Angewandte Chemie International Edition,
Год журнала:
2024,
Номер
63(15)
Опубликована: Апрель 1, 2024
in
their
Research
Article
(e202319162).Within
such
coordination
polymers
on
the
close-packed
silver
surface,
thermally
activated
switches
from
trans
to
cis
indigo
are
triggered
and
result
isomeric
indigo-Fe
polymers.Click
Chemistry
In
(e202318534),
Wei
Hou,
Hongtao
Xu
et
al.
put
forward
concept
of
selenium-nitrogen
exchange
(SeNEx)
chemistry
based
Abstract
The
design
and
fabrication
of
nanocatalysts
with
high
accessibility
sintering
resistance
remain
significant
challenges
in
heterogeneous
electrocatalysis.
Herein,
a
novel
catalyst
is
introduced
that
combines
electronic
pumping
alloy
crystal
facet
engineering.
At
the
nanoscale,
pump
leverages
chemical
potential
difference
to
drive
electron
migration
from
one
region
another,
separating
transferring
electron‐hole
pairs.
This
mechanism
accelerates
reaction
kinetics
improves
rate.
interface
structure
optimization
enables
CoFe/carbon
nanotube
(CNT)
exhibit
outstanding
oxygen
reduction
(ORR)
evolution
(OER)
performance.
Specifically,
this
achieves
an
ORR
half‐wave
(E₁/₂)
0.895
V,
outperforming
standard
Pt/C
RuO₂
electrocatalysts
terms
both
specific
activity
stability.
It
also
demonstrates
excellent
electrochemical
performance
for
OER,
overpotential
only
287
mV
at
current
density
10
mA
cm⁻
2
.
Theoretical
calculations
reveal
carefully
designed
facets
reduce
energy
barrier
rate‐determining
steps
optimizing
O₂
adsorption
promoting
capture
process.
study
highlights
developing
cost‐effective
bifunctional
ORR–OER
electrocatalysts,
offering
promising
strategy
advancing
Zn–air
battery
technology.
Advanced Functional Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Сен. 27, 2024
Abstract
Integrating
active
sites
for
oxygen
reduction
and
evolution
reactions
(ORR
OER)
is
pivotal
advancing
bifunctional
electrodes.
Addressing
the
geometric/electronic
properties
of
these
essential
to
disrupt
linear
scaling
relationship
between
adsorption
desorption
complex
intermediates.
Herein,
a
proof‐of‐concept
presented
constructing
asymmetric
trinuclear
employing
both
composition‐
size‐based
coupling
strategies.
These
comprise
ORR‐active
Fe
single
atom
(Fe
SA
),
OER‐active
atomically
clustered
species
AC
Ni
as
modulators.
This
AC‐SA
‐Ni
@N‐doped
carbon
exhibits
excellent
catalytic
activities,
with
narrow
potential
gap
0.661
V
an
ORR
half‐wave
0.931
OER
1.592
at
10
mA
cm
−2
.
The
Zn‐air
battery
this
material
achieves
peak
power
density
293
mW
,
specific
capacity
748
mAh
g
Zn
−1
remarkable
stability.
Experimental
findings
theoretical
simulations
reveal
that
induced
strong
electronic
among
centers,
facilitating
charge
redistribution
optimizing
barriers
enhances
rapid
release
*
OH
during
efficient
transformation
from
O
OOH
OER.
study
presents
novel
strategy
developing
robust
Advanced Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Сен. 9, 2024
Abstract
A
breakthrough
in
manufacturing
procedures
often
enables
people
to
obtain
the
desired
functional
materials.
For
field
of
energy
conversion,
designing
and
constructing
catalysts
with
high
cost‐effectiveness
is
urgently
needed
for
commercial
requirements.
Herein,
molten
salt‐assisted
synthesis
(MSAS)
strategy
emphasized,
which
combines
advantages
traditional
solid
liquid
phase
catalysts.
It
not
only
provides
sufficient
kinetic
accessibility,
but
effectively
controls
size,
morphology,
crystal
plane
features
product,
thus
possessing
promising
application
prospects.
Specifically,
selection
role
salt
system,
as
well
mechanism
assistance
are
analyzed
depth.
Then,
creation
catalyst
by
MSAS
electrochemical
conversion
related
introduced
detail.
