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Submitted on 1 Jan 1980

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BOSE CONDENSATION IN SPIN POLARIZED ATOMIC HYDROGEN

E. Siggia, A. Ruckenstein

To cite this version:

E. Siggia, A. Ruckenstein. BOSE CONDENSATION IN SPIN POLARIZED ATOMIC HYDROGEN.

Journal de Physique Colloques, 1980, 41 (C7), pp.C7-15-C7-18. �10.1051/jphyscol:1980703�. �jpa-

00220140�

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JOURNAL DE PHYSIQUE CoZZoque C 7 , suppZ&ment au n o 7 , Tome 41, j u i Z Z e t 1980, page ~ 7 - 1 5

BOSE CONDENSATION IN SPIN POLARIZED ATOMIC HYDROGEN

E.D. S i g g i a and A.E. Ruckenstein

Laboratory o f Atomic and SoZid S t a t e P h y s i c s , CorneZZ U n i v e r s i t y , I t h a c a , iVew Y o r k 14853, USA.

Resume.- Nous proposons une d e s c r i p t i o n phenom6nologique de l'hydrogene p o l a r i s e suggeree p a r l ' h a - m i l t o n i e n microscopique e t q u i i n c l u t deux p a r t i c u l e s de Bose q u i correspondent,

a

l a l i m i t e des f a i b l e s densites, aux deux e t a t s h y p e r f i n s l e s p l u s bas. On s ' a t t e n d ti ce que 1 'experience peuple i n i t i a l e m e n t l e s deux @ t a t s e t 8 ce que l e s temps d ' e q u i l i b r e s o i e n t longs. Quand l a condensation de Bose a l i e u dans chacun des deux & t a t s , il a p p a r a i t une aimantation coherente spontanee perpen- d i c u l a i r e m e n t au champ de s t a b i l i s a t i o n ; c e c i d e v r a i t C t r e f a c i l e m e n t observable par une simple experience de resonance magnetique. Les inhomogenei t e s de champ ne d e v r a i e n t pas

e l

a r g i r 1 e s i g n a l de resonance dans une t e l l e experience, contrairement

a

ce q u i se passe avec des systemes non condenses.

A b s t r a c t . - A phenomenological d e s c r i p t i o n o f s p i n - p o l a r i z e d hydrogen, suggested by t h e microscopic Hamiltonian, i s proposed t h a t i n c l u d e s two Bose p a r t i c l e s which correspond i n t h e low d e n s i t y l i m i t t o t h e two lowest hyperfine states. Experiments a r e expected t o i n i t i a l l y populate b o t h s t a t e s , and e q u i l i b r a t i o n times w i l l be long. When Bose condensation occurs i n both s t a t e s a spontaneous cohe- r e n t magnetization perpendicular t o t h e s t a b i l i z i n g f i e l d w i l l appear ; t h a t should be r e a d i l y observable i n a simple magnetic resonance experiment, F i e l d inhomogeneities should n o t broaden t h e resonance s i g n a l i n such an experiment, c o n t r a r y t o one's experience w i t h uncondensed systems.

Should i t prove p o s s i b l e t o s t a b i l i z e s p i n a f i e l d , we w i l l assume h e r e f o r t h o f order 100 kG, p o l a r i z e d atomic hydrogen, H+, a t d e n s i t i e s , ( n t h e s p i n dependence of t h e low energy s t a t e s i s 10'' h i g h enough t o observe Bose Condensa- l a > = (1

-

+>

- r l +

- > ) /

w

t i o n , t h e q u e s t i o n o f how t o unambiguously d e t e c t I b > =

I -

- > (1

1

t h e condensed phases w i l l a r i s e . Atomic hydrogen where w i t h i n each k e t t h e signs r e f e r t o t h e d i r e c - w i l l be a t b e s t metastable i n any a t t a i n a b l e l a b o r a - t i o n o f e l e c t r o n and proton spins r e s p e c t i v e l y . t o r y f i e l d and recombination r a t e s a r e very d i f f i - The parameter F i s the r a t i o o f t h e h y p e r f i n e con- c u l t t o a n t i c i p a t e . Thus, t h e canonical ~ e ~ super- s t a n t , a, t o t h e Zeeman energy 2ileHZ and i s of o r - f l c w experiments may n o t be p o s s i b l e . Our a t t e n t i o n der 2 x Also, E,,

-

Ea

.

