PLoS ONE,
Год журнала:
2024,
Номер
19(4), С. e0297677 - e0297677
Опубликована: Апрель 18, 2024
A
nitrogen-phosphorus
dual-doped
porous
spore
carbon
(NP-PSC)
positive
electrode
matrix
was
prepared
using
native
auricularia
auricula
as
solid
medium
based
on
the
principle
of
biomass
rot.
Yeast
introduce
and
cultured
by
medium.
The
freeze-drying
carbonization
activation
processes
made
materials
present
a
three-dimensional
aerogel
properties.
fermentation
transformed
from
blocky
structure
to
introduced
dual-doping.
physical
chemical
properties
were
characterized
in
detail.
Electrochemical
performance
NP-PSC
Li-S
batteries
systematically
investigated.
Porous
heteroatom-doping
improved
electrochemical
performance,
which
is
much
superior
conventional
activated
materials.
Energy & Environmental Science,
Год журнала:
2023,
Номер
17(1), С. 49 - 113
Опубликована: Ноя. 7, 2023
This
perspective
highlights
recent
advancements
in
innovative
strategies
to
provide
valuable
insights
into
the
potential
for
energy-saving
hydrogen
production
through
water
electrolysis.
Nano-Micro Letters,
Год журнала:
2024,
Номер
16(1)
Опубликована: Янв. 11, 2024
Constructing
the
efficacious
and
applicable
bi-functional
electrocatalysts
establishing
out
mechanisms
of
organic
electro-oxidation
by
replacing
anodic
oxygen
evolution
reaction
(OER)
are
critical
to
development
electrochemically-driven
technologies
for
efficient
hydrogen
production
avoid
CO
Angewandte Chemie International Edition,
Год журнала:
2024,
Номер
63(20)
Опубликована: Март 8, 2024
Abstract
Large‐scale
energy
storage
devices
play
pivotal
roles
in
effectively
harvesting
and
utilizing
green
renewable
energies
(such
as
solar
wind
energy)
with
capricious
nature.
Biphasic
self‐stratifying
batteries
(BSBs)
have
emerged
a
promising
alternative
for
grid
owing
to
their
membraneless
architecture
innovative
battery
design
philosophy,
which
holds
promise
enhancing
the
overall
performance
of
system
reducing
operation
maintenance
costs.
This
minireview
aims
provide
timely
review
such
emerging
technology,
including
its
fundamental
principles,
existing
categories,
prototype
architectures.
The
challenges
opportunities
this
undergoing
research
topic
will
also
be
systematically
highlighted
discussed
guidance
subsequent
R&D
superior
BSBs
while
conducive
bridging
gap
future
practical
application.
Nature Communications,
Год журнала:
2024,
Номер
15(1)
Опубликована: Ноя. 14, 2024
The
low-potential
aldehyde
oxidation
reaction
can
occur
at
low
potential
(~0
VRHE)
and
release
H2
the
anode,
enabling
hydrogen
production
with
less
than
one-tenth
of
energy
consumption
required
for
water
splitting.
Nevertheless,
activity
stability
Cu
catalysts
remain
inadequate
due
to
oxidative
deactivation
Cu-based
materials.
Herein,
we
elucidate
reactivation
cycle
electrocatalyst
develop
a
self-reactivating
PdCu
catalyst
that
exhibits
significantly
enhanced
stability.
Initially,
in-situ
Raman
spectroscopy
confirm
involved
in
electrochemical
non-electrochemical
reduction.
Subsequently,
X-ray
absorption
fine
structure
reveal
Pd
component
accelerates
rate
reduction,
thereby
enhancing
electrocatalyst.
Finally,
bipolar
device
is
assembled
utilizing
electrocatalyst,
which
deliver
current
400
mA
cm−2
0.42
V
operate
continuously
120
h.
This
work
offers
guidance
enhance
system.
A
dual-side
system
more
efficient
splitting
but
suffers
from
issues.
Here,
authors
report
operates
stably
h,
offering
an
alternative
solution
energy-efficient
production.
Proceedings of the National Academy of Sciences,
Год журнала:
2025,
Номер
122(8)
Опубликована: Фев. 20, 2025
Electrocatalytic
reduction
(ECR)
of
furfural
represents
a
sustainable
route
for
biomass
valorization.
Unfortunately,
traditional
Cu-catalyzed
ECR
suffers
from
diversified
product
distribution
and
industrial-incompatible
production
rates,
mainly
caused
by
the
intricate
mechanism-performance
relationship.
Here,
we
manipulate
hydrogenation
pathways
on
Cu
introducing
ceria
as
an
auxiliary
component,
which
enables
mechanism
switching
proton-coupled
electron
transfer
to
electrochemical
hydrogen-atom
(HAT)
thus
high-speed
furfural-to-furfuryl
alcohol
electroconversion.
Theoretical
kinetic
analyses
show
that
oxygen-vacancy-rich
delivers
efficient
formation-diffusion-hydrogenation
chain
H*
diminishing
adsorption.
Spectroscopic
characterizations
indicate
Cu/ceria
interfacial
perimeter
enriches
local
furfural,
synergistically
lowering
barrier
rate-determining
HAT
step
across
perimeter.
Our
catalyst
realizes
high-rate
HAT-dominated
electrosynthesis
single-product
furfuryl
alcohol,
achieving
high
rate
19.1
±
0.4
mol
h-1
m-2
Faradaic
efficiency
97
1%
at
economically
viable
partial
current
density
over
0.1
A
cm-2.
results
demonstrate
highly
biofeedstock
valorization
with
enhanced
techno-economic
feasibility.
