17 Some Structural and Magnetic Properties of
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AxVIIxVIII1-xF3Compounds Y . F . LEE, R . F .
WILLIAMSON,
and W . O . J .
BOO
1
Department of Chemistry, T h e University of Mississippi, University, M S 38677
Tungsten
bronze-like
studied changes
on
hexagonal
structure
KxVF
dimensions
with
observed (x =
to be
have lattice
dimensions
or ferrimagnetic
A single
spontaneous
moment
with the
x.
lattice was
Hexagonal
KxVF
(x =
3
that change
ordering
Pseudo-
change
a superstructure
small
compounds
spontaneous
dependent.
for
were
composition
properties.
does not
but
and tetragonal
All of the
systems,
parallel
composition
0.19-0.31)
sition.
magnetic
0.19-0.27)
optimum
compounds
3
the effects of small
and
(x =
3
xF
AxVIIxVIII1
in order to determine
smoothly
reported
Cs VF x
with
displayed
compoantiferro
above 4.2 K. In each of the
magnetic
moments
crystal
of
K .20VF3
only
when
its
0
were
three
composition
revealed
c axis
3
0.450-4.558)
was
a
small aligned
field.
T ) h a s e d i a g r a m s of m i x e d - v a l e n c e systems o f t e n are r e p o r t e d to h a v e single p h a s e d regions that e x t e n d o v e r b r o a d c o m p o s i t i o n ranges. W i t h i n these r e g i o n s , the ratios of m i x e d - v a l e n c e ions, as w e l l as c o m positions of other c o m p o n e n t s , m a y c h a n g e . T h e h e x a g o n a l K WF W
0.19-0.27) a n d C s ^ V F g (x = K a ? V F (x = 3
0.19-0.31) systems (1,2)
0.450-0.558) system (3,4)
S
(x
=
a n d the tetragonal
are r e p o r t e d l y r e l a t e d s t r u c t u r a l l y
to the t u n g s t e n bronzes. A l t h o u g h t h e structures are s i m i l a r , differences exist i n t h e A V F a ?
3
c o m p o u n d s s u c h as superlattices, l a t t i c e d i s t o r t i o n s ,
a n d e v e n space groups. 1
Author to whom correspondence should be addressed. 0-8412-0472-l/80/33-186-315$05.00/l © 1980 American Chemical Society Holt et al.; Solid State Chemistry: A Contemporary Overview Advances in Chemistry; American Chemical Society: Washington, DC, 1980.
316
SOLID S T A T E
T h e purpose
CHEMISTRY: A CONTEMPORARY OVERVIEW
o f this c h a p t e r i s t o r e p o r t s u b t l e , b u t i n t e r e s t i n g ,
structural a n d magnetic properties of the A . V a
I I
a
.V
I I I
i- .F a
3
p h a s e systems.
I t e m p h a s i z e s t h e fact t h a t p h y s i c a l changes w h i c h often
accompany
c o m p o s i t i o n changes w i t h i n a n a p p a r e n t single p h a s e p r o v i d e a n interest i n g area o f i n v e s t i g a t i o n f o r the s o l i d state c h e m i s t . Experimental Stoichiometric mixtures of K F or C s F , V F , a n d V F were m i x e d t h o r o u g h l y i n s i d e a n i n e r t a t m o s p h e r e g l o v e box. S a m p l e s o f these mixtures were v a c u u m encapsulated i n m o l y b d e n u m b y electron-beam w e l d i n g t e c h n i q u e s . T h e capsules w e r e fired a t 8 0 0 ° C f o r 30 days i n a n e v a c u a t e d stainless steel t u b e i n s i d e a H e v i D u t y f u r n a c e . V F a n d V F w e r e p r e p a r e d i n this l a b o r a t o r y b u t o p t i c a l - g r a d e K F a n d C s F w e r e o b t a i n e d c o m m e r c i a l l y . C h e m i c a l analyses of p r o d u c t s w e r e i n a g r e e m e n t w i t h c a l c u l a t e d v a l u e s w i t h i n e x p e r i m e n t a l error. S m a l l q u a n t i t i e s o f i m p u r i t y phases w e r e s e p a r a t e d f r o m b u l k samples b y Pasteur's m e t h o d u n d e r a n A m e r i c a n O p t i c s stereoscopic m i c r o s c o p e . F i n a l p r o d u c t s w e r e i n s p e c t e d u n d e r a L e i t z D i a l u x p o l a r i z i n g m i c r o s c o p e . S i n g l e crystals o f c o m p o s i t i o n K . 