ACS Materials Letters,
Journal Year:
2024,
Volume and Issue:
6(2), P. 566 - 571
Published: Jan. 9, 2024
We
provide
direct
evidence
for
a
spin-active
V4+
defect
center,
likely
in
the
form
of
VO2+
complex,
predominantly
introduced
single
crystals
vanadium-doped
Cs2NaInCl6
halide
double
perovskites
grown
by
solution-processed
hydrothermal
method.
The
has
C4v
point
group
symmetry,
exhibiting
an
electron
paramagnetic
resonance
(EPR)
spectrum
arising
from
effective
spin
S
=
1/2
and
nuclear
I
7/2
(corresponding
to
51V
with
nearly
100%
natural
abundance).
determined
g-factor
hyperfine
parameter
values
are
g⊥=
1.973,
g∥
1.945,
A⊥
180
MHz,
A∥
504
principal
axis
z
along
⟨001⟩
crystallographic
axis.
controlled
growth
V-doped
oxygen-free
environment
is
shown
suppress
EPR
signal.
model
suggested
have
VOCl5
octahedral
coordination,
where
one
nearest-neighbor
Cl–
V
replaced
O2–,
compression
V–O
This
VO
complex
formation
competes
isolated
V3+
substitution
In3+,
which
turn
provides
means
charge-state
tuning
ions.
finding
calls
better
understanding
control
solution-grown
perovskites,
critical
optimizing
tailoring
material
design
solution-processable
optoelectronics
spintronics.
Inorganic Chemistry,
Journal Year:
2024,
Volume and Issue:
63(23), P. 10756 - 10766
Published: May 29, 2024
The
lead-free
halide
perovskites
possess
nontoxicity
and
excellent
chemical
stability,
whereas
relatively
weak
luminescence
intensity
limits
their
potential
in
practical
applications.
Therefore,
strengthening
the
expanding
application
fields
are
urgent
tasks
for
development
of
perovskites.
In
this
paper,
antimony-doped
Cs2NaScCl6
crystals
synthesized
by
a
solvothermal
method
emit
bright,
deep
blue
photoluminescence
at
447
nm.
(PL),
excitation
(PLE),
absorption
spectra
demonstrate
that
Sb3+
doping
effectively
activate
intrinsic
"dark
self-trapped
exciton
(STE),"
leading
to
an
impressive
quantum
yield
(PLQY)
value
78.31%
1%
doping.
Furthermore,
remains
above
92%
compared
with
fresh
sample
without
secondary
phases
detected
even
after
90
days
under
environmental
conditions.
To
expand
emission
spectra,
rare-earth
Sm3+
is
further
incorporated
into
Cs2NaScCl6:1%
crystals.
results
show
Sb
ions
not
only
enhance
STE
but
also
serve
as
sensitizers
boost
red-light
Sm3+,
significant
500-fold
increase
red
intensity.
Finally,
PLQY
reaches
stunning
86.78%.
These
findings
provide
valuable
insights
design
ion-doped
double
perovskites,
broadening
various
optoelectronic
devices.
Advanced Optical Materials,
Journal Year:
2023,
Volume and Issue:
12(6)
Published: Oct. 6, 2023
Abstract
Chalcogenide
perovskites
are
an
emerging
family
of
perovskite
materials,
which
possess
excellent
optoelectronic
properties
comparable
with
halide
perovskites,
avoiding
the
drawbacks
toxicity
and
poor
stability.
Due
to
superiorities
strong
light
absorption,
direct
bandgaps,
carrier
transport
abilities,
high
defect
tolerance,
robust
stability,
non‐toxicity,
chalcogenide
have
been
extensively
studied
as
photovoltaic
materials.
However,
emitting
potential
is
ignored
or
less
explored.
In
this
work,
Eu
2+
doping
strategy
proposed
activate
abilities
perovskite.
The
synthesized
SrHfS
3
:Eu
powder
exhibits
intense
red
emission
through
relaxation
4f
6
5d
1
7
0
.
interband
absorption
,
a
distinct
character
perovskite,
harvests
optical
energy
funnels
it
luminescent
center
Besides,
characterized
by
superior
semiconducting
properties,
suggesting
its
suitable
emitters
in
light‐emitting
diodes.
Moreover,
obtained
luminescence
remain
stable
under
ultraviolet
irradiation,
water,
temperature
testing.
above
observations
open
new
frontier
for
exploring
highlighting
their
great
lighting
displays,
rather
than
being
limited
devices.
ACS Materials Letters,
Journal Year:
2024,
Volume and Issue:
6(2), P. 566 - 571
Published: Jan. 9, 2024
We
provide
direct
evidence
for
a
spin-active
V4+
defect
center,
likely
in
the
form
of
VO2+
complex,
predominantly
introduced
single
crystals
vanadium-doped
Cs2NaInCl6
halide
double
perovskites
grown
by
solution-processed
hydrothermal
method.
The
has
C4v
point
group
symmetry,
exhibiting
an
electron
paramagnetic
resonance
(EPR)
spectrum
arising
from
effective
spin
S
=
1/2
and
nuclear
I
7/2
(corresponding
to
51V
with
nearly
100%
natural
abundance).
determined
g-factor
hyperfine
parameter
values
are
g⊥=
1.973,
g∥
1.945,
A⊥
180
MHz,
A∥
504
principal
axis
z
along
⟨001⟩
crystallographic
axis.
controlled
growth
V-doped
oxygen-free
environment
is
shown
suppress
EPR
signal.
model
suggested
have
VOCl5
octahedral
coordination,
where
one
nearest-neighbor
Cl–
V
replaced
O2–,
compression
V–O
This
VO
complex
formation
competes
isolated
V3+
substitution
In3+,
which
turn
provides
means
charge-state
tuning
ions.
finding
calls
better
understanding
control
solution-grown
perovskites,
critical
optimizing
tailoring
material
design
solution-processable
optoelectronics
spintronics.