Finally,
key
problems
countermeasures
faced
breakthroughs
discussed
look
forward
future.
Undoubtedly,
this
systematical
review
insights
here
will
promote
comprehensive
understanding
further
stimulate
generation
new
efficiency
Heteroatom
immobilization
engineering
(HAIE)
is
becoming
a
forefront
approach
in
materials
science
and
engineering,
focusing
on
the
precise
control
manipulation
of
atomic-level
interactions
within
heterogeneous
systems.
HAIE
has
emerged
as
an
efficient
strategy
to
fabricate
single-atom
sites
for
enhancing
performance
metal-based
batteries.
Despite
significant
progress
achieved
through
metal
anodes
batteries,
several
critical
challenges
such
dendrites,
side
reactions,
sluggish
reaction
kinetics
are
still
present.
In
this
review,
we
delve
into
fundamental
principles
underlying
heteroatom
anodes,
aiming
elucidate
its
role
electrochemical
We
systematically
investigate
how
facilitates
uniform
nucleation
inhibits
reactions
at
anode-electrolyte
interface,
promoting
desolvation
ions
accelerating
Finally,
discuss
various
strategies
implementing
electrode
materials,
high-temperature
pyrolysis,
vacancy
reduction,
molten-salt
etching
anchoring.
These
include
selecting
appropriate
heteroatoms,
optimizing
methods,
constructing
material
architectures.
They
can
be
utilized
further
refine
enhance
capabilities
facilitate
widespread
application
next-generation
battery
technologies.
Journal of the American Chemical Society,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 7, 2025
Metal–nitrogen-carbon
(M–N-C)
single-atom
catalysts
(SACs)
have
been
widely
applied
in
catalyzing
electrochemical
redox
reactions.
However,
their
long-term
catalytic
stabilities
greatly
limit
practical
applications.
This
work
investigates
the
dynamic
evolution
of
two
model
Cu–N–C
SACs
with
different
Cu–N
coordinations,
namely
Cu1/Npyri-C
and
Cu1/Npyrr-C,
CO
reduction
reaction
(CORR),
based
on
a
collection
situ
characterizations
including
attenuated
total
reflectance
surface-enhanced
infrared
absorption
spectroscopy,
X-ray
quasi-in
electron
paramagnetic
resonance
spectroscopy
ultraviolet–visible
complemented
by
theoretical
calculations.
Our
findings
reveal
that
Cu
nanoparticle
formation
rate
over
Cu1/Npyrr-C
is
more
than
6
times
higher
during
CORR.
Quasi-in
UV–vis
measurements
demonstrate
hydrogen
radicals
can
be
produced
CORR,
which
will
attack
bonds
SACs,
causing
leaching
Cu2+
followed
subsequent
to
form
nanoparticles.
Kinetic
calculations
show
displays
better
stability
resulting
from
stronger
Cu–Npyri
bonds.
study
deepens
understanding
deactivation
mechanism
reactions
provides
guidance
for
design
next-generation
enhanced
durability.
Chinese Journal of Chemistry,
Год журнала:
2024,
Номер
42(20), С. 2520 - 2535
Опубликована: Июнь 19, 2024
Comprehensive
Summary
The
electrochemical
processes
of
oxygen
reduction
reaction
(ORR)
and
evolution
(OER)
play
a
crucial
role
in
various
energy
storage
conversion
systems.
However,
the
inherently
slow
kinetics
reversible
reactions
present
an
urgent
demand
for
development
efficient
electrocatalysts.
Recently,
metal‐organic
framework
(MOF)
derivatives
have
attracted
extensive
attention
electrocatalysis
research
due
to
their
unique
porous
structure,
abundant
active
sites,
tunable
structural
properties.
Especially,
optimization
electronic
structure
sites
MOF
has
been
proven
as
effective
strategy
enhance
catalytic
activity.
In
this
review,
we
provide
overview
strategies
advanced
catalysts
O—O
bond
activation
reactions,
including
construction
synergistic
effects
between
multiple
heterogeneous
interfaces,
utilization
metal
support
interactions,
precise
modulation
organic
ligands
surrounding
at
atomic
level.
Furthermore,
review
offers
theoretical
insights
into
mechanisms
derivatives,
well
identification
sites.
Finally,
potential
challenges
prospects
are
discussed.
This
contributes
understanding
advancement
Key
Scientists