50 mK. When the

has focused on t h e magnetic p r o p e r t i e s o f t h e d e n s i t y i n atomic u n i t s i s low, and t r a n s l a t i o n a l s u p e r f l u i d phases o f H+ which i n many respects a r e energies l e s s than atomic e x c i t a t i o n energies we expected t o resemble those o f a s p i n 1/2 Boson ( i .e. can t r e a t s t a t e s a and b as Bosons. The c o r r e - a Boson w i t h two i n t e r n a l s t a t e s ) . The s t a b i l i z i n g sponding second q u a n t i t i z e d f i e l d operators w i l l be f i e l d i s ready made f o r a magnetic resonance e x p e r i - denoted by @a,

$.

ment t h a t i s non-invasive and can be done on a much Most o f t h e physics we w i l l discuss f o l l o w s s h o r t e r t i m e s c a l e than t h e t r a d i t i o n a l s u p e r f l u i d from t h e Hamiltonian:

f l o w experiments. We w i l l describe one e f f e c t which 1

H = H

+ - I

V ( r 1

i? i j D i j ) +

7 fj

VE(rij)Si'Sj

i s unique t o s u p e r f l u i d

H +

and whose magnitude

(2)

should render i t e a s i l y measurable. where Ho includes t h e k i n e t i c and i n t r a a t o m i c It i s expected t h a t a magnetic f i e l d can be energies as w e l l as t h e i n t e r a c t i o n w i t h t h e e x t e r - used t o s e l e c t j u s t t h e two lowest h y p e r f i n e s t a t e s n a l f i e l d /2/. The e l e c t r o n s p i n i s denoted by

-

1

o f atomic hydrogen /I/. The upper two, whose e l e c - S and VD = (VS + 3VT). VE = VT

-

VS, where V,. and t r o n s p i n i s predominately p a r a l l e l t o t h e f i e l d , VS a r e t h e w e l l known t r i p l e t and s i n g l e t poten- w i l l be r e j e c t e d f r o m t h e experimental region. I n t i a l s between hydrogen atoms.

Article published online by EDP Sciences and available at http://dx.doi.org/10.1051/jphyscol:1980703

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C7.- 16 J O U R N A L DE PHYSIQUE

We can r e w r i t e ( 2 ) w i t h i n t h e space o f s t a t e s

$ a , $ b i n t h e form presented i n ( 3 ) below. ( A more c a r e f u l d i s c u s s i o n of t h e e f f e c t s o f c o u p l i n g t o t h e upper h y p e r f i n e s t a t e s i s contained i n Refer- ence /3/. See a l s o 121. )

+ C J ( E ~ )

,

( 3 )

+ +

where t h e operators P = QbQb and S+ -

a,b -

+ -

Sx

+ i S = +,'Lb, Numerical arguments a r e i n t e - - Y

grated over a l l space. Along w i t h (31, we can w r i t e the magnetization d e n s i t y , mi, as

mx,y = uJx,y mz = uzSZ

w i t h Sz = L ( D - 0 ) and

2 a b

We have neglected i n m a background p i ~ c e rroynr- z

t i o n a l t o t h e t o t a l d e n s i t y .

There i s an i m p o r t a n t s e p a r a t i o n o f time scales i m p l i c i t i n ( 3 ) . The t h e r m a l i z a t i o n time Tth o f t h e c e n t e r of mass motions i s s e t by t h e l a r g e s t term i n (31, (VT

- 2

VE). The l a s t term i n ( 3 ) a c t s l i k e an a n t i f e r r o m a g n e t i c exchange i n t h e x-y d i r e c t i o n and commutes w i t h t h e i n t e g r a l o f SZ b u t n o t Sx o r S I t thus c o n t r i b u t e s t o t h e t r a n s -

Y'

verse magnetization r e l a x a t i o n time, Tp. F i n a l l y the d i p o l a r i n t e r a c t i o n s we have o m i t t e d from ( 3 ) f a i l t o comnute w i t h a l l t h e components of t h e s p i n and e n t e r b o t h t h e r e l a x a t i o n time, T1 o f t h e r e l a - t i v e populations pa

-

p b and t h e t r a n s v e r s e

r e l a x a t i o n time T2. A t low temperatures we expect Tth < < T2 << T1

.

