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HAL Id: jpa-00208242

https://hal.archives-ouvertes.fr/jpa-00208242

Submitted on 1 Jan 1975

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Contribution of the central peak to the ultrasonic attenuation in structural phase transitions

C. Tsallis, A. Bachellerie

To cite this version:

C. Tsallis, A. Bachellerie. Contribution of the central peak to the ultrasonic attenuation in structural phase transitions. Journal de Physique, 1975, 36 (2), pp.171-174. �10.1051/jphys:01975003602017100�.

�jpa-00208242�

(2)

CONTRIBUTION OF THE CENTRAL PEAK TO THE ULTRASONIC

ATTENUATION IN STRUCTURAL PHASE TRANSITIONS

C. TSALLIS and A. BACHELLERIE

(*)

Service de

Physique

du Solide et de Résonance

Magnétique

Centre d’Etudes Nucléaires de

Saclay,

BP

2,

91190

Gif-sur-Yvette,

France

(Reçu

le 30

juillet 1974, révisé

le 30

septembre 1974)

Résumé. 2014 On calcule l’atténuation ultrasonore 03C3 au dessus de T0 en supposant : (a) une inter-

action non résonante entre les ultrasons et les phonons critiques ; (b) une forme lorentzienne pour le pic central; (c) une forme assez

générale

pour sa largeur

(d) une

procédure

au

premier

ordre pour calculer 03C3. On obtient deux régimes (03A9 ~ a ou 03A9 ~ a)

et les exposants x et ~ (03C3 ~ 03A9x a-~) sont calculés dans les deux régimes en fonction de la dimension d et des exposants { ni }. On montre que

l’anisotropie

dans

l’espace

k ne joue pas un rôle déterminant.

On compare les résultats obtenus avec ceux expérimentaux pour

SrTiO3.

Abstract. 2014 The ultrasonic attenuation 03C3 is calculated above T0 assuming : (a) a non resonant

interaction between ultrasonic and critical phonons ; (b) a lorentzian shape for the central peak ; (c) a quite general from for its width

(d) a first-order procedure to calculate 03C3. There are two distinct regimes, 03A9 ~ a, and 03A9 ~ a and

the x- and ~-exponents (03C3 ~ 03A9x a-~) are determined in both

regimes

as a function of the dimen-

sionality d

and exponents {

ni }.

Anisotropy in k-space is shown to be irrelevant.

Comparison

is

made with available experimental results for SrTiO3.

Classification

Physics Abstracts

7.270

1. Introduction. - In recent years much work has been devoted to the

study

of the central

peak

appear-

ing

in the time - and

space-Fourier -

transformed correlation function

S(k, cv)

of several structural

phase

transitions

(SrTi03, KMnF3, Tb2(MOO4)3, Gd2(MO04)3, etc.).

The main

goal

is of course to

obtain

knowledge

about the form and width of this central

peak, particularly

above the transition tempe-

rature

To.

At the present date this

problem

remains

quite unsolved,

at least from the

experimental

stand-

point. Quasi-elastic

neutron

scattering experiments [1-4] give

a direct pattern of the central

peak,

but

unfortunately adequate

resolution near

Tc

has not yet been achieved. An alternative method

might

be to

measure the critical contribution Q to the ultrasonic attenuation because a

change

in

regime

is

expected

when the central

peak’s

width becomes

comparable

with ultrasonic

frequency

Q. A certain amount of

work

[5-13]

has

already

been done within this frame

and if we define the x- and

q’-exponents by writing

.

Typical experimental

values are 1

x, il’

2.

The main theoretical contributions have been

presented by

Tani and Tsuda

[14] (x

=

1, il’

=

3/2) ; by Pytte [15]

who critisizes Tani and Tsuda’s

results,

and

assuming

a soft mode with constant mean life

T-1

obtains two

regimes :

F > Q

leading

to x = 2 and

il = 2,

and r « Q

leading

to x = 2 and

r’

=

t) ;

by

Rehwald

[8] (with assumptions

similar to those

of Pytte he

obtains x =

2 and il’

=

t or ’1’

=

5 accord-

ing

to two kinds of

k-dependence

of the soft

mode)

and

by

Schwabl

[16] (in

the

mode-mode, coupling

framework he obtains two

regimes,

very close to and

relatively

far from

To, leading

to x =

2, il’ = 4

and

q’

= yd -

dVd

+ 2

respectively,

where Yd

and vd

are

the usual

susceptibility

and correlation

length

d-

(*) Laboratoire d’Ultrasons, Université de Paris VI, Tour 13, 4, place Jussieu, 75005 Paris, France.