2 o V F , s u i t a b l e for m a g n e t i c s u s c e p t i b i l i t y m e a s u r e m e n t s , w e r e o b t a i n e d f r o m a n i n d e p e n d e n t e x p e r i m e n t b y the f o l l o w i n g p r o cedure: a mixture of K F , V F , a n d V F was heated to 1000°C inside a g r a p h i t e - f i n e d n i c k e l f u r n a c e t u b e u n d e r a c o n t r o l l e d gas f l o w o f H F , H , a n d A r . S e v e r a l l a r g e single crystals, w h i c h h a d g r o w n f r o m t h e v a p o r phase, w e r e d e p o s i t e d d o w n s t r e a m i n the cooler p o r t i o n o f t h e f u r n a c e . F r o m these, one s i n g l e c r y s t a l e l o n g a t e d a l o n g its c axis a n d w e i g h i n g 5.0 m g w a s chosen f o r m a g n e t i c a n i s o t r o p y measurements.
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2
3
2
0
3
3
2
3
2
T h e samples w e r e c h a r a c t e r i z e d b y X - r a y d i f f r a c t i o n m e t h o d s . B o t h D e b y e - S c h e r r e r and G u i n i e r - H a g g techniques were used o n powder samples. S i n g l e crystals, w h e r e a v a i l a b l e , w e r e s t u d i e d b y W e i s s e n b e r g m e t h o d s f o r s u p e r s t r u c t u r e s , d o m a i n structures, a n d o t h e r s t r u c t u r a l anomalies. A P A R v i b r a t i n g sample magnetometer equipped w i t h a l i q u i d h e l i u m d e w a r a n d g a l l i u m a r s e n i d e t h e r m o m e t e r w a s u s e d for m a g n e t i c s u s c e p t i b i l i t i e s f r o m 2 . 8 - 3 0 0 K a t a constant field o f 10,000 G o n r a n d o m l y o r i e n t e d p o w d e r samples, as w e l l as o n a s i n g l e c r y s t a l o f h e x a g o n a l K . o V F o r i e n t e d w i t h its c axis p a r a l l e l a n d p e r p e n d i c u l a r t o t h e field. Spontaneous m o m e n t s w e r e d e t e r m i n e d a t constant t e m p e r a t u r e s i n fields r a n g i n g f r o m 10,000-1,000 G a n d e x t r a p o l a t e d t o zero field. I n e v e r y e x p e r i m e n t , samples w e r e c o o l e d i n a field o f 10,000 G . Slopes o n plots o f X ^ " versus T w e r e o b t a i n e d b y l i n e a r regression. A D e c - 1 0 c o m p u t e r w a s u s e d t o r e d u c e the X - r a y d a t a . 0
2
3
1
Results and
Discussion A hexagonal
lattice c a n b e described
easily b y a set o f o r t h o r h o m b i c base vectors.
Pseudohexagonal Ka.VF .
I f these vectors are c h o s e n
3
s u c h t h a t ao — 1 / 2 a + b , b = 1 / 2 a*, a n d c = c ; t h e n \a \ = h
h
0
|a | — 2|b | a n d |a |/V3|b | = 0
0
0
0
G
h
h
2/\/3
1.00Q. T h e r e are t w o s i m p l e p o s s i b i l i t i e s
Holt et al.; Solid State Chemistry: A Contemporary Overview Advances in Chemistry; American Chemical Society: Washington, DC, 1980.
17.
A V
LEE E T AL.
x
7 /
x
V
317
i - ^3
7 / /
for d i s t o r t i o n f r o m h e x a g o n a l s y m m e t r y b y w h i c h the l a t t i c e r e m a i n s orthorhombic.
