Chemical Science,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 2, 2024
While
lithium-oxygen
batteries
have
a
high
theoretical
specific
energy,
the
practical
discharge
capacity
is
much
lower
due
to
passivation
of
solid
product,
Li
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
36(32)
Published: May 27, 2024
Abstract
Light‐assisted
Li‐O
2
batteries
exhibit
a
high
round‐trip
efficiency
attributable
to
the
assistance
of
light‐generated
electrons
and
holes
in
oxygen
reduction
evolution
reactions.
Nonetheless,
excitonic
effect
arising
from
Coulomb
interaction
between
impedes
carrier
separation,
thus
hindering
efficient
utilization
photo‐energy.
Herein,
porphyrinic
metal‐organic
frameworks
with
(Fe
Ni)O(COO)
6
clusters
are
used
as
photocathodes
accelerate
exciton
dissociation
into
charge
carriers
for
light‐assisted
batteries.
The
coupling
Ni
3d
Fe
orbitals
boosts
ligand‐to‐metal
cluster
transfer,
hence
drives
activates
O
superoxide
(
•
−
)
radicals,
rather
than
singlet
1
under
photoexcitation.
These
enable
low
total
overvoltage
0.28
V
92%
light
irradiation
100
mW
cm
−2
.
This
work
highlights
photoelectrochemical
processes
provides
insights
photocathode
design
Energy & Fuels,
Journal Year:
2024,
Volume and Issue:
38(11), P. 10324 - 10332
Published: May 24, 2024
The
lithium
carbon
dioxide
(Li-CO2)
battery
is
regarded
as
an
attractive
electrochemical
energy
storage
system
on
account
of
its
high
density
(∼1876
Wh
kg–1)
and
utilization
"greenhouse
gas"
CO2.
main
discharge
product
carbonate
(Li2CO3)
decomposed
along
with
the
inevitable
formation
superoxide
radicals
(O2•–),
it
results
in
irreversible
side
reactions,
such
deterioration
electrolytes
oxidation
cathode,
which
lead
to
unfavorable
cycle
life.
Herein,
sodium
lignosulfonate
(LSS)
introduced
a
radical
capture
agent
reduce
reactivity
generated
O2•–
Li-CO2
battery.
Combined
adsorption
calculation,
found
that
can
be
preferentially
adsorbed
LSS.
It
favors
suppression
reactions
between
cathode/electrolyte
during
charge.
discharge/charge
voltage
gap
significantly
reduced
by
0.23
V
long
lifespan
over
200
cycles.
This
investigation
demonstrates
manipulation
essential
construct
stable
efficient
Inorganic Chemistry Frontiers,
Journal Year:
2024,
Volume and Issue:
11(12), P. 3538 - 3547
Published: Jan. 1, 2024
Li–O
2
batteries
have
attracted
much
attention
due
to
its
ultra-high
theoretical
energy
density;
however,
an
overpotential
of
large
charging/discharging
limits
development.
Energy & Fuels,
Journal Year:
2024,
Volume and Issue:
38(14), P. 12472 - 12486
Published: June 29, 2024
Sodium-ion
batteries
(SIBs)
are
expected
to
become
attractive
large-scale
energy
storage
technologies
owing
their
abundant
resources
and
low
cost.
However,
sluggish
reaction
kinetics
at
the
interface
poor
thermodynamic
stability
of
organic
electrolytes
lead
inferior
cycle/rate
performance
a
density
SIBs.
The
electrolyte
engineering,
including
salt
concentration
adjustment,
molecule
design,
additive
utilization,
has
been
demonstrated
effectively
optimize
solvation
structures
construct
stable
interfaces,
resulting
in
accelerated
Na+
transport
suppressed
decomposition.
This
review
focuses
on
recent
advances
fundamental
design
principles
terms
sodium
salts,
solvents,
functional
additives.
Furthermore,
crucial
challenges
for
SIBs,
high
operating
voltage,
wide
working
temperature
range,
fast
charge
rate,
discussed.
corresponding
solution
strategies
introduced
desired
high-performance
Finally,
several
perspectives
future
development
presented
practical
Nanoscale,
Journal Year:
2024,
Volume and Issue:
16(37), P. 17324 - 17337
Published: Jan. 1, 2024
Reaction
mechanisms
of
CO
2
reduction
and
evolution
at
cathode/electrolyte
interface
are
discussed,
highlighting
the
relationship
between
electrochemical
performance
Li–CO
batteries
properties
different
discharge
products.
Journal of the American Chemical Society,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 19, 2025
Li-O2
batteries
have
aroused
considerable
interest
due
to
high
theoretical
energy
density;
however,
the
singlet
oxygen
(1O2)
generated
in
both
discharge
and
charge
processes
induces
severe
parasitic
reactions
leads
their
low
round-trip
efficiency
poor
rechargeability.
Herein,
a
universal
heavy
atom-induced
quenching
mechanism
is
proposed
suppress
1O2
related
side
reactions.
Br
tris(4-bromophenyl)amine
(TBPA)
strong
spin-orbit
coupling
(SOC),
enhancing
interaction
between
spin
angular
momentum
orbital
of
electron.
It
enables
TBPA
capture
electrophilic
form
complex
then
effectively
drives
spin-forbidden
spin-flip
process
triplet
complex.
This
accelerates
conversion
ground-state
3O2
through
intersystem
crossing
mechanism,
it
efficiently
eliminates
its
attack
on
organic
solvents
carbon
cathodes.
These
endow
battery
with
reduced
overvoltages
prolonged
lifespan
for
over
350
cycles
when
coupled
RuO2
catalyst.
work
highlights
SOC
quench
evolution
reaction-related
devices.
Lithium–oxygen
(Li–O2)
batteries
have
high
theoretical
energy
density,
but
the
discharge
product
Li2O2
of
Li–O2
is
difficult
to
decompose,
resulting
in
undesirably
charging
potential.
The
use
soluble
redox
mediators
(RMs)
can
usually
reduce
potential
batteries,
RM
on
cathode
side
diffuse
Li
metal
anode
and
react
with
it,
leading
continuous
loss
causing
damage
fragile
interface.
So,
it
necessary
develop
a
bifunctional
mediator
(BRM)
that
simultaneously
protect
anode.
Herein,
we
introduced
4-bromomethyl-phenylboronic
acid
(BPLA)
as
BRM.
Br–
ions
be
dissociated
from
BPLA
during
cycling
serve
an
effective
component
RM,
thereby
significantly
facilitating
reduction
batteries.
Meanwhile,
boronic
groups
capability
engage
cross-linking
reactions
Li-metal
surface,
forming
flexible
solid-electrolyte
interphase
(SEI)
layer.
More
importantly,
SEI
layer
contains
reversible
dynamic
B–O
covalent
bond,
which
possesses
characteristic
dissociation
rearrangement.
Thereby
shape
adaptability,
inhibits
growth
dendrites,
suppresses
reaction
between
Li.
Consequently,
our
BPLA,
serving
BRM,
enable
achieve
stable
cycle
life
180
cycles
under
low
charge
up
4.0
V.