For t h e t i m e being, l e t us t a k e t h e TI due t o atomic processes i n f i n i t e i n comparison t o Tth.

Then as a m i x t u r e o f H+ i n t h e s t a t e s a and b w i t h

d e n s i t i e s na, nb i s cooled, we expect Bose conden- s a t i o n t o occur s e p a r a t e l y i n t h e two s t a t e s a t temperatures s e t by t h e i d e a l Bose gas formulae.

I n thermodynamic e q u i l i b r i u m Bose condensation i s c h a r a c t e r i z e d by an o r d e r parameter <,I]> = .oe'e, ($, =

1 <$>I

) , t h a t i s complex and u n i f o r m i n space. I f our ensemble corresponds t o l o n g range order i n b o t h s t a t e s a and b t h e e x p e c t a t i o n value o f t h e operators mx i n ( 4 ) r e p r e s e n t i n g t h e

YY

perpendicular magnetization d e n s i t y w i l l have a non-zero magnitude very n e a r l y equal:

a b o l = U $ $

L O 0 ( 5 )

and a d i r e c t i o n i n t h e x,y plane s e t by

(Whether one regards t h e s t a t e i m p l i c i t i n (5) as having two condensates o r a s i n g l e condensate formed by superimposing t h e two " s p i n " s t a t e s a,b i s a moot p o i n t . )

I f t h e r e l a t i v e p o p u l a t i o n s o f a t o b a r e n o t themselves i n e q u i l i b r i u m , t h e perpendicular mag- n e t i z a t i o n n, w i l l r o t a t e a t a r a t e

va,b = (u,

-

Yb)/h %

l o 9

hz (6)

where ua,b a r e t h e chemical p o t e n t i a l s o f hydrogen atoms in t h e two h y p e r f i n e l e v e l s a,b. (Micro- scopic c o n s i d e r a t i o n s suggest q u i t e s t r o n g l y t h a t one can n o t have Bose condensation i n b o t h s t a t e s a and b and p a = ub.) T h i s i s t h e e f f e c t t o which we a l l u d e d i n t h e I n t r o d u c t i o n . A sample o f 10 19 c o h e r e n t l y r o t a t i n g spins w i t h a magnetic moment s e v e r a l times t h e p r o t o n ' s should be observable i n a magnetic resonance experiment.

A number o f complications have t o be ad- dressed b e f o r e we can a s s e r t t h a t t h e above e f f e c t w i l l be measurable / 3 / .

1. Inhomogeneous Broadening

S u p e r f l u i d 84 i s a r a t h e r i n t e r e s t i n g system i n t h i s r e s p e c t s i n c e t h e s i g n a l , ( 6 ) , apuears as t h e d i f f e r e n c e o f two chemical p o t e n t i a l s . The chemical p o t e n t i a l must be uniform i n any s t a t e i n

(4)

mechanical e q u i l i b r i u m . A f i e l d inhomogeneity w i l l induce a pressure g r a d i e n t and u l t i m a t e l y l e a d t o uniform values o f ua, ub. Thus, we expect no inhomogeneous broadening o f t h e l i n e ( 6 ) .

2. R e l a x a t i o n Times

I n i t i a l l y a m i x t u r e o f hydrogen atoms i n t h e a, b s t a t e s w i l l have a zero value o f nL. When such a m i x t u r e i s quenched t o below t h e Bose con- densation temperatures o f n what a r e t h e t i m e

a,b

scales o f t h e k i n e t i c processes t h a t l e a d t o t h e appearance of oJ i n ( 5 ) ? Are t h e y of order t h e atomic Tz times o r because a, i s t i e d t o t h e o r d e r parameter w i l l i t develop on a t i m e s c a l e s e t by VT (e.g. Tth) i n ( 3 ) ? We have addressed t h i s ques- t i o n by doing a v i c r o s c o p i c c a l c u l a t i o n t o f i x t h e parameters i n a mode c o u p l i n g Ginzburg-Landau

