We present a simple model together with its physical implementation which allows one to generate multipartite entanglement between several spatial modes of the electromagnetic field. It is based on parametric down-conversion with N pairs of symmetric
ally-tilted plane waves serving as a pump. The characteristics of this spatial entanglement are investigated in the cases of zero as well as nonzero phase mismatch. Furthermore, the phenomenon of entanglement localization in just two spatial modes is studied in detail and results in an enhancement of the entanglement by a factor square root of N.
Most investigations of multipartite entanglement have been concerned with temporal modes of the electromagnetic field, and have neglected its spatial structure. We present a simple model which allows to generate tripartite entanglement between spatia
l modes by parametric down-conversion with two symmetrically-tilted plane waves serving as a pump. The characteristics of this entanglement are investigated. We also discuss the generalization of our scheme to 2N+1-partite entanglement using 2N symmetrically-tilted plane pump waves. Another interesting feature is the possibility of entanglement localization in just two spatial modes.
An investigation of field-free molecular alignment produced by elliptically polarized laser pulses is reported. Experiments are conducted in CO$_2$ at room temperature. A non invasive all-optical technique, based on the cross defocusing of a probe pu
lse, is used to measure the alignment along two orthogonal directions that is sufficient to provide a 3 dimensional characterization. The field-free molecular alignment produced by a laser of elliptical polarization is in good agreement in terms of amplitude and shape with theoretical predictions. It turns out to be almost equivalent to the superposition of the effects that one would obtain with two individual cross-polarized pulses. The investigation highlights notably the occurrence of field-free two-direction alignment alternation for a suitably chosen degree of ellipticity. The analogy between this specific ellipticity and the well known magic angle used in time resolved spectroscopy to prevent rotational contributions is discussed.