Article published online by EDP Sciences and available at http://dx.doi.org/10.1051/jphys:01975003602017100

(3)

172

dimensional critical

exponents).

In the present paper

some

simple assumptions

are made which lead to two

regimes,

whose

respective

x- and

il-values

are calcu-

lated as functions of

dimensionality d,

which is known

to be a relevant parameter near

To; 17

is defined

by

(J oc Q’ a - "

(one

should note

that q

and

il’

are not

necessarily

the

same).

2. Model. - Let us describe our system

by

a

hamiltonian

where

Hcr, Jeus

and

Jeint

are the

crystal,

ultrasonic

and interaction hamiltonian

respectively.

anharmonic terms where 2013 k runs

throughout

the interior of the first Brillouin zone whose

origin

is defined

by

the wave

vector

(corresponding

to k =

0)

which is

going

to

freeze

in the ordered

phase (hence

k = 0 is not

necessarily

at the centre of the usual Brillouin zone ;

-

ak+ ,

ak are the creation and annihilation boson operators

concerning

the

phonon

branch

responsible

for the

transition ;

- (Ok is

supposed

to have a

relatively

smooth

departure

from the non

vanishing

value coo corres-

ponding

to k =

0 ;

- the anharmonic terms are of course

responsible

for the appearance of the central

peak

near

To ;

- the

crystal

is assumed to be

simple cubic,

but this

assumption

is

completely

irrelevant in this

theory

and may be

easily

removed.

Thus,

where

- q runs

throughout

the usual first Brillouin zone

and is measured from its centre.

Typically,

where c is the

crystalline

parameter ;

-

Qq

is the ultrasonic normal

coordinate ;

- Qq

= vq where v is the ultrasonic

velocity.

As interaction hamiltonian we consider the first

non

vanishing

term.

which,

because of conservation

laws,

is

given by

where

U(k, q)

is

given by

usual

quasi-harmonic approximation (1)

in our case

(1) U(k, q) is a Hamiltonian’s coefficient and should not be consi- dered as a thermally renormalised one.

This last

approximation

is due to the fact that

only

modes with k - 0 are

important.

Therefore we

adopt U(k, q)

=

WQ

=

Wvq,

where W is a constant.

The ultrasonic attenuation is

given

to a first order

approximation by (see

for

example [17])

where

n(w) = (eP1J(J) - 1 ) -1

and

x"(k, w)

is the ima-

ginary

part of the

susceptibility.

We now assume a Lorentzian

shape

for the corre-

lation function

S(k, cv)

which is

presently

conside-

red

[4, 16, 18]

as the most realistic one. Since at

high

temperatures

(which

is

usually

the

experimental case) S(k, co) ( ) oc1 (O ;("(k, co) (see )(

for

example

p

[ ]) [19]),

we have

at once

where the

norm Yk

which is a smooth function of k and

T,

is a real number of the order of

unity,

and the

width is

given by :

where a, bi, ni

> 0

Vi,

and a - 0 when T -

To.

The

particular

form

proposed

in papers

[4]

and

[18]

corresponds

to d = 3, ni =

2, Vi,

and

b

1 :0

b2 = b3.

If

we have

and, by complex-plane integration (or by remarking

that this is a convolution

product),

we obtain

where

Y

is a mean

value, 1 W 12

an energy and u

the inverse of a

length.

(2) This restriction is sufficient but it might be uncessarily strong.

(4)

If we

define bs

= sup

( { bi } ) and ns

the corres-

ponding

value of

the ni ’s (3),

two

regimes

are

phy- sically important :

(easily

attainable in ultrasonic

experiments

and called

from now on the

far regime).

(difficultly

attainable in ultrasonic

experiments

and

called from now on the close

regime).

In this case we may take the limit Q - 0 in the interior

of E

in

expression (1),

hence

k

On the other

hand,

which,

in the limit a - 0 and as

long as bi

=1= 0

Vi,

becomes

We may summarize the results in the

far regime

as follows :

where

( + 0)

means a

logarithmic dependence.