theory. 'The magnitude of t h e o r d e r parameter should r e l a x t o a constant uniform value i n a t i m e o f order sec. T ~ E phase o f i h c order para- meter, and thuscrL, evolves d i f f u s i v e l y w i t h a d i f f u s i o n constant of order cm /sec. 2 I n a t i m e measured i n seconds. m i l l i m e t e r s i z e domains o f o L w i l l develop. I n each domain, oL r o t a t e s u n i f o r m l y a t a r a t e given by ( 6 ) . I t s average o v e r t h e e n t i r e system i s zero u n t i l e f f e c t s t h a t break t h e conservation o f S come i n t o p l a y . The sub-

x ,Y

sequent e v o l u t i o n of ,lf i s determined by t h e magni- tude o f T2 and t h e l o n g range d i p o l a r f o r c e s .

3. Domain E n e r g e t i c s

When macroscopic regions o f n e a r l y u n i f o r m o, develop, we must enquire as t o what l i m i t s t h e domain s i z e . Domain formation i s favored by t h e small d i p o l e f i e l d s of o r d e r 47uLn 7 . G ( f o r n

-

10'' C K - ~ ) . Normally, domain s i z e s a r e s e t by balancing exchange a g a i n s t d i p o l a r energies w i t h ' t h e t h i c k n e s s of domain w a l l s determined by t h e a n i s o t r o p y energy. There i s no i n t r i n s i c aniso-

t r o p y energy i n H4 soo, w i l l vary smoothly i n space. The o n l y analogue o f t h e exchange energy i s t h o s u p e r f l u i d d e n s i t y t h a t a c t s as a s t i f f n e s s c o n s t a n t a g a i n s t changes i n 6, o r gb. An o r d e r o f magnitude estimate y i e l d s domains o f s i z e % 0.1 cm.

A more p r e c i s e c a l c u l a t i o n has been done f o r a l o n g c y l i n d e r o f r a d i u s R, p a r a l l e l t o t h e s t a - b i l i z i n g f i e l d w i t h b a

-

t~,, = kz. (The phase v a r i e s l i n e a r l y w i t h z s i n c e although t h e s u p e r f l u i d velo- c i t y may be nonzero i n thermodynamic equi 1 i brium t h e divergence o f t h e mass c u r r e n t must be zero; so i f P ! ~a r e uniform, v G a , b ~ = 0 ) . A p r e c i s e calcu- l a t i o n o f t h e magnetostatic energy as a f u n c t i o n o f k g i v e s

-

v o l *;

ti2

m n t Z

+

4n ( U , ~ ) ~ K ~ ( t n ) ~ , ( k ~ ) (7) and a minimum a t

e

=

!$

5 .28 cm f o r na = n b = n = 10'' and R = 1 cm. (Above K1, I1 a r e m o d i f i e d Bes- s e l f u n c t i o n s o f t h e f i r s t o r d e r ) .

A c t u a l l y t h i s i s s t i l l an underestimate o f t h e doa;ain s ? z e s i n c e we have n o t imposed t h e t-oundary c o n d i t i o n s on v z , vb on t h e ends o f t h e c y l i n d e r .

S

The g l o b a l f l o w f i e l d w i l l be c o n s i d e r a b l y more com- p l i c a t e d than we have assumed and t h e i n t r o d u c t i o n o f v o r t i c e s w i l l probably be r e q u i r e d i n thermal e q u i l i b r i u m .

