In this reply we show that the criticisms raised by J. Noronha are based on a misapplication of the model we have proposed in [A. Jaouadi, M. Telmini, E. Charron, Phys. Rev. A 83, 023616 (2011)]. Here we explicitly discuss the range of validity of th
e approximations underlying our analytical model. We also show that the discrepancies pointed out for very small atom numbers and for very anisotropic traps are not surprising since these conditions exceed the range of validity of the model.
We determine the optical response of a thin and dense layer of interacting quantum emitters. We show that in such a dense system, the Lorentz redshift and the associated interaction broadening can be used to control the transmission and reflection sp
ectra. In the presence of overlapping resonances, a Dipole-Induced Electromagnetic Transparency (DIET) regime, similar to Electromagnetically Induced Transparency (EIT), may be achieved. DIET relies on destructive interference between the electromagnetic waves emitted by quantum emitters. Carefully tuning material parameters allows to achieve narrow transmission windows in otherwise completely opaque media. We analyze in details this coherent and collective effect using a generalized Lorentz model and show how it can be controlled. Several potential applications of the phenomenon, such as slow light, are proposed.
We explore the laser-induced ionization dynamics of N2 and CO2 molecules subjected to a few-cycle, linearly polarized, 800,nm laser pulse using effective two-dimensional single active electron time-dependent quantum simulations. We show that the elec
tron recollision process taking place after an initial tunnel ionization stage results in quantum interference patterns in the energy resolved photo-electron signals. If the molecule is initially aligned perpendicular to the field polarization, the position and relative heights of the associated fringes can be related to the molecular geometrical and orbital structure, using a simple inversion algorithm which takes into account the symmetry of the initial molecular orbital from which the ionized electron is produced. We show that it is possible to extract inter-atomic distances in the molecule from an averaged photon-electron signal with an accuracy of a few percents.
Bose-Einstein condensation (BEC) of an ideal gas is investigated, beyond the thermodynamic limit, for a finite number $N$ of particles trapped in a generic three-dimensional power-law potential. We derive an analytical expression for the condensation
temperature $T_c$ in terms of a power series in $x_0=epsilon_0/k_BT_c$, where $epsilon_0$ denotes the zero-point energy of the trapping potential. This expression, which applies in cartesian, cylindrical and spherical power-law traps, is given analytically at infinite order. It is also given numerically for specific potential shapes as an expansion in powers of $x_0$ up to the second order. We show that, for a harmonic trap, the well known first order shift of the critical temperature $Delta T_c/T_c propto N^{-1/3}$ is inaccurate when $N leqslant 10^{5}$, the next order (proportional to $N^{-1/2}$) being significant. We also show that finite size effects on the condensation temperature cancel out in a cubic trapping potential, e.g. $V(mathbi{r}) propto r^3$. Finally, we show that in a generic power-law potential of higher order, e.g. $V(mathbi{r}) propto r^alpha$ with $alpha > 3$, the shift of the critical temperature becomes positive. This effect provides a large increase of $T_c$ for relatively small atom numbers. For instance, an increase of about +40% is expected with $10^4$ atoms in a $V(mathbi{r}) propto r^{12}$ trapping potential.
We address the feasibility of imaging geometric and orbital structure of a polyatomic molecule on an attosecond time-scale using the laser induced electron diffraction (LIED) technique. We present numerical results for the highest molecular orbitals
of the CO2 molecule excited by a near infrared few-cycle laser pulse. The molecular geometry (bond-lengths) is determined within 3% of accuracy from a diffraction pattern which also reflects the nodal properties of the initial molecular orbital. Robustness of the structure determination is discussed with respect to vibrational and rotational motions with a complete interpretation of the laser-induced mechanisms.
We investigate theoretically an original route to achieve Bose-Einstein condensation using dark power-law laser traps. We propose to create such traps with two crossing blue-detuned Laguerre-Gaussian optical beams. Controlling their azimuthal order $
ell$ allows for the exploration of a multitude of power-law trapping situations in one, two and three dimensions, ranging from the usual harmonic trap to an almost square-well potential, in which a quasi-homogeneous Bose gas can be formed. The usual cigar-shaped and disk-shaped Bose-Einstein condensates obtained in a 1D or 2D harmonic trap take the generic form of a finger or of a hockey puck in such Laguerre-Gaussian traps. In addition, for a fixed atom number, higher transition temperatures are obtained in such configurations when compared with a harmonic trap of same volume. This effect, which results in a substantial acceleration of the condensation dynamics, requires a better but still reasonable focusing of the Laguerre-Gaussian beams.
