used
prepare
LiNi
0.9
Co
0.05
Mn
O
2
(NCM9055)
material
with
dense,
ultrathin,
robust
lithium
fluoride
(LiF)
protective
layer.
Compared
traditional
methods,
this
approach
allows
precise
control
over
thickness
rate
of
deposited
LiF
layer,
producing
uniform
layer
that
enhances
stability.
This
not
only
effectively
reduces
direct
contact
between
electrolyte
electrode
surface,
mitigating
corrosion
reactions,
but
also
strengthens
structural
integrity
cathode,
thereby
significantly
improving
cycling
The
NCM9055
10
nm
exhibits
enhanced
electrochemical
performance,
especially
at
cut‐off
voltages
4.3
4.5
V,
excellent
performance
1
C.
Additionally,
introduction
improves
thermal
stability
NCM9055,
further
enhancing
safety
high‐nickel
batteries.
study
demonstrates
combination
processing
fast
effective
modification
technique
highlights
advantages
in
forming
homogeneous
which
essential
rapid
production
density
HNCM
advanced
LIBs.
Language: Английский