F o r the first k i n d , | a | / \ / 3 |b | is greater t h a n u n i t y , a n d G
0
for t h e s e c o n d k i n d it is less t h a n u n i t y . F o r distortions of either k i n d , the h e x a g o n a l M i l l e r i n d i c i e s are t r a n s f o r m e d to o r t h o r h o m b i c i n d i c i e s b y the m a t r i c i e s
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V4 VS 0'
1 0 0
0 0 1
V2 V4 V i VT.
0
T h e h e x a g o n a l (hOhl) r h o m b i c reflections (h/2,
0
0 0 1
T 0 0
, and
Vi V4 0
0 0 1
reflections are t r a n s f o r m e d i n t o t h r e e o r t h o h/2, I), (71/2, h/2, I), and (TiOZ). T h e
reflections are t r a n s f o r m e d i n t o ( 3 / 2 7 i , h/2, I) (Ohl),
(hh2hl)
a n d (3/2h, h/2,
I n b o t h cases, t w o of t h e three o r t h o r h o m b i c reflections are
I).
degenerate
a n d , i n p o w d e r d i f f r a c t i o n e x p e r i m e n t s , one observes a d o u b l e t of w h i c h one r e f l e c t i o n is t w i c e t h e i n t e n s i t y of t h e other. F o r a d i s t o r t i o n of t h e first k i n d , the (hOhl)
reflections s p l i t i n t o d o u b l e t s of w h i c h t h e first reflec
t i o n (larger d) is h a l f as intense as t h e second, a n d t h e (hh2hl)
reflections
s p l i t i n t o d o u b l e t s of w h i c h the first reflection is t w i c e as intense as t h e second.
F o r a d i s t o r t i o n of the s e c o n d k i n d , the o r d e r of intensities
o b v i o u s l y w o u l d be r e v e r s e d . G u i n i e r - H a g g photographs
s h o w that t h e lattices of K . 2 o V F 0
K0.25VF3 are d i s t o r t e d to a n o r t h o r h o m b i c s t r u c t u r e of the T a b l e I shows X - r a y p o w d e r
d a t a of K0.25VF3.
The hexagonal
i n d i c i e s i n the first c o l u m n w e r e those assigned to l o w - a n g l e
and
3
first
kind. Miller
Debye-
S c h e r r e r d a t a . O n e s u p e r l a t t i c e reflection i n d e x e d as ( 2 1 3 3 ) makes t h e h e x a g o n a l a v a l u e a p p e a r to d o u b l e . T h e s e c o n d c o l u m n i n T a b l e I gives M i l l e r i n d i c i e s of the m u l t i p l e o r t h o r h o m b i c reflections w h i c h are g e n erated f r o m Guinier-Hagg agreement
t h e h e x a g o n a l reflections. films
w i t h the
The
observed
d values
from
are s h o w n i n the t h i r d c o l u m n a n d are i n g o o d calculated values.
A l l of
reflections that w e r e r e s o l v a b l e are o b s e r v e d i n t e n s i t y 1:2, w h e r e a s , a l l (hh2hl)
the hexagonal
(hOhl)
to s p l i t i n t o d o u b l e t s
of
reflections are split i n t o d o u b l e t s
of
i n t e n s i t y 2 : 1 . A d e t a i l e d analysis of this system is p u b l i s h e d elsewhere (2). F i g u r e 1 d i s p l a y s the inverse s u s c e p t i b i l i t y versus t e m p e r a t u r e of a single c r y s t a l of K 0 . 2 0 V F 3 o r i e n t e d p a r a l l e l a n d p e r p e n d i c u l a r to a m a g n e t i c field of 10,000 G over the 4.2-100 K t e m p e r a t u r e r a n g e . T h e insert of F i g u r e 1 is a p l o t of spontaneous m o m e n t s e x t r a p o l a t e d to zero field at fixed
temperatures.
T h e s e m e a s u r e m e n t s r e v e a l a spontaneous
o n l y w h e n t h e c r y s t a l is o r i e n t e d w i t h its C axis p a r a l l e l to t h e
moment
field.
