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Bose-Einstein Condensates in Rotating Traps and Optical ... - BEC

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6.2 Tight b<strong>in</strong>d<strong>in</strong>g regime 81<br />

The lead<strong>in</strong>g contribution yields the s<strong>in</strong>gle particle harmonic oscillator groundstate where σ =<br />

s−1/4d/π = ¯h/m˜ω for the harmonic well with frequency ˜ω =2 √ sER/¯h, while the second<br />

term is a small correction aris<strong>in</strong>g from the anharmonicity which slightly <strong>in</strong>creases the width σ<br />

of the groundstate.<br />

Insert<strong>in</strong>g the gaussian ansatz <strong>in</strong>to the expressions (6.30) <strong>and</strong> (6.33) for the on-site contribution<br />

to the energy <strong>and</strong> the chemical potential, we obta<strong>in</strong><br />

ε0<br />

ER<br />

µ0<br />

ER<br />

= d2<br />

2π 2<br />

<br />

1 1π2 + s<br />

σ2 2d2 σ2 − 1π4<br />

σ4<br />

4d4 <br />

+ 1 gn d 1<br />

√ , (6.51)<br />

8π ER π σ<br />

= ε0<br />

+<br />

ER<br />

1 gn d 1<br />

√ . (6.52)<br />

8π ER π σ<br />

With<strong>in</strong> the gaussian approximation, the <strong>in</strong>verse compressibility (6.44) can be rewritten as<br />

κ −1 = gnd<br />

√ 2πσ<br />

<strong>and</strong> the tight b<strong>in</strong>d<strong>in</strong>g effective coupl<strong>in</strong>g constant (6.45) takes the form<br />

˜g = gd<br />

√ 2πσ<br />

(6.53)<br />

(6.54)<br />

with σ given by (6.50). For s =10,gn=0.5ER the approximation κ −1 =˜gn with ˜g given by<br />

Eq.(6.54) differs from the exact value of κ −1 by less than 1%.<br />

In section 5.4, we have found that the average density at the central site of a condensate<br />

loaded <strong>in</strong> the comb<strong>in</strong>ed potential of optical lattice <strong>and</strong> harmonic trap decreases like nl=0 ∼<br />

(˜g/g) −3/5 ∼ s −3/20 . As already mentioned there, the decrease of the average density at<br />

the trap center (5.31) is to be contrasted with the <strong>in</strong>crease of the non-averaged peak density<br />

n(r⊥ =0,z =0)∼ (˜g/g) 2/5 ∼ s 1/10 . We can now prove the latter statement us<strong>in</strong>g the<br />

gaussian ansatz (6.46) with σ given by (6.49): The peak density then reads<br />

n(r⊥ =0,z =0)=f(z =0) 2 nl=0(r⊥ =0;s) = 1<br />

π1/2 (µ − µgn=0)<br />

, (6.55)<br />

σ ˜g<br />

where we have used the approximative solution (µ − µgn=0)/˜g for the average density profile<br />

(see Eq.(5.31)) with µ − µgn=0 <strong>and</strong> ˜g given by Eqs.(5.29) <strong>and</strong> (6.54) respectively. At s =0,<br />

the density at the center is given by n(r⊥ =0,z =0)=µ/g where µ is the usual TF-value<br />

of the chemical potential (see Eq.(5.29) with ˜g = g <strong>and</strong> µgn=0 =0). It follows that the ratio<br />

between the peak densities at large s <strong>and</strong> at s =0equals √ 2(˜g/g) 2/5 .Fors =20<strong>and</strong> s =50,<br />

this amounts to a 32% <strong>and</strong> 46% <strong>in</strong>crease respectively.

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