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THE SCATTERING FUNCTION S33 (q, ω) OF DILUTE HeII-He3 MIXTURES
W. Götze, M. Lücke, A. Szprynger
To cite this version:
W. Götze, M. Lücke, A. Szprynger. THE SCATTERING FUNCTION S33 (q, ω) OF DI- LUTE HeII-He3 MIXTURES. Journal de Physique Colloques, 1978, 39 (C6), pp.C6-196-C6-197.
�10.1051/jphyscol:1978687�. �jpa-00218367�
JOURNAL DE PHYSIQUE
Colloque C6, supplbment au no 8, Tome 39, aotit 1978, page C6-196
THE SCATTERING FUNCTION
Sg3(q,w) OF DILUTE H ~ I I - H e 3 MIXTURES W. G6tze, M. Liicke and A. Szprynger
Max-Planck-Institut
filrPhysik and Physik Department der Teehnischen Universit?it, Milnehe, Germany I n s t i t u t e of
LowTemperature and Structure Research, Polish Academy
o fSciences, Wroclaw, Poland
Resum6.- La fonction de diff~action S33 (q,w) des melanges de H~II-He3
1 tempgrature zdro est cal-culde dans la limite de concentration zdro de ~e~ dans le cadre d'une thdorie des modes couplds. La masse effective de He3 dependant du vecteur d'onde et la structure du spectre des excitations conti- nues sont d6terminges.
Abstract
,-The scattering function S33 (q,w) of H~II-He3 mixtures at zero temperature is calculated in the zero He3 concentration limit wlthin a mode coupling theory. The momentum dependence of the effective He3 mass and the structure of the continuous excitation spectrum is predicted.
A He3 atom is He11 experiences a considera- ble mass enhancement by inducing motion in the HeII part of which consists of backflow
/ I / .One common- ly views this motion in terms of density excita- tions /2/ created by and coupled to the He3 movement.
These concepts have been extended /3/ to a nonli- near, first principles theory for the He3 motion coupled selfconsistently to He11 density excita- tions at T
= 0K by adopting mode coupling methods which proved to be successfui for pure He11 f4/.
The motion of a single He3 particle is des- cribed by the dynamical susceptibility x(q,z) for the He3 density fluctuation. Its spectrum is given by the zero concentration contribution of the dyna- mica1 He3 structure function to the scattering law of the mixture
X" (q,w)
=lim Sg3 (q,w
;x) .
( 1X
+o
The susceptibility
tion of a He3 density fluctuation and a He11 densi- ty fluctuation
W
W
N ~ I (q,~) J % J d
E\ v
~ & % ) , 2x;=(~,E)
0
xtt (Z-Z,
WE)(4)
This golden rule type formula contains the emission probability for HeII modes of momentum k -+
and energy
Eby the He3 atom. The decay vertex can be expressed /3,4/ approximately in terms of liquid structure factors which were taken from the lite- rature /5/. In the limit x
+ 0the He11 spectrum X;I(q,w) is unchanged. For it we use the results of our previous theory 141.
Equations (2-4) are, together with the Kramers-Kronig formula for M, a system of nonlinear integral equations for X (q,z). The solution descri- bing the motion of a ~e~ atom coupled selfconsis- tently via M to a hybridization of a "dressed" He3 particle and He11 density excitations has been ob- tained by iteration.
can be expressed by a polarization kernel M(q,z)
As expected there are, for wavenumbers below and a characteristic frequency Oo(q) which is, for
a threshold qc, undamped elementary excitations given M(q,z), most conveniently determined by the
defined bv voles of - .
(2).
.on the real axis spectrums normalization
'
0MIt ( q , ~ (q))
= 0 .
(5b)
The absorptive part of the relaxation Kernel
Mn(q,u) is approximated within mode coupling theory The excitation energy
E(q) of these He3 by the decay of the IIe3 motion into a pair excita- quasiparticles defines their effective mass m*(q)
Article published online by EDP Sciences and available at http://dx.doi.org/10.1051/jphyscol:1978687 Article published online by EDP Sciences and available at http://dx.doi.org/10.1051/jphyscol:1978687
according t o E (q) = q2/ (2m2(q)). I n a d d i t i o n t o t h e
&-functions from t h e s e He3 s i n g l e modes o f energy
~ ( q ) , t h e r e a r e broad c o n t r i b u t i o n s t o t h e spectrum
2" (q,w) from m u l t i p l e mode e x c i t a t i o n s . T h e i r in-
t e n s i t y i n c r e a s e s with i n c r e a s i n g wavenumber on c o s t of t h e s i n g l e mode i n t e n s i t y u n t i l f o r q
qc s i n g l e mode He3 e x c i t a t i o n s a r e no longer p o s s i b l e .
can a l s o be t r a c e d back t o s p e c i f i c combinations of He3 and He11 e x c i t a t i o n s .