In the limit a -> 0 and if u --> oo we may take k = 0 and a = 0

everywhere

in

expression (1)

except in the factor

1/Yk’

hence

With the definition

we have . and

if q -

0 then :

where nI- = inf

( {ni

such

as bi e i =1= 0 } ) (4)

and

bI, Oh

is the associated coefficient.

Hence

(independent

of

Q)

if

Furthermore

performing

a calculation similar to that of part

a)

we obtain

(this

result must be

rejected

as inconsistent with the

assumption

u -+

oo)

(5)

174

We may summarize the results in the close

regime

as follows :

and and and

and

and

Conclusion. - We may remark that for all fixed values of d

and {ni}

we have

il

(close regime) r (far regime) .

This fact seems to be confirmed

by experiments [7, 12].

We also see that

k-anisotropy (at

least two différent

bg s) plays

a minor role as

long

as all

bg

s are

sufficiently large

so

that,

for

pratical

purposes, the

dimensionality

of the

problem

is not

changed.

Finally,

let us make a

quantitative comparison

with

the

experimental

results.

Following

Ref.

[4]

and

[18]

we way propose for

SrTi03

where a =

A(T - To)

in the range

Numerical values deduced from estimates in ref.

[4]

are

hence the smallest value of a in the temperature domain considered is a ~ 1.6 x 109 s-1 and

On the other hand ultrasonic

experiments reported

in ref.

[5]

and

[8]

were done in the same temperature domain with 0.3 x

10g s-1 Q

2 x 108

s-1,

so

Q « a and we are indeed in the

far regime.

Our

theory gives

in this case

(where d

= 3 and ni = 2

Vi)

ri

= YI’

=

.;i 21 X

=

2,

which are in

good

agreement with the

experimental

results

[5, 8]

for

longitudinal

waves :

We have the

pleasure

to

acknowledge

fruitful

comments from B.

Jouvet,

R.

Pick,

R.

Bidaux,

J. M.

Courdille and J.

Dumas,

and critical

reading

of the

manuscript by

A. Levelut and J. Joffrin.

References [1] RISTE, T., SAMUELSEN, E. J., OTNES, K., FEDER, J., Solid State

Commun. 9 (1971) 1455.

[2] AXE, J. D., DORNER, B., SHIRANE, G., Phys. Rev. Lett. 26 (1971) 519.

[3] DORNER, B., AXE, J. D., SHIRANE, G., Phys. Rev. B6 (1972)

1950.

[4] SHAPIRO, S. M., AXE, J. D., SHIRANE, G., RISTE, T., Phys.

Rev. B6 (1972) 4332. ,

[5] BERRE, B., FOSSHEIM, K., MÜLLER, K. A., Phys. Rev. Lett.

23 (1969) 589.

[6] FURUKAWA, M., FUJIMORI, Y., HIRAKAWA, K., J. Phys. Soc.

Japan 29 (1970) 1528.

[7] COURDILLE, J. M., DUMAS, J., Doctoral Thesis and Solid State Commun. 9 (1971) 609.

[8] REHWALD, W., Phys. Kondens. Materie 14 (1971) 21. Ed. by Springer-Verlag 1971.

[9] CHIZHIKOV, S. I., SOROKIN, N. G., OSTROVSKII, B. I., MELE-

SHINA, V. A., Zhetf Pis. Red. 14 (1971) 490.

[10] DOMB, E. R., MIHALISIN, T., SKALYO Jr, J., Phys. Rev. B8 (1973) 5837.

[11] COURDILLE, J. M., DUMAS, J., to be published.

[12] FOSSHEIM, K., MARTINSEN, D., NAESO, A. (See ref. [10].) FOSSHEIM, K., MARTINSEN, D., LINZ, A., Proceedings of the

NATO A.S.I. Meeting 1973.

[13] GOLDING, B., Phys. Rev. Lett. 25 (1970) 1439.

[14] TANI, K., TSUDA, N., J. Phys. Soc. Japan 26 (1969) 113.

[15] PYTTE, E., Phys. Rev. B 1 (1970) 924.

[16] SCHWABL, F., Phys. Rev. B 7 (1973) 2038.

[17] BACHELLERIE, A., JOFFRIN, J., LEVELUT, A., J. Physique 32 (1971) 993.

[18] FEDER, J., Proceedings of International School of Physics

Enrico Fermi on « Local properties at Phase transitions »

9-21, July, 1972.

[19] KwoK, P. C., Sol. Stat. Phys. 20, 213.

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