Advanced Energy Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 9, 2025
Abstract
The
rechargeable
Zn‐redox
battery
represents
a
promising,
efficient,
and
sustainable
energy
storage
technology.
Herein,
novel
4‐nitrobenzyl
alcohol
(4‐NBA)‐assisted
battery,
driven
by
NiSe─Cu
2
Se/NF
bifunctional
electrocatalysts
is
developed.
different
redox
activities
of
─NO
─OH
groups
in
4‐NBA
allow
conversion
for
chemical
production
during
the
whole
discharge/charge
process,
maximizing
economic
value
technologies.
Detailed
charge
analyses
indicate
that
internal
electric
field
within
Se
heterostructure
modulates
d‐band
center,
optimizes
adsorption/desorption
strength
intermediates,
reduces
reaction
barriers
4‐NBA.
This
electrocatalyst
enables
selective
to
4‐aminobenzyl
discharge
process
4‐nitrobenzoic
acid
with
Faradaic
efficiencies
above
96%.
Consequently,
4‐NBA‐assisted
achieves
high
power
density
16.13
mW
cm
−2
maintains
stable
yield
rate
15.92
µmol
h
−1
22.84
acid.
work
presents
an
appealing
strategy
integrating
the‐whole‐process
production,
paving
way
developing
multifunctional
systems.
Angewandte Chemie,
Год журнала:
2024,
Номер
136(22)
Опубликована: Март 15, 2024
Abstract
Chiral
carboxylic
acid
production
from
renewable
biomass
by
chemocatalysis
is
vitally
important
for
reducing
our
carbon
footprint,
but
remains
underdeveloped.
We
herein
establish
a
strategy
that
make
use
of
stereogenic
center
to
achieve
rare
example
D‐glyceric
with
the
highest
yield
(86.8
%)
reported
date
as
well
an
excellent
ee
value
(>99
%).
Unlike
traditional
asymmetric
catalysis,
chiral
catalysts/additives
are
not
required.
Ample
experiments
combined
quantum
chemical
calculations
established
origins
and
catalyst
performance.
The
chirality
at
C4
in
D‐xylose
was
proved
be
retained
successfully
delivered
C2
during
C−C
cleavage.
remarkable
cooperative‐roles
Ag
+
0
constructed
Ag/γ‐Al
2
O
3
disclosed
crucial
contributors.
responsible
low‐temperature
activation
D‐xylose,
while
facilitated
generation
active
O*
.
cooperatively
promoted
precise
cleavage
C2−C3
bond,
more
importantly
allowed
immediate
fast
oxidization
D‐glyceraldehyde
intermediate
stabilize
acid,
thereby
inhibiting
side
reaction
induced
racemization.
This
makes
significant
breakthrough
overcoming
limitation
poor
enantioselectivity
current
chemocatalytic
conversion
biomass.
Abstract
Electricity
generation
and
chemical
production
are
both
critical
cornerstone
for
modern
society.
Integrating
electricity
output
high
value
in
an
electrochemical
system
is
highly
attractive
environmentally
sustainably.
In
this
review,
we
summarize
the
recent
advances
development
of
these
multifunctional
devices
(electrocatalytic
flow
batteries)
that
could
generate
chemicals
through
rational
coupling
half‐electrode
reactions,
covering
basic
principles,
device
configurations,
applications.
We
also
discuss
current
challenges
suggest
potential
research
directions.
Angewandte Chemie International Edition,
Год журнала:
2024,
Номер
63(22)
Опубликована: Март 15, 2024
Abstract
Chiral
carboxylic
acid
production
from
renewable
biomass
by
chemocatalysis
is
vitally
important
for
reducing
our
carbon
footprint,
but
remains
underdeveloped.
We
herein
establish
a
strategy
that
make
use
of
stereogenic
center
to
achieve
rare
example
D‐glyceric
with
the
highest
yield
(86.8
%)
reported
date
as
well
an
excellent
ee
value
(>99
%).
Unlike
traditional
asymmetric
catalysis,
chiral
catalysts/additives
are
not
required.
Ample
experiments
combined
quantum
chemical
calculations
established
origins
and
catalyst
performance.
The
chirality
at
C4
in
D‐xylose
was
proved
be
retained
successfully
delivered
C2
during
C−C
cleavage.
remarkable
cooperative‐roles
Ag
+
0
constructed
Ag/γ‐Al
2
O
3
disclosed
crucial
contributors.
responsible
low‐temperature
activation
D‐xylose,
while
facilitated
generation
active
O*
.
cooperatively
promoted
precise
cleavage
C2−C3
bond,
more
importantly
allowed
immediate
fast
oxidization
D‐glyceraldehyde
intermediate
stabilize
acid,
thereby
inhibiting
side
reaction
induced
racemization.
This
makes
significant
breakthrough
overcoming
limitation
poor
enantioselectivity
current
chemocatalytic
conversion
biomass.
Chemical Communications,
Год журнала:
2024,
Номер
unknown
Опубликована: Янв. 1, 2024
This
study
presents
the
synthesis
and
electrocatalytic
performance
of
amorphous
Fe-O-P
nanocages
derived
from
Fe-MOFs
for
water
ethylene
glycol
(EG)
oxidation.
Despite
structural
compositional
changes,
electrocatalyst
in
an
electrolytic
cell
with
Pt/C
shows
high
activity
reduced
voltage,
efficiently
generating
H