4. E x t e r n a l Josephson E f f e c t

We have chosen t h i s term by analogy w i t h L e g g e t t ' s " i n t e r n a l Josephson E f f e c t " , which he used t o e x p l a i n t h e l o n g i t u d i n a l resonance i n super- f l u i d H ~ ~ - A /4/. I n

H+,

t h e r e appear t o be no b u l k energies, i r r e s p e c t i v e of size, t h a t p i c k o u t a d i r e c t i o n f o r

+ -

+b even i f i t w e r e n ' t r o t a t i n g .

a

The l o n g range d i p o l e energy w i l l couple $a- tJb t o t h e shape o f t h e sample and i f the r e s u l t i n g de- magnetizing f i e l d s a r e i n s e r t e d back i n t o B l o c h ' s equations, c h a r a c t e r i s t i c , thounh very small, harmonics of va,b w i l l appear. There w i l l be a

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C7-- 10 JOURNAL DE P H Y S I Q U E

corresponding small o s c i l l a t i o n i n t h e r e l a t i v e

~ o p u l a t i o n s b u t no r e l a x a t i o n .

A more i m p o r t a n t source o f c o u p l i n g between t h e a-b p o p u l a t i o n s i s an e x t e r n a l c o i l . I f i t i s resonant, energy w i l l o s c i l l a t e between t h e f i e l d and sample. The c o u p l i n g t o t h e c o i l plays t h e same r o l e here as t h e d i p o l a r c o u p l i n g d i d i n Leg- g e t t ' s theory. The r e s i s t a n c e o f t h e c o i l w i l l probably s e t the t h e r m a l i z a t i o n t i m e o f na/nb as long as b o t h phases a r e s u p e r f l u i d although r e a l r a d i a t i o n damping i s a l s o p o s s i b l e .

We can now r e t u r n t o t h e q u e s t i o n o f whether t h e s i g n a l ( 6 ) w i l l be measurable i n Bose condensed H+. L e t us assume we can s t a b i l i z e a d e n s i t y o f 10" atoms f o r a t l e a s t several seconds. Domains w i l l form,

q

l o c a l l y w i l l r o t a t e a t the same frequency (61, b u t t h e volume average o f a, may be zero. I f t h e frequency o f a surrounding c o i l whose f i e l d exceeds vLn i s swept through v ~ , ~ , t h e v a r i o u s aamains w i l l be p u l l e d i n t o a1 iynnent.

I f t h e Q o f the c o i l i s s u f f i c i e n t l y h i g h and if i t remains locked cn resonance, t h e e x t e r n a l r.f.

source can be t u r n e d o f f . The sample o f hydrogen w i t h i t s r o t a t i n g magnetization w i l l induce a s u f f i c i e n t f i e l d i n t h e c o i l t o keep the domains a1 igned.

One p o s s i b l e c o m p l i c a t i o n i s t h a t v w i l l a ,b change w i t h na

-

nb i n a c a l c u l a b l e way. The resonant c o i l has t h e r e f o r e t o t r a c k a v a r i a b l e frequency. I n a d d i t i o n , p o p u l a t i o n s should be changed s u f f i c i e n t l y s l o w l y so t h a t t h e l o c a l e q u i l i b r i u m arguments we have used remain v a l i d . The small r a t i o bewteen t h e d i p o l a r f i e l d and Hz i n s u r e s a l l transverse r.f. sources can be k e p t small and r o t a t i o n r a t e o f t h e z component of the magnetization slow.

We have a l s o i n v e s t i g a t e d t h e hydrodynamics o f s u p e r f l u i d H+ and developed a s u i t a b l e mode c o u p l i n g theory t h a t i n c l u d e s 0, (which i s n o t a

hydrodynal-ic v a r i a b l e ) and reduces t o Bloch's equations i n t h e a p p r o p r i a t e l i m i t .

The work described h e r e i n was supported by t h e N a t i o n a l Science Foundation through Grant #DMR-77- 18329.. AER would a l s o l i k e t o thank t h e Graduate School o f Cornel 1 U n i v e r s i t y f o r Fellowship Sup- p o r t .

REFERENCES

A more complete l i s t o f references appears i n /3/.

/1/ I.F. S i l v e r a and J.T.M. Walraven, Phys. Rev.

L e t t .

44,

164 (1980).

/2/ A.J. B e r l i n s k y , Phys. Rev. L e t t .

3,

359 (1977).

/3/ E.D. S i g g i a and A. Ruckenstein, submitted t o Phys. Rev. L e t t .

/4/ A.J. Leggett, Rev. Mod. Phys.

3,

331 (1975).

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