Angewandte Chemie International Edition,
Journal Year:
2020,
Volume and Issue:
60(9), P. 4448 - 4463
Published: April 21, 2020
Abstract
Single‐atom
catalysts
(SACs)
with
highly
active
sites
atomically
dispersed
on
substrates
exhibit
unique
advantages
regarding
maximum
atomic
efficiency,
abundant
chemical
structures,
and
extraordinary
catalytic
performances
for
multiple
important
reactions.
In
particular,
M–N–C
SACs
(M=transition
metal
atom)
demonstrate
optimal
electrocatalytic
activity
the
oxygen
reduction
reaction
(ORR)
have
attracted
extensive
attention
recently.
Despite
substantial
efforts
in
fabricating
various
SACs,
principles
regulating
intrinsic
of
their
not
been
sufficiently
studied.
this
Review,
we
summarize
regulation
strategies
promoting
ORR
by
modulation
center
atoms,
coordinated
environmental
guest
groups.
Theoretical
calculations
experimental
investigations
are
both
included
to
afford
a
comprehensive
understanding
structure–performance
relationship.
Finally,
future
directions
developing
advanced
other
analogous
reactions
proposed.
ACS Catalysis,
Journal Year:
2019,
Volume and Issue:
9(12), P. 11042 - 11054
Published: Sept. 23, 2019
On-site
production
of
hydrogen
peroxide
(H2O2)
using
electrochemical
methods
could
be
more
efficient
than
the
current
industrial
process.
However,
due
to
existence
scaling
relations
for
adsorption
reaction
intermediates,
there
is
a
long
established
trade-off
between
activity
and
selectivity
catalysts,
as
enhancement
catalytic
typically
accompanied
by
four-electron
O2
reduction
(ORR),
leading
reduced
H2O2
production.
Herein,
means
density
functional
theory
(DFT)
computations,
we
reported
feasibility
several
classes
important
representative
experimentally
achievable
single-atom
catalysts
(SACs)
toward
two-electron
ORR,
paying
attention
their
stability,
selectivity,
at
acidic
medium.
Starting
from
210
two-dimensional
(2D)
SACs,
demonstrated
that
31
SACs
have
potential
break
metal-based
simultaneously
achieve
high
screened
out
7
with
higher
PtHg4
in
media.
Especially,
noble
metal-free
SAC,
namely,
single
Zn
atom
centered
phthalocyanine
(Zn@Pc-N4),
has
remarkable
improvement
small
overpotential
0.15
V.
Moreover,
multivariable
analysis
machine-learning
techniques,
provided
comprehensive
understanding
underlying
origin
unveiled
intrinsic
correlations
structure
performance.
This
work
may
pave
way
design
discovery
promising
materials
Advanced Energy Materials,
Journal Year:
2020,
Volume and Issue:
10(21)
Published: April 17, 2020
Abstract
The
electrochemical
reduction
of
O
2
via
a
two‐electron
reaction
pathway
to
H
provides
possibility
for
replacing
the
current
anthraquinone
process,
enabling
sustainable
and
decentralized
production.
Here,
nitrogen‐rich
few‐layered
graphene
(N‐FLG)
with
tunable
nitrogen
configuration
is
developed
generation.
A
positive
correlation
between
content
pyrrolic‐N
selectivity
experimentally
observed.
critical
role
elucidated
by
variable
intermediate
adsorption
profiles
as
well
dependent
negative
shifts
peak
on
X‐ray
near
edge
structure
spectra.
By
virtue
optimized
N
doping
unique
porous
structure,
as‐fabricated
N‐FLG
electrocatalyst
exhibits
high
toward
synthesis
superior
long‐term
stability.
To
achieve
high‐value
products
both
anode
cathode
energy
efficiency,
practical
device
coupling
generation
furfural
oxidation
assembled,
simultaneously
yield
rate
at
(9.66
mol
h
−1
g
cat
)
2‐furoic
acid
(2.076
m
−2
under
small
cell
voltage
1.8
V.
Advanced Powder Materials,
Journal Year:
2021,
Volume and Issue:
1(1), P. 100013 - 100013
Published: Nov. 15, 2021
Various
metal-based
electrocatalysts
from
nanocrystals,
to
clusters
and
single-atoms,
have
been
well-discovered
towards
high-efficient
power
devices
electrocatalytic
conversion.
To
accelerate
energy
transformation
materials
discovery,
developing
high-throughput
DFT
calculations
machine-learning
techniques
is
of
great
necessity.
This
review
comprehensively
outlines
the
latest
progress
theory-guided
design
advanced
materials.
Especially,
we
focus
on
study
single
atoms
in
various
devices,
such
as
fuel
cell
(oxygen
reduction
reaction,
ORR;
acid
oxidation
reaction;
alcohol
reaction),
other
reactions
for
energy-related
conversion
small
molecules,
H2O2
evolution
(2e−
ORR),
water
splitting
(H2
reaction/O2
HER/OER),
N2
reaction
(NRR),
CO2
(CO2RR).