T h e i n v e r s e s u s c e p t i b i l i t y a n d spontaneous m a g n e t i c m o m e n t versus t e m p e r a t u r e of a r a n d o m l y o r i e n t e d p o w d e r s a m p l e of K . 2 o V F is s h o w n 0
i n F i g u r e 2, a n d t h a t of K
0
5VF
2
3
i n F i g u r e 3.
3
S m a l l corrections
Holt et al.; Solid State Chemistry: A Contemporary Overview Advances in Chemistry; American Chemical Society: Washington, DC, 1980.
for
318
SOLID S T A T E C H E M I S T R Y :
Table I.
Hexagonal (Wi\) (2020)
OVERVIEW
G u i n i e r - H a g g D a t a f o r K0.25VF3: a = 12.88 ± b = 7.39 ± 0.01; c = 7.52 ± 0.01
0.01;
Orthorhombic ^•observed
((200
((no
6.448 6.419
l-observed
w w
+
^calculated
6.438 6.409
(002
3.763
M
{(310 { (020;
3.715 3.698
w
3.246
w
1(220
3.224 3.205
w
((312 {(022
2.643 2.638
W"
1
(4260)
f(510; \ (420
2.438
W"
2
T2.432 •j 2.427 [2.419
(3361)
(031
2.339
W"
3
2.341
((203
2.335
w
-s
(2.336 {2.334
(0002)
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A CONTEMPORARY
(2240) (2022) (4040) (2242)
(2023)
((202
1(112 ((400
1(130
1(113
3.760 1
W"
2
3.711 3.694 (3.247 {3.243 3.219 3.204
+
M
2.641 2.635
(4261)
f(511 \ (421
2.314
W"
3
T2.314 •(2.310 (2.303
(2133)
(213
2.229
W"
4
2.227
((600
2.146 2.136
1(131
W
- 3
2.146 2.136
(6060)
1 (330
(2243)
{(313 {(023
2.075
W
(0004)
(004
1.880
w
1.865
W"
1.856
M
1.847
W"
2
(2024)
1.805
W"
3
(1.805 {1.804
(6280)
1.787
W"
4
fl.785 -U.780 [1.776
(6062) (4480)
W"
2
(2.077 {2.074
- 3
1.880 4
1.864 (1.857 {1.855 1.847
Holt et al.; Solid State Chemistry: A Contemporary Overview Advances in Chemistry; American Chemical Society: Washington, DC, 1980.
17.
A^V"^/ " .
LEE E T AL.
1
319
F,
t
X
Table I. Hexagonal fhkiU
Orthorhombic (hkl)
(2224)
^•observed
-l -2
1.664 1.658
1.622
w
((800)
1.610 1.602
w w
(1.623 {1.622
{(802)
1(442)
1.479 1.474
f(822) \(732)
1.374
{(622)
1.664 1.658
1(440)
(8082) _ (64152)
1(152)
W
W W
1(044)
1.610 1.602
2 2
-3 w
1.480 1.474
W
1
W"
1.321 1.319
{(624)
(4484)
W
h e x a g o n a l samples. T h e v a l u e 6 X on V F
magnetic
region
3
fl.374 \ 1.372 U-368
4
1.321 1.318
-3
t e m p e r a t u r e - i n d e p e n d e n t o r b i t a l p a r a m a g n e t i s m of V et a l . ( 5 )
dca'cwlcrted
(1.677 {1.676
1.677
1(042)
(8080)
^•observed -4
{(314)
1(024)
(448*2)
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Continued
10" e m u / ( m o l V 4
were made on a l l
+ 3
+ 3
) used by Gossard
w h e n a p p l i e d to o u r d a t a g a v e l i n e a r i t y to the p a r a of
X M ' V S . T p l o t s of 1
a l l of
the h e x a g o n a l
Aa.VF
3
compounds. F o r m i x e d - v a l e n c e c o m p o u n d s of the t y p e A . V f l
C u r i e constant c a n b e expressed and V
+ 3
M
+ 2
V
I I I
i . . F , the molar a
3
as the s u m of c o m p o n e n t s
= xC )
+
i+2
from V
+ 2
(1 - x )
C
( + 3
)
, w h i c h is a s p i n o n l y s y s t e m , A ^
n C ( + 2 )
a n d for V
+ 3
(
+
2
)
W
(3/2)
(3/2 +
1)
3fc
=
i n w h i c h the o r b i t a l m o m e n t is q u e n c h e d ,
W(i)
r
^ f+3)
———
=
w h e r e N is A v o g a d r o s n u m b e r , g Lande
a ;
b y the e q u a t i o n C
For V
I I
s p l i t i n g factors
for V
+ 2
(+2
)
(i + i)
3/c and g
and V
+ 3
( + 3 )
are average v a l u e s of the
, r e s p e c t i v e l y , / A is the b
Holt et al.; Solid State Chemistry: A Contemporary Overview Advances in Chemistry; American Chemical Society: Washington, DC, 1980.