F i g u r e l a shows a l s o t h e c u r v e 92 (q)/w - w whose i n t e r s e c t i o n w i t h M' ( q , w ) y i e l d s according t o
(5a) t h e z e r o s i n t h e r e a l p a r t of t h e denominator o r ( 2 ) . F i . r s t t h e r e i s a t w = 6.7 K t h e undamped He3 e x c i t a t i o n (arrow a ) which c a r r i e s i n our example 59 % o f t h e t o t a l s p e c t r a l weight of X" (q,w).There i s a second i n t e r s e c t i o n (arrow b) where Mv'(q,w) i s f i n i t e . T h i s y i e l d s a resonance i n X" (q,w) (Fig. Ib) near 25 K. A t a t h i r d frequency (arrow c ) e q u a t i o n
(5a) i s n e a r l y f u l f i l l e d w i t h M" (q,u) simultaneous- l y being small. The r e s u l t i s a n o t h e r resonance i n
X"
(q,w) l o c a t e d n e a r 35 K. Note t h a t t h e i n t e r s e c -The s t r u c t u r e i n MU(q,w), shown f o r t h e re- p r e s e n t a t i v e example q = 1.5 !-I i n f i g u r e 1 , i s due t o phase space kinematics of opening and c l o - s i n g decay channels and t o t h e momentum dependence of t h e v e r t e x . Since energy and moment9 conserva- t i o n does n o t a l l o w two-mode s t a t e s with frequencies
t i o n a t 16 K does not l e a d t o a resonance s i n c e MI' i s l a r g e t h e r e and M' shows anomalous d i s p e r s i o n . The s t r u c t u r e i n X" (q,w), consequently, i s due t o t h e kinematics of He11 d e n s i t y f l u c t u a t i o n s b e i n g generated by t h e movement of t h e "dressed" He3 atom.
Fig. 1 : M" (q,u) ( f u l l curve) and M' (q,w) (dasked curve) a s a f u n c t i o n of frequency f o r q = 1.5 A-l.
The dash-dotted curve i n d i c a t e s t h e f u n c t i o n
a:
(Q) /w-wFig. Ib : Normalized spectrum X I ' (q,w) /.T f o r q = 1.5 A - ~
l e s s than t h e s i n g l e mode energy
-
i n our exampleE = 6.7 K
-
one f i n d s M " ( q , w l ~ ( q ) ) = 0. The smooth i n c r e a s e of M"(q,u) j u s t above E ( q ) i s cau- sed by s o f t phonon emission by t h e moving He3 atom.The s t r o n g peak a t w = 15 K i s due t o h y b r i d i z a t i o n with He11 maxons 9 f o r which t h e phase space t u r n s o u t t o be l a r g e s t . The o r i g i n o f t h e o t h e r l e s s conspi- cuous f e a t u r e s of t h e coupled mode spectrum M1'(q,w)
The elementary e x c i t a t i o n d i s p e r s i o n E (q) t u r n s o u t t o b e a monotonously i n c r e a s i n g f u n c t i o n of momentum w i t h an approximate p a r a m e t r i z a t i o n f o r t h e e f f e c t i v e mass
& ( q ) = m S ( I
+
a q ) ; a = 0.1 (6) The v a l u e of m* = 2.35 m a g r e e s w e l l w i t h t h e one known from thermodynamical d a t a f o r d i l u t e H~II-He3 s o l u t i o n s . It h a s been o b t a i n e d e a r l i e r by q u i t e a d i f f e r e n t t h e o r e t i c a l approach / 6 / . The undamped ~e~q u a s i p a r t i c l e e x c i t a t i o n s c e a s e t o e x i s t f o r
q + q c % 2
1-I
w i t h t h e d i s p e r s i o n having a P i t a e v s k i endpoint /7/ a t qc. For q > qc, however, t h e spec- trum c o n t i n u e s a s a resonance o f X" (q,w)References
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