Firstly,
electronic
structure,
interaction
mechanism,
activation
path
are
discussed
provide
an
overall
blueprint
electrocatalysis
batteries
mentioned
above.
Thereafter,
experimental
synthesis
strategies,
structural
recognition,
performance
figured
out.
Finally,
some
viewpoints
into
current
issues
future
concept
provided.
ACS Catalysis,
Journal Year:
2020,
Volume and Issue:
10(14), P. 7495 - 7511
Published: June 10, 2020
Hydrogen
peroxide
is
a
valuable
chemical
oxidant
with
wide
range
of
applications
in
variety
industrial
processes,
especially
water
sanitization.
Electrochemical
synthesis
hydrogen
(H2O2)
through
two-electron
oxygen
reduction
reaction
(2e-ORR)
or
oxidation
(2e-WOR)
has
emerged
as
an
appealing
process
for
onsite
production
this
chemically
oxidant.
On-site
produced
H2O2
can
be
applied
wastewater
treatment
remote
locations
any
where
needed
oxidizing
agent.
This
Review
studies
the
theoretical
efforts
understanding
challenges
catalysis
electrochemical
well
providing
design
principles
more
efficient
catalyst
materials.
Nature Communications,
Journal Year:
2021,
Volume and Issue:
12(1)
Published: July 9, 2021
Abstract
Oxygen
reduction
reaction
towards
hydrogen
peroxide
(H
2
O
)
provides
a
green
alternative
route
for
H
production,
but
it
lacks
efficient
catalysts
to
achieve
high
selectivity
and
activity
simultaneously
under
industrial-relevant
production
rates.
Here
we
report
boron-doped
carbon
(B-C)
catalyst
which
can
overcome
this
activity-selectivity
dilemma.
Compared
the
state-of-the-art
oxidized
catalyst,
B-C
presents
enhanced
(saving
more
than
210
mV
overpotential)
currents
(up
300
mA
cm
−2
while
maintaining
(85–90%).
Density-functional
theory
calculations
reveal
that
boron
dopant
site
is
responsible
due
low
thermodynamic
kinetic
barriers.
Employed
in
our
porous
solid
electrolyte
reactor,
demonstrates
direct
continuous
generation
of
pure
solutions
with
95%)
partial
~400
),
illustrating
catalyst’s
great
potential
practical
applications
future.
Advanced Science,
Journal Year:
2021,
Volume and Issue:
8(15)
Published: May 27, 2021
Shifting
electrochemical
oxygen
reduction
reaction
(ORR)
via
two-electron
pathway
becomes
increasingly
crucial
as
an
alternative/green
method
for
hydrogen
peroxide
(H2
O2
)
generation.
Here,
the
development
of
2e-
ORR
catalysts
in
recent
years
is
reviewed,
aspects
mechanism
exploration,
types
high-performance
catalysts,
factors
to
influence
catalytic
performance,
and
potential
applications
ORR.
Based
on
previous
theoretical
experimental
studies,
underlying
firstly
unveiled,
aspect
pathway,
thermodynamic
free
energy
diagram,
limiting
potential,
volcano
plots.
Then,
various
efficient
producing
H2
are
summarized.
Additionally,
active
sites
catalysts'
such
electronic
structure,
carbon
defect,
functional
groups
(O,
N,
B,
S,
F
etc.),
synergistic
effect,
others
(pH,
pore
steric
hindrance
etc.)
discussed.
The
electrogeneration
also
has
wastewater
treatment,
disinfection,
organics
degradation,
storage.
Finally,
future
directions
prospects
electrochemically
examined.
These
insights
may
help
develop
highly
active/selective
shape
application
this
method.
Nature Communications,
Journal Year:
2020,
Volume and Issue:
11(1)
Published: May 1, 2020
Abstract
Electrochemical
synthesis
of
H
2
O
through
a
selective
two-electron
(2e
−
)
oxygen
reduction
reaction
(ORR)
is
an
attractive
alternative
to
the
industrial
anthraquinone
oxidation
method,
as
it
allows
decentralized
production.
Herein,
we
report
that
synergistic
interaction
between
partially
oxidized
palladium
(Pd
δ+
and
oxygen-functionalized
carbon
can
promote
2e
ORR
in
acidic
electrolytes.
An
electrocatalyst
synthesized
by
solution
deposition
amorphous
Pd
clusters
3
4
onto
mildly
nanotubes
-OCNT)
shows
nearly
100%
selectivity
toward
positive
shift
onset
potential
~320
mV
compared
with
OCNT
substrate.
A
high
mass
activity
(1.946
mg
−1
at
0.45
V)
-OCNT
achieved.
Extended
X-ray
absorption
fine
structure
characterization
density
functional
theory
calculations
suggest
nearby
oxygen-containing
groups
key
for
ORR.