Bohr
320
CHEMISTRY:
A
CONTEMPORARY
OVERVIEW
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SOLID S T A T E
Figure 1. Inverse molar susceptibilities and spontaneous moments versus temperature of a single crystal of K VFg oriented parallel and perpendicular to the field 0t20
m a g n e t o n , a n d k is the B o l t z m a n n constant.
I t has b e e n e s t a b l i s h e d that
g 2) is i s o t r o p i c a n d has a v a l u e of 1.97 i n a n o c t a h e d r a l (+
m e n t (6,7).
F o r V F , the a v e r a g e v a l u e of g ) 3
(+3
is 1.80
s i n g l e - c r y s t a l d a t a of K . 2 o V F , a n average v a l u e of g 0
3
( + 3 )
fluoride
environ
(5).
F r o m the
was
calculated
Holt et al.; Solid State Chemistry: A Contemporary Overview Advances in Chemistry; American Chemical Society: Washington, DC, 1980.
17.
AJ/ ^/ .
LEE E T AL.
to b e 1.75.
n
321
F
m
t
X
S
C u r i e constants f o r p o w d e r e d samples of K0.20VF3, K0.25VF3,
CS0.25VF3, a n d C s . 3 i V F , c a l c u l a t e d w i t h g > == 1.97 a n d g ) 0
3
(+2
(+3
=
1.75,
are i n excellent a g r e e m e n t w i t h m e a s u r e d v a l u e s as seen i n T a b l e I I . T h i s e v i d e n c e s t r o n g l y supports the c o n c l u s i o n t h a t the o r b i t a l m o m e n t of V
+ 3
is q u e n c h e d
largely i n the hexagonal A V F X
3
compounds
as is
t y p i c a l of t r a n s i t i o n m e t a l ions i n solids. H o w e v e r , some o r b i t a l c o n t r i b u t i o n reduces the effective g v a l u e b e l o w 2.0 o w i n g to s p i n - o r b i t c o u p l i n g . Hexagonal Cs*VF .
Debye-Scherrer and G u i n i e r - H a g g X-ray pow
3
d e r d a t a r e v e a l that C s . 5 V F Downloaded by UNIV OF SOUTHERN CALIFORNIA on June 18, 2016 | http://pubs.acs.org Publication Date: June 1, 1980 | doi: 10.1021/ba-1970-0186.ch017
0
2
3
and C s . 3 i V F 0
3
retain hexagonal symmetry
b u t h a v e l a t t i c e constants that increase s l i g h t l y w i t h x.
These are: a
T,°K
Figure 2.
Inverse molar susceptibility and spontaneous moments versus temperature of a powder sample of K VF 0
20
S
Holt et al.; Solid State Chemistry: A Contemporary Overview Advances in Chemistry; American Chemical Society: Washington, DC, 1980.
=
322
A
CONTEMPORARY OVERVIEW
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SOLID S T A T E C H E M I S T R Y :
7.50 ±
0.01 A , c — 7.67 ±
dz 0.01 A , respectively.
0.01 A a n d a =
7.51 ±
p e r a t u r e of CS0.25VF3, s h o w n i n F i g u r e 4, i n d i c a t e s a n t r a n s i t i o n at 22 material.
Like
K.
