Atomic N00N state generation in distant cavities by virtual excitations

A general scheme of generating NOON states of virtually-excited 2N atoms is proposed. The two cavities are fibre-connected with N atoms in each cavity. Although we focus on the case of N = 2, the system can be extended to a few atoms with N 〉2. It is found that all 2N atoms can be entangled in the form of NOON states if the atoms in the first cavity are initially in the excited states and atoms in the second cavity are all in the ground states. The feasibility of the scheme is carefully discussed, it shows that the NOON state with a few atoms can be generated with good fidelity and the scheme is feasible in experiment.

Temporal electronic structure of non-resonant Raman excited virtual state of P-nitroaniline by 514 nm excitation via bond polarisabilities

We have studied the temporal bond polarisabilities of para-nitroaniline from the Raman intensities by the algorithm proposed by Wu et al. in 1987 （Tian B, Wu G, Liu G 1987 J. Chem. Phys. 87 7300）. The bond polarisabilities provide much information concerning the electronic structure of the non-resonant Raman excited virtual state. At the initial moment by the 514.5 nm excitation, the tendency of the excited electrons （mapped out by the bond polarisabilities） is to spread to the molecular periphery, and the electronic structure of the Raman virtual state is close to the pseudoquinonoidic state. When the final stage of relaxation is approached, the bond polarisabilities of those peripheral bonds relax faster than those closer to the molecular core, the phenyl ring. The molecule is in the benzenoidic form as demonstrated by the bond polarisabilities after relaxation.

Scheme for implementing frequency up-conversion between two collective atomic modes

This paper presents a scheme for realizing the frequency up-conversion between two collective atomic modes. In the scheme two atomic samples are coupled to a cavity mode. Under the large detuning condition, the two collective atomic modes are coupled via the virtual excitation of the cavity mode and the effective Hamiltonian corresponds to the frequency up-conversion. In the scheme the cavity mode is only virtually excited and thus the process is insensitive to cavity decay.