No
0.01 A , c —
7.69
T h e inverse m a g n e t i c s u s c e p t i b i l i t y versus t e m spontaneous m o m e n t was
K0.20VF3 a n d
K0.25VF3, t h e
inverse
antiferromagnetic o b s e r v e d for susceptibility
this of
C s . 3 i V F , s h o w n i n F i g u r e 5, indicates no m a g n e t i c o r d e r i n g t r a n s i t i o n . 0
3
( M a t e r i a l s that o r d e r f e r r i m a g n e t i c a l l y u s u a l l y do not d i s p l a y m a x i m a
Holt et al.; Solid State Chemistry: A Contemporary Overview Advances in Chemistry; American Chemical Society: Washington, DC, 1980.
LEE ET AL. Table II.
X
X
X
Magnetic Constants of Aa.VF
CM
^served)
Compound
(cm
3
K0.20VF3 K0.25VF3 CS0.25VF3
Cs .3iVF Downloaded by UNIV OF SOUTHERN CALIFORNIA on June 18, 2016 | http://pubs.acs.org Publication Date: June 1, 1980 | doi: 10.1021/ba-1970-0186.ch017
0
3
K0.450VF3 K0.498VF3 K0.558VF3
323
A V" V"V F,
0.99 1.02 1.02 1.09 1.39 1.49 1.51
deg
(
CM
calculated)
3
Compounds a
© K
TV K
MB
-10 - 3 -20 -11 -65 -75 -78
8 10 22 12 48 47 45
0.05 0.13 0.00 0.06 0.28 0.010 0.004
mol' ) 1
0.98 1.03 1.03 1.10
—
300 T, K
Figure 4.
Inverse susceptibility versus temperature of Cs . VF 0 25
of a powder
3
Holt et al.; Solid State Chemistry: A Contemporary Overview Advances in Chemistry; American Chemical Society: Washington, DC, 1980.
sample
324
CHEMISTRY: A
CONTEMPORARY OVERVIEW
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SOLID S T A T E
in
)
H o w e v e r , a r e m n a n t m a g n e t i c m o m e n t w h i c h appears b e l o w T
N
,
a n d d i s a p p e a r s a b o v e T , gives e v i d e n c e o f m a g n e t i c o r d e r i n g a n d defines N
t h e o r d e r i n g t e m p e r a t u r e v e r y w e l l . A s u m m a r y of t h e m a g n e t i c constants is g i v e n i n T a b l e I I . Tetragonal Ka.VF . 3
T h e l a t t i c e constants of t h e t e t r a g o n a l K a . V F
3
p h a s e r e p o r t e d l y c h a n g e s m o o t h l y w i t h x (4)
a n d a superstructure w i t h
d i m e n s i o n s \a
was observed for the com
\ = 2\/2Ja
suvteT
position x = Ka.VF
3
0.558.
B U b
|; c ' s
upe
r = 2 c
s u b
T h e i n v e r s e m a g n e t i c s u s c e p t i b i l i t y of t e t r a g o n a l
indicated long-range magnetic ordering near 45 K
(4).
Holt et al.; Solid State Chemistry: A Contemporary Overview Advances in Chemistry; American Chemical Society: Washington, DC, 1980.
The
17.
LEEETAL.
A V" V x
x
I 7 /
325
i -J?3
d e p e n d e n c e of spontaneous m o m e n t o n c o m p o s i t i o n , d i s p l a y e d i n F i g u r e 6, is a n i m p o r t a n t effect t h a t has not b e e n r e p o r t e d p r e v i o u s l y . T h e d i m e n s i o n s |a er| = 2 2|a |; c = 2 c was observed for the c o m r e m n a n t m o m e n t s o n r a n d o m l y o r i e n t e d p o w d e r samples of c o m p o s i t i o n x — 0.558 a n d 0.498 are s m a l l , b u t for x — 0.450 the m a g n i t u d e of t h e m o m e n t p e r v a n a d i u m a t o m is 0.28 PB- A s u m m a r y of t h e m a g n e t i c constants of t e t r a g o n a l K z V F is i n c l u d e d i n T a b l e I I . sub
BllP
s u p e r
s u b
3
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Conclusions T h e b r o n z e - l i k e A ^ V F a structures are p e r o v s k i t e - l i k e , as V - F - V b o n d angles are a l l close to 180°.
T h e y are u n l i k e perovskites, h o w e v e r , i n
0.30 _
0.20 _